Category Archives: Cell Biology

New Worthington Enzyme and Biochemical Product Catalog Features Solutions for Life Science Research and Bulk Requirements – Newswise

LAKEWOOD, NJ (December 9, 2020) Worthington, the leading supplier of specialty enzymes for over 70 years, announces today the publication of an expanded, 2021-22 Enzyme and Biochemical Product Catalog. As a primary enzyme producer for biochemistry, cell biology, molecular biology, pre-clinical research and bioprocessing applications, Worthington is the go-to expert in enzyme technology.

Even with COVID restrictions in place, Worthington employees have been diligently working to support our customers needs, said Jim Zacka, vice president at Worthington. Releasing a number of new products this year, we continue our legacy of advancing research through innovation in enzyme development for both research, OEM and bioprocessing customers.

The new catalog is available in two easy-to-use formats, a downloadable PDF and an easy-to-navigate, digital catalog for online browsing and purchasing.

To request a PDF, go to: Worthington-Biochem.com

About Worthington Biochemical Corporation

Founded in 1947, Worthington Biochemical Corporation is an industry leader in the development and production of high-quality purified enzymes, proteins, nucleic acids and cell isolation kits for life science research, diagnostics and biotechnology applications. An ISO9001 Certified, primary manufacturer Worthington meets enzyme requirements from research to scale-up bulk bioprocessing and OEM applications. Products extensively cited in peer-review journals and open-access publications, the company is committed to supporting STEM education. Worthington Biochemical Corporation is a privately held company, headquartered in Lakewood, NJ and has worldwide distribution through a network of exclusive distributors.

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New Worthington Enzyme and Biochemical Product Catalog Features Solutions for Life Science Research and Bulk Requirements - Newswise

Repair protein may prevent damage to healthy cells during cancer therapy – News-Medical.net

A key way radiation therapy and chemotherapy work is by making highly lethal double-strand breaks in the DNA of cancer cells. A Georgia Cancer Center scientist wants to help those therapies work better by better understanding the complex DNA damage repair process, because sometimes these therapies can inadvertently contribute to cancer.

We are trying to identify a repair protein that can help healthy cells avoid dying or becoming cancerous."

Dr. Chunhong Yan, Molecular Biologist, Cancer center, Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta University

ATF3, a sensor of cell stress which Yan's team has shown is an early and important player in DNA damage repair, may be that protein. A new $1.7 million grant (R01CA240966) from the National Cancer Institute is helping them find out.

Our hereditary material is contained in the nucleus of our cells, and is constantly bombarded by factors like sunlight and oxidative stress, even chemicals in our food. Our healthy cells are mostly adept at DNA damage repair, but cancer cells have a defect in their DNA damage repair mechanism that should leave them more vulnerable to chemotherapy and radiation. In fact, our healthy cells' natural, rapid ability to repair DNA damage is considered a natural cancer barrier because incomplete repairs can accumulate and become cancer, Yan says. That's one of the reasons cancer risk generally increases with age.

One of the problems with radiation and chemotherapy is the collateral damage it does to healthy cells. Despite efforts at more targeted delivery, the treatments also can produce serious, double-strand breaks in the DNA of healthy cells, putting them at risk of dying or becoming part of the tumor, one of the unfortunate side effects of these therapies and key reasons for Yan's interest. "If we can find something that specifically only kills cancer cells, but keeps normal cells healthy, that could be very beneficial to patients," he says.

So Yan and his lab are dissecting this important "genome maintenance" of DNA repair. If their findings continue to hold, their ultimate goal is new cancer therapies that make increased use of the ATF3's skill at stopping spontaneous tumor production.

They have already shown that the protein ATF3 is essential to efficient, complete access to DNA and its repair. That without it mice get more tumors, which suggests that ATF3 is important in suppressing tumor formation, he says. That includes establishing a direct link between ATF3 and the established tumor suppressor p53. They found ATF3 can bind to p53 and increase expression of this protein which also has a role in DNA damage response, including going to the scene and putting the cell in a state of rest to ease repair. The other side of the coin is that when a cell can't repair, p53 enables it to commit suicide. Without ATF3, there is a better chance the cell will just become cancer, Yan says.

But good repair first requires access. To get our long DNA to fit inside our compact cells, proteins called histones provide a sort of spool, called a nucleosome, around which the iconic double-stranded DNA is wound. Chromatin is the biological packaging. In the snug confines of chromatin, the familiar classic double helix that resembles a twisted ladder is more of an X-shape resembling a clothespin.

When a cell senses DNA damage, the histones need to modify the chromatin so repair proteins can get inside and do their work and the DNA needs to relax its grip on the nucleosome. One they gain access to the damage, repair proteins enable what is called non-homologous end-joining by essentially trimming the broken ends of the damaged DNA and patching them back together.

