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S Acierno

Showing results (21-30 of 34) with videos related to

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Urology|January 14, 1998
Vitamin D inhibition of prostate adenocarcinoma growth and metastasis in the Dunning rat prostate model systemR H Getzenberg, B W Light, P E Lapco, et al.
Human Molecular Genetics|October 13, 2000
Mucolipidosis type IV is caused by mutations in a gene encoding a novel transient receptor potential channelM Sun, E Goldin, S Stahl, et al.
Molecular and Cellular Endocrinology|June 13, 2006
Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypesNelly Pitteloud, Astrid Meysing, Richard Quinton, et al.
Neuroendocrinology|February 20, 2020
Congenital Hypogonadotropic Hypogonadism with Anosmia and Gorlin Features Caused by a PTCH1 Mutation Reveals a New Candidate Gene for Kallmann SyndromeSara Barraud, Brigitte Delemer, Céline Poirsier-Violle, et al.
Human Reproduction Open|March 24, 2026
Clinical and genetic basis of congenital gonadotropin deficiencyYi Wang, Jing Zhai, Imen Habibi, et al.
Genomics|April 25, 2001
A physical and transcript map of the MCOLN1 gene region on human chromosome 19p13.3-p13.2J S Acierno, J C Kennedy, J L Falardeau, et al.
JCI Insight|April 20, 2017
β-Klotho deficiency protects against obesity through a crosstalk between liver, microbiota, and brown adipose tissueEmmanuel Somm, Hugues Henry, Stephen J Bruce, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 12, 2006
Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadismNelly Pitteloud, James S Acierno, Astrid Meysing, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 30, 2020
Pathogenic mosaic variants in congenital hypogonadotropic hypogonadismJames S Acierno, Cheng Xu, Georgios E Papadakis, 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.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Urology|January 14, 1998
Vitamin D inhibition of prostate adenocarcinoma growth and metastasis in the Dunning rat prostate model systemR H Getzenberg, B W Light, P E Lapco, et al.
Human Molecular Genetics|October 13, 2000
Mucolipidosis type IV is caused by mutations in a gene encoding a novel transient receptor potential channelM Sun, E Goldin, S Stahl, et al.
Molecular and Cellular Endocrinology|June 13, 2006
Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypesNelly Pitteloud, Astrid Meysing, Richard Quinton, et al.
Neuroendocrinology|February 20, 2020
Congenital Hypogonadotropic Hypogonadism with Anosmia and Gorlin Features Caused by a PTCH1 Mutation Reveals a New Candidate Gene for Kallmann SyndromeSara Barraud, Brigitte Delemer, Céline Poirsier-Violle, et al.
Human Reproduction Open|March 24, 2026
Clinical and genetic basis of congenital gonadotropin deficiencyYi Wang, Jing Zhai, Imen Habibi, et al.
Genomics|April 25, 2001
A physical and transcript map of the MCOLN1 gene region on human chromosome 19p13.3-p13.2J S Acierno, J C Kennedy, J L Falardeau, et al.
JCI Insight|April 20, 2017
β-Klotho deficiency protects against obesity through a crosstalk between liver, microbiota, and brown adipose tissueEmmanuel Somm, Hugues Henry, Stephen J Bruce, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 12, 2006
Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadismNelly Pitteloud, James S Acierno, Astrid Meysing, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 30, 2020
Pathogenic mosaic variants in congenital hypogonadotropic hypogonadismJames S Acierno, Cheng Xu, Georgios E Papadakis, 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.
Pageof 4