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Smaller, faster, stronger: NSF grant will help Tvrdy develop the electronics of the future – Communique

Each year, consumers demand more from their electronic devices smaller sizes, faster processing and better performance. As engineers scramble to meet these demands with standard silicon-based transistors, another school of thought has emerged: using carbon nanotubes.

The cylindrical molecules that make up carbon nanotubes look like rolled-up tubes of chicken wire under a microscope. Strong, flexible, lightweight, thermally conductive and chemically stable, nanotubes are useful for a wide range of electronic and biomedical purposes.

Indeed, they may represent the future of electronic devices. But its deceptively difficult to grow nanotubes pure enough for research, not to mention real-world applications. During the growth process, many different types of carbon nanotubes are produced, necessitating purification that has remained elusive for these otherwise promising materials.

Now, a $250,000 National Science Foundation grant will allow Kevin Tvrdy, associate professor of chemistry & biochemistry at UCCS, to advance the process of creating and purifying these molecules for the benefit of nanoscience worldwide.

Tvrdys proposal, titled Synthesis and Characterization of Novel Hydrogel Formulations for the Single Chirality Purification of Single-Walled Carbon Nanotubes, has a specific focus: creating hydrogels tailored for the purification of nanotubes, thereby helping to allow the scientific community to research and apply nanotubes at scale.

The advancement of carbon nanotube purification stands to enable the development of next-generation devices and schemes that take full advantage of nanotube properties, Tvrdy said. Some examples include the fabrication of ultrasmall carbon-based electronics, solar cells capable of harvesting the infrared region of the spectrum, and imaging schemes capable of simultaneously sensing and mapping with nanoscale precision.

In other words, the future of phones, wearable electronics, solar cells, biomedical devices and more could rest on the carbon nanotube purification schemes under development by researchers and developers like Tvrdy.

Tvrdy and his research team, consisting of graduate and undergraduate students, will work to devise different formulations of hydrogel that target specific properties within carbon nanotubes. By developing both high- and low-cost formulation of the gel, their hope is to expand the number of pure, single-walled carbon nanotube species available to the scientific community for research and applied use.

They will publicly report their research progress within the Colorado Springs Science on Tap lecture series and results from this work will be integrated into Tvrdys nanoscience.

And perhaps, in the near future, we will have Tvrdy and his team to thank for electronic devices that are smaller, faster and stronger than we ever imagined.

Kevin Tvrdy is an associate professor of chemistry & biochemistry within the College of Letters, Arts and Sciences at UCCS. His research interests lie in the synthesis, purification and characterization of low dimensional materials and their use in novel devices. Of particular interest are the optical and electronic properties of single walled carbon nanotubes and semiconducting quantum dots. Learn more about Tvrdy and the Tvrdy Lab at UCCS online.

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Smaller, faster, stronger: NSF grant will help Tvrdy develop the electronics of the future - Communique

Libraries to Receive $25000 Grant from National Endowment for the Arts – University of Arkansas Newswire

FAYETTEVILLE, Ark. The University of Arkansas Libraries have been approved for a $25,000 grant through the Grants for Arts Projects, which will support Arkansas Folk and Traditional Arts Community Scholars Program.

Arkansas Folk and Traditional Arts is a statewide outreach program of the University of Arkansas Libraries. This project will provide free training across the state centered on equipping and empowering Arkansas communities to document, present and sustain their traditional culture and arts.

As the country and the arts sector begin to imagine returning to a post-pandemic world, the National Endowment for the Arts is proud to announce funding that will help arts organizations such as Arkansas Folk and Traditional Arts reengage fully with partners and audiences, said Ann Eilers, acting chair for the National Endowment for the Arts. Although the arts have sustained many during the pandemic, the chance to gather with one another and share arts experiences is its own necessity and pleasure.

Arkansas Folk and Traditional Arts Community Scholars Program will be modeled after the Kentucky Arts Councils longstanding and successful training of the same name.

Arkansas Folk and Traditional Arts will host three trainings throughout the project year in different geographic regions of Arkansas in partnership with hosting organizations and/or individuals. Each training will include five sessions designed to introduce folklore and folk art, teach oral history and fieldwork skills and provide examples for how communities can archive or showcase their research.

