Results 201 to 210 of about 84,383 (263)

Comprehensive whole-genome sequencing reveals origins of mutational signatures associated with aging, mismatch repair deficiency and temozolomide chemotherapy. [PDF]

open access: yesNucleic Acids Res
Hwang T   +13 more
europepmc   +1 more source

Unravelling the instability of mutational signatures extraction via archetypal analysis. [PDF]

open access: yesFront Genet, 2022
Pancotti C   +5 more
europepmc   +1 more source

An Exon Signature to Estimate the Tumor Mutational Burden of Right-sided Colon Cancer Patients [PDF]

open access: gold, 2019
Wenbing Guo   +9 more
openalex   +1 more source

PCSK9 Promotes the Malignancy of Triple‐negative Breast Cancer Cells by Reducing Cholesterol Levels at the Plasma Membrane to Activate EGFR and HER3

open access: yesAdvanced Science, EarlyView.
By decreasing cholesterol and lipid raft levels in the plasma membrane, proprotein convertase subtilisin/kexin type 9 (PCSK9) boosts human epidermal growth factor receptor 1 and 3 (EGFR and HER3) activation, driving tumor growth and metastasis in triple‐negative breast cancer (TNBC).
Tianhong Li, Renfei Wu, Kathy Qian Luo
wiley   +1 more source

Mutational signatures in upper tract urothelial carcinoma define etiologically distinct subtypes with prognostic relevance [PDF]

open access: green, 2019
Xuesong Li   +15 more
openalex   +1 more source

AAVR Expression is Essential for AAV Vector Transduction in Sensory Hair Cells

open access: yesAdvanced Science, EarlyView.
Decreased sensitivity to AAV vector transduction in the outer hair cells (OHCs) of adult mice is primarily attributed to reduction of AAVR (Kiaa0319l; Au040320). Knockout of AAVR reduces AAV vector transduction efficiency in both inner hair cells (IHCs) and OHCs in neonatal mice.
Fan Wu   +8 more
wiley   +1 more source

GDC: Integration of Multi‐Omic and Phenotypic Resources to Unravel the Genetic Pathogenesis of Hearing Loss

open access: yesAdvanced Science, EarlyView.
Overview of the Genetic Deafness Commons (GDC), integrating data from the Chinese Deafness Genetics Consortium (CDGC) and 51 public databases. The GDC provides tools for variant search, functional predictions, and gene‐disease visualization, offering insights into 201 hearing loss genes and facilitating novel gene discovery and clinical applications ...
Hui Cheng   +11 more
wiley   +1 more source

Mutational signatures of colorectal cancers according to distinct computational workflows. [PDF]

open access: yesBrief Bioinform
Battuello P   +8 more
europepmc   +1 more source

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