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Page 1
Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M.
Bakker ST, van de Vrugt HJ, Rooimans MA, Oostra AB, Steltenpool J, Delzenne-Goette E, van der Wal A, van der Valk M, Joenje H, te Riele H, de Winter JP. Bakker ST, et al. Among authors: steltenpool j. Hum Mol Genet. 2009 Sep 15;18(18):3484-95. doi: 10.1093/hmg/ddp297. Epub 2009 Jun 26. Hum Mol Genet. 2009. PMID: 19561169
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. Among authors: steltenpool j. Blood. 2004 Apr 1;103(7):2498-503. doi: 10.1182/blood-2003-08-2915. Epub 2003 Nov 20. Blood. 2004. PMID: 14630800 Free 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: steltenpool j. Nat Genet. 2005 Sep;37(9):934-5. doi: 10.1038/ng1625. Epub 2005 Aug 21. Nat Genet. 2005. PMID: 16116423
The nuclear accumulation of the Fanconi anemia protein FANCE depends on FANCC.
Léveillé F, Ferrer M, Medhurst AL, Laghmani el H, Rooimans MA, Bier P, Steltenpool J, Titus TA, Postlethwait JH, Hoatlin ME, Joenje H, de Winter JP. Léveillé F, et al. Among authors: steltenpool j. DNA Repair (Amst). 2006 May 10;5(5):556-65. doi: 10.1016/j.dnarep.2006.01.005. Epub 2006 Feb 28. DNA Repair (Amst). 2006. PMID: 16513431
Evidence for subcomplexes in the Fanconi anemia pathway.
Medhurst AL, Laghmani el H, Steltenpool J, Ferrer M, Fontaine C, de Groot J, Rooimans MA, Scheper RJ, Meetei AR, Wang W, Joenje H, de Winter JP. Medhurst AL, et al. Among authors: steltenpool j. Blood. 2006 Sep 15;108(6):2072-80. doi: 10.1182/blood-2005-11-008151. Epub 2006 May 23. Blood. 2006. PMID: 16720839 Free PMC article.
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: steltenpool j. Cell Oncol. 2007;29(3):211-8. doi: 10.1155/2007/151968. Cell Oncol. 2007. PMID: 17452773 Free PMC article.
Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M.
Singh TR, Bakker ST, Agarwal S, Jansen M, Grassman E, Godthelp BC, Ali AM, Du CH, Rooimans MA, Fan Q, Wahengbam K, Steltenpool J, Andreassen PR, Williams DA, Joenje H, de Winter JP, Meetei AR. Singh TR, et al. Among authors: steltenpool j. Blood. 2009 Jul 2;114(1):174-80. doi: 10.1182/blood-2009-02-207811. Epub 2009 May 7. Blood. 2009. PMID: 19423727 Free PMC article.
Isolation of a cDNA representing the Fanconi anemia complementation group E gene.
de Winter JP, Léveillé F, van Berkel CG, Rooimans MA, van Der Weel L, Steltenpool J, Demuth I, Morgan NV, Alon N, Bosnoyan-Collins L, Lightfoot J, Leegwater PA, Waisfisz Q, Komatsu K, Arwert F, Pronk JC, Mathew CG, Digweed M, Buchwald M, Joenje H. de Winter JP, et al. Among authors: steltenpool j. Am J Hum Genet. 2000 Nov;67(5):1306-8. doi: 10.1016/S0002-9297(07)62959-0. Epub 2000 Sep 19. Am J Hum Genet. 2000. PMID: 11001585 Free PMC article.
12 results