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H Peretz

Showing results (31-40 of 59) with videos related to

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Blood|August 9, 2001
Identification of a region in glycoprotein IIIa involved in subunit association with glycoprotein IIb: further lessons from Iraqi-Jewish Glanzmann thrombastheniaR Yatuv, N Rosenberg, A Zivelin, et al.
Journal of Thrombosis and Haemostasis : JTH|July 2, 2011
Point mutations regarded as missense mutations cause splicing defects in the factor XI geneM Zucker, N Rosenberg, H Peretz, et al.
Blood|May 15, 1997
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 founderN Rosenberg, R Yatuv, Y Orion, et al.
American Journal of Human Genetics|March 26, 1999
Age estimates of two common mutations causing factor XI deficiency: recent genetic drift is not necessary for elevated disease incidence among Ashkenazi JewsD B Goldstein, D E Reich, N Bradman, et al.
Journal of Thrombosis and Haemostasis : JTH|January 22, 2013
Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi JewsH Peretz, O Salomon, R Mor-Cohen, et al.
Blood|September 9, 1999
The human platelet alphaIIb gene is not closely linked to its integrin partner beta3M A Thornton, M Poncz, M Korostishevsky, et al.
Life Sciences|February 9, 2005
Time dependent protection of amifostine from renal and hematopoietic cisplatin induced toxicityN Asna, H Lewy, I E Ashkenazi, et al.
Blood|January 15, 1995
Glanzmann's thrombasthenia associated with deletion-insertion and alternative splicing in the glycoprotein IIb geneH Peretz, N Rosenberg, S Usher, et al.
British Journal of Haematology|August 8, 1998
Prenatal diagnosis of Glanzmann thrombasthenia using the polymorphic markers BRCA1 and THRA1 on chromosome 17D L French, B S Coller, S Usher, et al.
Kidney International|June 9, 2000
XDH gene mutation is the underlying cause of classical xanthinuria: a second reportD Levartovsky, A Lagziel, O Sperling, et al.
Pageof 6

Showing results (31-40 of 59) with videos related to

Sort By:
Pageof 6
Blood|August 9, 2001
Identification of a region in glycoprotein IIIa involved in subunit association with glycoprotein IIb: further lessons from Iraqi-Jewish Glanzmann thrombastheniaR Yatuv, N Rosenberg, A Zivelin, et al.
Journal of Thrombosis and Haemostasis : JTH|July 2, 2011
Point mutations regarded as missense mutations cause splicing defects in the factor XI geneM Zucker, N Rosenberg, H Peretz, et al.
Blood|May 15, 1997
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 founderN Rosenberg, R Yatuv, Y Orion, et al.
American Journal of Human Genetics|March 26, 1999
Age estimates of two common mutations causing factor XI deficiency: recent genetic drift is not necessary for elevated disease incidence among Ashkenazi JewsD B Goldstein, D E Reich, N Bradman, et al.
Journal of Thrombosis and Haemostasis : JTH|January 22, 2013
Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi JewsH Peretz, O Salomon, R Mor-Cohen, et al.
Blood|September 9, 1999
The human platelet alphaIIb gene is not closely linked to its integrin partner beta3M A Thornton, M Poncz, M Korostishevsky, et al.
Life Sciences|February 9, 2005
Time dependent protection of amifostine from renal and hematopoietic cisplatin induced toxicityN Asna, H Lewy, I E Ashkenazi, et al.
Blood|January 15, 1995
Glanzmann's thrombasthenia associated with deletion-insertion and alternative splicing in the glycoprotein IIb geneH Peretz, N Rosenberg, S Usher, et al.
British Journal of Haematology|August 8, 1998
Prenatal diagnosis of Glanzmann thrombasthenia using the polymorphic markers BRCA1 and THRA1 on chromosome 17D L French, B S Coller, S Usher, et al.
Kidney International|June 9, 2000
XDH gene mutation is the underlying cause of classical xanthinuria: a second reportD Levartovsky, A Lagziel, O Sperling, et al.
Pageof 6