Anatomy of a Song: Willow Parker, ‘Wild’ – Bend Bulletin

Artist: Willow Parker

Featured song: Wild

Singer-songwriter Willow Parker grew up in Bend and started performing at local open mic nights about five years ago. Shes still a frequent open mic performer, and can be regularly heard at the Astro Lounges open mic nights on Mondays and M&J Taverns Wednesday open mic. This song, Wild, is one of her originals.

Q: Whats the story behind this song how was it written, recorded, etc.?

A: (The process) varies from song to song. Sometimes Ill come up with themes first, sometimes I really like poetry, so sometimes Ill have the lyrics first. Most of my originals are written in standard tuning, and I was getting a little bored, so I decided to branch out a little bit. The first one I did was open E (tuning). I loved it, I did a few riffs, I thought I was gonna write maybe a couple different songs with it, but they ended up flowing all together, and so the music part came first and then I put lyrics to it.

Q: Whats the story inside this song whats it about?

A: Well, its pretty self-explanatory when you hear it. Basically (its) just about a relationship, love and lust and feeling confident in a relationship with affirmation and attention.

Brian McElhiney, The Bulletin

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Anatomy of a Song: Willow Parker, 'Wild' - Bend Bulletin

OPINION: How Marines can better predict human behavior – Marine Corps Times

The term human terrain is often used within the military. Individual Marines are encouraged to understand more about a local population they interact with, either on a deployment or while on liberty.

At the Marine Corps' Combat Hunter course, we specifically dive into this topic to help Marines better understand, to identify, and most importantly to predict human behavior.

For several hundreds of years scientists have studied our behavior as a species. Unilaterally, they conclude that we are predictable as creatures of habit that set patterns and are driven, at times, by uncontrollable responses in the brain.

Combat Hunter highlights these patterns to help recognize and explain why we act or react in a specific predictive pattern. Behavior that is consistent becomes predictable, which directly relates to military operations overseas or while on leave and liberty at home.

Imagine a popular singer visits your local diner and the fuss that creates. People are swarming and asking for autographs and selfies. We call this a Proxemic pull: We are pulled into situations we are interested in or feel safe around.

Conversely, if a crowd of Marines having a smoke see the first sergeant walking toward them, they scatter quickly. This is a Proxemic push: We push away from encounters we dont like or when we sense danger.

A crowd of people conducting normal business in a market overseas will show the same pushes and pulls that can be recognized and observed. When these occur, they have meaning and are not just random.

Thats where the so what? comes in. Why did the locals grab their kids and bolt? What caused the men to congregate only around a car that just pulled up? How come yesterday the locals were smiling and shaking our hands, yet today they keep their distance and are quickly closing up the market?

Every one of us knows we like our space. We dont like strangers getting too close to us, so we move out of the way or cross the street to get away from them. Remember the last time you were in an elevator: Where did the next person stand when they entered? Typically they take a position furthest from another person, and so on as others enter the elevator.

This is another example of proximity or how we use the space around us. It is predictable, and a Marine can observe when a meeting takes place between more than one person: Do they know each other or not? Is one acting submissive or dominant over the other? Are they interested or uninterested? Are they acting comfortable or uncomfortable? This behavior can be seen in a crowd or in an individual and give a read to the others intent.

Anybody can practice this by taking the time to observe people around them in their daily life. The next time you are in a mall, for example, take a seat in the food court or a bench and just watch people. Pick out who is together, who are just dating, the loners, who seems to be in a hurry, how most patrons dress, who is acting a bit odd, and determine why they stand out to you. By practicing this, you will be surprised how quickly you build file folders, or memories, of specific behavior. When you notice it again during one of your future travels, you will key in on it instantly.

People across the globe are wired the same on the inside-the culture may be different, but understanding what to expect behaviorally from people will help you to predict what they will do.

Human behavior is consistent and predictable.Understanding and studying this behavior will equip a Marine with a better understanding of the human terrain they are faced with no matter where they are deployed.

Gus Mingus is a retired Force Recon Marine and infantry officer who currently teaches profiling as an instructor at Combat Hunter, Advanced Infantry Training Battalion, School of Infantry-East, Camp Geiger, North Carolina. Opinions expressed in this commentary are his own.

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OPINION: How Marines can better predict human behavior - Marine Corps Times

Regulators holding fistful of livestock genetics magic at the gate – Agri-Pulse

WASHINGTON, April 19, 2017- A mounting wave of new genetics technology is on its way, promising improved health and growth to farm animals, along with improved management tools and profits to livestock owners.

Still, use of this new channel of technological wonders, called gene or genome editing (see text box) apparently awaits the Trump administrations decisions about what kind of regulations theyll impose.

Bubbling up from technology companies and universities, and research collaborators in both, are gene editing techniques to breed cattle and swine immunity to foot-and-mouth disease, cattle that produce antibodies for fighting cancer in people, poultry resistant to highly pathological bird flu and, for example, improved heat-tolerance into cattle breeds that built their genomes in cool, northern-European climates.

The world market for shares of promising genome editing products in human and animal physiology, immune responses and other medical and agricultural applications is likely to grow to $8.1 billion by 2025, according to a projections by Grand View Research of California.

In the agricultural arena, for example, already at least two developers, Acceligen (the agricultural genetics subsidiary of Recombinetics) and a collaborative of university and Genus researchers, can offer genome editing technology to ensure strong resistance to PRRSV (the disastrous porcine reproductive and respiratory syndrome virus).

But thats just one item on Acceligens gene-editing menu of marvels. For the dairy sector, it has the right stuff for hornless (polled) cattle. It is a trait dairy farmers have long been able to select for Holsteins, which would relieve cattle from the stressful removal of horns or horn buds plus save dairy farm labor. However, unfortunately, choosing the trait has meant sacrificing other desired traits for health, milk production and more.

So, says Tad Sonstegard, Acceligens chief scientific officer: How do you get polled cattle without having to physically dehorn the animal or backcross in polled genetics, slowing your genetic improvement program? That is where our technology comes in.

With its new gene editing for hornless cattle, we could make (the genetics for) that animal tomorrow in a laboratory . . . and move it into an animal once we validated that it has been properly edited, Sonstegard explains. His company secured a USDA grant to edit the cattle genome for the polled trait, qualifying for the funds because the trait is associated with both animal welfare and safety for people handling cattle. Acceligen then hired scientists at the University of California, Davis, to produce the technology.

