Results 191 to 200 of about 5,289 (294)
Using mathematical constraints to explain narrow ranges for allele-sharing dissimilarities. [PDF]
Liu X, Ahsan Z, Rosenberg NA.
europepmc +1 more source
Loss of IGF‐1R impairs DNA‐PKcs recruitment to chromatin leading to defective end‐joining
IGF‐1R promotes radioresistance by facilitating DNA‐PKcs recruitment to chromatin, enabling non‐homologous end‐joining (NHEJ) repair of double‐strand breaks. Inhibition or loss of IGF‐1R disrupts this recruitment to damage sites, driving compensatory reliance on microhomology‐mediated end‐joining (MMEJ) repair.
Matthew O. Ellis +3 more
wiley +1 more source
Given two vectors of real components, we say that one vector (say u) majorizes or dominates the other vector (say v) if the components of u are more spread-out than the components of v.
Zhang, Fuzhen
core +1 more source
A Majorization-Minimization Gauss-Newton Method for 1-Bit Matrix Completion. [PDF]
Liu X, Han X, Chi EC, Nadler B.
europepmc +1 more source
gmcoda: Graphical model for multiple compositional vectors in microbiome studies. [PDF]
Fang H.
europepmc +1 more source
We identify USP29 as the only DUB mirroring CA9 expression, a marker of hypoxia and HIF pathway activation associated with PCA aggressiveness. USP29 stabilizes HIF‐1α and HIF‐2α via a noncanonical mechanism that is independent of PHD/pVHL activity yet relies on proteasomal regulation, establishing USP29 as a previously unrecognized regulator of hypoxic
Amelie S Schober +16 more
wiley +1 more source
Enhanced Inversion for Distributed Acoustic Sensing: A Robust Approach with HOLp-OGS Regularization. [PDF]
Xu W, Li J, Wu Y, Geng W, Gao B, Han L.
europepmc +1 more source
Finding novel vulnerabilities of hypomorphic BRCA1 alleles
Synthetic lethality screens performed to identify novel vulnerabilities often model complete gene loss, thereby overlooking patient‐derived hypomorphic mutations. In this study, we have performed genome‐wide CRISPR screens on BRCA1 hypomorphic mutations, showing BRCA1I26A behaves like wild‐type, while BRCA1R1699Q mimics deficiency. Furthermore, we have
Anne Schreuder +10 more
wiley +1 more source
A citation index bridging Hirsch's <i>h</i> and Egghe's <i>g</i>. [PDF]
Nuermaimaiti R, Bogachev L, Voss J.
europepmc +1 more source
MITF maintains genome stability in nonmelanocyte lineages
MITF is essential for melanocyte survival and acts as an oncogene in 10%–20% of melanomas. We show that MITF depletion causes genome instability in nonmelanocytic cells, leading to LATS2‐mediated P53 activation, cell cycle arrest, and apoptosis. This study highlights the role of MITF as a genome maintenance factor beyond the melanocyte lineage. Created
Drifa H. Gudmundsdottir +13 more
wiley +1 more source

