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Developmental Biology
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February 28, 2015
IFT46 plays an essential role in cilia development
Mi-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 Syndrome
Kang-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 disorders
Afif 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 interneurons
Melanie May, Kyu-Seok Hwang, Judith Miles, et al.
Nature Methods
|
September 18, 2023
Statistically unbiased prediction enables accurate denoising of voltage imaging data
Minho 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 syndrome
Hyung-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 autism
Hyung-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 responses
Jung-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 syndrome
Mi-Ae Jang, Eun Kyoung Kim, Hesung Now, et al.
Nature Communications
|
July 25, 2020
Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathy
Yu-Ri Lee, Kamal Khan, Kim Armfield-Uhas, et al.
Page
of 23
Search research articles
Search
Showing results (211-220 of 225) with videos related to
Sort By:
Page
of 23
Developmental Biology
|
February 28, 2015
IFT46 plays an essential role in cilia development
Mi-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 Syndrome
Kang-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 disorders
Afif 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 interneurons
Melanie May, Kyu-Seok Hwang, Judith Miles, et al.
Nature Methods
|
September 18, 2023
Statistically unbiased prediction enables accurate denoising of voltage imaging data
Minho 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 syndrome
Hyung-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 autism
Hyung-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 responses
Jung-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 syndrome
Mi-Ae Jang, Eun Kyoung Kim, Hesung Now, et al.
Nature Communications
|
July 25, 2020
Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathy
Yu-Ri Lee, Kamal Khan, Kim Armfield-Uhas, et al.
Page
of 23