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Reposted by Günter Schneider
Lyssiotis Lab
@lyssiotislab.bsky.social
· Aug 28
Assistant/Associate Professor - Tenure Track - Physiology - University of Michigan, Ann Arbor job with University of Michigan Department of Molecular & Integrative Physiology | 674815
Tenure track assistant/associate professor in the Department of Molecular & Integrative Physiology at the University of Michigan Medical School.
jobs.sciencecareers.org
Reposted by Günter Schneider
Reposted by Günter Schneider
Quinn Sievers
@quinnsievers.bsky.social
· Jul 27
A neomorphic protein interface catalyzes covalent inhibition of RASG12D aspartic acid in tumors
Mutant RAS proteins are among the most prevalent drivers of human cancer, and the glycine to aspartic acid mutation at codon 12 (G12D) is the most common variant. Mutation-selective covalent inhibitor...
www.science.org
Reposted by Günter Schneider
Lyssiotis Lab
@lyssiotislab.bsky.social
· Jul 18
Lyssiotis awarded Stephenson Global Scholar Grant for pancreatic cancer research
Costas Lyssiotis, Ph.D., co-director of the Rogel and Blondy Center for Pancreatic Cancer at the Rogel Cancer Center, was one of six researchers to receive inaugural grants from the Stephenson Global ...
michmed.org
Günter Schneider
@schneiderg.bsky.social
· Jan 29
Reposted by Günter Schneider
Günter Schneider
@schneiderg.bsky.social
· Dec 28
KRAS inhibitors: resistance drivers and combinatorial strategies
In 1982, the RAS genes HRAS and KRAS were discovered as the first human cancer genes, with KRAS later identified as one of the most frequently mutated oncogenes. Yet, it took nearly 40 years to develop clinically effective inhibitors for RAS-mutant cancers. The discovery in 2013 by Shokat and colleagues of a druggable pocket in KRAS paved the way to FDA approval of the first covalently binding KRASG12C inhibitors, sotorasib and adagrasib, in 2021 and 2022, respectively. However, rather than marking the end of a successful assault on the Mount Everest of cancer research, this landmark only revealed new challenges in RAS drug discovery. In this review, we highlight the progress on defining resistance mechanisms and developing combination treatment strategies to improve patient responses to KRAS therapies.
www.cell.com
Reposted by Günter Schneider
Reposted by Günter Schneider
Reposted by Günter Schneider
Hans Clevers
@hansclevers.bsky.social
· Dec 3
Long-term in vitro expansion of a human fetal pancreas stem cell that generates all three pancreatic cell lineages
Identification of an LGR5 as a marker for a tripotent stem/progenitor cell of the
human fetal pancreas. Organoids derived from single LGR5+ cells are capable of long-term
expansion in vitro and genera...
www.cell.com
Reposted by Günter Schneider
Reposted by Günter Schneider
Dan Nomura
@dannomura.bsky.social
· Nov 28
An engineered cereblon optimized for high throughput screening and molecular glue discovery
Due to challenges in studying molecular interactions of CRBN, identification of CRBN
based molecular glues has remained underexplored. Here, Bailey et al designed an easy-to-handle
CRBN construct and ...
www.cell.com
Reposted by Günter Schneider
Günter Schneider
@schneiderg.bsky.social
· Nov 25