Study uncovers molecular mechanism linking nonsense-mediated RNA decay to microcephaly
News Medical » CRISPR NEWS AND RESEARCH
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2d ago
Nonsense-mediated RNA decay, or NMD, is an evolutionarily conserved molecular mechanism in which potentially defective messenger RNAs, or mRNAs (genetic material that instructs the body on how to make proteins), are degraded ..read more
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RNA editing using CRISPRs shows promise for genetic disease treatment
News Medical » CRISPR NEWS AND RESEARCH
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4d ago
A team at Montana State University published research this week that shows how RNA, the close chemical cousin to DNA, can be edited using CRISPRs ..read more
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Leveraging CRISPR/Cas technology to address antimicrobial resistance
News Medical » CRISPR NEWS AND RESEARCH
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6d ago
In the second new research review on this subject, Assistant Prof. Ibrahim Bitar, Department of Microbiology, Faculty of Medicine and University Hospital in Plzen, Charles University in Prague, Plzen, Czech Republic, will give an overview of the molecular biology of CRISPR technology in explaining how it can used to tackle antimicrobial resistance ..read more
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New research lays foundation for targeted therapies to inhibit NF-κB activation
News Medical » CRISPR NEWS AND RESEARCH
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1w ago
A new paper by Dana-Farber Cancer Institute scientists lays the foundation for targeted therapies to inhibit activation of nuclear factor kappa B (NF-κB), a transcription factor that plays a role in various autoimmune and inflammatory diseases and cancers ..read more
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Timelapse breakthrough: Scientists capture secrets of early embryonic cell division
News Medical » CRISPR NEWS AND RESEARCH
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1w ago
The beginning of life is shrouded in mystery. While the intricate dynamics of mitosis is well-studied in the so-called somatic cells – the cells that have a specialized function, like skin and muscle cells – they remain elusive in the first cells of our bodies, the embryonic cells ..read more
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CASGEVY gene therapy eliminates vaso-occlusive crises in sickle cell patients
News Medical » CRISPR NEWS AND RESEARCH
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1w ago
In a landmark study, an international consortium led by researchers at Children's Hospital of Philadelphia (CHOP) published the final results of a key clinical trial of the gene therapy CASGEVY (exagamglogene autotemcel) for the treatment of sickle cell disease in patients 12 years and older with recurrent vaso-occlusive crises (VOCs ..read more
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Researchers receive NIH grant to help develop gene therapy for HIV
News Medical » CRISPR NEWS AND RESEARCH
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1w ago
Researchers at Washington University School of Medicine in St. Louis have received a $6.2 million grant from the National Institutes of Health (NIH) to develop a gene therapy that would modify the immune system's B cells to spur them to produce broadly neutralizing antibodies against HIV ..read more
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U-M study reveals potential pathway to reverse lung fibrosis
News Medical » CRISPR NEWS AND RESEARCH
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2w ago
The most common type of lung fibrosis -; scarring of the lungs -- is idiopathic, meaning of unknown cause ..read more
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Fluent BioSciences awarded NIH SBIR grant to commercialize low-cost million-cell transcriptome profiling kits
News Medical » CRISPR NEWS AND RESEARCH
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3w ago
Fluent BioSciences, a cutting-edge life sciences company leading the charge in revolutionizing single-cell analysis through simple, cost-effective, and highly scalable single-cell RNA sequencing solutions is thrilled to announce the award of an NIH Small Business Innovation Research (SBIR) Phase II grant, funded by the National Institute of General Medical Sciences (NIGMS, 2 R44 GM137648 ..read more
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Gene defect associated with argininosuccinic aciduria corrected using CRISPR-Cas9 technique
News Medical » CRISPR NEWS AND RESEARCH
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3w ago
Argininosuccinate lyase deficiency (ASLD), also known as argininosuccinic aciduria, is a disease that has been enriched in the Finnish genetic heritage ..read more
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