Hanenberg H - Search Results

1

A 20-year perspective on the International Fanconi Anemia Registry (IFAR).

Kutler DI, Singh B, Satagopan J, Batish SD, Berwick M, Giampietro PF, Hanenberg H, Auerbach AD. Kutler DI, et al. Among authors: hanenberg h. Blood. 2003 Feb 15;101(4):1249-56. doi: 10.1182/blood-2002-07-2170. Epub 2002 Sep 26. Blood. 2003. PMID: 12393516 Free article.

2

Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemia.

Offit K, Levran O, Mullaney B, Mah K, Nafa K, Batish SD, Diotti R, Schneider H, Deffenbaugh A, Scholl T, Proud VK, Robson M, Norton L, Ellis N, Hanenberg H, Auerbach AD. Offit K, et al. Among authors: hanenberg h. J Natl Cancer Inst. 2003 Oct 15;95(20):1548-51. doi: 10.1093/jnci/djg072. J Natl Cancer Inst. 2003. PMID: 14559878

3

Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia.

Wagner JE, Tolar J, Levran O, Scholl T, Deffenbaugh A, Satagopan J, Ben-Porat L, Mah K, Batish SD, Kutler DI, MacMillan ML, Hanenberg H, Auerbach AD. Wagner JE, et al. Among authors: hanenberg h. Blood. 2004 Apr 15;103(8):3226-9. doi: 10.1182/blood-2003-09-3138. Epub 2004 Jan 8. Blood. 2004. PMID: 15070707 Free article.

4

Spectrum of sequence variations in the FANCA gene: an International Fanconi Anemia Registry (IFAR) study.

Levran O, Diotti R, Pujara K, Batish SD, Hanenberg H, Auerbach AD. Levran O, et al. Among authors: hanenberg h. Hum Mutat. 2005 Feb;25(2):142-9. doi: 10.1002/humu.20125. Hum Mutat. 2005. PMID: 15643609

5

Spectrum of sequence variation in the FANCG gene: an International Fanconi Anemia Registry (IFAR) study.

Auerbach AD, Greenbaum J, Pujara K, Batish SD, Bitencourt MA, Kokemohr I, Schneider H, Lobitzc S, Pasquini R, Giampietro PF, Hanenberg H, Levran O; International Fanconi Anemia Registry. Auerbach AD, et al. Among authors: hanenberg h. Hum Mutat. 2003 Feb;21(2):158-68. doi: 10.1002/humu.10166. Hum Mutat. 2003. PMID: 12552564

6

A rapid method for retrovirus-mediated identification of complementation groups in Fanconi anemia patients.

Chandra S, Levran O, Jurickova I, Maas C, Kapur R, Schindler D, Henry R, Milton K, Batish SD, Cancelas JA, Hanenberg H, Auerbach AD, Williams DA. Chandra S, et al. Among authors: hanenberg h. Mol Ther. 2005 Nov;12(5):976-84. doi: 10.1016/j.ymthe.2005.04.021. Epub 2005 Aug 9. Mol Ther. 2005. PMID: 16084127 Free article.

7

The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia.

Levran O, Attwooll C, Henry RT, Milton KL, Neveling K, Rio P, Batish SD, Kalb R, Velleuer E, Barral S, Ott J, Petrini J, Schindler D, Hanenberg H, Auerbach AD. Levran O, et al. Among authors: hanenberg h. Nat Genet. 2005 Sep;37(9):931-3. doi: 10.1038/ng1624. Epub 2005 Aug 21. Nat Genet. 2005. PMID: 16116424

8

GST genotype may modify clinical phenotype in patients with Fanconi anaemia.

Davies SM, Radloff GA, DeFor TE, Levran O, Batish SD, Hanenberg H, Auerbach AD. Davies SM, et al. Among authors: hanenberg h. Br J Haematol. 2005 Oct;131(1):118-22. doi: 10.1111/j.1365-2141.2005.05721.x. Br J Haematol. 2005. PMID: 16173971 Free article.

9

Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer.

Reid S, Schindler D, Hanenberg H, Barker K, Hanks S, Kalb R, Neveling K, Kelly P, Seal S, Freund M, Wurm M, Batish SD, Lach FP, Yetgin S, Neitzel H, Ariffin H, Tischkowitz M, Mathew CG, Auerbach AD, Rahman N. Reid S, et al. Among authors: hanenberg h. Nat Genet. 2007 Feb;39(2):162-4. doi: 10.1038/ng1947. Epub 2006 Dec 31. Nat Genet. 2007. PMID: 17200671

10

FANCI is a second monoubiquitinated member of the Fanconi anemia pathway.

Sims AE, Spiteri E, Sims RJ 3rd, Arita AG, Lach FP, Landers T, Wurm M, Freund M, Neveling K, Hanenberg H, Auerbach AD, Huang TT. Sims AE, et al. Among authors: hanenberg h. Nat Struct Mol Biol. 2007 Jun;14(6):564-7. doi: 10.1038/nsmb1252. Epub 2007 Apr 25. Nat Struct Mol Biol. 2007. PMID: 17460694

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