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Rivka Yatuv
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Journal Articles

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

Nurit Rosenberg, Rivka Yatuv, Vladimir Sobolev, Hava Peretz, Ariella Zivelin, Uri Seligsohn
Journal: Blood
Blood (2003) 101 (12): 4808–4815.
https://doi.org/10.1182/blood-2002-08-2452
Published: 2003
Journal Articles

Factor XI deficiency in French Basques is caused predominantly by an ancestral Cys38Arg mutation in the factor XI gene

Ariella Zivelin, Frederic Bauduer, Louis Ducout, Hava Peretz, Nurit Rosenberg, Rivka Yatuv, Uri Seligsohn
Journal: Blood
Blood (2002) 99 (7): 2448–2454.
https://doi.org/10.1182/blood.V99.7.2448
Published: 2002
Journal Articles

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

Rivka Yatuv, Nurit Rosenberg, Ariella Zivelin, Hava Peretz, Rima Dardik, Luba Trakhtenbrot, Uri Seligsohn
Journal: Blood
Blood (2001) 98 (4): 1063–1069.
https://doi.org/10.1182/blood.V98.4.1063
Published: 2001
Journal Articles

Glanzmann Thrombasthenia Caused by an 11.2-kb Deletion in the Glycoprotein IIIa (β 3 ) Is a Second Mutation in Iraqi Jews That Stemmed From a Distinct Founder

Nurit Rosenberg, Rivka Yatuv, Yael Orion, Ariella Zivelin, Rima Dardik, Hava Peretz, Uri Seligsohn
Journal: Blood
Blood (1997) 89 (10): 3654–3662.
https://doi.org/10.1182/blood.V89.10.3654
Published: 1997