Shochat C - Search Results

1

Genotype/phenotype correlation in primary congenital glaucoma patients from different ethnic groups of the Israeli population.

Geyer O, Wolf A, Levinger E, Harari-Shacham A, Walton DS, Shochat C, Korem S, Bercovich D. Geyer O, et al. Among authors: shochat c. Am J Ophthalmol. 2011 Feb;151(2):263-71.e1. doi: 10.1016/j.ajo.2010.08.038. Epub 2010 Dec 18. Am J Ophthalmol. 2011. PMID: 21168818

2

A novel BRCA-1 mutation in Arab kindred from east Jerusalem with breast and ovarian cancer.

Kadouri L, Bercovich D, Elimelech A, Lerer I, Sagi M, Glusman G, Shochat C, Korem S, Hamburger T, Nissan A, Abu-Halaf N, Badrriyah M, Abeliovich D, Peretz T. Kadouri L, et al. Among authors: shochat c. BMC Cancer. 2007 Jan 18;7:14. doi: 10.1186/1471-2407-7-14. BMC Cancer. 2007. PMID: 17233897 Free PMC article.

3

Mutation spectrum in HNPCC in the Israeli population.

Goldberg Y, Porat RM, Kedar I, Shochat C, Sagi M, Eilat A, Mendelson S, Hamburger T, Nissan A, Hubert A, Kadouri L, Pikarski E, Lerer I, Abeliovich D, Bercovich D, Peretz T. Goldberg Y, et al. Among authors: shochat c. Fam Cancer. 2008;7(4):309-17. doi: 10.1007/s10689-008-9191-y. Epub 2008 Apr 4. Fam Cancer. 2008. PMID: 18389388

4

An Ashkenazi founder mutation in the MSH6 gene leading to HNPCC.

Goldberg Y, Porat RM, Kedar I, Shochat C, Galinsky D, Hamburger T, Hubert A, Strul H, Kariiv R, Ben-Avi L, Savion M, Pikarsky E, Abeliovich D, Bercovich D, Lerer I, Peretz T. Goldberg Y, et al. Among authors: shochat c. Fam Cancer. 2010 Jun;9(2):141-50. doi: 10.1007/s10689-009-9298-9. Fam Cancer. 2010. PMID: 19851887

5

Homozygosity of MSH2 c.1906G-->C germline mutation is associated with childhood colon cancer, astrocytoma and signs of Neurofibromatosis type I.

Toledano H, Goldberg Y, Kedar-Barnes I, Baris H, Porat RM, Shochat C, Bercovich D, Pikarsky E, Lerer I, Yaniv I, Abeliovich D, Peretz T. Toledano H, et al. Among authors: shochat c. Fam Cancer. 2009;8(3):187-94. doi: 10.1007/s10689-008-9227-3. Epub 2008 Dec 20. Fam Cancer. 2009. PMID: 19101824

6

The association of common SNPs and haplotypes in the CETP and MDR1 genes with lipids response to fluvastatin in familial hypercholesterolemia.

Bercovich D, Friedlander Y, Korem S, Houminer A, Hoffman A, Kleinberg L, Shochat C, Leitersdorf E, Meiner V. Bercovich D, et al. Among authors: shochat c. Atherosclerosis. 2006 Mar;185(1):97-107. doi: 10.1016/j.atherosclerosis.2005.05.025. Epub 2005 Jul 5. Atherosclerosis. 2006. PMID: 16002074 Clinical Trial.

7

A protocol for genetic evaluation of patients with multiple colorectal adenomas and without evidence of APC gene mutation.

Rosner G, Rozen P, Bercovich D, Shochat C, Solar I, Strul H, Kariv R, Halpern Z. Rosner G, et al. Among authors: shochat c. Isr Med Assoc J. 2010 Sep;12(9):549-53. Isr Med Assoc J. 2010. PMID: 21287799 Free article. Clinical Trial.

8

Interleukin 7 and thymic stromal lymphopoietin: from immunity to leukemia.

Tal N, Shochat C, Geron I, Bercovich D, Izraeli S. Tal N, et al. Among authors: shochat c. Cell Mol Life Sci. 2014 Feb;71(3):365-78. doi: 10.1007/s00018-013-1337-x. Epub 2013 Apr 27. Cell Mol Life Sci. 2014. PMID: 23625073 Free PMC article. Review.

9

Gain-of-function mutations in interleukin-7 receptor-α (IL7R) in childhood acute lymphoblastic leukemias.

Shochat C, Tal N, Bandapalli OR, Palmi C, Ganmore I, te Kronnie G, Cario G, Cazzaniga G, Kulozik AE, Stanulla M, Schrappe M, Biondi A, Basso G, Bercovich D, Muckenthaler MU, Izraeli S. Shochat C, et al. J Exp Med. 2011 May 9;208(5):901-8. doi: 10.1084/jem.20110580. Epub 2011 May 2. J Exp Med. 2011. PMID: 21536738 Free PMC article.

10

Mutations of JAK2 in acute lymphoblastic leukaemias associated with Down's syndrome.

Bercovich D, Ganmore I, Scott LM, Wainreb G, Birger Y, Elimelech A, Shochat C, Cazzaniga G, Biondi A, Basso G, Cario G, Schrappe M, Stanulla M, Strehl S, Haas OA, Mann G, Binder V, Borkhardt A, Kempski H, Trka J, Bielorei B, Avigad S, Stark B, Smith O, Dastugue N, Bourquin JP, Tal NB, Green AR, Izraeli S. Bercovich D, et al. Among authors: shochat c. Lancet. 2008 Oct 25;372(9648):1484-92. doi: 10.1016/S0140-6736(08)61341-0. Epub 2008 Sep 19. Lancet. 2008. PMID: 18805579

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