Amid the stream of such animal gene editing magic, the Food and Drug Administration posted its intent in January to regulate genome editing as it has transgenic processes, generally called genetic engineering. It is part of a move that the FDA, USDA and the Environmental Protection Agency took at the end of the Obama administration to modernize the regulatory system for biotechnology products, as then-President Obama had suggested in a 2015 memorandum. FDAs proposed guidance would specifically apply regulatory authority over animals intentionally altered through use of genome editing techniques.

Sonstegard says that, even though the agency has no regulation on use of gene editing products currently, its proposed guidance leaves commercial use of gene editing of farm animals in limbo until FDA moves to waive regulation, or require pre-market or post-market regulation.

That may not be helpful for industry, he says, because we made animals (genetic changes) two to three years ago in some cases. So at a minimum, the regulation is three years behind the technology. And, he says, I just dont know if . . . they (FDA) have reached the place where that approach is equal to their proposed regulation. And, he worries, If its too expensive and it takes too long, it wont fit into the (livestock) system.

Meanwhile, Kellye Eversole, a veteran biotechnology policy consultant in Bethesda, Md., doesnt agree that commercial production of gene-edited animals must wait for FDA to act. The agency doesnt regulate genome editing now, and it would be a change in FDA principles if they did look at what technology was used. Instead, theyve always been very product oriented. That is, she says, the results of gene editing arent different than what is done every day in conventional breeding practices . . . modifications that go on all the time within an organisms genetic makeup.

Regulators would be unable to differentiate with certainty the products of gene editing from other conventionally bred specimens because gene editing involves no introductions of foreign genetic matter, according to Eversole and Sonstegard.

Brad Shurdut, an Intrexon vice president for regulatory and government affairs, emphasizes that a product-based approach is needed by FDA. Intrexon is known for developing a host of transgenic products, including male mosquitos that cause female mosquitos offspring to die before adulthood. A subsidiary, AquaBounty, is developing a fast-growing freshwater salmon calledAquAdvantage. Intrexon is also editing the genomes of tilapia, for example, to produce large, higher-quality fillets, so genome editing looms large, for that company, too.

FDAs regulations must ensure that products are safe and effective, Shurdut says. But also, it is important to us and to agriculture that we have a transparent, predictable regulatory system so we can understand . . . the regulatory pathway. Obviously that has impact on our ability to bring innovation forward.

#30

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Regulators holding fistful of livestock genetics magic at the gate - Agri-Pulse

NewLink Genetics: Initiating Coverage With Buy Rating And First … – Seeking Alpha

NewLink Genetics (NASDAQ:NLNK) is Ames, Iowa, based emerging biotechnology company in the field of immuno-oncology. The company's common stock sank last year after the failure of two Phase 3 trials of its HyperAcute cellular immunotherapy in metastatic pancreatic cancer. Afterwards, the stock more than doubled from its 2016 lows in anticipation of data from its IDO inhibitor pipeline and has pulled back from the recent highs, thus providing an attractive long entry point.

(NewLink Genetics, common stock price chart. Source: Bloomberg)

Product Pipeline:

(NewLink Genetics, IDO inhibitor immuno-oncology product pipeline)

The company's immuno-oncology pipeline is focused on the inhibition of IDO (indoleamine-2, 3-dioxygenase) pathway which is believed to be an immune checkpoint similar to PD-1 and CTLA-4 pathways. It is one of the handful of companies which are developing IDO inhibitors (and the one of two public ones). The IDO pathway regulates the immune response by suppressing T cell activation, which enables the tumor cells to evade the host immune response. IDO inhibitors are believed to be the next potential blockbuster class of checkpoint inhibitors. Incyte (NASDAQ:INCY)'s direct IDO enzyme inhibitor epacadostat is being tested in various solid tumors in partnership with Merck's (NYSE:MRK) Keytruda. Peak sales estimates for epacadostat are as high as $9 billion in various solid tumor indications.

(Mechanisms of actions of Indoximod and GDC-0919)

Indoximod: It acts on the T cells by mimicking tryptophan and, thus, signals the activation of T cells. It, thus, acts as an indirect inhibitor of IDO pathway. Indoximod attracted widespread investor attention after its recent data release in the treatment of advanced melanoma at the recently concluded AACR meeting. In an ongoing Phase 1b/2 trial in 60 patients enrolled so far, Indoximod and Keytruda combination resulted in 59% overall response rate (ORR) and 74% disease control rate (DCR). The cohort also included ocular melanoma patients (which have poor treatment response) and when these were excluded, ORR was 59% and DCR was 80%. The results were spectacular considering that Keytruda alone has shown ORR of only 33% in this patient population. A combination of Bristol-Myers Squibb's (NYSE:BMY) Opdivo and Yervoy (anti-CTLA-4) resulted in 58% ORR in advanced melanoma but had higher incidence of Grade 3 and 4 treatment-related adverse events (58% in the combination vs. 21% in Opdivo alone).

In a smaller Phase 1 study of 19 patients with advanced melanoma, Incyte's epacadostat and Keytruda combination resulted in 58% ORR, 26% complete remission rate (CR) and 74% DCR. The CR was lower in the above mentioned Phase 1b/2 trial of Indoximod+Keytruda (10%). However, Indoximod+Keytruda have shown efficacy and safety in the largest patient population of advanced melanoma treated with anti-PD1+anti-IDO combination so far, and till Incyte and Merck show efficacy and safety in a similar sized patient population, we like Indoximod in this indication so far.

In a Phase 1/2 trial, Indoximod+gemcitabine+abraxane resulted in impressive 45% ORR in metastatic pancreatic cancer (compared with 34% for Folfirinox regime and 9.4% for gemcitabine).

Indoximod is also being tested in various other cancers, and data from these indications is expected to be released over next 12 months. NewLink Genetics hold all worldwide commercialization rights to Indoximod. It will pay royalty payments on net sales of Indoximod (single-digit percentage) to Lankenau Institute of Medical Research, Augusta University, and Iowa State Department of Economic Development (ISDED). Various patents for Indoximod extend till 2027.

GDC-0919: It is a direct IDO enzyme inhibitor. Roche/Genentech (OTCQX:RHHBY) has licensed its worldwide commercial rights, thus showing confidence in its potential. In exchange, NewLink Genetics received $150 million of upfront payment and may receive up to $1 billion in future milestone payments and double-digit percentage of net sales as royalty payments.

A combination of GDC-0919 and Roche's anti-PDL1 Tecentriq is being tested in an ongoing Phase 1b, open-label study in various solid tumors like melanoma, NSCLC, head & neck squamous cell cancer, gastric cancer, ovarian cancer, Merkel cell cancer, cervical cancer, endometrial cancer, renal cell cancer, triple-negative breast cancer, and urothelial/bladder cancer. About 305 patients are planned to be enrolled. The estimated completion date of the trial is December 2018, but interim data is expected in mid-2017.

