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Yuval Itan

Showing results (61-70 of 116) with videos related to

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Nature Metabolism|February 23, 2021
Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbiditiesLam O Huang, Alexander Rauch, Eugenia Mazzaferro, et al.
Nature Genetics|January 3, 2024
Development of a human genetics-guided priority score for 19,365 genes and 399 drug indicationsÁine Duffy, Ben Omega Petrazzini, David Stein, et al.
Nature Metabolism|April 6, 2023
Genetic susceptibility to diabetic kidney disease is linked to promoter variants of XORQin Wang, Haiying Qi, Yiming Wu, et al.
Journal of the American College of Cardiology|April 1, 2017
Autosomal Recessive Cardiomyopathy Presenting as Acute MyocarditisSerkan Belkaya, Amy R Kontorovich, Minji Byun, et al.
The Journal of Experimental Medicine|April 29, 2015
Inherited IL-17RC deficiency in patients with chronic mucocutaneous candidiasisYun Ling, Sophie Cypowyj, Caner Aytekin, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2025
Acute cold exposure in humans shifts the circulating proteome to a cardioprotective and anti-aging profileKaja Plucińska, Zsu-Zsu Chen, Ruijie Xiang, et al.
The Journal of Clinical Investigation|June 16, 2020
Human CRY1 variants associate with attention deficit/hyperactivity disorderO Emre Onat, M Ece Kars, Şeref Gül, et al.
The Journal of Experimental Medicine|July 8, 2015
Reticular dysgenesis-associated AK2 protects hematopoietic stem and progenitor cell development from oxidative stressAlberto Rissone, Katja Gabriele Weinacht, Giancarlo la Marca, et al.
Clinical Immunology (Orlando, Fla.)|October 4, 2016
Gain-of-function mutation in PIK3R1 in a patient with a narrow clinical phenotype of respiratory infectionsMaría Teresa Martínez-Saavedra, Sonia García-Gomez, Ana Domínguez Acosta, et al.
Research Square|July 23, 2024
Molecular and clinical characterization of a founder mutation causing G6PC3 deficiencyXin Zhen, Michael Betti, Meltem Ece Kars, et al.
Pageof 12

Showing results (61-70 of 116) with videos related to

Sort By:
Pageof 12
Nature Metabolism|February 23, 2021
Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbiditiesLam O Huang, Alexander Rauch, Eugenia Mazzaferro, et al.
Nature Genetics|January 3, 2024
Development of a human genetics-guided priority score for 19,365 genes and 399 drug indicationsÁine Duffy, Ben Omega Petrazzini, David Stein, et al.
Nature Metabolism|April 6, 2023
Genetic susceptibility to diabetic kidney disease is linked to promoter variants of XORQin Wang, Haiying Qi, Yiming Wu, et al.
Journal of the American College of Cardiology|April 1, 2017
Autosomal Recessive Cardiomyopathy Presenting as Acute MyocarditisSerkan Belkaya, Amy R Kontorovich, Minji Byun, et al.
The Journal of Experimental Medicine|April 29, 2015
Inherited IL-17RC deficiency in patients with chronic mucocutaneous candidiasisYun Ling, Sophie Cypowyj, Caner Aytekin, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2025
Acute cold exposure in humans shifts the circulating proteome to a cardioprotective and anti-aging profileKaja Plucińska, Zsu-Zsu Chen, Ruijie Xiang, et al.
The Journal of Clinical Investigation|June 16, 2020
Human CRY1 variants associate with attention deficit/hyperactivity disorderO Emre Onat, M Ece Kars, Şeref Gül, et al.
The Journal of Experimental Medicine|July 8, 2015
Reticular dysgenesis-associated AK2 protects hematopoietic stem and progenitor cell development from oxidative stressAlberto Rissone, Katja Gabriele Weinacht, Giancarlo la Marca, et al.
Clinical Immunology (Orlando, Fla.)|October 4, 2016
Gain-of-function mutation in PIK3R1 in a patient with a narrow clinical phenotype of respiratory infectionsMaría Teresa Martínez-Saavedra, Sonia García-Gomez, Ana Domínguez Acosta, et al.
Research Square|July 23, 2024
Molecular and clinical characterization of a founder mutation causing G6PC3 deficiencyXin Zhen, Michael Betti, Meltem Ece Kars, et al.
Pageof 12