Kết quả tìm kiếm - David Zangen

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  1. 1
    Exercise stimulates the mitogen-activated protein kinase pathway in human skeletal muscle.

    Exercise stimulates the mitogen-activated protein kinase pathway in human skeletal muscle. Bằng Doron Aronson, Mariona Violán, Scott D. Dufresne, David Zangen, Roger A. Fielding, Laurie J. Goodyear

    Được phát hành 1997
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    Artigo
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  2. 2
    CFTR potentiator therapy ameliorates impaired insulin secretion in CF patients with a gating mutation

    CFTR potentiator therapy ameliorates impaired insulin secretion in CF patients with a gating mutation Bằng Reuven Tsabari, Hila Iron Elyashar, Malena Cohen Cymberknowh, Oded Breuer, S. Armoni, Galit Livnat, Eitan Kerem, David Zangen

    Được phát hành 2015
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    Artigo
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  3. 3
    Mutations in DDR2 Gene Cause SMED with Short Limbs and Abnormal Calcifications

    Mutations in DDR2 Gene Cause SMED with Short Limbs and Abnormal Calcifications Bằng Ruth Bargal, Valérie Cormier‐Daire, Ziva Ben‐Neriah, Martine Le Merrer, Jacob Sosna, Judith Melki, David Zangen, Sarah Smithson, Zvi Borochowitz, Ruth Belostotsky, Annick Raas‐Rothschild

    Được phát hành 2008
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    Artigo
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  4. 4
    XX Ovarian Dysgenesis Is Caused by a PSMC3IP/HOP2 Mutation that Abolishes Coactivation of Estrogen-Driven Transcription

    XX Ovarian Dysgenesis Is Caused by a PSMC3IP/HOP2 Mutation that Abolishes Coactivation of Estrogen-Driven Transcription Bằng David Zangen, Yotam Kaufman, Sharon Zeligson, Shira Perlberg, Hila Fridman, Moien Kanaan, Maha Abdulhadi‐Atwan, Abdulsalam Abu‐Libdeh, Ayal B. Gussow, Irit Kisslov, Liran Carmel, Paul Renbaum, Ephrat Levy‐Lahad

    Được phát hành 2011
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    Artigo
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  5. 5
    Haploseek: a 24-hour all-in-one method for preimplantation genetic diagnosis (PGD) of monogenic disease and aneuploidy

    Haploseek: a 24-hour all-in-one method for preimplantation genetic diagnosis (PGD) of monogenic disease and aneuploidy Bằng Daniel Backenroth, Fouad Zahdeh, Yehuda Kling, Aharon Peretz, Tzvia Rosen, Dina Kort, Sharon Zeligson, Tal Dror, Sophie Kirshberg, Efrat Burak, Reeval Segel, Ephrat Levy‐Lahad, David Zangen, Gheona Altarescu, Shai Carmi, David A. Zeevi

    Được phát hành 2018
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    Artigo
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  6. 6
    A mutation in the nucleoporin-107 gene causes XX gonadal dysgenesis

    A mutation in the nucleoporin-107 gene causes XX gonadal dysgenesis Bằng Ariella Weinberg‐Shukron, Paul Renbaum, Rachel Kalifa, Sharon Zeligson, Ziva Ben‐Neriah, Amatzia Dreifuss, Amal Abu Rayyan, Noa Maatuk, Nilly Fardian, Dina Rekler, Moien Kanaan, Abraham O. Samson, Ephrat Levy‐Lahad, Offer Gerlitz, David Zangen

    Được phát hành 2015
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    Artigo
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  7. 7
    GLP-1-RA Corrects Mitochondrial Labile Iron Accumulation and Improves β-Cell Function in Type 2 Wolfram Syndrome

    GLP-1-RA Corrects Mitochondrial Labile Iron Accumulation and Improves β-Cell Function in Type 2 Wolfram Syndrome Bằng Liron Danielpur, Yang‐Sung Sohn, Ola Karmi, Chen Fogel, Adar Zinger, Abdulsalam Abu‐Libdeh, Tal Israeli, Yael Riahi, Orit Pappo, Ruth Birk, David Zangen, Ron Mittler, Zvi-Ioav Cabantchik, Erol Cerasi, Rachel Nechushtai, Gil Leibowitz

    Được phát hành 2016
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    Artigo
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  8. 8
    Essential Role of<i>BRCA2</i>in Ovarian Development and Function

    Essential Role of<i>BRCA2</i>in Ovarian Development and Function Bằng Ariella Weinberg‐Shukron, Marianna Rachmiel, Paul Renbaum, Süleyman Gülsüner, Tom Walsh, Orit Lobel, Amatzia Dreifuss, Avital Ben-Moshe, Sharon Zeligson, Reeval Segel, Tikva Shorê, Rachel Kalifa, Michal Goldberg, Mary‐Claire King, Offer Gerlitz, Ephrat Levy‐Lahad, David Zangen

    Được phát hành 2018
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    Artigo
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  9. 9
    Hyperinsulinism of Infancy: Novel ABCC8 and KCNJ11 Mutations and Evidence for Additional Locus Heterogeneity

    Hyperinsulinism of Infancy: Novel ABCC8 and KCNJ11 Mutations and Evidence for Additional Locus Heterogeneity Bằng Sharona Tornovsky, Ana Crane, Karen E. Cosgrove, Khalid Hussain, Judith Lavie, Maayan Heyman, Yaron Nesher, Na’ama Kuchinski, Etti Ben-Shushan, Olga Shatz, Efrat Nahari, Tamara Potikha, David Zangen, Yardena Tenenbaum‐Rakover, Liat de Vries, Jesús Argente, Ricardo Gracía, Heddy Landau, Alon Eliakim, Keith Lindley, Mark J. Dunne, Lydia Aguilar‐Bryan, Benjamin Gläser

