Peretz H - 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: peretz h. Blood. 1999 Sep 15;94(6):2039-47. Blood. 1999. PMID: 10477733 Free article.

2

Glanzmann's thrombasthenia associated with deletion-insertion and alternative splicing in the glycoprotein IIb gene.

Peretz H, Rosenberg N, Usher S, Graff E, Newman PJ, Coller BS, Seligsohn U. Peretz H, et al. Blood. 1995 Jan 15;85(2):414-20. Blood. 1995. PMID: 7529063 Free article.

3

Factor VIII gene rearrangement in hemophilia A carrier detection: a word of caution.

Peretz H, Usher S, Martinovitz U, Seligsohn U. Peretz H, et al. Blood. 1994 Aug 15;84(4):1351-2. Blood. 1994. PMID: 7914105 Free article. No abstract available.

4

Glanzmann thrombasthenia caused by an 11.2-kb deletion in the glycoprotein IIIa (beta3) is a second mutation in Iraqi Jews that stemmed from a distinct founder.

Rosenberg N, Yatuv R, Orion Y, Zivelin A, Dardik R, Peretz H, Seligsohn U. Rosenberg N, et al. Among authors: peretz h. Blood. 1997 May 15;89(10):3654-62. Blood. 1997. PMID: 9160670 Free article.

5

The two common mutations causing factor XI deficiency in Jews stem from distinct founders: one of ancient Middle Eastern origin and another of more recent European origin.

Peretz H, Mulai A, Usher S, Zivelin A, Segal A, Weisman Z, Mittelman M, Lupo H, Lanir N, Brenner B, Shpilberg O, Seligsohn U. Peretz H, et al. Blood. 1997 Oct 1;90(7):2654-9. Blood. 1997. PMID: 9326232 Free article.

6

Prenatal diagnosis of Glanzmann thrombasthenia using the polymorphic markers BRCA1 and THRA1 on chromosome 17.

French DL, Coller BS, Usher S, Berkowitz R, Eng C, Seligsohn U, Peretz H. French DL, et al. Among authors: peretz h. Br J Haematol. 1998 Jul;102(2):582-7. doi: 10.1046/j.1365-2141.1998.00798.x. Br J Haematol. 1998. PMID: 9695977 Free article.

7

Identification of a region in glycoprotein IIIa involved in subunit association with glycoprotein IIb: further lessons from Iraqi-Jewish Glanzmann thrombasthenia.

Yatuv R, Rosenberg N, Zivelin A, Peretz H, Dardik R, Trakhtenbrot L, Seligsohn U. Yatuv R, et al. Among authors: peretz h. Blood. 2001 Aug 15;98(4):1063-9. doi: 10.1182/blood.v98.4.1063. Blood. 2001. PMID: 11493452 Free article.

8

Major mutations in calf-1 and calf-2 domains of glycoprotein IIb in patients with Glanzmann thrombasthenia enable GPIIb/IIIa complex formation, but impair its transport from the endoplasmic reticulum to the Golgi apparatus.

Rosenberg N, Yatuv R, Sobolev V, Peretz H, Zivelin A, Seligsohn U. Rosenberg N, et al. Among authors: peretz h. Blood. 2003 Jun 15;101(12):4808-15. doi: 10.1182/blood-2002-08-2452. Epub 2003 Feb 27. Blood. 2003. PMID: 12609844 Free article.

9

One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of Jews.

Shpilberg O, Peretz H, Zivelin A, Yatuv R, Chetrit A, Kulka T, Stern C, Weiss E, Seligsohn U. Shpilberg O, et al. Among authors: peretz h. Blood. 1995 Jan 15;85(2):429-32. Blood. 1995. PMID: 7811996 Free article.

10

Molecular genetics aspects of factor XI deficiency and Glanzmann thrombasthenia.

Seligsohn U, Peretz H. Seligsohn U, et al. Among authors: peretz h. Haemostasis. 1994 Mar-Apr;24(2):81-5. doi: 10.1159/000217088. Haemostasis. 1994. PMID: 7959366 Review.

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