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Annals of Neurology
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January 22, 2022
Muscle Transcriptomics Shows Overexpression of Cadherin 1 in Inclusion Body Myositis
Chiseko Ikenaga, Hidetoshi Date, Motoi Kanagawa, et al.
Journal of the Neurological Sciences
|
December 27, 2016
Slowly progressive d-bifunctional protein deficiency with survival to adulthood diagnosed by whole-exome sequencing
Takashi Matsukawa, Kagari Mano Koshi, Jun Mitsui, et al.
Cerebellum (London, England)
|
September 13, 2017
Novel De Novo KCND3 Mutation in a Japanese Patient with Intellectual Disability, Cerebellar Ataxia, Myoclonus, and Dystonia
Masanori Kurihara, Hiroyuki Ishiura, Takuya Sasaki, et al.
Gene
|
June 16, 2012
Extremely slow rate of evolution in the HOX cluster revealed by comparison between Tanzanian and Indonesian coelacanths
Koichiro Higasa, Masato Nikaido, Taro L Saito, et al.
Neurogenetics
|
August 21, 2020
Splice-site mutations in KIF5A in the Japanese case series of amyotrophic lateral sclerosis
Hiroya Naruse, Hiroyuki Ishiura, Jun Mitsui, et al.
Scientific Reports
|
June 10, 2022
Early prediction of functional prognosis in neurofibromatosis type 2 patients based on genotype-phenotype correlation with targeted deep sequencing
Yu Teranishi, Satoru Miyawaki, Hirofumi Nakatomi, et al.
Bioinformatics (Oxford, England)
|
June 19, 2016
AgIn: measuring the landscape of CpG methylation of individual repetitive elements
Yuta Suzuki, Jonas Korlach, Stephen W Turner, et al.
Genome Research
|
May 25, 2019
Recompleting the <i>Caenorhabditis elegans</i> genome
Jun Yoshimura, Kazuki Ichikawa, Massa J Shoura, et al.
Journal of the Neurological Sciences
|
March 22, 2017
Ataxic form of autosomal recessive PEX10-related peroxisome biogenesis disorders with a novel compound heterozygous gene mutation and characteristic clinical phenotype
Toru Yamashita, Jun Mitsui, Nobuyuki Shimozawa, et al.
Molecular Brain
|
October 8, 2016
Modeling neurological diseases with induced pluripotent cells reprogrammed from immortalized lymphoblastoid cell lines
Koki Fujimori, Toshiki Tezuka, Hiroyuki Ishiura, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 52) with videos related to
Sort By:
Page
of 6
Annals of Neurology
|
January 22, 2022
Muscle Transcriptomics Shows Overexpression of Cadherin 1 in Inclusion Body Myositis
Chiseko Ikenaga, Hidetoshi Date, Motoi Kanagawa, et al.
Journal of the Neurological Sciences
|
December 27, 2016
Slowly progressive d-bifunctional protein deficiency with survival to adulthood diagnosed by whole-exome sequencing
Takashi Matsukawa, Kagari Mano Koshi, Jun Mitsui, et al.
Cerebellum (London, England)
|
September 13, 2017
Novel De Novo KCND3 Mutation in a Japanese Patient with Intellectual Disability, Cerebellar Ataxia, Myoclonus, and Dystonia
Masanori Kurihara, Hiroyuki Ishiura, Takuya Sasaki, et al.
Gene
|
June 16, 2012
Extremely slow rate of evolution in the HOX cluster revealed by comparison between Tanzanian and Indonesian coelacanths
Koichiro Higasa, Masato Nikaido, Taro L Saito, et al.
Neurogenetics
|
August 21, 2020
Splice-site mutations in KIF5A in the Japanese case series of amyotrophic lateral sclerosis
Hiroya Naruse, Hiroyuki Ishiura, Jun Mitsui, et al.
Scientific Reports
|
June 10, 2022
Early prediction of functional prognosis in neurofibromatosis type 2 patients based on genotype-phenotype correlation with targeted deep sequencing
Yu Teranishi, Satoru Miyawaki, Hirofumi Nakatomi, et al.
Bioinformatics (Oxford, England)
|
June 19, 2016
AgIn: measuring the landscape of CpG methylation of individual repetitive elements
Yuta Suzuki, Jonas Korlach, Stephen W Turner, et al.
Genome Research
|
May 25, 2019
Recompleting the <i>Caenorhabditis elegans</i> genome
Jun Yoshimura, Kazuki Ichikawa, Massa J Shoura, et al.
Journal of the Neurological Sciences
|
March 22, 2017
Ataxic form of autosomal recessive PEX10-related peroxisome biogenesis disorders with a novel compound heterozygous gene mutation and characteristic clinical phenotype
Toru Yamashita, Jun Mitsui, Nobuyuki Shimozawa, et al.
Molecular Brain
|
October 8, 2016
Modeling neurological diseases with induced pluripotent cells reprogrammed from immortalized lymphoblastoid cell lines
Koki Fujimori, Toshiki Tezuka, Hiroyuki Ishiura, et al.
Page
of 6