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Gen Tamiya

Showing results (21-30 of 169) with videos related to

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ISRN Neurology|October 3, 2012
UBR5 Gene Mutation Is Associated with Familial Adult Myoclonic Epilepsy in a Japanese FamilyTakeo Kato, Gen Tamiya, Shingo Koyama, et al.
Infection and Immunity|January 18, 2002
Association of a determinant on mouse chromosome 18 with experimental severe Plasmodium berghei malariaEiji Nagayasu, Koichi Nagakura, Mayumi Akaki, et al.
American Journal of Human Genetics|July 11, 2006
Genomewide association analysis of human narcolepsy and a new resistance geneMinae Kawashima, Gen Tamiya, Akira Oka, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|January 8, 2025
Idiopathic infantile hypercalcemia with a <i>CYP24A1</i> variant triggered by vitamin D supplementation in fortified milk: A case reportSota Iwafuchi, Nao Uchida, Naoya Saijo, et al.
Journal of Human Genetics|October 2, 2007
Refinement of a locus for autosomal dominant hereditary motor and sensory neuropathy with proximal dominancy (HMSN-P) and genetic heterogeneityKouji Maeda, Ryuji Kaji, Katsuhito Yasuno, et al.
Genetics|December 13, 2007
Genetic analysis of craniofacial traits in the medakaTetsuaki Kimura, Atsuko Shimada, Noriyoshi Sakai, et al.
Genome Biology and Evolution|March 5, 2014
Divergence of East Asians and Europeans estimated using male- and female-specific genetic markersYoshio Tateno, Tomoyoshi Komiyama, Toru Katoh, et al.
Molecular Genetics & Genomic Medicine|June 17, 2025
A Japanese Case of Lenz-Majewski Syndrome With a Novel PTDSS1 VariantYasuko Kobari, Non Miyata, Jun Takayama, et al.
Gene|December 14, 2004
Identification, expression analysis and polymorphism of a novel RLTPR gene encoding a RGD motif, tropomodulin domain and proline/leucine-rich regionsYasunari Matsuzaka, Koichi Okamoto, Tomotaka Mabuchi, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 28, 2005
Identification and characterization of novel variants of the thioredoxin reductase 3 new transcript 1 TXNRD3NT1Yasunari Matsuzaka, Koichi Okamoto, Tomotaka Mabuchi, et al.
Pageof 17

Showing results (21-30 of 169) with videos related to

Sort By:
Pageof 17
ISRN Neurology|October 3, 2012
UBR5 Gene Mutation Is Associated with Familial Adult Myoclonic Epilepsy in a Japanese FamilyTakeo Kato, Gen Tamiya, Shingo Koyama, et al.
Infection and Immunity|January 18, 2002
Association of a determinant on mouse chromosome 18 with experimental severe Plasmodium berghei malariaEiji Nagayasu, Koichi Nagakura, Mayumi Akaki, et al.
American Journal of Human Genetics|July 11, 2006
Genomewide association analysis of human narcolepsy and a new resistance geneMinae Kawashima, Gen Tamiya, Akira Oka, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|January 8, 2025
Idiopathic infantile hypercalcemia with a <i>CYP24A1</i> variant triggered by vitamin D supplementation in fortified milk: A case reportSota Iwafuchi, Nao Uchida, Naoya Saijo, et al.
Journal of Human Genetics|October 2, 2007
Refinement of a locus for autosomal dominant hereditary motor and sensory neuropathy with proximal dominancy (HMSN-P) and genetic heterogeneityKouji Maeda, Ryuji Kaji, Katsuhito Yasuno, et al.
Genetics|December 13, 2007
Genetic analysis of craniofacial traits in the medakaTetsuaki Kimura, Atsuko Shimada, Noriyoshi Sakai, et al.
Genome Biology and Evolution|March 5, 2014
Divergence of East Asians and Europeans estimated using male- and female-specific genetic markersYoshio Tateno, Tomoyoshi Komiyama, Toru Katoh, et al.
Molecular Genetics & Genomic Medicine|June 17, 2025
A Japanese Case of Lenz-Majewski Syndrome With a Novel PTDSS1 VariantYasuko Kobari, Non Miyata, Jun Takayama, et al.
Gene|December 14, 2004
Identification, expression analysis and polymorphism of a novel RLTPR gene encoding a RGD motif, tropomodulin domain and proline/leucine-rich regionsYasunari Matsuzaka, Koichi Okamoto, Tomotaka Mabuchi, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 28, 2005
Identification and characterization of novel variants of the thioredoxin reductase 3 new transcript 1 TXNRD3NT1Yasunari Matsuzaka, Koichi Okamoto, Tomotaka Mabuchi, et al.
Pageof 17