Yan is learning more about those modifications to the histones and the ones needed to recruit those repair proteins, which already are in the nucleus, right to the damage site.

Their goals including learning more about how ATF3, also already present in the cell nucleus, gets to the actual DNA damage site. They have evidence that yet another histone, called H2AX, may be part of that.

H2AX is in the chromatin, and when there is a double-strand break in the DNA, it gets modified within seconds into? H2AX, which Yan's lab has evidence recruits ATF3 to the damage site. Yan notes that while he cannot yet say that these are the first changes, he can say they are very early ones.

"What we have found is ATF3 can come to the damage site pretty quickly, and promote the chromatin change," Yan says. They've found ATF3 binding to and stabilizing the enzymes Tip60 and p300/CBP can help provide direct access to the DNA damage site so repair proteins can move in.

This so-called histone acetylation is considered a principal way DNA damage repair happens, so identifying the genes that regulate this important intersection so that cells can be properly repaired and avoid becoming cancerous is important, Yan says.

Yan's lab has shown that ATF3 can activate the natural tumor suppressor p53 while getting Tip60 to activate the major DNA damage response kinase ATM, which provides a sort of framework for the team of repair proteins that will be recruited. p53 also is an early arriver, like a master engineer, helping make decisions on whether or not the DNA is a loss or can be repaired.

Now they want to learn more about how ATF3 promotes p300/CBP that ultimately brings on multiple repair proteins. That includes learning more about how ATF3 alters chromatin's structure to help recruit these repair proteins. A mouse missing ATF3 is enabling them to better see the roles of ATF3 including exploring further whether cancer increases when it is MIA.

Yan has documented lower ATF3 levels in people with cancer; and how taking down ATF3 levels decreases DNA repair and increases susceptibility to radiation. His research team also has found ATF3 is important in stopping damaged cells from becoming cancer. Yan and others additionally have shown that ATF3 can suppress spread of lung, colon and bladder cancers.

DNA damage is one of the most common sources of cell stress.

Like many body functions, the DNA repair mechanism tends to get less efficient with age. DNA damage, unrepaired or incompletely repaired, can lead to mutations, which increase the risk of the cell becoming cancer; or, with the help of p53, cell death from apoptosis, the innate ability of a cell to kill itself, when an injury likely cannot be repaired.

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Cell Biology, Molecular Biology, Biotechnology And The Man Who Is Connecting It All: Felix Paul Joe – Outlook India

Thats the philosophy of Felix Paul Joe and preferably the biggest explanation one can have for his unflinching crusade in the field of biotech research. Felix founded GeneX India Bioscience Pvt. Ltd. in 2004 but, the journey before it prepared him for everything that came next.

After earning a Masters in Life Science and Post Graduate Diploma in Business Administration from the University of Madras and Madras Productivity Council, Felix was all set to create his own path in biotechnology. But, revolution is a way paved stone by stone. Before realizing his passion and dream to become an entrepreneur, Felix completed a nine-year run in different biotech companies. As a National Sales & Product Manager, he embarked on a journey that shaped his understanding of what the industry is and what it needs.

He attended a plethora of application training on varied subjects like molecular biology, cellular microscopy, interphase chromosome profiling and Proteomics. His learnings from these teachings formed a crucial part of his ventures growth model in the later years. He also completed exclusive product training and lab sessions at many international labs and forums during his days as a manager. Working with many Centres for Excellence labs across India, Felix perceived the need for a bridge between the Indian and global standards.

In 2004, when Felix established GeneX India Bioscience, the company only started as a distributor of cell culture products. Molecular biology and biotechnology were then added to widen the spectrum. Today, the company focusses in the fields of bio-science research institutes, molecular diagnostic labs, biopharmaceutical R&D, biotech contract research and development centres.

Over the years, the organization created a line of products and solutions, namely Cell Biology, Real-Time PCR, Epigenetics, Next Generation Sequencing and Protein Biology. The private company is a full-fledged service provider for cell biology, flowcytometry and proteomics. As envisioned by Felix, GeneX also acts as a middleman nurturing quality products, scientific and technical support between biotech solution providers in Europe, USA, UK and Indian researchers who work across the relevant fields.

GeneX India has an experienced team of 33 scientifically-qualified professionals who possess the capability to market, conduct workshops, seminars. They cumulatively provide solutions to scientists and research scholars, helping them complete their research. The team works in constant collaboration mode to ensure a zero-defect product and service range. The stringent quality standard and client-centric approach have made the enterprise synonymous to the word biotech all across the world.

Following this unprecedented rise, GeneX India has been recognized for its efforts via major accolades like the Biotech Excellence and the APJ Abdul Kalam Excellence Award. The CEO magazine also noted GeneX as one of the 25 fastest growing biotechnology companies in India recently. Moreover, Felix himself has been the recipient of multiple national and international awards such as the Mahatma Gandhi Samman at the House of Commons, UK.

