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Virginia Hughes

Showing results (41-50 of 46) with videos related to

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Angiogenesis|November 23, 2019
The potassium channel Kcne3 is a VEGFA-inducible gene selectively expressed by vascular endothelial tip cellsRon A Deckelbaum, Ivan B Lobov, Eunice Cheung, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 25, 2011
Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadismJanne Tornberg, Gerasimos P Sykiotis, Kimberly Keefe, et al.
The Journal of Clinical Investigation|January 20, 2007
Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadismNelly Pitteloud, Richard Quinton, Simon Pearce, et al.
The Journal of Clinical Investigation|July 4, 2008
Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and miceJohn Falardeau, Wilson C J Chung, Andrew Beenken, et al.
The Journal of Clinical Endocrinology and Metabolism|September 2, 2011
GnRH-deficient phenotypes in humans and mice with heterozygous variants in KISS1/Kiss1Yee-Ming Chan, Sarabeth Broder-Fingert, Sophia Paraschos, et al.
American Journal of Human Genetics|December 5, 2017
Monoallelic BMP2 Variants Predicted to Result in Haploinsufficiency Cause Craniofacial, Skeletal, and Cardiac Features Overlapping Those of 20p12 DeletionsTiong Yang Tan, Claudia Gonzaga-Jauregui, Elizabeth J Bhoj, et al.
Pageof 5

Showing results (41-50 of 46) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 46 results.
Angiogenesis|November 23, 2019
The potassium channel Kcne3 is a VEGFA-inducible gene selectively expressed by vascular endothelial tip cellsRon A Deckelbaum, Ivan B Lobov, Eunice Cheung, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 25, 2011
Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadismJanne Tornberg, Gerasimos P Sykiotis, Kimberly Keefe, et al.
The Journal of Clinical Investigation|January 20, 2007
Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadismNelly Pitteloud, Richard Quinton, Simon Pearce, et al.
The Journal of Clinical Investigation|July 4, 2008
Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and miceJohn Falardeau, Wilson C J Chung, Andrew Beenken, et al.
The Journal of Clinical Endocrinology and Metabolism|September 2, 2011
GnRH-deficient phenotypes in humans and mice with heterozygous variants in KISS1/Kiss1Yee-Ming Chan, Sarabeth Broder-Fingert, Sophia Paraschos, et al.
American Journal of Human Genetics|December 5, 2017
Monoallelic BMP2 Variants Predicted to Result in Haploinsufficiency Cause Craniofacial, Skeletal, and Cardiac Features Overlapping Those of 20p12 DeletionsTiong Yang Tan, Claudia Gonzaga-Jauregui, Elizabeth J Bhoj, et al.
Pageof 5