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Aritoshi Iida

Showing results (31-40 of 106) with videos related to

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Journal of Human Genetics|July 12, 2002
Catalog of 605 single-nucleotide polymorphisms (SNPs) among 13 genes encoding human ATP-binding cassette transporters: ABCA4, ABCA7, ABCA8, ABCD1, ABCD3, ABCD4, ABCE1, ABCF1, ABCG1, ABCG2, ABCG4, ABCG5, and ABCG8Aritoshi Iida, Susumu Saito, Akihiro Sekine, et al.
Journal of Human Genetics|October 12, 2002
Catalog of 86 single-nucleotide polymorphisms (SNPs) in three uridine diphosphate glycosyltransferase genes: UGT2A1, UGT2B15, and UGT8Aritoshi Iida, Susumu Saito, Akihiro Sekine, et al.
Acta Neuropathologica Communications|December 8, 2022
Intranuclear inclusions in muscle biopsy can differentiate oculopharyngodistal myopathy and oculopharyngeal muscular dystrophyMasashi Ogasawara, Nobuyuki Eura, Aritoshi Iida, et al.
Journal of Human Genetics|October 27, 2004
Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn diseaseKeiko Yamazaki, Masakazu Takazoe, Torao Tanaka, et al.
Journal of Human Genetics|March 28, 2002
Thirteen single-nucleotide polymorphisms (SNPs) in the alcohol dehydrogenase 4 (ADH4) gene locusAritoshi Iida, Susumu Saito, Akihiro Sekine, et al.
Neuromuscular Disorders : NMD|October 12, 2021
An autopsied case of ADSSL1 myopathyAtsuko Motoda, Tetsuya Takahashi, Chigusa Watanabe, et al.
Journal of Human Genetics|February 7, 2002
Catalog of 77 single-nucleotide polymorphisms (SNPs) in the carbohydrate sulfotransferase 1 (CHST1) and carbohydrate sulfotransferase 3 (CHST3) genesAritoshi Iida, Susumu Saito, Akihiro Sekine, et al.
Neurology. Genetics|December 22, 2021
<i>TNNI1</i> Mutated in Autosomal Dominant Proximal ArthrogryposisYukako Nishimori, Aritoshi Iida, Masashi Ogasawara, et al.
The Journal of Clinical Endocrinology and Metabolism|February 10, 2015
A case of functional growth hormone deficiency and early growth retardation in a child with IFT172 mutationsAngela K Lucas-Herald, Esther Kinning, Aritoshi Iida, et al.
Molecular Genetics & Genomic Medicine|March 19, 2019
Three novel MTM1 pathogenic variants identified in Japanese patients with X-linked myotubular myopathyAtsuko Nishikawa, Aritoshi Iida, Shinichiro Hayashi, et al.
Pageof 11

Showing results (31-40 of 106) with videos related to

Sort By:
Pageof 11
Journal of Human Genetics|July 12, 2002
Catalog of 605 single-nucleotide polymorphisms (SNPs) among 13 genes encoding human ATP-binding cassette transporters: ABCA4, ABCA7, ABCA8, ABCD1, ABCD3, ABCD4, ABCE1, ABCF1, ABCG1, ABCG2, ABCG4, ABCG5, and ABCG8Aritoshi Iida, Susumu Saito, Akihiro Sekine, et al.
Journal of Human Genetics|October 12, 2002
Catalog of 86 single-nucleotide polymorphisms (SNPs) in three uridine diphosphate glycosyltransferase genes: UGT2A1, UGT2B15, and UGT8Aritoshi Iida, Susumu Saito, Akihiro Sekine, et al.
Acta Neuropathologica Communications|December 8, 2022
Intranuclear inclusions in muscle biopsy can differentiate oculopharyngodistal myopathy and oculopharyngeal muscular dystrophyMasashi Ogasawara, Nobuyuki Eura, Aritoshi Iida, et al.
Journal of Human Genetics|October 27, 2004
Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn diseaseKeiko Yamazaki, Masakazu Takazoe, Torao Tanaka, et al.
Journal of Human Genetics|March 28, 2002
Thirteen single-nucleotide polymorphisms (SNPs) in the alcohol dehydrogenase 4 (ADH4) gene locusAritoshi Iida, Susumu Saito, Akihiro Sekine, et al.
Neuromuscular Disorders : NMD|October 12, 2021
An autopsied case of ADSSL1 myopathyAtsuko Motoda, Tetsuya Takahashi, Chigusa Watanabe, et al.
Journal of Human Genetics|February 7, 2002
Catalog of 77 single-nucleotide polymorphisms (SNPs) in the carbohydrate sulfotransferase 1 (CHST1) and carbohydrate sulfotransferase 3 (CHST3) genesAritoshi Iida, Susumu Saito, Akihiro Sekine, et al.
Neurology. Genetics|December 22, 2021
<i>TNNI1</i> Mutated in Autosomal Dominant Proximal ArthrogryposisYukako Nishimori, Aritoshi Iida, Masashi Ogasawara, et al.
The Journal of Clinical Endocrinology and Metabolism|February 10, 2015
A case of functional growth hormone deficiency and early growth retardation in a child with IFT172 mutationsAngela K Lucas-Herald, Esther Kinning, Aritoshi Iida, et al.
Molecular Genetics & Genomic Medicine|March 19, 2019
Three novel MTM1 pathogenic variants identified in Japanese patients with X-linked myotubular myopathyAtsuko Nishikawa, Aritoshi Iida, Shinichiro Hayashi, et al.
Pageof 11