The NEAs support will help us grow a network of Community Scholars across the state who are aligned with our own mission to document, present and sustain Arkansas rich cultural heritage, said Virginia Siegel, coordinator for Arkansas Folk and Traditional Arts. Community Scholars are already the experts of their communities and we hope this program will provide resources to strengthen these experts toolkits.

About Arkansas Folk and Traditional Arts:AFTA is a statewide folk arts program of the University of Arkansas Libraries dedicated to building cross-cultural understanding by documenting, presenting, and sustaining Arkansas living traditional arts and cultural heritage. AFTA is supported in part by the National Endowment for the Arts and works in partnership with stakeholder organizations and individuals, including the Arkansas Arts Council, Mid-America Arts Alliance, and Arkansas State University.

About the University Libraries: Located in the heart of campus, the David W. Mullins Library is the university's main research library. Branch libraries include the Chemistry and Biochemistry Library, the Fine Arts Library, the Physics Library, and the Robert A. and Vivian Young Law Library. The Libraries provide access to more than 3.1 million volumes and more than 180,000 journals and offer research assistance, study spaces, computer labs with printing and scanning, interlibrary loan and delivery services, and cultural exhibits and events. The Libraries' Special Collections division acquires, preserves, and provides access to materials on Arkansas and the region, its customs and people, and its cultural, physical, and political climate. Visit the Libraries' website at libraries.uark.edu to learn more about services and collections.

About the University of Arkansas: The University of Arkansas provides an internationally competitive education for undergraduate and graduate students in more than 200 academic programs.

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Libraries to Receive $25000 Grant from National Endowment for the Arts - University of Arkansas Newswire

Bio-Based Itaconic Acid Market | Key Opportunities, Trends, Business Demand And Key Players Analysis | Itaconix Corporation, Qingdao Kehai…

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Bio-Based Itaconic Acid Market | Key Opportunities, Trends, Business Demand And Key Players Analysis | Itaconix Corporation, Qingdao Kehai...

Portable Veterinary Biochemistry Analyzer Market Global Demand, Research and Top Leading Player to 2026 Covid-19 Analysis KSU | The Sentinel…

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Global Portable Veterinary Biochemistry Analyzer Market Revenue, 2016-2021, 2022-2027, ($ millions)

Global Portable Veterinary Biochemistry Analyzer Market Sales, 2016-2021, 2022-2027, (K Units)

Global top five Portable Veterinary Biochemistry Analyzer companies in 2020 (%)

The global Portable Veterinary Biochemistry Analyzer market was valued at xx million in 2020 and is projected to reach US$ xx million by 2027, at a CAGR of xx% during the forecast period.

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Global Portable Veterinary Biochemistry Analyzer Market, By Type, 2016-2021, 2022-2027 ($ Millions) & (K Units)

Global Portable Veterinary Biochemistry Analyzer Market Segment Percentages, By Type, 2020 (%)

Automatic

Semi-Automatic

Global Portable Veterinary Biochemistry Analyzer Market, By Application, 2016-2021, 2022-2027 ($ Millions) & (K Units)

Global Portable Veterinary Biochemistry Analyzer Market Segment Percentages, By Application, 2020 (%)

Veterinary Hospitals

Veterinary Clinics

Others

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Global Portable Veterinary Biochemistry Analyzer Market Segment Percentages, By Region and Country, 2020 (%)

North America

US

Canada

Mexico

Europe

Germany

France

U.K.

Italy

Russia

Nordic Countries

Benelux

Rest of Europe

Asia

China

Japan

South Korea

Southeast Asia

India

Rest of Asia

South America

Brazil

Argentina

Rest of South America

Middle East & Africa

Turkey

Israel

Saudi Arabia

UAE

Rest of Middle East & Africa

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Key companies Portable Veterinary Biochemistry Analyzer revenues share in global market, 2020 (%)

Key companies Portable Veterinary Biochemistry Analyzer sales in global market, 2016-2021 (Estimated), (K Units)

Key companies Portable Veterinary Biochemistry Analyzer sales share in global market, 2020 (%)

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Samsung

Randox

Alphatecscientific

Genrui

KPM Analytics(AMS Alliance)

Woodleyequipment

Idexx

Zoetis(Abaxis)

Seamaty

YSENMED

MNCHIP

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Portable Veterinary Biochemistry Analyzer Market Global Demand, Research and Top Leading Player to 2026 Covid-19 Analysis KSU | The Sentinel...

