Korostishevsky M - Search Results

1

The human platelet alphaIIb gene is not closely linked to its integrin partner beta3.

Thornton MA, Poncz M, Korostishevsky M, Yakobson E, Usher S, Seligsohn U, Peretz H. Thornton MA, et al. Among authors: korostishevsky m. Blood. 1999 Sep 15;94(6):2039-47. Blood. 1999. PMID: 10477733 Free article.

2

An ancestral variant causing type I xanthinuria in Turkmen and Arab families is predicted to prevail in the Afro-Asian stone-forming belt.

Peretz H, Korostishevsky M, Steinberg DM, Kabha M, Usher S, Krause I, Shalev H, Landau D, Levartovsky D. Peretz H, et al. Among authors: korostishevsky m. JIMD Rep. 2019 Dec 5;51(1):45-52. doi: 10.1002/jmd2.12077. eCollection 2020 Jan. JIMD Rep. 2019. PMID: 32071838 Free PMC article.

3

Ala244Val is a common, probably ancient mutation causing factor VII deficiency in Moroccan and Iranian Jews.

Tamary H, Fromovich Y, Shalmon L, Reich Z, Dym O, Lanir N, Brenner B, Paz M, Luder AS, Blau O, Korostishevsky M, Zaizov R, Seligsohn U. Tamary H, et al. Among authors: korostishevsky m. Thromb Haemost. 1996 Sep;76(3):283-91. Thromb Haemost. 1996. PMID: 8883260

4

Localization of the gene for congenital dyserythropoietic anemia type I to a <1-cM interval on chromosome 15q15.1-15.3.

Tamary H, Shalmon L, Shalev H, Halil A, Dobrushin D, Ashkenazi N, Zoldan M, Resnitzky P, Korostishevsky M, Bonne-Tamir B, Zaizov R. Tamary H, et al. Among authors: korostishevsky m. Am J Hum Genet. 1998 May;62(5):1062-9. doi: 10.1086/301834. Am J Hum Genet. 1998. PMID: 9545404 Free PMC article.

5

Genotype and allele frequencies of C3435T polymorphism of the MDR1 gene in various Jewish populations of Israel.

Ostrovsky O, Nagler A, Korostishevsky M, Gazit E, Galski H. Ostrovsky O, et al. Among authors: korostishevsky m. Ther Drug Monit. 2004 Dec;26(6):679-84. doi: 10.1097/00007691-200412000-00015. Ther Drug Monit. 2004. PMID: 15570194

6

Characterization of HPSE gene single nucleotide polymorphisms in Jewish populations of Israel.

Ostrovsky O, Korostishevsky M, Levite I, Leiba M, Galski H, Gazit E, Vlodavsky I, Nagler A. Ostrovsky O, et al. Among authors: korostishevsky m. Acta Haematol. 2007;117(1):57-64. doi: 10.1159/000096790. Epub 2006 Nov 8. Acta Haematol. 2007. PMID: 17095861

7

Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins.

Adato A, Weil D, Kalinski H, Pel-Or Y, Ayadi H, Petit C, Korostishevsky M, Bonne-Tamir B. Adato A, et al. Among authors: korostishevsky m. Am J Hum Genet. 1997 Oct;61(4):813-21. doi: 10.1086/514899. Am J Hum Genet. 1997. PMID: 9382091 Free PMC article.

8

Common ancestral origin of pemphigus vulgaris in Jews and Spaniards: a study using microsatellite markers.

Loewenthal R, Slomov Y, Gonzalez-Escribano MF, Goldberg I, Korostishevsky M, Brenner S, Nunez-Roldan A, Conejo-Mir JS, Gazit E. Loewenthal R, et al. Among authors: korostishevsky m. Tissue Antigens. 2004 Apr;63(4):326-34. doi: 10.1111/j.0001-2815.2004.00191.x. Tissue Antigens. 2004. PMID: 15009804

9

The VKORC1 Asp36Tyr variant and VKORC1 haplotype diversity in Ashkenazi and Ethiopian populations.

Sominsky S, Korostishevsky M, Kurnik D, Aklillu E, Cohen Y, Ken-Dror G, Loebstein R, Halkin H, Gak E. Sominsky S, et al. Among authors: korostishevsky m. J Appl Genet. 2014 May;55(2):163-71. doi: 10.1007/s13353-013-0189-2. Epub 2014 Jan 15. J Appl Genet. 2014. PMID: 24425227

10

Erroneous identification in a mixed population: simulation using Israeli STR data.

Korostishevsky M, Loewenthal R, Slomov Y, Gazit E. Korostishevsky M, et al. Int J Legal Med. 2004 Apr;118(2):111-4. doi: 10.1007/s00414-003-0401-8. Epub 2003 Dec 24. Int J Legal Med. 2004. PMID: 14704802

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