Even during the COVID pandemic, Felix and his company have been dedicated to aiding ICMR approved testing labs and kit manufacturers. Vaccine research labs and producers are being helped in complete sync too.

As the future entails, Felix is now set on scaling the firm to global benchmarks and giving Indian research the world stage it deserves. A plan to support the bioprocess and vaccine development has been put in place as well. He also aims to produce affordable molecular diagnostic kits using the latest technology like the CRISPR Cas9 Genome editing tool. A Contract Research Lab that acts as a high-end core facility with its primary focus on Genomics and DNA sequencing for molecular diagnostics is also in the works. The end goal is to provide services to biotech researchers and in turn, become a parallel economic solution provider for the high throughput, time-bound turnkey biotech projects and diagnostic labs.

A reputable part of the significant science congresses across the country, Felix has always had the vision to create a sustainable future for the world. He has a strong conviction that the firms business model should make a profound and positive impact on the lives of all the researchers it touches. His every step has been towards building his own pathway that treads towards this purpose.

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Cell Biology, Molecular Biology, Biotechnology And The Man Who Is Connecting It All: Felix Paul Joe - Outlook India

Molecular Biology of the Cell seeks early-career editors to focus on curating preprints – Newswise

Newswise Molecular Biology of the Cell (MBoC) is assembling an editorial board of early-career researchers dedicated to curating and classifying the impact of new articles published in MBoC and preprints posted on bioRxiv. Supported by a Learned Society Curation Awardfrom the Wellcome Trust and the Howard Hughes Medical Institute awarded to MBoCs publisher, the American Society for Cell Biology (ASCB), this new board of diverse, young editors will contribute to curation and recognition of research works across the subjects covered by MBoC.

The recent growth of preprint servers and rapid pace of research dissemination can pose a challenge for researchers and evaluators, says ASCB Curation Manager Michael Lacy. It is sometimes difficult to discover the most interesting articles to read or to assess the significance and potential impact of new research. Our curators will be a valuable addition to the journal and ASCBs community, helping to spotlight important work for a broader audience.

Early-career editors should meet the following criteria:

Responsibilities of early-career editors include:

Early-career editors receive:

Applications should be submitted by Monday January 18, 2021 and must include 1) a CV, 2) a brief description of their research topic, interest in the position and future career plans (1 page total), and 3) a letter of recommendation. We are especially interested in recruiting a diverse group of candidates including those from under-represented backgrounds, across international regions, and from a broad range of research topics.

For more information and instructions to apply, visit our web pageor contact Michael Lacy (mlacy@ascb.org)

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Molecular Biology of the Cell seeks early-career editors to focus on curating preprints - Newswise

20 ways UM-Flint CAS innovated in 2020 (Part 1) – University of Michigan Flint News

It goes without saying: This year has been filled with unprecedented hardships. Students, faculty, and staff across the UM-Flint community have encountered countless challenges that often change from week to week.

Despite these challenges, UM-Flint remains committed to keeping students safe while continuing to provide a world-class education. UM-Flint has developed a culture of innovation to meet that goal. Solutions that were once hard to imagine are now embraced to help create the best experiences for students and community members.

This culture of innovation has spread to every school, college, and unit across the university, producing so many examples that they would be impossible to list in their entirety. This two-part series presents, in no particular order, 20 innovative highlights from the College of Arts & Sciences in 2020.

Students in AST 120: Survey of Astronomy, taught by Lecturer II Michele Stark, are learning by playing the video game "The University of Mars." While exploring the solar system, astronomy students discover more about elemental particles, moon phases, planetary orbits and more. It's easy to stay engaged with an online asynchronous course when you're having fun!

Assistant Professor of Biology You-shin Chen wanted to be sure her Cell Biology students got hands-on experience while studying from home. That's why she set up a drive-through on campus where students could pick up laboratory materials. Then they conducted numerous experiments away from the lab, including extracting DNA from fruits & vegetables and separating plant pigments to study photosynthesis. She says, "We are trying to be as a creative as possible to cultivate students' desire for learning."

After travel restrictions forced the Department of History to cancel their Wyatt Global Exploration Program, faculty began thinking of other ways they could support their students. That resulted in more than $70,000 in additional scholarships being awarded to every eligible History major and minor.

Performances from the Department of Theatre & Dance continued in new formats to keep students and audiences safe. The first performance of the season was Poof!, recorded in a socially distanced format and released online. In Poof!, a housewife comes to the end of her rope with an abusive husband, but she doesn't expect him to spontaneously combust.

