Որոնման արդյունքները - David Zangen
- Ցուցադրվում են 1 - 12 արդյունքները 12
-
1
-
2
CFTR potentiator therapy ameliorates impaired insulin secretion in CF patients with a gating mutation Reuven Tsabari, Hila Iron Elyashar, Malena Cohen Cymberknowh, Oded Breuer, S. Armoni, Galit Livnat, Eitan Kerem, David Zangen
Հրապարակվել է 2015Artigo -
3
Mutations in DDR2 Gene Cause SMED with Short Limbs and Abnormal Calcifications 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
Հրապարակվել է 2008Artigo -
4
XX Ovarian Dysgenesis Is Caused by a PSMC3IP/HOP2 Mutation that Abolishes Coactivation of Estrogen-Driven Transcription 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
Հրապարակվել է 2011Artigo -
5
Haploseek: a 24-hour all-in-one method for preimplantation genetic diagnosis (PGD) of monogenic disease and aneuploidy 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
Հրապարակվել է 2018Artigo -
6
A mutation in the nucleoporin-107 gene causes XX gonadal dysgenesis 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
Հրապարակվել է 2015Artigo -
7
GLP-1-RA Corrects Mitochondrial Labile Iron Accumulation and Improves β-Cell Function in Type 2 Wolfram Syndrome 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
Հրապարակվել է 2016Artigo -
8
Essential Role of<i>BRCA2</i>in Ovarian Development and Function 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
Հրապարակվել է 2018Artigo -
9
Hyperinsulinism of Infancy: Novel ABCC8 and KCNJ11 Mutations and Evidence for Additional Locus Heterogeneity 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
Հրապարակվել է 2004Artigo -
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 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
Հրապարակվել է 2008Artigo -
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 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
Հրապարակվել է 2025Artigo -
12
Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex development 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
Հրապարակվել է 2024Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Biology
Medicine
Genetics
Endocrinology
Gene
Internal medicine
Insulin
Mutation
Phenotype
Cell biology
Computational biology
Diabetes mellitus
Disorders of sex development
Gonadal dysgenesis
Insulin resistance
Missense mutation
Transcription factor
Allele
Aneuploidy
Basal (medicine)
Biochemistry
Bioinformatics
Bolus (digestion)
Cancer research
Chemistry
Chromosome
Coactivation
Coding region
Cohort
Congenital hyperinsulinism