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Human Mutation|November 1, 2020
De novo variants in CELF2 that disrupt the nuclear localization signal cause developmental and epileptic encephalopathyToshiyuki Itai, Kohei Hamanaka, Kazunori Sasaki, et al.
Nature Medicine|January 22, 2020
Visualization of AMPA receptors in living human brain with positron emission tomographyTomoyuki Miyazaki, Waki Nakajima, Mai Hatano, et al.
Brain : a Journal of Neurology|March 31, 2022
Repeat conformation heterogeneity in cerebellar ataxia, neuropathy, vestibular areflexia syndromeSatoko Miyatake, Kunihiro Yoshida, Eriko Koshimizu, et al.
Science Translational Medicine|June 22, 2022
Molecular signatures of long-term hepatocellular carcinoma risk in nonalcoholic fatty liver diseaseNaoto Fujiwara, Naoto Kubota, Emilie Crouchet, 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.
Journal of Medical Genetics|August 1, 2020
Prenatal clinical manifestations in individuals with COL4A1/2 variantsToshiyuki Itai, Satoko Miyatake, Masataka Taguri, et al.
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