Stablix Therapeutics Launches with $63 Million Series A Financing – BioSpace

--Versant Ventures leads investment in first-in-category company with targeted protein stabilization platform --

--Foundational know-how establishes leadership in the field--

NEW YORK--(BUSINESS WIRE)-- Stablix Therapeutics, a biotechnology company pioneering the field of Targeted Protein Stabilization (TPS), today announced a $63 million Series A financing led by founding investor Versant Ventures together with NEA, Cormorant, Euclidean Capital and Alexandria Real Estate Equities.

Many inherited and acquired diseases are caused by insufficient levels of specific proteins. With inherited diseases such as cystic fibrosis, mutations in the CFTR gene produce a protein that remains functional but is subject to excessive ubiquitination, leading to its rapid degradation via the proteasome. Excess ubiquitination is also a feature of cancer, where E3 ubiquitin ligases enzymes that add ubiquitin to proteins are frequently upregulated or amplified, driving the degradation of tumor suppressor proteins.

Until now, it has not been possible to inhibit the ubiquitin-proteasome system in a target-selective manner. Stablixs RESTORED platform generates heterobifunctional small molecules (RESTORACS) that recruit deubiquitinase enzymes to remove ubiquitin from targeted proteins and consequently stabilize or increase target protein levels and activity. The company initially is leveraging the platform to develop programs to treat rare diseases, cancer and immunological disorders.

Stablix possesses a first-in-category platform that can restore protein stability and function in a target-selective manner, said Carlo Rizzuto, Ph.D., partner at Versant and acting CEO of Stablix. We are very pleased to launch this company to address this important therapeutic white space for numerous devastating diseases.

Targeted Protein Stabilization (TPS)

Protein stabilization can be thought of as the inverse of protein degradation. The underlying concept of augmenting protein stabilization has been validated in nature. Many viruses encode their own E3 ligases and deubiquitinases to coopt the ubiquitin-proteasome system as part of their life cycles. This demonstrates that the system can be manipulated via exogenous intervention.

The therapeutic value of augmenting protein stabilization has also been demonstrated with proteasome inhibitors. These inhibitors are potent cancer therapeutics but have also been profiled for activity in Mendelian diseases in multiple animal and patient studies. In these studies, proteasome inhibitors were able to increase levels of deficient proteins across a range of targets and organ systems. However, because proteasome inhibitors globally inhibit protein degradation in a non-specific manner, their use outside of oncology is limited by poor tolerability, highlighting the need for targeted approaches.

The Stablix platform originated in the laboratory of Henry Colecraft, Ph.D., John C. Dalton Professor of Physiology and Cellular Biophysics at Columbia University. Co-founders Dr. Colecraft and Scott Kanner, Ph.D., developed an approach to selectively recruit deubiquitinases (DUBs) to proteins of interest. Their pioneering work demonstrated the functional rescue of CFTR and of a second target, KCNQ1, a gene that when mutated causes Long QT syndrome.

It is gratifying to see the work on precise stabilization of proteins now being translated into new therapies, said Dr. Colecraft. I look forward to working closely with the Stablix team to bring these treatments to patients.

The companys RESTORED platform has two primary components. The first is a library of binding moieties capable of recruiting selected DUBs. These recruiting moieties are conjugated with linkers to targeting ligands to create bispecific molecules that co-localize a DUB and a target. Second, a suite of biochemical and functional assays is used to monitor the ubiquitination and functional status of target proteins in cells. Stablix will initially focus pipeline development on rare diseases, oncology and immunology.

Operating plans and scientific leadership

Stablix plans to use the proceeds from the Series A financing to build out its platform and advance a portfolio of protein stabilizers towards the clinic. In addition, the company has established a lab facility in New York City, where it is building a research team led by co-founders Brian Bowman, Ph.D., head of in vitro pharmacology, and Kevin Sprott, Ph.D., head of drug discovery, with Dr. Kanner, head of platform development, leading technology transfer.

For its Scientific Advisory Board, Stablix has recruited a leading group of researchers with extensive experience in DUB biology and chemistry. In addition to Dr. Colecraft, SAB members include Benedikt Kessler, professor of biochemistry and mass spectrometry at the Target Discovery Institute, University of Oxford; Andrew Turnbull, senior principal scientist at Cancer Research UK; Chris Dinsmore, CSO at Kronos Bio; and Chris Roberts, CSO at Black Diamond Therapeutics.

