Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Cheol-Hee Kim

Showing results (211-220 of 225) with videos related to

Pageof 23
Sort By:
Developmental Biology|February 28, 2015
IFT46 plays an essential role in cilia developmentMi-Sun Lee, Kyu-Seok Hwang, Hyun-Woo Oh, et al.
Biorxiv : the Preprint Server for Biology|June 3, 2024
Complimentary vertebrate <i>Wac</i> models exhibit phenotypes relevant to DeSanto-Shinawi SyndromeKang-Han Lee, April M Stafford, Maria Pacheco-Vergara, et al.
Frontiers in Molecular Neuroscience|October 24, 2022
A rigorous <i>in silico</i> genomic interrogation at 1p13.3 reveals 16 autosomal dominant candidate genes in syndromic neurodevelopmental disordersAfif Ben-Mahmoud, Kyung Ran Jun, Vijay Gupta, et al.
Human Molecular Genetics|June 10, 2015
ZC4H2, an XLID gene, is required for the generation of a specific subset of CNS interneuronsMelanie May, Kyu-Seok Hwang, Judith Miles, et al.
Nature Methods|September 18, 2023
Statistically unbiased prediction enables accurate denoising of voltage imaging dataMinho Eom, Seungjae Han, Pojeong Park, et al.
American Journal of Human Genetics|October 5, 2010
WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndromeHyung-Goo Kim, Jang-Won Ahn, Ingo Kurth, et al.
Molecular Autism|October 26, 2019
Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autismHyung-Goo Kim, Jill A Rosenfeld, Daryl A Scott, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 18, 2018
Targeted knockout of a chemokine-like gene increases anxiety and fear responsesJung-Hwa Choi, Yun-Mi Jeong, Sujin Kim, et al.
American Journal of Human Genetics|January 27, 2015
Mutations in DDX58, which encodes RIG-I, cause atypical Singleton-Merten syndromeMi-Ae Jang, Eun Kyoung Kim, Hesung Now, et al.
Nature Communications|July 25, 2020
Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathyYu-Ri Lee, Kamal Khan, Kim Armfield-Uhas, et al.
Pageof 23

Showing results (211-220 of 225) with videos related to

Sort By:
Pageof 23
Developmental Biology|February 28, 2015
IFT46 plays an essential role in cilia developmentMi-Sun Lee, Kyu-Seok Hwang, Hyun-Woo Oh, et al.
Biorxiv : the Preprint Server for Biology|June 3, 2024
Complimentary vertebrate <i>Wac</i> models exhibit phenotypes relevant to DeSanto-Shinawi SyndromeKang-Han Lee, April M Stafford, Maria Pacheco-Vergara, et al.
Frontiers in Molecular Neuroscience|October 24, 2022
A rigorous <i>in silico</i> genomic interrogation at 1p13.3 reveals 16 autosomal dominant candidate genes in syndromic neurodevelopmental disordersAfif Ben-Mahmoud, Kyung Ran Jun, Vijay Gupta, et al.
Human Molecular Genetics|June 10, 2015
ZC4H2, an XLID gene, is required for the generation of a specific subset of CNS interneuronsMelanie May, Kyu-Seok Hwang, Judith Miles, et al.
Nature Methods|September 18, 2023
Statistically unbiased prediction enables accurate denoising of voltage imaging dataMinho Eom, Seungjae Han, Pojeong Park, et al.
American Journal of Human Genetics|October 5, 2010
WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndromeHyung-Goo Kim, Jang-Won Ahn, Ingo Kurth, et al.
Molecular Autism|October 26, 2019
Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autismHyung-Goo Kim, Jill A Rosenfeld, Daryl A Scott, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 18, 2018
Targeted knockout of a chemokine-like gene increases anxiety and fear responsesJung-Hwa Choi, Yun-Mi Jeong, Sujin Kim, et al.
American Journal of Human Genetics|January 27, 2015
Mutations in DDX58, which encodes RIG-I, cause atypical Singleton-Merten syndromeMi-Ae Jang, Eun Kyoung Kim, Hesung Now, et al.
Nature Communications|July 25, 2020
Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathyYu-Ri Lee, Kamal Khan, Kim Armfield-Uhas, et al.
Pageof 23