The Role of Reactive Oxygen Species in Diabetes-Induced Anomalies in Embryos of Cohen Diabetic Rats

Por Zangen, Sarah W., Yaffe, Pirhiya, Shechtman, Svetlana, Zangen, David H., Ornoy, Asher
Publicado em 2002

Novel De Novo Mutation in Sulfonylurea Receptor 1 Presenting as Hyperinsulinism in Infancy Followed by Overt Diabetes in Early Adolescence

Por Abdulhadi-Atwan, Maha, Bushmann, Jeremy, Tornovsky-Babaey, Sharona, Perry, Avital, Abu-Libdeh, Abdulsalam, Glaser, Benjamin, Shyng, Show-Ling, Zangen, David H.
Publicado em 2008

Relative Expression of a Dominant Mutated ABCC8 Allele Determines the Clinical Manifestation of Congenital Hyperinsulinism

Por Shemer, Ruth, Avnon Ziv, Carmit, Laiba, Efrat, Zhou, Qing, Gay, Joel, Tunovsky-Babaey, Sharona, Shyng, Show-Ling, Glaser, Benjamin, Zangen, David H.
Publicado em 2012

A Novel Familial Mutation in the PCSK1 Gene That Alters the Oxyanion Hole Residue of Proprotein Convertase 1/3 and Impairs Its Enzymatic Activity

Por Wilschanski, Michael, Abbasi, Montaser, Blanco, Elias, Lindberg, Iris, Yourshaw, Michael, Zangen, David, Berger, Itai, Shteyer, Eyal, Pappo, Orit, Bar-Oz, Benjamin, Martín, Martin G., Elpeleg, Orly
Publicado em 2014

Testicular differentiation factor SF-1 is required for human spleen development

Por Zangen, David, Kaufman, Yotam, Banne, Ehud, Weinberg-Shukron, Ariella, Abulibdeh, Abdulsalam, Garfinkel, Benjamin P., Dweik, Dima, Kanaan, Moein, Camats, Núria, Flück, Christa, Renbaum, Paul, Levy-Lahad, Ephrat
Publicado em 2014

Mutations in DDR2 Gene Cause SMED with Short Limbs and Abnormal Calcifications

Por Bargal, Ruth, Cormier-Daire, Valerie, Ben-Neriah, Ziva, Le Merrer, Martine, Sosna, Jacob, Melki, Judith, Zangen, David H., Smithson, Sarah F., Borochowitz, Zvi, Belostotsky, Ruth, Raas-Rothschild, Annick
Publicado em 2009

XX Ovarian Dysgenesis Is Caused by a PSMC3IP/HOP2 Mutation that Abolishes Coactivation of Estrogen-Driven Transcription

Por Zangen, David, Kaufman, Yotam, Zeligson, Sharon, Perlberg, Shira, Fridman, Hila, Kanaan, Moein, Abdulhadi-Atwan, Maha, Abu Libdeh, Abdulsalam, Gussow, Ayal, Kisslov, Irit, Carmel, Liran, Renbaum, Paul, Levy-Lahad, Ephrat
Publicado em 2011

A mutation in the nucleoporin-107 gene causes XX gonadal dysgenesis

Por Weinberg-Shukron, Ariella, Renbaum, Paul, Kalifa, Rachel, Zeligson, Sharon, Ben-Neriah, Ziva, Dreifuss, Amatzia, Abu-Rayyan, Amal, Maatuk, Noa, Fardian, Nilly, Rekler, Dina, Kanaan, Moien, Samson, Abraham O., Levy-Lahad, Ephrat, Gerlitz, Offer, Zangen, David
Publicado no J Clin Invest (2015)