The Department of Political Science didn't let remote learning stop Coffee & Conversation, an event series that invites the UM-Flint community to discuss current issues with faculty. On Nov. 11, they held a virtual election debrief, facilitating dialogue on the presidential election process. Many Political Science faculty have also contributed their expertise to media coverage of the election season; Lecturer IV Kim Saks-McManaway provided insight on election vote counts and Associate Professor Jason Kosnoski shed light on possible timelines for election results.

Our student chapter of the American Society of Mechanical Engineers designed, built, and tested an original drone design, in preparation for the national IAM3D competition. The pandemic forced the competition online, but they weren't deterred. The team developed a video showcasing their design process, earning them second place in just their second year competing.

In Shelley Spivack's CRJ 388/588: Corrections A Critical Perspective course, socially distanced learning has not stopped community leaders and working professionals from enhancing the experience for students. Among the guest speakers this year were Judge Mark Latchana of the 7th Circuit Court, Judge Jessica Hammon of 67th District Court, Leon El- Amin from the M.A.D.E. Institute, Dr. Denise Smith Allen, a retired state probation officer, and Chad Sharpe, Director of the Genesee Valley Regional Center.

36 high school teams competed in UM-Flint's High School Programming Competition, hosted by Computer Science & Information Systems. The event took place virtually in May despite the pandemic preventing in-person meetings. The high school competitors were treated to a keynote address from Dr. Mark Guzdial of UM-Ann Arbor.

Created by Assistant Professor of Biochemistry Besa Xhabija, the "Keeping COVID-19 Out of Flint" initiative provided both the protective equipment and knowledge necessary to help slow the spread of COVID-19. Xhabija collaborated with recent graduate Miguel Strawn to create informational videos and pamphlets. Miguel managed the delivery of 300 care packages containing masks, gloves, and soap to Flint Residents.

The 61,00 sq. ft. Expansion to the Murchie Science Building is on track to open in winter semester 2021. The MSB Expansion not only enhances the experience for STEM majorslearners in all disciplines will enjoy the benefits of a space that features a student-centered design that removes barriers to instruction.

Stay tuned for ten more innovations in part two of this series.

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20 ways UM-Flint CAS innovated in 2020 (Part 1) - University of Michigan Flint News

Immunicum AB (publ) Provides Additional Information on the Proposed Transaction and Virtual Investor Event Summary – GlobeNewswire

Press Release

8 December 2020

Immunicum AB (publ) Provides Additional Information on the Proposed Transaction and Virtual Investor Event Summary

Immunicum AB (publ; IMMU.ST) provided today an overview and details on the topics to be covered during the previously announced Investor Event regarding the proposed combination between Immunicum and DCprime. The live presentation and Q&A session will be led by members of the Immunicum and DCprime management teams during the webcast tomorrow, Wednesday, December 9th at 3.00 pm CET. To view the livestream of the event, click here: https://bit.ly/36V9VAQ

Questions can be sent before and during the event to ir@immunicum.com. The presentation is now available on Immunicums website.

The business combination with DCprime is a rare and exciting opportunity through which we gain improved control of the entire value chain of development for ilixadencel while adding a complementary clinical-stage program to our pipeline. This transaction is an essential step to generating shareholder value, commented Sven Rohmann, MD, Ph.D., CEO of Immunicum. Through this additional information and tomorrows Investor Event, our objective is to provide a more extensive overview of this proposed transaction to the Immunicum shareholders. Speaking for the combined leadership, we are convinced that this is a truly transformative opportunity for the Company.

Merger RationaleAs announced on November 18th, combining forces with DCprime will establish a leading company built on decades of combined immuno-oncology and cell therapy expertise in the field of allogeneic dendritic cell biology.

Building a Fully Integrated Company & Leveraging Value

Complementary Organizations & Clinical Pipeline

Broadening Shareholder Base & Financing

Transaction Process

Next Steps

Scientific BackgroundFrom a scientific perspective, both Immunicum and DCprime share the therapeutic approach of using allogeneic, off-the-shelf dendritic cell biology to enable a patients immune system to more effectively fight cancer.

Cancer Treatment in the Age of Immunotherapy

Dendritic Cells, Immunicum & DCprime

Clinical Pipeline UpdateThe combination of Immunicum and DCprime will enable the newly unified organization to advance a synergistic pipeline spanning both large and orphan indications in solid as well as blood-borne tumors, with two programs in Phase II clinical development and multiple near-term value inflection points as well as a portfolio of preclinical programs and research capabilities to fuel future pipeline expansion.

Combined Pipeline Overview & Upcoming Clinical Milestones

ASH Oral Presentation Update

Pipeline Expansion Opportunities

Transaction SummaryThe business combination of Immunicum and DCprime is first and foremost based on the shared and unique biology of allogeneic, off-the-shelf dendritic cell-based therapies and the complementary therapeutic approaches of intratumoral priming and cancer relapse vaccination. From this foundation, the unified company can build and expand a strong pipeline in solid and blood-borne tumors which will establish Immunicums position as a leading cell therapy player. This pipeline will also facilitate near- and long-term clinical development progress and value creation.

