Kerem B - Search Results

1

Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24.

Lerer B, Segman RH, Hamdan A, Kanyas K, Karni O, Kohn Y, Korner M, Lanktree M, Kaadan M, Turetsky N, Yakir A, Kerem B, Macciardi F. Lerer B, et al. Among authors: kerem b. Mol Psychiatry. 2003 May;8(5):488-98. doi: 10.1038/sj.mp.4001322. Mol Psychiatry. 2003. PMID: 12808429

2

Evidence of genetic heterogeneity in the long QT syndrome.

Benhorin J, Kalman YM, Medina A, Towbin J, Rave-Harel N, Dyer TD, Blangero J, MacCluer JW, Kerem BS. Benhorin J, et al. Among authors: kerem bs. Science. 1993 Jun 25;260(5116):1960-2. doi: 10.1126/science.8316839. Science. 1993. PMID: 8316839 No abstract available.

3

An interstitial nucleolus organizer region in the long arm of human chromosome 7: cytogenetic characterization and familial segregation.

Guttenbach M, Nassar N, Feichtinger W, Steinlein C, Nanda I, Wanner G, Kerem B, Schmid M. Guttenbach M, et al. Among authors: kerem b. Cytogenet Cell Genet. 1998;80(1-4):104-12. doi: 10.1159/000014964. Cytogenet Cell Genet. 1998. PMID: 9678342

4

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: kerem b. 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.

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: kerem b. 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

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: kerem b. 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.

7

Screening of CFTR mutations in an isolated population: identification of carriers and patients.

Chiba-Falek O, Nissim-Rafinia M, Argaman Z, Genem A, Moran I, Kerem E, Kerem B. Chiba-Falek O, et al. Among authors: kerem b, kerem e. Eur J Hum Genet. 1998 Mar-Apr;6(2):181-4. doi: 10.1038/sj.ejhg.5200174. Eur J Hum Genet. 1998. PMID: 9781064

8

Cellular and viral splicing factors can modify the splicing pattern of CFTR transcripts carrying splicing mutations.

Nissim-Rafinia M, Chiba-Falek O, Sharon G, Boss A, Kerem B. Nissim-Rafinia M, et al. Among authors: kerem b. Hum Mol Genet. 2000 Jul 22;9(12):1771-8. doi: 10.1093/hmg/9.12.1771. Hum Mol Genet. 2000. PMID: 10915765

9

The splicing machinery is a genetic modifier of disease severity.

Nissim-Rafinia M, Kerem B. Nissim-Rafinia M, et al. Among authors: kerem b. Trends Genet. 2005 Sep;21(9):480-3. doi: 10.1016/j.tig.2005.07.005. Trends Genet. 2005. PMID: 16039004 Review.

10

Nonsense-mediated mRNA decay and cystic fibrosis.

Linde L, Kerem B. Linde L, et al. Among authors: kerem b. Methods Mol Biol. 2011;741:137-54. doi: 10.1007/978-1-61779-117-8_10. Methods Mol Biol. 2011. PMID: 21594783

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