Related Experiment Videos

NRAS hypermutability in familial melanoma with CDKN2A mutations--cause and effect?

Kenneth H Kraemer

Journal of the National Cancer Institute

|June 5, 2003

Abstract

No abstract available in PubMed .

Related Concept Videos

Articles linked to this work by shared authors, journal, and citation graph.

RNA Lariat-Debranching Enzyme (DBR1) Variations in Sabinas Brittle Hair Syndrome Form of Trichothiodystrophy: A Trichothiodystrophy-Causing Gene.

The Journal of investigative dermatology·2025

Co-infection of HSV-1 amplicons containing the XPC gene and a human artificial chromosome vector into primary XPC deficient fibroblast cells.

Biochemistry and biophysics reports·2024

Different germline variants in the XPA gene are associated with severe, intermediate, or mild neurodegeneration in xeroderma pigmentosum patients.

PLoS genetics·2024

Retrospective study of efficacy and adverse events of immune checkpoint inhibitors in 22 xeroderma pigmentosum patients with metastatic or unresectable cancers.

Frontiers in oncology·2023

Debilitating hip degeneration in trichothiodystrophy: Association with ERCC2/XPD mutations, osteosclerosis, osteopenia, coxa valga, contractures, and osteonecrosis.

American journal of medical genetics. Part A·2022

Trichothiodystrophy hair shafts display distinct ultrastructural features.

Experimental dermatology·2022

See all related articles