Various patents for GDC-0919 extend till 2032.

NLG802: NewLink Genetics is also developing NLG802, a prodrug of Indoximod to increase bioavailability and exposure. An IND was filed in 2017, and Phase 1 trial is expected to start this year.

Potential competition:

Other companies developing IDO inhibitors include Incyte, iTeos Therapeutics, and Redx Pharma.

HyperAcute Cellular Immunotherapy Program:

Despite failing in metastatic pancreatic cancer, a tough to treat cancer, this program is not dead yet. A combination of Tergenpumatucel with Indoximod and docetaxel is being tested in a Phase 1b trial in advanced non-small cell lung cancer (NSCLC). Dorgenmeltucel-C is being tested in combination with checkpoint inhibitors in a Phase 2 trial in advanced melanoma. Results from these trials are expected in 2018. Various patents for this program extend till 2029.

Vaccine program:

The company's Ebola Zaire vaccine has Breakthrough therapy designation from FDA. Interim data from a Phase 3 trial showed the vaccine's efficacy in preventing Ebola infection. Merck has licensed worldwide commercial rights to the rVSVG-ZEBOV GP vaccine (Ebola). NewLink Genetics received upfront $30 million and $20 million in milestone payments so far. It may also receive royalty payments on net sales of the vaccine.

Leadership:

CEO, chief scientific officer, and chairman of the board, Charles J. Link Jr. MD: He co-founded NewLink Genetics in 1999 and was a practicing oncologist for 18 years. He also served as the director of the Human Gene Therapy Research Institute at the Iowa Methodist Medical Center.

Co-founder and chief medical officer, Nicholas Vahanian, MD: He has led the algenpantucel-L (HyperAcute Cellular) program and worked at the National Cancer Institute and National Center for Human Genome Research Institute (both at the NIH).

Lead Director, Thomas Raffin, MD: He was the faculty member at the Stanford University School of Medicine for 30 years where he was the Colleen and Robert Haas Professor Emeritus of Medicine and Biomedical Ethics.

Director of the board, Paul R. Edick: He was the CEO of Durata Therapeutics, GANIC Pharmaceuticals, and MedPointe Healthcare.

Director of the board, Paolo Pucci: He is the current CEO of ArQule, Inc. He also worked as the senior VP of Bayer-Schering Global Oncology/Specialized Therapeutics Business Unit at Bayer AG.

Director of the board, Lota S. Zoth: She worked as the senior VP and CFO of MedImmune.

Financials and valuation:

NewLink Genetics is expected to have $131.5 million in cash reserves at the end of 2016. The operating cash burn was $65.9 million in 2016. The management expects to end 2017 with cash reserves of $75 million. We don't see any risk of equity dilution in 2017. The company has long-term debt of about $0.5 million and $6 million of royalty obligation to ISDED.

The size of melanoma market is $2.06 billion globally in the US and is expected to grow to $4.7 billion globally by 2020. About 76,000 new cases of melanoma are seen every year in the US and another 80,000 cases per year are seen in the EU. About 10% of these are diagnosed at advanced stage, thus providing our target market for Indoximod+Keytruda combination in advanced melanoma = 7,600 cases/year in the US and 8,000 cases/year in the EU. A combination of Opdivo and Yervoy is priced at average wholesale price = $256,000 in the US. Opdivo alone is priced at AWP of $150,000 in the US. We expect Indoximod to be priced in a similar range, thus providing us AWP = $106,000 in the US. At average sales price = 74% of AWP (average per Pharmagellan guide), we input ASP = $78,440 in the US. ASP of drugs in the EU and Japan is about 50% of that in the US. We input ASP = $39,220 in the EU. We input probability of reaching the market = 65% for the combination at this stage (average for drugs who passed Phase 2). The biggest competition for the combination in the melanoma market is Keytruda+epacadostat and Opdivo+Yervoy combinations. We input peak 20% market penetration in this indication for Indoximod+Keytruda combination in this combination in a base conservative scenario. Using these inputs, we modeled peak $106 million risk-adjusted revenue in this indication in the US+EU in 2024. Peak estimates for Opdivo+Yervoy combination in advanced melanoma is $350 million.

Peak sales estimate for epacadostat in various cancers is expected to be as high as $9 billion. Peak sales estimate for Tecentriq in various cancers is $3.5 billion in 2020. We are optimistic that GDC-0919 can achieve $1 billion in worldwide sales at the peak in combination with Tecentriq in various cancer mentioned above. Using probability of reaching the market = 60% at this stage and 20% of revenue as royalty payments for NewLink Genetics, we modeled peak $120 million risk-adjusted royalty revenue from GDC-0919 in 2024.

We also added NPV of potential $1 billion milestone payment from Genentech (equally distributed from 2017 to 2024, risk-adjusted at 60% probability and discounted at 15% for NPV of $336.5 million).

Using rNPV method (20% cost of capital), we calculated fair value of equity = $850.3 million after adjusting for non-operating assets, operating loss carry-forwards, and liabilities (using diluted share count) or $23.80 per share.

We are initiating coverage on NewLink Genetics common stock with Buy rating and first price target = $24.

We have not yet modeled revenue from Indoximod in other non-melanoma indications mentioned above, revenue from HyperAcute cellular immunotherapy pipeline, and Ebola vaccine program, which could add to further upside. We will adjust our model for these indications as we get more data.

Bristol-Myers acquired Flexus Therapeutics, another company developing IDO inhibitor pipeline (in preclinical stage) for $1.25 billion in 2015. In 2016, Merck acquired IOmet Pharma for its preclinical stage IDO inhibitor pipeline for $400 million.

OrbiMed Advisors, one of the largest healthcare institutional investors in the world, is the second largest investor in NewLink Genetics, and owns $33 million worth of stock (6.8% of the outstanding shares).

Several sell-side analysts reiterated Buy ratings on the stock recently, including Cantor Fitzgerald (PT = $20, April 4), and Stifel (PT = $26, April 4). SunTrust Robinson Humphrey considers NewLink Genetics as a takeover target and has price target of $30 on the stock.

Upcoming catalysts:

Risks in the investment:

It is possible that the ongoing clinical trials may fail, regulatory agencies might not approve the products, unexpected side effects might be seen in the future, clinicians might not widely prescribe the products, or insurers might not reimburse them. Competing products from other companies might gain significant market share in the planned clinical indications. The company may also need to raise additional capital in future.