In addition, as two synergistic organizations, Immunicum and DCprime will bring together and further develop strong in-house research and process development capabilities.

Van Herk and AP4, two leading institutional investors, have expressed their support to the combined entity.

For more information, please contact:

Sven Rohmann, MD, Ph.D., CEOTelephone: +46 8 732 8400E-mail: info@immunicum.com

Investor Relations

Jonas Rodny and Carolin WikenPaues berg CommunicationsTelephone: +46 190 90 51 E-mail:ir@immunicum.com

Media Relations

Joanne Tudorica and Sophia Hergenhan, Ph.D.Trophic CommunicationsTelephone: +49 171 351 2733E-mail:ir@immunicum.com

About Immunicum AB (publ)

Immunicum is establishing a unique immuno-oncology approach through the development of allogeneic, off-the-shelf cell-based therapies. Our goal is to improve survival outcomes and quality of life by priming the patients own immune system to fight cancer. The Companys lead product ilixadencel, consisting of pro-inflammatory allogeneic dendritic cells, has the potential to become a backbone component of modern cancer combination treatments in a variety of solid tumor indications. Immunicum has evaluated ilixadencel in several clinical trials including the recently completed exploratory Phase II MERECA study in kidney cancer and the Company is moving towards late-stage clinical development. Founded and based in Sweden, Immunicum is publicly traded on the Nasdaq Stockholm. http://www.immunicum.com

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Immunicum AB (publ) Provides Additional Information on the Proposed Transaction and Virtual Investor Event Summary - GlobeNewswire

Enara Bio relocates to The Oxford Science Park’s newest facility to expand R&D capabilities in the search for novel cancer immunotherapies -…

Oxford and London, UK 9th December 2020. Enara Bio, a biotechnology company leveraging its proprietary T-cell/T-cell receptor (TCR) discovery and Dark Antigen platforms to deliver targeted cancer immunotherapies, announces its expansion and move to the new Bellhouse Building at The Oxford Science Park. Enara Bios move from the Oxford BioEscalator to one of the UK's largest biomedical innovation centres is in preparation for its future growth and ambition to transform cancer care. The dedicated research facility will enable the company to accelerate the preclinical development of its lead MR1-targeting T-cell therapy program while continuing to drive the discovery of novel cancer antigens and TCRs for immunotherapy.

The move, which will see the company occupy over 5,000 sq. ft of office and laboratory space in the Bellhouse Building, is a key milestone in Enara Bios growth and development. The purpose-built facility will enable Enara Bio to bring together key personnel with world-leading capabilities in bioinformatics, immunopeptidomics, cell therapy process development, and immunology to discover and develop novel TCR-based immunotherapies.

Kevin Pojasek, President and CEO of Enara Bio, said:

We are delighted to be expanding and moving into The Oxford Science Park. As pioneers of TCR-directed T-cell immunotherapies, it seems fitting that we will be the first occupier of the Bellhouse Building, the parks latest, state-of-the-art facility. Our current growth is fuelled by the interest generated by our innovation platform and its transformative potential. The move will enable us to scale up our research and development efforts and hopefully realize this potential as we explore novel targets such as Dark Antigens and MR1, which hold great promise in the search for next generation cancer immunotherapies.

Piers Scrimshaw-Wright, CEO of The Oxford Science Park, added:

Enara Bios exciting work on novel immunotherapies makes it the ideal first occupier of the Bellhouse Building, named after one of the University of Oxfords earliest entrepreneurs. Professor Brian Bellhouse formed PowderJect in 1993, and based the company at The Oxford Science Park, where Enara Bio can now continue its own pioneering research. We are delighted to welcome the company to the Park and look forward to supporting its development in the coming years.

About Enara Bio

Enara Bio (formerly Ervaxx) is a science-led company targeting the T-cell/cancer-cell interface (the immune synapse) to develop new targeted cancer immunotherapies designed to treat a broad patient population. Enara Bio is exploring the hidden depths of cancer and T-cell biology to discover and characterize novel immunotherapy targets, such as Dark Antigens and MR1-presented ligands. We are pioneering approaches to exploit these targets with TCR-directed T-cell immunotherapy and therapeutic vaccines. To achieve our mission, we are leveraging our differentiated Dark Antigen and TCR discovery platforms that integrate bioinformatics, immunopeptidomics, metabolomics and immunology in our Oxford, UK-based research lab. Enara Bio is backed by leading life science investors, including SV Health Investors. We have partnerships with world-class academic institutions, including the Francis Crick Institute, Cardiff University, Johns Hopkins School of Medicine and the University of Oxford, to help drive the leading edge of these new areas of science.

