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Mitsuko Nakashima

Showing results (201-210 of 208) with videos related to

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Cell Reports|January 19, 2018
Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum DisorderAtsushi Takata, Noriko Miyake, Yoshinori Tsurusaki, et al.
American Journal of Medical Genetics. Part A|August 6, 2013
MLL2 and KDM6A mutations in patients with Kabuki syndromeNoriko Miyake, Eriko Koshimizu, Nobuhiko Okamoto, et al.
Science Advances|March 25, 2021
De novo ATP1A3 variants cause polymicrogyriaSatoko Miyatake, Mitsuhiro Kato, Takuma Kumamoto, et al.
Brain : a Journal of Neurology|October 21, 2017
Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophySteffen Syrbe, Frederike L Harms, Elena Parrini, et al.
Molecular Psychiatry|March 28, 2026
A key gene modulating oxytocin efficacy in autism: genome-wide discovery and verification in randomized controlled trials datasetsHitoshi Kuwabara, Masaki Kojima, Seico Benner, et al.
Human Genetics|May 4, 2021
Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsyIlaria Parenti, Daphné Lehalle, Caroline Nava, et al.
Nature Communications|June 9, 2019
Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathyAtsushi Takata, Mitsuko Nakashima, Hirotomo Saitsu, et al.
Journal of Medical Genetics|August 1, 2020
Prenatal clinical manifestations in individuals with <i>COL4A1/2</i> variantsToshiyuki Itai, Satoko Miyatake, Masataka Taguri, et al.
Pageof 21

Showing results (201-210 of 208) with videos related to

Sort By:
Pageof 21
You have reached the last page of results.This site can display upto 208 results.
Cell Reports|January 19, 2018
Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum DisorderAtsushi Takata, Noriko Miyake, Yoshinori Tsurusaki, et al.
American Journal of Medical Genetics. Part A|August 6, 2013
MLL2 and KDM6A mutations in patients with Kabuki syndromeNoriko Miyake, Eriko Koshimizu, Nobuhiko Okamoto, et al.
Science Advances|March 25, 2021
De novo ATP1A3 variants cause polymicrogyriaSatoko Miyatake, Mitsuhiro Kato, Takuma Kumamoto, et al.
Brain : a Journal of Neurology|October 21, 2017
Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophySteffen Syrbe, Frederike L Harms, Elena Parrini, et al.
Molecular Psychiatry|March 28, 2026
A key gene modulating oxytocin efficacy in autism: genome-wide discovery and verification in randomized controlled trials datasetsHitoshi Kuwabara, Masaki Kojima, Seico Benner, et al.
Human Genetics|May 4, 2021
Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsyIlaria Parenti, Daphné Lehalle, Caroline Nava, et al.
Nature Communications|June 9, 2019
Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathyAtsushi Takata, Mitsuko Nakashima, Hirotomo Saitsu, et al.
Journal of Medical Genetics|August 1, 2020
Prenatal clinical manifestations in individuals with <i>COL4A1/2</i> variantsToshiyuki Itai, Satoko Miyatake, Masataka Taguri, et al.
Pageof 21