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Disclosure: This article represents my own opinion and is not a substitute for professional investment advice. It does not represent solicitation to buy or sell any security. Investors should do their own research and consult their financial adviser before making any investment.

Disclosure: I am/we are long NLNK, INCY, BMY.

I wrote this article myself, and it expresses my own opinions. I am not receiving compensation for it (other than from Seeking Alpha). I have no business relationship with any company whose stock is mentioned in this article.

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Closer look at brain circuits reveals important role of genetics – Medical Xpress

April 19, 2017 A serial electron microscopy reconstruction of a single synaptic connection. Credit: Anton Maximov

Scientists at The Scripps Research Institute (TSRI) in La Jolla have revealed new clues to the wiring of the brain. A team led by Associate Professor Anton Maximov found that neurons in brain regions that store memory can form networks in the absence of synaptic activity.

"Our results imply that assembly of neural circuits in areas required for cognition is largely controlled by intrinsic genetic programs that operate independently of the external world," Maximov explained.

A similar phenomenon was observed by the group of Professor Nils Brose at the Max Planck Institute for Experimental Medicine in Germany. The two complementary studies were co-published as cover stories in the April 19, 2017, issue of the journal Neuron.

The "Nature vs. Nurture" Question

Experience makes every brain unique by changing the patterns and properties of neuronal connections. Vision, hearing, smell, taste and touch play particularly important roles during early postnatal life when the majority of synapses is formed. New synapses also appear in the adult brain during learning. These activity-dependent changes in neuronal wiring are driven by chemical neurotransmitters that relay signals from one neuron to another. Yet, animals and humans have innate behaviors whose features are consistent across generations, suggesting that some synaptic connections are genetically predetermined.

The notion that neurons do not need to communicate to develop networks has also been supported by earlier discoveries of synapses in mice that lacked transmitter secretion in the entire brain. These studies were performed in the laboratory of Professor Thomas Sdhof, who won the 2013 Nobel Prize in Physiology or Medicine.

"We thought these experiments were quite intriguing," Maximov said, "but they also had a major limitation: mice with completely disabled nervous systems became paralyzed and died shortly after birth, when circuitry in the brain is still rudimental."

The TSRI team set out to investigate if neurons can form and maintain connections with appropriate partners in genetically engineered animals that live into adulthood with virtually no synaptic activity in the hippocampus, a brain region that is critical for learning and memory storage. "While the idea may sound crazy at the first glance," Maximov continued, "several observations hinted that this task is technically feasible." Indeed, mammals can survive with injuries and developmental abnormalities that result in a massive loss of brain tissue.

Inspired by these examples, Richard Sando, a graduate student in the Maximov lab, generated mice whose hippocampus permanently lacked secretion of glutamate, a neurotransmitter that activates neurons when a memory is formed. Despite apparent inability to learn and remember, these animals could eat, walk around, groom, and even engage in rudimental social interactions.

Working closely with Professor Mark Ellisman, who directs the National Center for Microscopy and Imaging Research at the University of California, San Diego, Sando and his co-workers then examined the connectivity in permanently inactive areas. Combining contemporary genetic and imaging tools was fruitful: the collaborative team found that several key stages of neural circuit development widely believed to require synaptic activity were remarkably unaffected in their mouse model.

The outcomes of ultra-structural analyses were particularly surprising: it turns out that neurotransmission is unnecessary for assembly of basic building blocks of single synaptic connections, including so-called dendritic spines that recruit signaling complexes that enable neurons to sense glutamate.

Maximov emphasized that the mice could not function normally. In a way, their hippocampus can be compared to a computer that goes though the assembly line, but never gets plugged to a power source and loaded with software. As the next step, the team aims to exploit new chemical-genetic approaches to test if intrinsically-formed networks can support learning.

Explore further: Mice offer a window into sleep's role in memory

More information: "Assembly of excitatory synapses in the absence of glutamatergic neurotransmission," Neuron (2017). DOI: 10.1016/j.neuron.2017.03.047

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Scientists at The Scripps Research Institute (TSRI) in La Jolla have revealed new clues to the wiring of the brain. A team led by Associate Professor Anton Maximov found that neurons in brain regions that store memory can ...

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Cattle producers offered intro to genetic technology – Tri-State Neighbor

Cattle produers can learn about using genetic technology to improve cattle herds at a program offered in Rapid City by the King Ranch Institute for Ranch Management in May.

Sessions on Application of Advanced Genetic Technology in Beef Cattle will be offered May 11-12 at the Rushmore Inn and Suites in Rapid City. South Dakota State University West River Ag Center is co-hosting the lectureships. The cost is $300, which covers materials and meals.

"We hear many of our producers are beginning or wanting to use genetic technology to improve their herds. Some question if they are using it correctly; some feel it is information overload," said Kristi Cammack, director of the West River Ag Center.

Keeping up with genetic selection and evaluation innovations can be challenging. Early adopters who have been trying the technology as well as those who are interested but don't know where to start can learn from the classes.

The sessions are meant to strengthen the understanding of the genetic principles and help attendees build on the information. Faculty contracted by the King Institute will share how to apply advanced genetic technologies in the real world of seedstock and commercial cattle production.

Instructors will be Bob Weaber, Ph.D., extension specialist in animal sciences and industry from Kansas State University and Matt Spangler, Ph.D., beef genetics extension specialist in the animal science department at the University of Nebraska-Lincoln. Along with the basics, they will look at the application of advanced genetic tools including genomically enhanced expected progeny differences and marker assisted management in genetic advancement.

Cammack expects that the sessions will appeal to both commercial and seed stock producers from across the state, region and throughout the country.

Information will focus on developing breeding objectives for the herd and determining the economics relative for each operation as that may vary within a region. Owners want to know what will work for them at their location, taking into consideration different feedstuffs and different markets.

The tools have advanced so they are producer friendly. Cammack said the speakers will share knowledge that producers can apply and use in their operation, including an applied understanding of how to use genomic selection tools.

Cattle producers will get a lot out of the 1 -day program, she said. Producers will participate in interactive sire selection scenarios where they will break out into groups and practice how to pick sires.

"We hope the result is that cattle producers will learn to use advanced genetics. Applying these tools, in the correct way, will pay off with improved genetics. Producers will find it advancing herd genetics really pays it forward," Cammack said.

Contact Cammack at 605-394-2236, or email Kristi.Cammack@sdstate.edu. To see the agenda and make a reservation, go to the King Ranch Institute website.