For more information visit: http://www.enarabio.com

About The Oxford Science Park

The Oxford Science Park is owned and managed by Magdalen College, Oxford. Created in 1991, the Park upholds the Colleges heritage and provides one of the most influential science & technology environments in the UK. There is approaching 750,000 square feet of workspace accommodation across the Park, which is now home to 2,700 people and more than 130 businesses. These range from start-ups based in the Magdalen Centre innovation hub to major international companies and include Blue Earth Diagnostics, MiroBio, OrganOx, OxSonics Therapeutics, Oxford Nanopore Technologies, OXGENE, ProImmune, Oxford Sciences Innovation, Evox Therapeutics, Vaccitech, Exscientia, Sensyne Health and Intuitive Surgical.

In addition to being a key property investment, the Park is at the heart of Magdalen College's strategy to support discovery, innovation and entrepreneurship. It will continue to develop The Oxford Science Park as a long-term strategic asset, with ambitious plans to create an additional 500,000+ sq ft of office and laboratory space on the remaining 12 acres of land over the next 3-5 years. This additional capacity will support the growth of businesses already based on the Park, providing flexible workspace accommodation, and enabling new companies to enjoy the Parks exceptional environment and collegiate and collaborative ethos. The Oxford Science Park is located approximately four miles south-east of Oxford city centre, just off the Citys southern ring road. It has easy access to the M40 and A34, as well as to Heathrow Airport and mainline train services. For further information, please visit: http://www.oxfordsp.com or follow us on twitter @OxfordSciencePK

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Enara Bio relocates to The Oxford Science Park's newest facility to expand R&D capabilities in the search for novel cancer immunotherapies -...

University researchers scoop over 4 million in EU funding competition – Deadline News

A SCOTTISH university projects have been awarded millions in a prestigious EU funding competition.

Two projects led by the University of Dundee researchers were awarded 4m by the European Research Council (ERC).

The grant was awarded as part of the Consolidator Grant competition as part of universities frontier research in life sciences.

Dr Yogesh KulathuandDr Jorunn Bos, both of the UniversitysSchool of Life Sciences, have been awarded the grants for their research projects that look to investigate unexplored areas of cell biology and explore novel ways to provide plant protection, respectively.

Dr Kulathus project, StressHUb, aims to gain insights into the fundamental principles regulating stress at the cellular level.

The 2.1 million ERC funding will enable Dr Kulathu and his colleagues to develop new technologies and methodologies for use in understanding how unresolved stress results in disease.

The cells of the human body are constantly exposed to stresses, such as UV light and carcinogens, heat, and metabolic stresses.

Cells use intricate intracellular signalling pathways to translate these environmental challenges into appropriate cellular responses.

Currently, these signals and the reasons why they go wrong in disease are poorly understood due to the lack of tools and methods to study them.

Dr Kulathu, MRC Investigator and Group Leader at the Medical Research Council Protein Phosphorylation and Ubiquitylation Unit (MRC PPU), said, We are studying almost unexplored areas of cell biology which has immense potential for ground-breaking discoveries.

StressHUb will explore the functions of branched heterotypic ubiquitin chains (HUbs) in cellular stress responses.

These branched HUbs play important roles in the physiology of human cells, however, their functions have not been defined because of the complex nature of these modifications and the lack of ways to study them.

We will develop novel tools and methodologies which will reveal the cellular machinery that makes these modifications, how they are formed in response to stress, and their roles in resolving cellular stress.

This knowledge can then be used to develop drugs to treat various diseases where cellular stress is not resolved, such as neurodegeneration, chronic inflammatory diseases and cancer.

Dr Bos, a principal investigator in the Division of Plant Sciences and the James Hutton Institute based in Invergowrie, and her project, APHIDTRAP, will explore and develop new ways to provide crop protection against insects.

The grant, worth almost 2 million, will allow her research team to take new directions to answer important questions on how insects such as greenfly and blackfly, commonly known as aphids, are such successful pests.

Current aphid control relies almost exclusively on insecticides, which are costly, damaging to the environment and to which aphids develop resistance.

Dr Bos and her team are interested in understanding the molecular dialogue that takes place between plants and aphids to come up with new solutions.

Dr Bos said:This project is building on years of work by members of my team, past and present, and without them this would not have been possible,

The key questions that drive APHIDTRAP are building on previous findings that aphids can actively promote host susceptibility using effector proteins. The function of these effector proteins is based on association with host proteins and modification of their activity.

The next step is to try and understand how these protein-protein interactions take place, and what the downstream consequences are with regards to susceptibility.

