Work

Inactivation of Murine Usp1 Results in Genomic Instability and a Fanconi Anemia Phenotype

Year: 2009

Type: article

Source: Developmental Cell

DOI: 10.1016/j.devcel.2009.01.001

Authors: Jung Min Kim, Kalindi Parmar, Min Huang, David M. Weinstock, Carrie Ann Ruit, Jeffrey L. Kutok, Alan D. D'Andrea

Institutions: Harvard University, Dana-Farber Cancer Institute, Brigham and Women's Hospital

Language: English

Topic: DNA Repair Mechanisms

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: National Institutes of Health, U.S. Public Health Service, National Heart, Lung, and Blood Institute, National Institute of Allergy and Infectious Diseases, National Institute of Diabetes and Digestive and Kidney Diseases

Awards: G2097853161, Regulation of the Fanconi Anemia Pathway by Ubiquitination, Centers for Medical Countermeasures Against Radiation, Molecular Pathogenesis of Fanconi Anemia, Abnormalities/Signal Transduction/Hematopoietic Disease, G7167773382, G9000105278, G9000272554, G9000341670, Molecular Pathogenesis of Fanconi Anemia

OpenAlex ID: W1987871280

FWCI: 8.58

Cites: 32

Cited by: 248

Related to: 10