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Re Cases Y, Z, AA, AB & AC (Human Fertilisation and Embryology Act 2008) [2017] EWHC 784 (Fam) – Family Law Week

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Case summary coming soon

Case numbers omitted Neutral Citation Number: [2017] EWHC 784 (Fam) IN THE HIGH COURT OF JUSTICEFAMILY DIVISION

Royal Courts of Justice Strand, London, WC2A 2LL

Date: 12 April 2017

Before :

SIR JAMES MUNBY PRESIDENT OF THE FAMILY DIVISION

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In the Matter of the Human Fertilisation and Embryology Act 2008 (Cases Y, Z, AA, AB and AC)

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Ms Deirdre Fottrell QC (instructed by Goodman Ray Solicitors LLP) for the applicants

Hearing date: 21 March 2017

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Judgment This judgment was handed down in open court

Sir James Munby, President of the Family Division : 1.Since I handed down judgment in In re A and others (Legal Parenthood: Written Consents) [2015] EWHC 2602 (Fam), [2016] 1 WLR 1325, I have had to consider a number of cases raising issues very similar to those which confront me here. The most recent judgments were Re the Human Fertilisation and Embryology Act 2008 (Cases P, Q, R, S, T, U, W and X) [2016] EWHC 2273 (Fam) and Re the Human Fertilisation and Embryology Act 2008 (Case K) [2016] EWHC 2356 (Fam). They were the sixteenth to twenty-fourth of these cases in which I have given a final judgment. This judgment relates to another five cases, Cases Y, Z, AA, AB and AC. That amounts to 29 cases in all. There are at least another five cases in the pipeline, Cases AD, AE, AF, AG and AH.

2.For the purposes of this judgment I shall take as read the analysis in In re A and the summary of the background to all this litigation which appears in Re the Human Fertilisation and Embryology Act 2008 (Case O) [2016] EWHC 2273 (Fam).

The facts3.For reasons which will by now be familiar, I propose to be extremely sparing in what I say of the facts and the evidence in these cases.

4.All relate to treatment provided by Care Fertility Group Manchester, except Case X which relates to treatment provided by Care Fertility Group Manchester. Each of the clinics is and was regulated by the Human Fertilisation and Embryology Authority. I shall refer to the applicant in each case as X, the respondent as Y and the child as C. In each case X seeks a declaration pursuant to section 55A of the Family Law Act 1986 that he or she is, in accordance with sections 36 and 37 or, as the case may be, sections 43 and 44 of the Human Fertilisation and Embryology Act 2008, the legal parent of C. In each case Y is wholeheartedly supportive of X's application. In each case the clinic, the HFEA, the Secretary of State for Health and the Attorney General have all been notified of the proceedings. None has sought to be joined, although representatives of Care Fertility Group attended the hearing. In each case, given the nature of the issues (see below) I decided that there was no need for C to have a guardian appointed.

5.I heard the cases sequentially, in the order Case Y, Case AA, Case AC, Case AB and Case Z, on 21 March 2017. In each case X was represented by Ms Deirdre Fottrell QC. At the end of each of the hearings I indicated that I was making the orders sought. I now (xx April 2017) hand down judgment explaining my reasons.

6.Although I am acutely conscious of the stress, worry and anxiety burdening all the parents in these cases, and of the powerful human emotions that are inevitably engaged, each of these cases is, in terms of the applicable legal analysis, straight-forward and simple. They raise no new points. In each case the evidence, which there is no need for me to rehearse in detail, is compelling. In each case the answer is clear.

7.Just as in each of the other cases I have had to consider, so in each of these cases, having regard to the evidence before me, I find as a fact that:

i)The treatment which led to the birth of C was embarked upon and carried through jointly and with full knowledge by both the woman (that is, Y) and her partner (X).

ii)From the outset of that treatment, it was the intention of both X and Y that X would be a legal parent of C. Each was aware that this was a matter which, legally, required the signing by each of them of consent forms. Each of them believed that they had signed the relevant forms as legally required and, more generally, had done whatever was needed to ensure that they would both be parents.

iii)From the moment when the pregnancy was confirmed, both X and Y believed that X was the other parent of the child. That remained their belief when C was born.

iv)X and Y, believing that they were entitled to, and acting in complete good faith, registered the birth of their child, as they believed C to be, showing both of them on the birth certificate as C's parents, as they believed themselves to be.

v)The first they knew that anything was or might be 'wrong' was when, some while later, they were contacted by the clinic.

8.I add that there can be no suggestion that any consent given was not fully informed consent. Nor is there any suggestion of any failure or omission by the clinic in relation to the provision of information or counselling.

The facts: the individual cases9.In each of Cases Y, AA, AC and AB the applicant is a woman. In Case Z the applicant is a man. None of them was either in a civil partnership with or married to the respondent mother.

10.Case Y: Adopting the terminology I have used in previous cases, the problem in this case is very shortly stated. The Form PP was correctly completed. There is no Form WP in the clinic's records. X and Y do not assert any positive memory of a Form WP. Ms Fottrell invites me to proceed on the basis that there is a Form IC, signed by both X and Y, in a form which, on the basis of my judgments in previous cases, suffices to entitle X to the declaration she seeks. The relevant declaration, signed by X, reads as follows:

"I am the partner of [Y]. I acknowledge that she and I are being treated together In consenting to the course of treatment outlined above, I understand that I will become the legal parent of any resulting child(ren) subject to the completion of the appropriate HFEA consent forms [see page 1, section 4 of this consent]."

That cross-reference is to Forms WP and PP. But for the inclusion of the words "subject to the completion of the appropriate HFEA consent forms", there could be no question of this not being a Form IC sufficient to entitle X to the declaration she seeks. The only question is whether those words are fatal to the efficacy of the document for this purpose. In my judgment they are not. The document has to be read as a whole and, read as a whole, it is clear that both parties were signing a document which contemplated that X would be a parent. If X was not to be a parent, why sign the declaration at all? X is entitled to the declaration she seeks: see In re A, para 63(iii).