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University researchers scoop over 4 million in EU funding competition - Deadline News

Cytovia Therapeutics announces plans to initiate in 2021 Clinical Development of Universal iPSC NK Cell Therapy for Hematological and Solid Tumors -…

CAMBRIDGE, Mass., Dec. 08, 2020 (GLOBE NEWSWIRE) -- Cytovia Therapeutics, an emerging NK cell therapeutics company, announced today that it plans to file with the FDAin 2021an Investigational New Drug (IND) application and initiate clinical trials in hematological and solid tumors with its Universal iPSC NK cell therapy (U-iNK).

Cytovia's CEO, Dr. Daniel Teper commented: "Cytovia is among a select group of biotech companies developing Gene Edited iPSC NK and CAR NK cell therapeutics. We are aiming to be, in 2021, the second company to initiate clinical trials with an iPSC NK product. We are enthusiastic about the potential of U-iNK to prevent relapse in Acute Myeloid Leukemia, and in combination with PD1/ PDL-1 inhibitors and our own NK engager bispecific antibodies, to improve outcomes in solid tumors starting with hepatocellular carcinoma."

Cytovia will participate in the RBC Capital Markets Healthcare Private Company Conference on December 15-16, 2020. Daniel Teper, PharmD, CEO, Wei Li, PhD, CSO and Kaouthar Lbiati, MD, VP, Product Strategy will take part in a Fireside chat with RBC's Senior Analyst, Gregory Renza, MD, on December 16, 2020 at 10am ET. A link to the discussion will be available on Cytovias website and social media channels.

About Cytovia TherapeuticsCytovia Therapeutics Inc is an emerging biotechnology company that aims to accelerate patient access to transformational immunotherapies, addressing several of the most challenging unmet medical needs in cancer. Cytovia focuses on Natural Killer (NK) cell biology and is leveraging multiple advanced patented technologies, including an induced pluripotent stem cell (iPSC) platform for CAR (Chimeric Antigen Receptors) NK cell therapy, next-generation precision gene-editing to enhance targeting of NK cells, and NK engager multi-functional antibodies. Our initial product portfolio focuses on both hematological malignancies such as multiple myeloma and solid tumors including hepatocellular carcinoma and glioblastoma. The company partners with the University of California San Francisco (UCSF), the New York Stem Cell Foundation (NYSCF), the Hebrew University of Jerusalem, INSERM, and CytoImmune Therapeutics.

Learn more atwww.cytoviatx.comand follow Cytovia Therapeutics on Social MediaFacebook,LinkedIn,Twitter, Youtube

For more information, please contact:

Cytovia Therapeutics, IncSophieBadrVice President, Corporate Affairssophie.badre@cytoviatx.comCell: 1 (929) 317 1565

Anna Baran-DjokovicVice President, Investor Relationsanna@cytoviatx.comVP Investor RelationsCell: +44 7521083006

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Cytovia Therapeutics announces plans to initiate in 2021 Clinical Development of Universal iPSC NK Cell Therapy for Hematological and Solid Tumors -...

Bateman, Diamond, Hultgren named to National Academy of Inventors – Washington University School of Medicine in St. Louis

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School of Medicine scientists honored for innovation

Washington University School of Medicine in St. Louis faculty members (left to right) Randall J. Bateman, MD, Michael S. Diamond, MD, PhD, and Scott Hultgren, PhD, have been elected fellows of the National Academy of Inventors.

Neurologist Randall J. Bateman, MD, virologist and immunologist Michael S. Diamond, MD, PhD, and microbiologist Scott Hultgren, PhD all faculty members at Washington University School of Medicine in St. Louis have been named fellows of the National Academy of Inventors, the highest professional distinction accorded solely to academic inventors.

They are among 175 new fellows elected this year in recognition of their innovation in creating and facilitating outstanding inventions that have made a tangible impact on quality of life, economic development and the welfare of society. They will be honored at a ceremony during the academys annual meeting in June in Tampa, Fla.

Randall J. Bateman

Bateman, the Charles F. and Joanne Knight Distinguished Professor of Neurology, is being recognized for his pioneering work in diagnostics and clinical treatment for Alzheimers disease. His research into techniques to detect molecular signs of Alzheimers has led to the first blood test approved under the Clinical Laboratory Improvement Amendments (CLIA), to aid in the diagnosis of Alzheimers. The aim of the CLIA program, under the Centers for Medicare & Medicaid Services, is to ensure quality laboratory testing in people. The Alzheimers test, made by the startup company C2N Diagnostics, became available to patients and physicians in October.

Bateman co-founded C2N in 2007 with David Holtzman, MD, the Andrew B. and Gretchen P. Jones Professor and head of theDepartment of Neurology, to provide a technology the two had developed called SILK, or stable isotope labeling kinetics. The technology measures the breakdown and synthesis rates of neurological proteins important in Alzheimers disease, such as amyloid beta, tau and others, data that can be crucial for evaluating the effectiveness of potential Alzheimers drugs. Multiple large pharma companies have partnered with C2N to use SILK to help assess drugs in clinical development.

