Rahat A - Search Results

1

The molecular basis of disease variability among cystic fibrosis patients carrying the 3849+10 kb C-->T mutation.

Chiba-Falek O, Kerem E, Shoshani T, Aviram M, Augarten A, Bentur L, Tal A, Tullis E, Rahat A, Kerem B. Chiba-Falek O, et al. Among authors: rahat a. Genomics. 1998 Nov 1;53(3):276-83. doi: 10.1006/geno.1998.5517. Genomics. 1998. PMID: 9799593

2

The molecular basis of partial penetrance of splicing mutations in cystic fibrosis.

Rave-Harel N, Kerem E, Nissim-Rafinia M, Madjar I, Goshen R, Augarten A, Rahat A, Hurwitz A, Darvasi A, Kerem B. Rave-Harel N, et al. Among authors: rahat a. Am J Hum Genet. 1997 Jan;60(1):87-94. Am J Hum Genet. 1997. PMID: 8981951 Free PMC article.

3

Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instability.

Hellman A, Rahat A, Scherer SW, Darvasi A, Tsui LC, Kerem B. Hellman A, et al. Among authors: rahat a. Mol Cell Biol. 2000 Jun;20(12):4420-7. doi: 10.1128/MCB.20.12.4420-4427.2000. Mol Cell Biol. 2000. PMID: 10825205 Free PMC article.

4

Interplay between ATM and ATR in the regulation of common fragile site stability.

Ozeri-Galai E, Schwartz M, Rahat A, Kerem B. Ozeri-Galai E, et al. Among authors: rahat a. Oncogene. 2008 Apr 3;27(15):2109-17. doi: 10.1038/sj.onc.1210849. Epub 2007 Oct 15. Oncogene. 2008. PMID: 17934520

5

Molecular basis for expression of common and rare fragile sites.

Zlotorynski E, Rahat A, Skaug J, Ben-Porat N, Ozeri E, Hershberg R, Levi A, Scherer SW, Margalit H, Kerem B. Zlotorynski E, et al. Among authors: rahat a. Mol Cell Biol. 2003 Oct;23(20):7143-51. doi: 10.1128/MCB.23.20.7143-7151.2003. Mol Cell Biol. 2003. PMID: 14517285 Free PMC article.

6

Impaired replication stress response in cells from immunodeficiency patients carrying Cernunnos/XLF mutations.

Schwartz M, Oren YS, Bester AC, Rahat A, Sfez R, Yitzchaik S, de Villartay JP, Kerem B. Schwartz M, et al. Among authors: rahat a. PLoS One. 2009;4(2):e4516. doi: 10.1371/journal.pone.0004516. Epub 2009 Feb 18. PLoS One. 2009. PMID: 19223975 Free PMC article.

7

Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site.

Mishmar D, Rahat A, Scherer SW, Nyakatura G, Hinzmann B, Kohwi Y, Mandel-Gutfroind Y, Lee JR, Drescher B, Sas DE, Margalit H, Platzer M, Weiss A, Tsui LC, Rosenthal A, Kerem B. Mishmar D, et al. Among authors: rahat a. Proc Natl Acad Sci U S A. 1998 Jul 7;95(14):8141-6. doi: 10.1073/pnas.95.14.8141. Proc Natl Acad Sci U S A. 1998. PMID: 9653154 Free PMC article.

8

Identification of a new SCN5A mutation, D1840G, associated with the long QT syndrome. Mutations in brief no. 153. Online.

Benhorin J, Goldmit M, MacCluer JW, Blangero J, Goffen R, Leibovitch A, Rahat A, Wang Q, Medina A, Towbin J, Kerem B. Benhorin J, et al. Among authors: rahat a. Hum Mutat. 1998;12(1):72. doi: 10.1002/(SICI)1098-1004(1998)12:1<72::AID-HUMU19>3.0.CO;2-T. Hum Mutat. 1998. PMID: 10627139

9

Failure of origin activation in response to fork stalling leads to chromosomal instability at fragile sites.

Ozeri-Galai E, Lebofsky R, Rahat A, Bester AC, Bensimon A, Kerem B. Ozeri-Galai E, et al. Among authors: rahat a. Mol Cell. 2011 Jul 8;43(1):122-31. doi: 10.1016/j.molcel.2011.05.019. Mol Cell. 2011. PMID: 21726815 Free article.

10

Homologous recombination and nonhomologous end-joining repair pathways regulate fragile site stability.

Schwartz M, Zlotorynski E, Goldberg M, Ozeri E, Rahat A, le Sage C, Chen BP, Chen DJ, Agami R, Kerem B. Schwartz M, et al. Among authors: rahat a. Genes Dev. 2005 Nov 15;19(22):2715-26. doi: 10.1101/gad.340905. Genes Dev. 2005. PMID: 16291645 Free PMC article.

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