11.Case AA: Again, the problem is very shortly stated. The Form WP was properly completed. The Form PP contains two errors: first, Y's name, rather than X's, appears in section 1, and X's name, rather than Y's, appears in section 2; secondly, the declaration in section 5 has been signed by Y and not by X. However, and importantly, the consent box in section 3 has been ticked and the second page, which contains section 3, has been signed at the foot by X. Both errors are obvious. The first error, the transposition of the names, can be corrected by way of rectification: see In re A, para 47, Re the Human Fertilisation and Embryology Act 2008 (Case G) [2016] EWHC 729 (Fam) and Re the Human Fertilisation and Embryology Act 2008 (Cases P, Q, R, S, T, U, W and X) [2016] EWHC 2273 (Fam), paras 17 (Case S) and 18 (Case T). The second error is irrelevant: see Re the Human Fertilisation and Embryology Act 2008 (Cases P, Q, R, S, T, U, W and X) [2016] EWHC 2273 (Fam), paras 13 (Case Q) and 15 (Case R). X's signature at the foot of the second page is sufficient to satisfy the statutory requirement: see Re the Human Fertilisation and Embryology Act 2008 (Cases P, Q, R, S, T, U, W and X) [2016] EWHC 2273 (Fam), paras 13 (Case Q) and 15 (Case R). In these circumstances X is entitled to a decree of rectification and the declaration she seeks.

12.Case AC: Again, the problem is very shortly stated. The Form WP was properly completed. In the Form PP, Y's name, rather than X's, appears in section 1, and X's name, rather than Y's, appears in section 2. However, the consent box in section 3 has been ticked, the second page, which contains section 3, has been signed at the foot by X, as has the declaration in section 5. The error is obvious. The transposition of the names can be corrected by way of rectification: see the authorities referred to in paragraph 11 above. X is entitled to a decree of rectification and the declaration she seeks.

13.Moreover, there is again a quite separate ground on which X is entitled to the relief she seeks. Both Y and X signed a Form IC which, in all material respects, was in the same form as the Form IC considered in paragraph 10 above. In the circumstances, X is, in principle, entitled to the declaration she seeks on this ground also.

14.Case AB: Again, the problem is shortly stated. The Form PP was properly completed. In the Form WP, which was otherwise properly completed, the consent box in section 3 on the second page was not ticked. The omission of the ? in the consent box is not fatal to the validity either of a Form PP or, as here, of a Form WP: see Re the Human Fertilisation and Embryology Act 2008 (Case J) [2016] EWHC 1330 (Fam), para 15, followed by Peter Jackson J in D v D (Fertility Treatment: Paperwork Error) [2016] EWHC 2112 (Fam), and Re the Human Fertilisation and Embryology Act 2008 (Cases P, Q, R, S, T, U, W and X) [2016] EWHC 2273 (Fam), paras 11 (Case P) and 17 (Case S). X is entitled to the declaration she seeks.

15.Again, there is a quite separate ground on which X is entitled to the relief she seeks. Both Y and X signed a Form IC which, in all material respects, was in the same form as the Forms IC considered in paragraphs 10 and 13 above. In the circumstances, X is, in principle, entitled to the declaration she seeks on this ground also.

16.Case Z: Again, the problem is shortly stated. The Form WP was properly completed. In the Form PP, which was otherwise properly completed, the consent box in section 3 on the second page was not ticked. The omission of the ? in the consent box is not fatal to the validity either of a Form WP or, as here, of a Form PP: see the authorities referred to in paragraph 14 above. X is entitled to the declaration he seeks.

17.Again, there is again a quite separate ground on which X is entitled to the relief he seeks. Both Y and X signed a Form IC, indeed a number of Forms IC, which, in all material respects, were in the same form as the Forms IC considered in paragraphs 10, 13 and 15 above. X is, in principle, entitled to the declaration he seeks on this ground also.

Outcome18.It was for these reasons that at the conclusion of the hearing of each case I made a declaration in the terms sought by X.

Costs19.In each case the clinic has very properly agreed to pay the applicant's reasonable costs.

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Re Cases Y, Z, AA, AB & AC (Human Fertilisation and Embryology Act 2008) [2017] EWHC 784 (Fam) - Family Law Week

Researchers study secrets of aging via stem cells – Harvard Gazette

Third in an occasional series on how Harvard researchers are tackling the problematic issues of aging.

If only, wrote an ancient Japanese poet, when one heard that Old Age was coming one could bolt the door.

Science is working on it.

Aging is as much about the physical processes of repair and regeneration and their slow-motion failure as it is the passage of time. And scientists studying stem cell and regenerative biology are making progress understanding those processes, developing treatments for the many diseases whose risks increase as we get older, while at times seeming to draw close to a broader anti-aging breakthrough.

If stem cells offer potential solutions, theyre also part of the problem. Stem cells, which can differentiate into many cell types, are important parts of the bodys repair system, but lose regenerative potency as we age. In addition, their self-renewing ability allows the mutations that affect every cell to accumulate across cellular generations, and some of those mutations lead to disease.

We do think that stem cells are a key player in at least some of the manifestations of age, said Professor of Stem Cell and Regenerative Biology David Scadden, co-director of the Harvard Stem Cell Institute. The hypothesis is that stem cell function deteriorates with age, driving events we know occur with aging, like our limited ability to fully repair or regenerate healthy tissue following injury.

When it comes to aging, certain tissue types seem to lead the charge, according to Professor of Stem Cell and Regenerative Biology Lee Rubin, who directs the Harvard Stem Cell Institutes Therapeutic Screening Center. Particular tissues nerve cells appear to be one somehow signal to others that its time to age. This raises the prospect, Rubin said, that aging might be reversed by treating these key tissue categories, rather than designing individual treatments for the myriad tissue types that make up the body.

The process of aging involves all tissues in your body and, while different things go wrong in each tissue, they go wrong at basically the same rate, Rubin said. We can think of it as a process that is somehow coordinated, or there are fundamental processes in each tissue that play out.

In addition to key tissues, certain chemical pathways like insulin signaling seem to be able to control aging, said Rubin, whose work has received backing from the National Institute of Neurological Disorders and Stroke, as well as private foundations. The insulin signaling pathway is a chemical chain reaction in which the hormone insulin helps the body metabolize glucose. Reducing it has been shown to greatly extend life span in flies and worms, Rubin said. Also, signaling doesnt have to be reduced in all tissues.

If you just reduce it in neurons, the whole fly or worm lives longer, Rubin said. Certain key tissues in those organisms, if you selectively manipulate those tissues, have a positive effect on a number of processes in other tissues.

Because it circulates throughout the body, blood is an obvious place to look for controlling or signaling molecules that prompt or coordinate aging. A key carrier of oxygen and nutrients, blood is also rich with other compounds, some of which appear to play a role in decline linked to age.

Scadden described recent work done separately by Ben Ebert, a professor of medicine working at Harvard-affiliated Brigham and Womens Hospital, and Steve McCarroll, the Dorothy and Milton Flier Associate Professor of Biomedical Science and Genetics, that identified age-related changes in the blood that can increase the risk of diseases we dont typically think of as blood diseases.

