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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

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

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

Blood (2001) 98 (4): 1063–1069.

https://doi.org/10.1182/blood.V98.4.1063

Published: 2001

Journal Articles

A Single Genetic Origin for the Common Prothrombotic G20210A Polymorphism in the Prothrombin Gene

Ariella Zivelin, Nurit Rosenberg, Shlomit Faier, Nurit Kornbrot, Hava Peretz, Christine Mannhalter, Marie Helene Horellou, Uri Seligsohn

Blood (1998) 92 (4): 1119–1124.

https://doi.org/10.1182/blood.V92.4.1119

Published: 1998

Journal Articles

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

Hava Peretz, Avital Mulai, Sali Usher, Ariella Zivelin, Avihai Segal, Zahavi Weisman, Moshe Mittelman, Hannah Lupo, Naomi Lanir, Benjamin Brenner, Ofer Shpilberg, Uri Seligsohn

Blood (1997) 90 (7): 2654–2659.

https://doi.org/10.1182/blood.V90.7.2654

Published: 1997

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

Blood (1997) 89 (10): 3654–3662.

https://doi.org/10.1182/blood.V89.10.3654

Published: 1997

NARROW

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

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

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

A Single Genetic Origin for the Common Prothrombotic G20210A Polymorphism in the Prothrombin Gene

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

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

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ASH Publications

American Society of Hematology

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

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

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

A Single Genetic Origin for the Common Prothrombotic G20210A Polymorphism in the Prothrombin Gene

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

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

Email alerts

ASH Publications

American Society of Hematology

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