Stablixs unique approach presents the company with a massive opportunity to create an impact for patients with rare diseases, cancer or immunological disorders, said Ali Behbahani, M.D., general partner at NEA and a Stablix board member. We are pleased to join this high-quality syndicate and look forward to the continued development of Stablixs platform and programs.

About Stablix Therapeutics

Stablix Therapeutics is a biotechnology company pioneering the field of Targeted Protein Stabilization (TPS). The companys RESTORED platform generates heterobifunctional small molecules (RESTORACS) that recruit deubiquitinase enzymes to remove ubiquitin from targeted proteins and consequently stabilize or increase target protein levels and activity. Stablix initially is leveraging the platform to develop programs to treat rare diseases, cancer and immunological disorders.

About Versant Ventures

Versant Ventures is a leading healthcare venture capital firm committed to helping exceptional entrepreneurs build the next generation of great companies. The firms emphasis is on biotechnology companies that are discovering and developing novel therapeutics. With $4.2 billion under management and offices in the U.S., Canada and Europe, Versant has built a team with deep investment, operating and R&D expertise that enables a hands-on approach to company building. Since the firms founding in 1999, more than 85 Versant companies have achieved successful acquisitions or IPOs. For more information, please visit http://www.versantventures.com.

About NEA

New Enterprise Associates, Inc. (NEA) is a global venture capital firm focused on helping entrepreneurs build transformational businesses across multiple stages, sectors and geographies. With nearly $24 billion in cumulative committed capital since the firm's founding in 1977, NEA invests in technology and healthcare companies at all stages in a company's lifecycle, from seed stage through IPO. The firm's long track record of successful investing includes more than 230 portfolio company IPOs and more than 390 mergers and acquisitions. http://www.nea.com.

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Stablix Therapeutics Launches with $63 Million Series A Financing - BioSpace

Cell-Free DNA Guided Targeted Therapy Leads to Better Survival in Advanced Non-Small Cell Lung Cancer – Business Wire

SANTA CLARA, Calif.--(BUSINESS WIRE)--Agilent Technologies Inc. (NYSE: A) today announced a presentation by Memorial Sloan Kettering Cancer Center (MSK) at the upcoming annual meeting of the American Society of Clinical Oncology (ASCO) to discuss the Resolution ctDx Lung, a laboratory-developed test (LDT) developed by Resolution Bioscience.

The presentation titled Overall survival with circulating tumor DNA-guided therapy in advanced non-small cell lung cancer will present evidence for the clinical utility of Resolution ctDx Lung in detecting actionable mutations in non-small cell lung cancer (NSCLC) patients.

Previous findings have supported the clinical utility of the Resolution ctDx Lung for accurately selecting patients for targeted therapies.1 The latest study, involving the largest prospective liquid biopsy cohort (>1,000 patients) with 34 years of survival data, demonstrates that cell-free DNA guided targeted therapies help result in better overall survival.

This is the first and largest prospective study of ctDNA guided therapy to show an overall survival benefit in patients with lung cancers, providing evidence for the utility of liquid biopsy in clinical practice, said Bob Li, MD, PhD, MPH, Co-Director of the Thoracic Liquid Biopsy Program at MSK.

This large cohort highlights the utility of the Resolution ctDx Lung in helping guide therapy selection to improve patient outcomes, said Mark Li, CEO of Resolution Bioscience, now a part of Agilent. Significantly, the study highlighted important differences between liquid biopsies and tissue testing, including faster turnaround to reporting, while providing the benefits of guided targeted therapy."

The success of Resolution ctDx Lung further strengthens Agilent's ability to deliver precision oncology testing assays for patients worldwide and demonstrates the company's commitment as a partner in the development of powerful new clinical diagnostics solutions to expand the fight against cancer.

Resolution Bioscience is dedicated to developing a highly sensitive, non-invasive liquid biopsy platform that improves cancer diagnostics and monitoring for patients around the world. The company has developed core technology for circulating cell-free DNA NGS analysis. Resolution Biosciences Liquid Biopsy assays are powered by the companys cell-free DNA (cfDNA) analysis platform, which includes targeted capture next-generation sequencing (NGS) biochemistry and tightly coupled, cloud-based bioinformatics. The Resolution Bioscience homologous recombination deficiency (HRD) assay has received Breakthrough Device Designation from the U.S. Food and Drug Administration.