Another tantalizing study, published in 2013, used the blood of a young mouse to rejuvenate the organs of an older one. In these parabiotic experiments, conducted by Professor of Stem Cell and Regenerative Biology Richard Lee and Forst Family Professor of Stem Cell and Regenerative Biology Amy Wagers, the circulatory systems of the two mice were joined, allowing the blood of the young to flow through the older ones body. The older mouse showed improvements in muscle tone and heart function. Later, similar experiments done by Rubin also showed improvements in neuronal health and brain functioning.

The young mouses fate depended on the age of the older mouse, Rubin said. If the latter was middle-aged, the young mouse appeared to be fine. If the older mouse was very old, however, the young mouse did worse.

Rubin said the experiments suggest that blood contains both positive and negative factors that influence aging. It may be, he said, that both are always present, but that positive factors outweigh negative in the young and that negative factors increase as we age.

Researchers have identified but not yet confirmed candidate blood factors for the rejuvenating effects. What seems not in doubt is the overall effect of the young blood on the old mouse. Interest is intense enough that a California company, Alkahest, has begun experiments giving Alzheimers patients plasma from young blood in hopes of improving cognition and brain function.

Even if that approach works, Rubin said, there would be practical hurdles to the widespread administration of young peoples blood plasma to older patients. But with an active compound identified, a drug could be made available to restore at least some cognitive function in Alzheimers patients.

In addition to the overall process of aging, researchers at the Harvard Stem Cell Institute, as well as across the University and its affiliated institutions, are investigating an array of diseases whose incidence increases sometimes dramatically with age.

The list includes several of the countrys top causes of death heart disease, stroke, diabetes, and cancer as well as rarer conditions such as the lethal neurodegenerative disorder amyotrophic lateral sclerosis (ALS).

Two decades ago, when stem cell research hit mainstream consciousness, many thought its greatest promise would be in stem cells ability to grow replacement parts: organs and tissues for damage caused by trauma or disease.

The stem cell revolution is still developing, Scadden said, but so far has taken a different form than many expected. The dream of harnessing stem cells to grow replacement hearts, livers, and kidneys remains, but potentially powerful uses have emerged in modeling disease for drug discovery and in targeting treatment for personalized medicine.

We thought stem cells would provide mostly replacement parts. I think thats clearly changed very dramatically. Now we think of them as contributing to our ability to make disease models for drug discovery.

David Scadden

Researchers have taken from the sick easily accessible cells, such as skin or blood, and reprogrammed them into the affected tissue type nerve cells in the case of ALS, which most commonly strikes between 55 and 75, according to the National Institutes of Health (NIH).

These tissues are used as models to study the disease and test interventions. Work on ALS in the lab of Professor of Stem Cell and Regenerative Biology Kevin Eggan has identified a drug approved for epilepsy that might be effective against ALS. This application is now entering clinical trials, in collaboration with Harvard-affiliated Massachusetts General Hospital.

In the end, stem cells might have their greatest impact as a drug-discovery tool, Scadden said.

Much of stem cell medicine is ultimately going to be medicine, he said. Even here, we thought stem cells would provide mostly replacement parts. I think thats clearly changed very dramatically. Now we think of them as contributing to our ability to make disease models for drug discovery.

Also evolving is knowledge of stem cell biology. Our previous understanding was that once embryonic stem cells differentiated into stem cells for muscle, blood, skin, and other tissue, those stem cells remained flexible enough to further develop into an array of different cells within the tissue, whenever needed.

Recent work on blood stem cells, however, indicates that this plasticity within a particular tissue type may be more limited than previously thought, Scadden said. Instead of armies of similarly plastic stem cells, it appears there is diversity within populations, with different stem cells having different capabilities.

If thats the case, Scadden said, problems might arise in part from the loss of some of these stem cell subpopulations, a scenario that could explain individual variation in aging. Getting old may be something like the endgame in chess, he said, when players are down to just a few pieces that dictate their ability to defend and attack.

If were graced and happen to have a queen and couple of bishops, were doing OK, said Scadden, whose work is largely funded through the NIH. But if we are left with pawns, we may lose resilience as we age.

Scaddens lab is using fluorescent tags to mark stem cells in different laboratory animals and then following them to see which ones do what work. It might be possible to boost populations of particularly potent players the queens to fight disease.

Were just at the beginning of this, Scadden said. I think that our sense of stem cells as this highly adaptable cell type may or may not be true. What we observe when we look at a population may not be the case with individuals.

The replacement parts scenario for stem cells hasnt gone away. One example is in the work of Harvard Stem Cell Institute co-director and Xander University Professor Douglas Melton, who has made significant progress growing replacement insulin-producing beta cells for treatment of diabetes.

Another is in Lees research. With support from the NIH, Lee is working to make heart muscle cells that can be used to repair damaged hearts.

Trials in this area have already begun, though with cells not genetically matched to the patient. In France, researchers are placing partially differentiated embryonic stem cells on the outside of the heart as a temporary aid to healing. Another trial, planned by researchers in Seattle, would inject fully differentiated heart muscle cells into a patient after a heart attack as a kind of very localized heart transplant.

Lees approach will take longer to develop. He wants to exploit the potential of stem cell biology to grow cells that are genetically matched to the patient. Researchers would reprogram cells taken from the patient into heart cells and, as in the Seattle experiment, inject them into damaged parts of the heart. The advantage of Lees approach is that because the cells would be genetically identical to the patient, he or she could avoid antirejection drugs for life.

What were thinking about is longer-term but more ambitious, Lee said. Avoiding immune suppression could change the way we think about things, because it opens the door to many decades of potential benefit.

Change has been a constant in Lees career, and he says theres no reason to think that will slow. Patient populations are older and more complex, disease profiles are changing, and the tools physicians have at their disposal are more powerful and more targeted.

Many of our patients today wouldnt be alive if not for the benefit of research advances, he said. Cardiology has completely changed in the last 25 years. If you think its not going to change even more in the next 25 years, youre probably wrong.

When Lee envisions the full potential of stem cell science, he sees treatments and replacement organs with the power to transform how we develop and grow old.

It may not be there for you and me, but for our children or their children, ultimately, regenerative biology and stem cell biology have that kind of potential, he said. We imagine a world where it doesnt matter what mutations or other things youre born with, because we can give you a good life.

Lees not guessing at future longevity. Hes not even sure extending life span beyond the current record, 122, is possible. Instead, he cites surveys that suggest that most Americans target 90 as their expectation for a long, healthy life.

Thats about a decade more than we get now in America, Lee said. We have work to do.

