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Janet E Hall

Showing results (121-130 of 131) with videos related to

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JCI Insight|January 5, 2023
Heterozygous mutations in SOX2 may cause idiopathic hypogonadotropic hypogonadism via dominant-negative mechanismsJessica Cassin, Maria I Stamou, Kimberly W Keefe, et al.
The Science of the Total Environment|July 21, 2017
Health consequences of electric lighting practices in the modern world: A report on the National Toxicology Program's workshop on shift work at night, artificial light at night, and circadian disruptionRuth M Lunn, David E Blask, Andrew N Coogan, 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|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.
The Journal of Clinical Endocrinology and Metabolism|March 25, 2010
TAC3/TACR3 mutations reveal preferential activation of gonadotropin-releasing hormone release by neurokinin B in neonatal life followed by reversal in adulthoodElena Gianetti, Cintia Tusset, Sekoni D Noel, et al.
The Journal of Clinical Endocrinology and Metabolism|June 20, 2023
Prevalence of Deleterious Variants in MC3R in Patients With Constitutional Delay of Growth and PubertyKatie Duckett, Alice Williamson, John W R Kincaid, et al.
The Journal of Clinical Endocrinology and Metabolism|February 9, 2020
Insight Into the Ontogeny of GnRH Neurons From Patients Born Without a NoseAngela Delaney, Rita Volochayev, Brooke Meader, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|May 7, 2020
The COronavirus Pandemic Epidemiology (COPE) Consortium: A Call to ActionAndrew T Chan, David A Drew, Long H Nguyen, et al.
Nature Genetics|May 27, 2017
Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndromeNatalie D Shaw, Harrison Brand, Zachary A Kupchinsky, et al.
Nature Genetics|January 10, 2017
SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndromeNatalie D Shaw, Harrison Brand, Zachary A Kupchinsky, et al.
Pageof 14

Showing results (121-130 of 131) with videos related to

Sort By:
Pageof 14
JCI Insight|January 5, 2023
Heterozygous mutations in SOX2 may cause idiopathic hypogonadotropic hypogonadism via dominant-negative mechanismsJessica Cassin, Maria I Stamou, Kimberly W Keefe, et al.
The Science of the Total Environment|July 21, 2017
Health consequences of electric lighting practices in the modern world: A report on the National Toxicology Program's workshop on shift work at night, artificial light at night, and circadian disruptionRuth M Lunn, David E Blask, Andrew N Coogan, 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|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.
The Journal of Clinical Endocrinology and Metabolism|March 25, 2010
TAC3/TACR3 mutations reveal preferential activation of gonadotropin-releasing hormone release by neurokinin B in neonatal life followed by reversal in adulthoodElena Gianetti, Cintia Tusset, Sekoni D Noel, et al.
The Journal of Clinical Endocrinology and Metabolism|June 20, 2023
Prevalence of Deleterious Variants in MC3R in Patients With Constitutional Delay of Growth and PubertyKatie Duckett, Alice Williamson, John W R Kincaid, et al.
The Journal of Clinical Endocrinology and Metabolism|February 9, 2020
Insight Into the Ontogeny of GnRH Neurons From Patients Born Without a NoseAngela Delaney, Rita Volochayev, Brooke Meader, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|May 7, 2020
The COronavirus Pandemic Epidemiology (COPE) Consortium: A Call to ActionAndrew T Chan, David A Drew, Long H Nguyen, et al.
Nature Genetics|May 27, 2017
Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndromeNatalie D Shaw, Harrison Brand, Zachary A Kupchinsky, et al.
Nature Genetics|January 10, 2017
SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndromeNatalie D Shaw, Harrison Brand, Zachary A Kupchinsky, et al.
Pageof 14