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New targeted agent achieves impressive response rate in trial with patients with uterine serous carcinoma

Date Time New targeted agent achieves impressive response rate in trial with patients with uterine serous carcinoma In its first clinical trial in patients with a hard-to-treat form of uterine cancer, a targeted drug that subjects tumor cells to staggering levels of DNA damage caused tumors to shrink in nearly one-third of patients, investigators at Dana-Farber Cancer Institute reported. The results of a phase 2 study published today in the Journal of Clinical Oncology showed that a WEE1-direct...
United States Joyce Liu Dana Farber Cancer Institute Astrazeneca Externally Sponsored Research American Cancer Society Clinical Oncology

Spike protein mutations in SARS-CoV-2 variants help resist antibody neutralization

Researchers based in Beijing and Shenzhen, China, report that they have identified mutations in the spike protein of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that may allow variant strains to avoid neutralization by monoclonal antibodies and convalescent blood plasma.
South Africa United Kingdom South African Michael Burgessmar Michael Burgess Sars Cov 2

Structure and function of locked conformation of the SARS-CoV-2 spike protein identified

A new preprint research paper, posted to the bioRxiv* server, uncovered more information on the different structural conformations of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The findings suggest the spike protein turns into a locked state to stabilize the spike protein during virus egress.
Jocelyn Solis Moreiramar Jocelyn Solis Moreira Sars Cov 2 Spike Protein Corona Virus Coronavirus Disease Covid 19

A simple step to enhance CRISPR-Cas9 genome editing

Kyoto University The Hotta lab shows that protection from cellular RNA enhances the genome editing of iPS cells. The ability for scientists to edit human genomic DNA has been around for decades. Such research has revealed how a single mutation in just one of the billions of base pairs in the human genome can cause destructive diseases. In the past decade, advances in CRISPR-Cas9 technology have taken DNA editing a major step farther and promise to revolutionize regenerative medicine. One of t...
Takahiro Iguchi Peter Gee Miyuki Ono Akitsu Hotta Yuto Kita Huaigeng Xu

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Opinion: A postpandemic summer? Not this year

The Globe and Mail Bookmark Please log in to listen to this story. Also available in French and Mandarin. Log In Create Free Account Getting audio file ... This translation has been automatically generated and has not been verified for accuracy. Full Disclaimer To scientists in Oregon, it was as unsettling a discovery as there has been in the last year: a homegrown version of a highly transmissible COVID-19 variant that first surfaced in Britain last year. Only this one came with a mutat...
New York United States United Kingdom South Africa City Of South African

The E484K mutation - a 'backdoor' to undoing vaccine efforts - Mar 10 2021 - Professor Martin Michaelis and Dr Mark Wass - Life Science News Articles

Mar 11 2021 Read 1487 Times Author: Professor Martin Michaelis and Dr Mark Wass on behalf of University of Kent Free to read Unlock As we are seeing many novel Covid-19 variants around the world, Professor Martin Michaelis and Dr Mark Wass of University of Kent’s School of Biosciences explain why this may be happening and what these new variants may mean: ‘After almost a year, in which SARS-CoV-2, the coronavirus that causes COVID-19, has not seemed to change its propert...
South Africa United Kingdom South African Martin Michaelis Jindrich Cinatl Goethe Professor Martin Michaelis

Novel CRISPR-based gene editor developed to correct mutations that cause genetic disorders

Novel CRISPR-based gene editor developed to correct mutations that cause genetic disorders A team of researchers from the Agency for Science, Technology and Researchs (A*STAR) Genome Institute of Singapore (GIS) have developed a CRISPR-based gene editor, C-to-G Base Editor (CGBE), to correct mutations that cause genetic disorders. Their research was published in Nature Communications on 2 March 2021. One in seventeen people in the world suffers from some type of genetic disorder. Chances are, ...
Kwei Leong Emily Henderson Agency For Science Genome Institute Of Singapore Nature Communications Senior Research Scientist

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