More recently, Bateman has focused on developing sensitive techniques for detecting Alzheimers proteins in blood. The approved blood test is based on identifying the presence of amyloid beta, but he also is working on a promising blood test for tau.

Bateman earned his bachelors degree at Washington University in 1996, and his medical degree at Case Western Reserve University School of Medicine in Cleveland in 2000. He completed his residency at Barnes-Jewish Hospital and a clinical fellowship at Washington University School of Medicine before joining the faculty in 2005.

His many honors include the Chancellors Award for Innovation and Entrepreneurship, the MetLife Award in Medical Research and the Potamkin Prize for Research in Picks, Alzheimers, and Related Diseases, an international recognition sometimes referred to as the Nobel Prize for Alzheimers research. He is an elected fellow of the National Academy of Medicine.

Michael S. Diamond

Diamond, the Herbert S. Gasser Professor of Medicine, a professor of molecular microbiology, and of pathology and immunology, is being recognized for his accomplishments developing research tools and drug and vaccine candidates for emerging viruses such as West Nile, dengue, chikungunya, Zika and SARS-CoV-2, the virus that causes COVID-19.

Most recently, Diamond developed research tools to aid the international search for treatments and preventives for COVID-19, including a mouse model for COVID-19. He helped identify antibodies that are undergoing clinical testing as potential drugs for COVID-19, and developed two vaccine candidates that have shown promise in animal studies, one of which soon will be the focus of a vaccine trial in people.

During the Zika epidemic, Diamond helped develop the first mouse model and the first pregnant mouse model of Zika infection, enabling research into the devastating neurological damage seen in the fetuses of infected pregnant women. He conducted pivotal preclinical studies to advance a Zika vaccine, and identified antibodies against Zika virus that led to two novel diagnostic tests to detect Zika virus in patients.

Diamond earned his medical and doctoral degrees from Harvard in 1994. After completing a research fellowship in molecular and cell biology at the University of California, Berkeley, Diamond moved to the University of California, San Francisco, where he completed his residency in internal medicine and a clinical fellowship in infectious diseases. He returned to Berkeley to complete another research fellowship in infectious diseases in 2001, before joining Washington University School of Medicine that year.

Diamond is an elected fellow or member of the American Association for the Advancement of Science, the American Society for Clinical Investigation, the American Academy of Microbiology, the Association of American Physicians and the National Academy of Medicine.

Scott Hultgren

Hultgren, the Helen L. Stoever Professor of Molecular Microbiology, is being recognized for his pioneering research in nonantibiotic treatments and preventives for urinary tract infections (UTIs), one of the most common infections in women.

Current therapies use antibiotics to kill bacteria in the urinary tract, but they are often ineffective and can promote drug resistance. Hultgren discovered bacterial and host mechanisms that determine the onset, course and outcome of UTIs, including discovering how E. coli bacteria evade the immune system and form stable, protected bacterial communities known as biofilms. This work has led to the identification of alternative therapies based on preventing bacteria from causing disease without killing them, such as compounds that target bacterial attachment to human tissues. His work also has led to an investigational vaccine that has completed phase 1a/1b clinical trials and has been allowed by the U.S. Food and Drug Administration (FDA) for compassionate use in patients with multidrug-resistant UTI caused by E. coli.

Hultgren co-founded Fimbrion Therapeutics, which is developing decoy sugars known as mannosides as nonlethal antimicrobials to eliminate bacteria from the urinary tract. These compounds are in phase 1 clinical trials. He is also a cofounder of Quretech Bio, which is working to develop first-line drugs to combat infectious diseases and prevent antibiotic resistance.

Hultgren earned his doctoral degree from Northwestern University in 1987 before moving to Sweden to do postdoctoral research under Staffan Normark, PhD, at the University of Ume. Normark joined Washington University as head of the molecular microbiology department in 1989 and recruited Hultgren to join the faculty later that same year.

Hultgren holds 22 U.S. patents and has four pending patent applications. His many honors and awards include the Eli Lilly Microbiology Award and election to the National Academy of Medicine, the National Academy of Sciences and the American Association for the Advancement of Science.

Washington University School of Medicines 1,500 faculty physicians also are the medical staff of Barnes-Jewish and St. Louis Childrens hospitals. The School of Medicine is a leader in medical research, teaching and patient care, ranking among the top 10 medical schools in the nation by U.S. News & World Report. Through its affiliations with Barnes-Jewish and St. Louis Childrens hospitals, the School of Medicine is linked to BJC HealthCare.

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Bateman, Diamond, Hultgren named to National Academy of Inventors - Washington University School of Medicine in St. Louis