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Noam Adir

Showing results (81-90 of 88) with videos related to

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American Journal of Human Genetics|October 1, 2013
Cole Disease Results from Mutations in ENPP1Ori Eytan, Fanny Morice-Picard, Ofer Sarig, et al.
American Journal of Human Genetics|April 29, 2008
Alopecia, neurological defects, and endocrinopathy syndrome caused by decreased expression of RBM28, a nucleolar protein associated with ribosome biogenesisJanna Nousbeck, Ronen Spiegel, Akemi Ishida-Yamamoto, et al.
The ISME Journal|November 29, 2007
Viral photosynthetic reaction center genes and transcripts in the marine environmentItai Sharon, Shani Tzahor, Shannon Williamson, et al.
Molecular Brain|January 22, 2021
Rare functional missense variants in CACNA1H: What can we learn from Writer's cramp?Miaozhen Huang, Esther A R Nibbeling, Tjerk J Lagrand, et al.
The New England Journal of Medicine|February 15, 2019
Variant <i>PADI3</i> in Central Centrifugal Cicatricial AlopeciaLiron Malki, Ofer Sarig, Maria-Teresa Romano, et al.
Plos Genetics|October 14, 2016
Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle MorphogenesisAlon Peled, Ofer Sarig, Liat Samuelov, et al.
Brain : a Journal of Neurology|October 21, 2017
Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxiaEsther A R Nibbeling, Anna Duarri, Corien C Verschuuren-Bemelmans, et al.
The Journal of Investigative Dermatology|October 23, 2016
Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital IchthyosisRon Bochner, Liat Samuelov, Ofer Sarig, et al.
Pageof 9

Showing results (81-90 of 88) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 88 results.
American Journal of Human Genetics|October 1, 2013
Cole Disease Results from Mutations in ENPP1Ori Eytan, Fanny Morice-Picard, Ofer Sarig, et al.
American Journal of Human Genetics|April 29, 2008
Alopecia, neurological defects, and endocrinopathy syndrome caused by decreased expression of RBM28, a nucleolar protein associated with ribosome biogenesisJanna Nousbeck, Ronen Spiegel, Akemi Ishida-Yamamoto, et al.
The ISME Journal|November 29, 2007
Viral photosynthetic reaction center genes and transcripts in the marine environmentItai Sharon, Shani Tzahor, Shannon Williamson, et al.
Molecular Brain|January 22, 2021
Rare functional missense variants in CACNA1H: What can we learn from Writer's cramp?Miaozhen Huang, Esther A R Nibbeling, Tjerk J Lagrand, et al.
The New England Journal of Medicine|February 15, 2019
Variant <i>PADI3</i> in Central Centrifugal Cicatricial AlopeciaLiron Malki, Ofer Sarig, Maria-Teresa Romano, et al.
Plos Genetics|October 14, 2016
Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle MorphogenesisAlon Peled, Ofer Sarig, Liat Samuelov, et al.
Brain : a Journal of Neurology|October 21, 2017
Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxiaEsther A R Nibbeling, Anna Duarri, Corien C Verschuuren-Bemelmans, et al.
The Journal of Investigative Dermatology|October 23, 2016
Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital IchthyosisRon Bochner, Liat Samuelov, Ofer Sarig, et al.
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