Fanconi-Anemia-Complementation-Group-G-Protein, page 2

Search results for Fanconi-Anemia-Complementation-Group-G-Protein

Found 49 articles. Showing from 11 to 20.

Blood (2012-07-31)
Regulation of the Fanconi anemia pathway by a CUE ubiquitin-binding domain in the FANCD2 protein.

Experimental hematology (1998-02-04)
Expression of the Fanconi anemia group C gene in hematopoietic cells is not influenced by oxidative stress, cross-linking agents, radiation, heat, or mitotic inhibitory factors.

Oncogene (2012-01-19)
Regulation of the activation of the Fanconi anemia pathway by the p21 cyclin-dependent kinase inhibitor.

Experimental hematology (2002-05-28)
Phenotypic correction of primary Fanconi anemia T cells with retroviral vectors as a diagnostic tool.

Experimental hematology (2001-07-04)
Functional analysis of patient-derived mutations in the Fanconi anemia gene, FANCG/XRCC9.

Blood (2010-11-12)
Fanconi anemia group J mutation abolishes its DNA repair function by uncoupling DNA translocation from helicase activity or disruption of protein-DNA complexes.

Experimental hematology (1999-06-14)
A patient-derived mutant form of the Fanconi anemia protein, FANCA, is defective in nuclear accumulation.

Acta haematologica (2002-11-14)
Evolutionary clues to the molecular function of fanconi anemia genes.

Experimental hematology (1999-02-25)
The Fanconi anemia group C gene product modulates apoptotic responses to tumor necrosis factor-alpha and Fas ligand but does not suppress expression of receptors of the tumor necrosis factor receptor superfamily.

British journal of haematology (2007-01-19)
Human Fanconi A cells are susceptible to TRAIL-induced apoptosis.

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