References:

About Agilent Technologies

Agilent is a leader in life sciences, diagnostics, and applied chemical markets, delivering innovative technology solutions that provide trusted answers to researchers most challenging scientific questions. The company generated revenue of $5.34 billion in fiscal year 2020 and employs 16,400 people worldwide. Information about Agilent is available at http://www.agilent.com. To receive the latest Agilent news, please subscribe to the Agilent Newsroom. Follow Agilent on LinkedIn, Twitter, and Facebook.

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Cell-Free DNA Guided Targeted Therapy Leads to Better Survival in Advanced Non-Small Cell Lung Cancer - Business Wire

Cue Biopharma to Present at the 2021 Federation of Clinical Immunology Societies (FOCIS) Virtual Annual Meeting – Yahoo Finance

CAMBRIDGE, Mass., June 03, 2021 (GLOBE NEWSWIRE) -- Cue Biopharma, Inc. (Nasdaq: CUE), a clinical-stage biopharmaceutical company engineering a novel class of injectable biologics designed to selectively engage and modulate targeted T cells directly within the patients body, announced today it will give a presentation at the 2021 Federation of Clinical Immunology Societies (FOCIS) Annual Meeting, which is being held virtually from June 8-11, 2021.

Anish Suri, president and chief scientific officer of Cue Biopharma, will discuss preclinical data on CUE-401, the Companys most recent autoimmune drug product candidate. CUE-401, part of the CUE-400 series designed for differentiation and expansion of induced regulatory T cells (iTregs), is a bispecific molecule engineered to deliver the two signals, transforming growth factor beta (TGF-) and interleukin 2 (IL-2), required to induce iTregs in vivo.

Presentation DetailsSession Title: CUE-401: A Novel IL-2/TGF-beta Fusion Protein for the Induction of CD4+ FOXP3+ Regulatory T cellsPresenter: Anish Suri, Ph.D., president and chief scientific officer of Cue BiopharmaSession: Late Breaking Abstracts (Part II)Date and Time: Thursday, June 10, 2021 from 3:45 p.m. 4:00 p.m. PDT

The recorded presentation and poster will be available in the Investor & Media section of the Companys website under Scientific Publications and Presentations, following the presentation at FOCIS 2021 annual meeting.

Presentation data highlights include:

In vivo data show that CUE-401 can effectively induce FOXP3-expressing iTregs from T cells obtained from healthy donors as well as patients suffering from rheumatoid arthritis and inflammatory bowel diseases.

CUE-401 induced iTregs suppressed effector T cell responses.

A single dose of CUE-401 was shown effective at inducing Tregs in mice with active and ongoing autoimmunity.

Dr. Suri commented, We are very excited to share these promising preclinical data demonstrating CUE-401 has the ability to induce and expand regulatory T cells in vitro and in vivo. We believe this is an innovative and potentially effective means of suppressing chronic inflammatory diseases and may provide a more meaningful and lasting benefit to patients suffering from numerous autoimmune diseases, graft versus host disease (GVHD) and even transplant rejection.

About FOCIS Annual Meeting The Federation of Clinical Immunology Societies is a key forum where opinion leaders come together to chart the path to the next major breakthrough in disease therapy. Through FOCIS, researchers and clinicians share knowledge across traditional disease borders, and identify commonalities between treatments and therapies that are life-changing for those impacted by immune-mediated diseases. The FOCIS Annual Meeting educates clinicians, researchers and trainees in the broad discipline of clinical immunology. FOCIS is the worlds leader in immunology education and in training future generations of clinical immunologists. Initially established as a cross-disciplinary meeting, FOCIS held its first Annual Meeting in 2001. After two successful consecutive meetings, FOCIS was incorporated as a 501(c)3 organization in 2003. Today, FOCIS has 58 Member Societies, representing roughly 65,000 clinician scientists.

About Cue BiopharmaCue Biopharma, a clinical-stage biopharmaceutical company, is engineering a novel class of injectable biologics to selectively engage and modulate targeted T cells directly within the patients body to transform the treatment of cancer, infectious disease and autoimmune disease. The companys proprietary Immuno-STAT (Selective Targeting and Alteration of T cells) platform, is designed to harness the bodys intrinsic immune system without the need for ex vivo manipulation.Headquartered in Cambridge, Massachusetts, the company is led by an experienced management team and independent Board of Directors with deep expertise in immunology and immuno-oncology as well as the design and clinical development of protein biologics.

