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Showing results (121-130 of 128) with videos related to

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Nature Communications|September 10, 2017
Direct measurement of individual phonon lifetimes in the clathrate compound Ba<sub>7.81</sub>Ge<sub>40.67</sub>Au<sub>5.33</sub>Pierre-François Lory, Stéphane Pailhès, Valentina M Giordano, 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.
Human Molecular Genetics|December 5, 2017
DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron developmentJustine Bouilly, Andrea Messina, Georgios Papadakis, et al.
Endocrine Connections|March 12, 2015
FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficienciesFernanda A Correa, Ericka B Trarbach, Cintia Tusset, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 14, 2014
Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutationsCarine Villanueva, Elka Jacobson-Dickman, Cheng Xu, 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.
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 13

Showing results (121-130 of 128) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 128 results.
Nature Communications|September 10, 2017
Direct measurement of individual phonon lifetimes in the clathrate compound Ba<sub>7.81</sub>Ge<sub>40.67</sub>Au<sub>5.33</sub>Pierre-François Lory, Stéphane Pailhès, Valentina M Giordano, 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.
Human Molecular Genetics|December 5, 2017
DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron developmentJustine Bouilly, Andrea Messina, Georgios Papadakis, et al.
Endocrine Connections|March 12, 2015
FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficienciesFernanda A Correa, Ericka B Trarbach, Cintia Tusset, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 14, 2014
Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutationsCarine Villanueva, Elka Jacobson-Dickman, Cheng Xu, 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.
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 13