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Researchers study secrets of aging via stem cells - Harvard Gazette

Cell biologists discover crucial ‘traffic regulator’ in neurons – Medical Xpress

April 19, 2017 This is a scanning electron micrograph (false color) of a human induced pluripotent stem cell-derived neuron. Credit: Thomas Deerinck, UC San Diego

Cell biologists from Utrecht University have discovered the protein that may be the crucial traffic regulator for the transport of vital molecules inside nerve cells. When this traffic regulator is removed, the flow of traffic comes to a halt. 'Traffic jams' are reported to play a key role in neurodegenerative diseases such as Alzheimer's and Parkinson's disease. The results of their research will be published in the scientific journal Neuron on April 19.

Neurons are the main cells in the nervous system. They process information by sending, receiving, and combining signals from around the brain and the body. All neurons have a cell body where molecules vital for its functioning and maintenance are produced. The axon, a long and slender extension that can reach one metre in length in humans, sends information from the nerve cell to other nerve cells. Neuronal survival is highly dependent on the transport of vital molecules within this axon. Research has shown that defects in the transport function in the axons play a key role in degenerative brain diseases such as Alzheimer.

First comprehensive map

"Previous research examined transport processes in small areas of the axon, such as the very beginning or the very end. This left it unclear how the movement of molecules through the axon was regulated over long distances. In our study, we provide the first comprehensive map of transport in mammalian axons", says Casper Hoogenraad, Professor of Cell Biology at Utrecht University, explaining the relevance of this study.

Stumped

In most neurons, an area between the cell body and the axon called the 'axon initial segment' serves as a checkpoint: only some molecules can pass through it. This area has stumped scientists for more than a decade. Why should one type of molecule be able to pass through this area, while others cannot? The answer is to be found in the traffic regulator, a protein called MAP2. "With this discovery, we have answered a fundamental question about the unique functioning of nerve cells that has occupied scientists for a long time", lead author of the study Dr Laura Gumy says.

Driving force

The cell biologists from Utrecht first discovered that larger quantities of MAP2 accumulate between the cell body and the axon. When they removed MAP2 from the neuron, the normal pattern of molecule movement changed. Certain molecules suddenly ceased to enter the axon, whereas others accumulated in the axon instead of passing through to the cell body. This abnormal transport indicates that MAP2 is the driving force behind transport within the axon.

Car key

The cell biologists from Utrecht University went on to make another very important discovery. Since axons are so long, transport in the neurons is carried out by sets of proteins - known as 'motor proteins' - that carry packages of other proteins on their back. As it turns out, MAP2 is able to switch a specific 'motor protein' on or off, like a car key. This means that MAP2 actually controls which packages of molecules may enter the axon and which may not. Targeting the activity of the transport engine allowed the researchers to make another interesting discovery: MAP2 is also able to control the delivery of molecules at specific points along the axon.

New targets for therapies

"Transport within axons has been shown to fail in Alzheimer, Parkinson's disease and Huntington's disease, as well as in many other diseases. When the neuron is no longer able to control where molecules go, or is unable to get molecules to where they need to be, it cannot do its job. By understanding how transport works, we have laid the foundation for considering new targets and potential therapies for various neurodegenerative disorders", Casper Hoogenraad concludes.

Explore further: New technique can help understand neurodegenerative diseases

More information: Neuron (2017). DOI: 10.1016/j.neuron.2017.03.046

Journal reference: Neuron

Provided by: Utrecht University

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‘Filled with hate, filled with anger’: Anatomy of a shooting allegedly fueled by hatred of white people – Los Angeles Times

Fresno police said they believe a shooting rampage downtown Tuesday that left three white men dead was racially motivated.

Fresno Police Chief Jerry Dyer said the suspect, Kori Ali Muhammad, gave very specific, detailed information to police that led officers to believe this was a hate-motivated crime, but did not elaborate on what those statements were.

If in fact hes lashing out at white people white males in this case that would constitute a hate crime, Dyer said. We believe it is a hate crime, definitely a hate crime.

The chief said investigators dont believe Muhammad worked with anyone else in the attack, calling him an individual that is filled with hate, filled with anger.

Family members said Muhammad had spoken of a war going on between blacks and whites in America.

Heres a rundown of what happened:

Police believe Muhammad killed a Motel 6 security guard, Carl Williams. The unarmed 25-year-old was shot outside the motel on North Blackstone Avenue.

Muhammad cut off his braids and shaved his face, significantly changing his appearance, after Fresno police put out a news release about that killing.

After being aware of that media release, Muhammad made a decision to himself that he was not going to go to jail for shooting a security guard that he was going to kill as many people as he could today and thats what he set out to do, Dyer said.

Grandmother Glenestene Taylor said Muhammad was acting strangely when he visited her Sunday. He was crying, but she believed he was simply going out of town.

I thought thats why hes upset, because he thinks of me as a mother, said Taylor, 81. Hes always telling me, Ill take care of it. Ill protect you. Dont you worry about it. He really didnt want to go but he was going.

The shootings began around 10:30 a.m. in downtown Fresno.

Dyer said that Muhammad fired sixteen rounds in less than two minutes, but immediately surrendered when approached by Fresno Police Officer Frank Borrego, and made spontaneous statements.

Those statements were I did it. I shot them, Dyer said, adding that Muhammad identified himself and said, You guys are looking for me.

He yelled Allahu akbar from the back seat of the patrol car. Muhammad later said he made that statement in order to pledge allegiance to God in case anything happened to him, Dyer said.

The victims of Tuesdays shootings were a 34-year-old white man who was a passenger in a PG&E vehicle, a 37-year-old white man killed on the sidewalk and a 58-year-old man shot in the Catholic Charities parking lot. Another 59-year-old white man was shot at but not struck.

The gunman also approached two Latina women, a mother and daughter, in a vehicle. He pointed the gun directly at them but did not fire. They drove away from the location, hearing gunfire as they left.

Dyer said Muhammad gave very specific, detailed information to police which led officer to believe this was a hate-motivated crime, but did not elaborate on what those statements were.

Muhammad was in the area because of several abandoned houses in the vicinity; according to Dyer, Muhammad was living on the streets and was hoping to stay at one such house. Muhammads grandmother said she didnt believe he was homeless.

Mason and Marcum reported from Fresno, and Branson-Potts and Serna from Los Angeles. Times staff writers Richard Winton and Veronica Rocha contributed to this report.

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'Filled with hate, filled with anger': Anatomy of a shooting allegedly fueled by hatred of white people - Los Angeles Times