Levran O - Search Results

1

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: levran o. 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.

2

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. Hum Mutat. 2005 Feb;25(2):142-9. doi: 10.1002/humu.20125. Hum Mutat. 2005. PMID: 15643609

3

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: levran o. 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.

4

Identification of Alu-mediated deletions in the Fanconi anemia gene FAA.

Levran O, Doggett NA, Auerbach AD. Levran O, et al. Hum Mutat. 1998;12(3):145-52. doi: 10.1002/(SICI)1098-1004(1998)12:3<145::AID-HUMU2>3.0.CO;2-G. Hum Mutat. 1998. PMID: 9711872

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: levran o. Hum Mutat. 2003 Feb;21(2):158-68. doi: 10.1002/humu.10166. Hum Mutat. 2003. PMID: 12552564

6

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: levran o. 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.

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. Nat Genet. 2005 Sep;37(9):931-3. doi: 10.1038/ng1624. Epub 2005 Aug 21. Nat Genet. 2005. PMID: 16116424

8

Genetic heterogeneity among Fanconi anemia heterozygotes and risk of cancer.

Berwick M, Satagopan JM, Ben-Porat L, Carlson A, Mah K, Henry R, Diotti R, Milton K, Pujara K, Landers T, Dev Batish S, Morales J, Schindler D, Hanenberg H, Hromas R, Levran O, Auerbach AD. Berwick M, et al. Among authors: levran o. Cancer Res. 2007 Oct 1;67(19):9591-6. doi: 10.1158/0008-5472.CAN-07-1501. Cancer Res. 2007. PMID: 17909071 Free PMC article.

9

Sequence variation in the Fanconi anemia gene FAA.

Levran O, Erlich T, Magdalena N, Gregory JJ, Batish SD, Verlander PC, Auerbach AD. Levran O, et al. Proc Natl Acad Sci U S A. 1997 Nov 25;94(24):13051-6. doi: 10.1073/pnas.94.24.13051. Proc Natl Acad Sci U S A. 1997. PMID: 9371798 Free PMC article.

10

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: levran o. J Natl Cancer Inst. 2003 Oct 15;95(20):1548-51. doi: 10.1093/jnci/djg072. J Natl Cancer Inst. 2003. PMID: 14559878

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