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Angiogenesis
|
November 23, 2019
The potassium channel Kcne3 is a VEGFA-inducible gene selectively expressed by vascular endothelial tip cells
Ron 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 hypogonadism
Janne 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 hypogonadism
Nelly 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 mice
John 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/Kiss1
Yee-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 Deletions
Tiong Yang Tan, Claudia Gonzaga-Jauregui, Elizabeth J Bhoj, et al.
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of 5
Search research articles
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Showing results (41-50 of 46) with videos related to
Sort By:
Page
of 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 cells
Ron 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 hypogonadism
Janne 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 hypogonadism
Nelly 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 mice
John 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/Kiss1
Yee-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 Deletions
Tiong Yang Tan, Claudia Gonzaga-Jauregui, Elizabeth J Bhoj, et al.
Page
of 5