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Richard Quinton

Showing results (171-180 of 189) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|June 28, 2022
Transcriptome profiling of kisspeptin neurons from the mouse arcuate nucleus reveals new mechanisms in estrogenic control of fertilityBalázs Göcz, Éva Rumpler, Miklós Sárvári, et al.
The Journal of Clinical Endocrinology and Metabolism|June 30, 2012
When genetic load does not correlate with phenotypic spectrum: lessons from the GnRH receptor (GNRHR)Elena Gianetti, Janet E Hall, Margaret G Au, et al.
Human Molecular Genetics|July 10, 2012
An ancient founder mutation in PROKR2 impairs human reproductionMagdalena Avbelj Stefanija, Marc Jeanpierre, Gerasimos P Sykiotis, et al.
The Journal of Clinical Endocrinology and Metabolism|February 10, 2012
Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasiaTaneli Raivio, Magdalena Avbelj, Mark J McCabe, et al.
The Journal of Sexual Medicine|August 8, 2017
Quality of Life and Sexual Function Benefits of Long-Term Testosterone Treatment: Longitudinal Results From the Registry of Hypogonadism in Men (RHYME)Raymond C Rosen, Frederick Wu, Hermann M Behre, et al.
European Journal of Human Genetics : EJHG|January 14, 2026
Pleiotropic genes linking congenital hypogonadotropic hypogonadism and cleft lip/palate: evidence from a genomic CHH cohort studyFernanda de Azevedo Correa, Imen Habibi, Jing Zhai, et al.
European Journal of Endocrinology|June 22, 2017
In-frame seven amino-acid duplication in <i>AIP</i> arose over the last 3000 years, disrupts protein interaction and stability and is associated with gigantismRoberto Salvatori, Serban Radian, Yoan Diekmann, et al.
EMBO Molecular Medicine|July 30, 2017
<i>KLB</i>, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadismCheng Xu, Andrea Messina, Emmanuel Somm, et al.
Orphanet Journal of Rare Diseases|March 22, 2017
Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism, Corin Badiu, Marco Bonomi, et al.
American Journal of Human Genetics|May 7, 2013
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadismHichem Miraoui, Andrew A Dwyer, Gerasimos P Sykiotis, et al.
Pageof 19

Showing results (171-180 of 189) with videos related to

Sort By:
Pageof 19
Proceedings of the National Academy of Sciences of the United States of America|June 28, 2022
Transcriptome profiling of kisspeptin neurons from the mouse arcuate nucleus reveals new mechanisms in estrogenic control of fertilityBalázs Göcz, Éva Rumpler, Miklós Sárvári, et al.
The Journal of Clinical Endocrinology and Metabolism|June 30, 2012
When genetic load does not correlate with phenotypic spectrum: lessons from the GnRH receptor (GNRHR)Elena Gianetti, Janet E Hall, Margaret G Au, et al.
Human Molecular Genetics|July 10, 2012
An ancient founder mutation in PROKR2 impairs human reproductionMagdalena Avbelj Stefanija, Marc Jeanpierre, Gerasimos P Sykiotis, et al.
The Journal of Clinical Endocrinology and Metabolism|February 10, 2012
Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasiaTaneli Raivio, Magdalena Avbelj, Mark J McCabe, et al.
The Journal of Sexual Medicine|August 8, 2017
Quality of Life and Sexual Function Benefits of Long-Term Testosterone Treatment: Longitudinal Results From the Registry of Hypogonadism in Men (RHYME)Raymond C Rosen, Frederick Wu, Hermann M Behre, et al.
European Journal of Human Genetics : EJHG|January 14, 2026
Pleiotropic genes linking congenital hypogonadotropic hypogonadism and cleft lip/palate: evidence from a genomic CHH cohort studyFernanda de Azevedo Correa, Imen Habibi, Jing Zhai, et al.
European Journal of Endocrinology|June 22, 2017
In-frame seven amino-acid duplication in <i>AIP</i> arose over the last 3000 years, disrupts protein interaction and stability and is associated with gigantismRoberto Salvatori, Serban Radian, Yoan Diekmann, et al.
EMBO Molecular Medicine|July 30, 2017
<i>KLB</i>, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadismCheng Xu, Andrea Messina, Emmanuel Somm, et al.
Orphanet Journal of Rare Diseases|March 22, 2017
Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism, Corin Badiu, Marco Bonomi, et al.
American Journal of Human Genetics|May 7, 2013
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadismHichem Miraoui, Andrew A Dwyer, Gerasimos P Sykiotis, et al.
Pageof 19