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Hyung-Goo Kim

Showing results (1-10 of 107) with videos related to

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International Journal of Molecular Sciences|June 28, 2023
Editorial for the <i>IJMS</i> Special Issue on "Molecular Genetics of Autism and Intellectual Disability"Hyung-Goo Kim
Molecular and Cellular Endocrinology|August 23, 2011
The role of CHD7 and the newly identified WDR11 gene in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndromeHyung-Goo Kim, Lawrence C Layman
Neuro-Signals|February 7, 2008
Clinical manifestations of impaired GnRH neuron development and functionHyung-Goo Kim, Balasubramanian Bhagavath, Lawrence C Layman
Molecular Neurobiology|June 7, 2022
WDR5-HOTTIP Histone Modifying Complex Regulates Neural Migration and Dendrite Polarity of Pyramidal Neurons via Reelin SignalingMinhan Ka, Hyung-Goo Kim, Woo-Yang Kim
Biomaterials|January 25, 2015
Characterization and tissue incorporation of cross-linked human acellular dermal matrixJu Hee Lee, Hyung Goo Kim, Won Jai Lee
Experimental & Molecular Medicine|January 8, 2025
The WAVE complex in developmental and adulthood brain disordersHyung-Goo Kim, Clara Berdasco, Angus C Nairn, et al.
Frontiers of Hormone Research|April 15, 2010
Genotype and phenotype of patients with gonadotropin-releasing hormone receptor mutationsHyung-Goo Kim, Jennifer Pedersen-White, Balasubramanian Bhagavath, et al.
Frontiers of Hormone Research|April 15, 2010
Rarer syndromes characterized by hypogonadotropic hypogonadismMajid Aminzadeh, Hyung-Goo Kim, Lawrence C Layman, et al.
Molecular Cytogenetics|October 7, 2016
The presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disabilityKyungsoo Ha, Yiping Shen, Tyler Graves, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|November 28, 2012
The molecular basis of impaired follicle-stimulating hormone action: evidence from human mutations and mouse modelsEric T Siegel, Hyung-Goo Kim, Hiromi Koso Nishimoto, et al.
Pageof 11

Showing results (1-10 of 107) with videos related to

Sort By:
Pageof 11
International Journal of Molecular Sciences|June 28, 2023
Editorial for the <i>IJMS</i> Special Issue on "Molecular Genetics of Autism and Intellectual Disability"Hyung-Goo Kim
Molecular and Cellular Endocrinology|August 23, 2011
The role of CHD7 and the newly identified WDR11 gene in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndromeHyung-Goo Kim, Lawrence C Layman
Neuro-Signals|February 7, 2008
Clinical manifestations of impaired GnRH neuron development and functionHyung-Goo Kim, Balasubramanian Bhagavath, Lawrence C Layman
Molecular Neurobiology|June 7, 2022
WDR5-HOTTIP Histone Modifying Complex Regulates Neural Migration and Dendrite Polarity of Pyramidal Neurons via Reelin SignalingMinhan Ka, Hyung-Goo Kim, Woo-Yang Kim
Biomaterials|January 25, 2015
Characterization and tissue incorporation of cross-linked human acellular dermal matrixJu Hee Lee, Hyung Goo Kim, Won Jai Lee
Experimental & Molecular Medicine|January 8, 2025
The WAVE complex in developmental and adulthood brain disordersHyung-Goo Kim, Clara Berdasco, Angus C Nairn, et al.
Frontiers of Hormone Research|April 15, 2010
Genotype and phenotype of patients with gonadotropin-releasing hormone receptor mutationsHyung-Goo Kim, Jennifer Pedersen-White, Balasubramanian Bhagavath, et al.
Frontiers of Hormone Research|April 15, 2010
Rarer syndromes characterized by hypogonadotropic hypogonadismMajid Aminzadeh, Hyung-Goo Kim, Lawrence C Layman, et al.
Molecular Cytogenetics|October 7, 2016
The presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disabilityKyungsoo Ha, Yiping Shen, Tyler Graves, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|November 28, 2012
The molecular basis of impaired follicle-stimulating hormone action: evidence from human mutations and mouse modelsEric T Siegel, Hyung-Goo Kim, Hiromi Koso Nishimoto, et al.
Pageof 11