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Human Molecular Genetics
|
November 16, 2013
LRP4 third β-propeller domain mutations cause novel congenital myasthenia by compromising agrin-mediated MuSK signaling in a position-specific manner
Bisei Ohkawara, Macarena Cabrera-Serrano, Tomohiko Nakata, et al.
Plos One
|
May 3, 2014
Searching for genomic region of high-fat diet-induced type 2 diabetes in mouse chromosome 2 by analysis of congenic strains
Misato Kobayashi, Tamio Ohno, Kunio Ihara, et al.
Journal of Neurochemistry
|
November 23, 2023
Transcriptome profile of subsynaptic myonuclei at the neuromuscular junction in embryogenesis
Bisei Ohkawara, Masaomi Kurokawa, Akinori Kanai, et al.
The Journal of General Physiology
|
October 3, 2002
Naturally occurring mutations at the acetylcholine receptor binding site independently alter ACh binding and channel gating
Steven M Sine, Xing-Ming Shen, Hai-Long Wang, et al.
Journal of the Neurological Sciences
|
January 20, 2012
A novel mutation in SCN4A causes severe myotonia and school-age-onset paralytic episodes
Harumi Yoshinaga, Shunichi Sakoda, Jean-Marc Good, et al.
Scientific Reports
|
October 9, 2023
Development of machine learning models for predicting unfavorable functional outcomes from preoperative data in patients with chronic subdural hematomas
Yutaro Fuse, Yoshitaka Nagashima, Hiroshi Nishiwaki, et al.
Journal of Human Genetics
|
April 20, 2012
Four parameters increase the sensitivity and specificity of the exon array analysis and disclose 25 novel aberrantly spliced exons in myotonic dystrophy
Yoshihiro Yamashita, Tohru Matsuura, Jun Shinmi, et al.
Frontiers in Cell and Developmental Biology
|
February 4, 2022
Meclozine Attenuates the MARK Pathway in Mammalian Chondrocytes and Ameliorates FGF2-Induced Bone Hyperossification in Larval Zebrafish
Genta Takemoto, Masaki Matsushita, Takaaki Okamoto, et al.
EMBO Molecular Medicine
|
January 30, 2014
SIL1, a causative cochaperone gene of Marinesco-Söjgren syndrome, plays an essential role in establishing the architecture of the developing cerebral cortex
Yutaka Inaguma, Nanako Hamada, Hidenori Tabata, et al.
Parkinsonism & Related Disorders
|
December 26, 2021
Altered gut microbiota in Parkinson's disease patients with motor complications
Kai Takahashi, Hiroshi Nishiwaki, Mikako Ito, et al.
Page
of 25
Search research articles
Search
Showing results (201-210 of 245) with videos related to
Sort By:
Page
of 25
Human Molecular Genetics
|
November 16, 2013
LRP4 third β-propeller domain mutations cause novel congenital myasthenia by compromising agrin-mediated MuSK signaling in a position-specific manner
Bisei Ohkawara, Macarena Cabrera-Serrano, Tomohiko Nakata, et al.
Plos One
|
May 3, 2014
Searching for genomic region of high-fat diet-induced type 2 diabetes in mouse chromosome 2 by analysis of congenic strains
Misato Kobayashi, Tamio Ohno, Kunio Ihara, et al.
Journal of Neurochemistry
|
November 23, 2023
Transcriptome profile of subsynaptic myonuclei at the neuromuscular junction in embryogenesis
Bisei Ohkawara, Masaomi Kurokawa, Akinori Kanai, et al.
The Journal of General Physiology
|
October 3, 2002
Naturally occurring mutations at the acetylcholine receptor binding site independently alter ACh binding and channel gating
Steven M Sine, Xing-Ming Shen, Hai-Long Wang, et al.
Journal of the Neurological Sciences
|
January 20, 2012
A novel mutation in SCN4A causes severe myotonia and school-age-onset paralytic episodes
Harumi Yoshinaga, Shunichi Sakoda, Jean-Marc Good, et al.
Scientific Reports
|
October 9, 2023
Development of machine learning models for predicting unfavorable functional outcomes from preoperative data in patients with chronic subdural hematomas
Yutaro Fuse, Yoshitaka Nagashima, Hiroshi Nishiwaki, et al.
Journal of Human Genetics
|
April 20, 2012
Four parameters increase the sensitivity and specificity of the exon array analysis and disclose 25 novel aberrantly spliced exons in myotonic dystrophy
Yoshihiro Yamashita, Tohru Matsuura, Jun Shinmi, et al.
Frontiers in Cell and Developmental Biology
|
February 4, 2022
Meclozine Attenuates the MARK Pathway in Mammalian Chondrocytes and Ameliorates FGF2-Induced Bone Hyperossification in Larval Zebrafish
Genta Takemoto, Masaki Matsushita, Takaaki Okamoto, et al.
EMBO Molecular Medicine
|
January 30, 2014
SIL1, a causative cochaperone gene of Marinesco-Söjgren syndrome, plays an essential role in establishing the architecture of the developing cerebral cortex
Yutaka Inaguma, Nanako Hamada, Hidenori Tabata, et al.
Parkinsonism & Related Disorders
|
December 26, 2021
Altered gut microbiota in Parkinson's disease patients with motor complications
Kai Takahashi, Hiroshi Nishiwaki, Mikako Ito, et al.
Page
of 25