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For more information, visit https://www.cuebiopharma.com and follow us on Twitter at https://twitter.com/CueBiopharma.

Forward-Looking StatementsThis press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, that are intended to be covered by the safe harbor created by those sections. Such forward-looking statements include, but are not limited to, those regarding: the companys estimate of the period in which it expects to have cash to fund its operations; the companys belief that the Immuno-STAT platform stimulates targeted immune modulation through the selective engagement of disease-relevant T cells; and the companys business strategies, plans and prospects. Forward-looking statements, which are based on certain assumptions and describe the companys future plans, strategies and expectations, can generally be identified by the use of forward-looking terms such as believe, expect, may, will, should, would, could, seek, intend, plan, goal, project, estimate, anticipate, strategy, future, likely or other comparable terms, although not all forward-looking statements contain these identifying words. All statements other than statements of historical facts included in this press release regarding the companys strategies, prospects, financial condition, operations, costs, plans and objectives are forward-looking statements. Important factors that could cause the companys actual results and financial condition to differ materially from those indicated in the forward-looking statements include, among others, the companys limited operating history, limited cash and a history of losses; the companys ability to achieve profitability; potential setbacks in the companys research and development efforts including negative or inconclusive results from its preclinical studies, its ability to secure required U.S. Food and Drug Administration (FDA) or other governmental approvals for its product candidates and the breadth of any approved indication; adverse effects caused by public health pandemics, including COVID-19, including possible effects on the companys trials; negative or inconclusive results from the companys clinical trials or preclinical studies or serious and unexpected drug-related side effects or other safety issues experienced by participants in clinical trials; delays and changes in regulatory requirements, policy and guidelines including potential delays in submitting required regulatory applications to the FDA; the companys reliance on licensors, collaborators, contract research organizations, suppliers and other business partners; the companys ability to obtain adequate financing to fund its business operations in the future; operations and clinical the companys ability to maintain and enforce necessary patent and other intellectual property protection; competitive factors; general economic and market conditions and the other risks and uncertainties described in the Risk Factors and in Management's Discussion and Analysis of Financial Condition and Results of Operations sections of the companys most recently filed Annual Report on Form 10-K and any subsequently filed Quarterly Report(s) on Form 10-Q. Any forward-looking statement made by the company in this press release is based only on information currently available to the company and speaks only as of the date on which it is made. The company undertakes no obligation to publicly update any forward-looking statement, whether written or oral, that may be made from time to time, whether as a result of new information, future developments or otherwise.

Investor ContactGeorge B. Zavoico, Ph.D.VP, Investor Relations & Corporate Development Cue Biopharma, Inc. gzavoico@cuebio.com

Media ContactDarren Opland, Ph.D.LifeSci Communicationsdarren@lifescicomms.com

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Cue Biopharma to Present at the 2021 Federation of Clinical Immunology Societies (FOCIS) Virtual Annual Meeting - Yahoo Finance

The SSC Platelet Immunology Register of VITT and VIITP: Towards standardization of laboratory and clinical parameters – DocWire News

This article was originally published here

J Thromb Haemost. 2021 Jun 2. doi: 10.1111/jth.15402. Online ahead of print.

ABSTRACT

A severe syndrome of thrombosis and thrombocytopenia has been described in patients vaccinated against severe acute respiratory distress syndrome coronavirus 2 (SARSCoV2) with a chimpanzee adenovirus vector encoding Spike protein (ChAdOx1 nCov-19, AstraZeneca).[1-6] as well as (Ad26.COV2.S, Johnson & Johnson/Janssen).[7] Currently, this novel immune thrombosis syndrome is known as vaccine-induced immune thrombotic thrombocytopenia (VITT) but has been described as vaccine-induced prothrombotic immune thrombocytopenia (VIPIT) and thrombotic thrombocytopenia syndrome (TTS) elsewhere.

PMID:34076338 | DOI:10.1111/jth.15402

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The SSC Platelet Immunology Register of VITT and VIITP: Towards standardization of laboratory and clinical parameters - DocWire News