Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

109 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Connecting Fanconi anemia to BRCA1.
Joenje H, Arwert F. Joenje H, et al. Nat Med. 2001 Apr;7(4):406-7. doi: 10.1038/86458. Nat Med. 2001. PMID: 11283658 No abstract available.
Identification of the Fanconi anemia complementation group I gene, FANCI.
Dorsman JC, Levitus M, Rockx D, Rooimans MA, Oostra AB, Haitjema A, Bakker ST, Steltenpool J, Schuler D, Mohan S, Schindler D, Arwert F, Pals G, Mathew CG, Waisfisz Q, de Winter JP, Joenje H. Dorsman JC, et al. Among authors: arwert f. Cell Oncol. 2007;29(3):211-8. doi: 10.1155/2007/151968. Cell Oncol. 2007. PMID: 17452773 Free PMC article.
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J.
Levitus M, Waisfisz Q, Godthelp BC, de Vries Y, Hussain S, Wiegant WW, Elghalbzouri-Maghrani E, Steltenpool J, Rooimans MA, Pals G, Arwert F, Mathew CG, Zdzienicka MZ, Hiom K, De Winter JP, Joenje H. Levitus M, et al. Among authors: arwert f. Nat Genet. 2005 Sep;37(9):934-5. doi: 10.1038/ng1625. Epub 2005 Aug 21. Nat Genet. 2005. PMID: 16116423
Multiple TPR motifs characterize the Fanconi anemia FANCG protein.
Blom E, van de Vrugt HJ, de Vries Y, de Winter JP, Arwert F, Joenje H. Blom E, et al. DNA Repair (Amst). 2004 Jan 5;3(1):77-84. doi: 10.1016/j.dnarep.2003.09.007. DNA Repair (Amst). 2004. PMID: 14697762
A key step in the pathway involves the monoubiquitylation of FANCD2, which critically depends on a multi-subunit nuclear 'core complex' of at least six FANC proteins (FANCA, -C, -E, -F, -G, and -L). ...
A key step in the pathway involves the monoubiquitylation of FANCD2, which critically depends on a multi-subunit nuclear 'core complex' of a …
Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes.
Levitus M, Rooimans MA, Steltenpool J, Cool NF, Oostra AB, Mathew CG, Hoatlin ME, Waisfisz Q, Arwert F, de Winter JP, Joenje H. Levitus M, et al. Blood. 2004 Apr 1;103(7):2498-503. doi: 10.1182/blood-2003-08-2915. Epub 2003 Nov 20. Blood. 2004. PMID: 14630800
Nine genetic subtypes have been described for FA (A, B, C, D1, D2, E, F, G, and L), all of which have been connected to distinct disease genes, except B. ...
Nine genetic subtypes have been described for FA (A, B, C, D1, D2, E, F, G, and L), all of which have been connected to distinct dise …
Evolutionary clues to the molecular function of fanconi anemia genes.
Blom E, van de Vrugt HJ, de Winter JP, Arwert F, Joenje H. Blom E, et al. Acta Haematol. 2002;108(4):231-6. doi: 10.1159/000065659. Acta Haematol. 2002. PMID: 12432219
Breast cancer and Fanconi anemia: what are the connections?
Zdzienicka MZ, Arwert F. Zdzienicka MZ, et al. Trends Mol Med. 2002 Oct;8(10):458-60. doi: 10.1016/s1471-4914(02)02411-5. Trends Mol Med. 2002. PMID: 12383764
Oxygen-dependence of chromosomal aberrations in Fanconi's anaemia.
Joenje H, Arwert F, Eriksson AW, de Koning H, Oostra AB. Joenje H, et al. Nature. 1981 Mar 12;290(5802):142-3. doi: 10.1038/290142a0. Nature. 1981. PMID: 7207594
109 results
Jump to page
Feedback