    Được phát hành 2004
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    Artigo
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  10. 10
    Establishing glycaemic control with continuous subcutaneous insulin infusion in children and adolescents with type 1 diabetes: experience of the PedPump Study in 17 countries

    Establishing glycaemic control with continuous subcutaneous insulin infusion in children and adolescents with type 1 diabetes: experience of the PedPump Study in 17 countries Bằng Thomas Danne, Tadej Battelino, Przemysława Jarosz‐Chobot, Olga Kordonouri, Ewa Pańkowska, Johnny Ludvigsson, Edith Schober, Jaakko Kaprio, Tero Saukkonen, Marc Nicolino, Nadia Tubiana‐Rufi, Christof Klinkert, Holger Haberland, Andriani Vazeou, L Madácsy, David Zangen, Valentino Cherubini, Ivana Rabbone, Sonia Toni, Carine de Beaufort, Willie Bakker‐Van Waarde, N. van den Berg, И Э Волков, Rosa Barrio, Ragnar Hanås, Urs Zumsteg, Beatrice G. Kuhlmann, C. Aebi, U. Schumacher, Sylvia Gschwend, Peter C. Hindmarsh, M. Torres, Naim Shehadeh, Moshe Phillip

    Được phát hành 2008
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    Artigo
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  11. 11
    Oligogenic analysis across broad phenotypes of 46,XY differences in sex development associated with NR5A1/SF-1 variants: findings from the international SF1next study

    Oligogenic analysis across broad phenotypes of 46,XY differences in sex development associated with NR5A1/SF-1 variants: findings from the international SF1next study Bằng Chrysanthi Kouri, Idoia Martinez de la Piscina, Rawda Naamneh-Elzenaty, Grit Sommer, Kay‐Sara Sauter, Christa E. Flück, Saygın Abalı, Zehra Yavaş Abalı, S. Faisal Ahmed, Leyla Akın, Maricruz Almaraz, Laura Audí, Murat Aydın, Antonio Balsamo, Federico Baronio, Jillian Bryce, Kanetee Busiah, María Caimari, Núria Camats, Ariadna Campos-Martorell, Luís Castaño, Anna Casteràs, Semra Çeti̇nkaya, Hedi L. Claahsen‐van der Grinten, Martine Cools, Ines M. Costa, Fatma Darendeliler, Justin H. Davies, Isabel Esteva, Helena Fabbri‐Scallet, Courtney Finlayson, Emilio García García, B. García Cuartero, Alina German, Evgenia Globa, Gil Guerra‐Júnior, Júlio Guerrero, Tülay Güran, Sabine E Hannema, Olaf Hiort, Josephine Hirsch, Ieuan A. Hughes, Marco Janner, Uchenna Kennedy, Zofia Kolesińska, Katherine Lachlan, Anna Lauber-Biason, Jana Malíková, Dagmar l’Allemand, Nina Lenhnerr-Taube, Angela K Lucas‐Herald, Jamala Mammadova, Verónica Mericq, Isabel Mönig, Francisca Moreno, Julia Mührer, Marek Niedziela, Anna Nordenström, Burçe Orman, Şükran Poyrazoğlu, Jose M. Rial, Meilan M. Rutter, Amaia Rodrı́guez, Tara Schafer-Kalkhoff, Sumudu Nimali Seneviratne, Maria Sredkova-Ruskova, L. Tack, Rieko Tadokoro‐Cuccaro, Ajay Thankamony, Mónica Tomé, Amaia Vela, Małgorzata Waśniewska, David Zangen, Н. Б. Зелінська

    Được phát hành 2025
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    Artigo
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  12. 12
    Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex development

    Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex development Bằng Chrysanthi Kouri, Grit Sommer, Idoia Martinez de la Piscina, Rawda Naamneh Elzenaty, Lloyd Tack, Martine Cools, S. Faisal Ahmed, Christa E. Flück, Saygın Abalı, Zehra Yavaş Abalı, Leyla Akın, Maricruz Almaraz, Laura Audí, Murat Aydın, Antonio Balsamo, Federico Baronio, Jillian Bryce, Kanetee Busiah, María Caimari, Núria Camats, Ariadna Campos-Martorell, Luís Castaño, Anna Casteràs, Semra Çeti̇nkaya, Yee-Ming Chan, Hedi L. Claahsen‐van der Grinten, Ines M. Costa, Fatma Darendeliler, Justin H. Davies, Isabel Esteva, Helena Fabbri‐Scallet, Courtney Finlayson, Emilio García García, B. García Cuartero, Alina German, Evgenia Globa, Gil Guerra‐Júnior, Júlio Guerrero, Tülay Güran, Sabine E Hannema, Olaf Hiort, Josephine Hirsch, Leuan Hughes, Marco Janner, Zofia Kolesińska, Katherine Lachlan, Anna Lauber-Biason, Jana Malíková, Dagmar l’Allemand, Nina Lenhnerr-Taube, Angela K Lucas‐Herald, Jamala Mammadova, Kenneth MсElreavey, Verónica Mericq, Isabel Mönig, Francisca Moreno, Julia Mührer, Marek Niedziela, Anna Nordenström, Burçe Orman, Şükran Poyrazoğlu, Jose M. Rial, Meilan M. Rutter, Amaia Rodrı́guez, Tara Schafer-Kalkhoff, Kay‐Sara Sauter, Sumudu Nimali Seneviratne, Maria Sredkova-Ruskova, Rieko Tadokoro‐Cuccaro, Ajay Thankamony, Mónica Tomé, Amaia Vela, Małgorzata Waśniewska, David Zangen, Н. Б. Зелінська

    Được phát hành 2024
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    Artigo
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