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Gen Tamiya

Showing results (11-20 of 169) with videos related to

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Scientific Reports|January 14, 2021
Facial UV photo imaging for skin pigmentation assessment using conditional generative adversarial networksKaname Kojima, Kosuke Shido, Gen Tamiya, et al.
Plos Computational Biology|October 1, 2020
A genotype imputation method for de-identified haplotype reference information by using recurrent neural networkKaname Kojima, Shu Tadaka, Fumiki Katsuoka, et al.
Genomics|February 8, 2003
SLURP-2, a novel member of the human Ly-6 superfamily that is up-regulated in psoriasis vulgarisHitomi Tsuji, Koichi Okamoto, Yasunari Matsuzaka, et al.
The Journal of Medical Investigation : JMI|December 22, 2005
Molecular dissection and anatomical basis of dystonia: X-linked recessive dystonia-parkinsonism (DYT3)Ryuji Kaji, Satoshi Goto, Gen Tamiya, et al.
Plos One|August 23, 2012
HLA-A*0206 with TLR3 polymorphisms exerts more than additive effects in Stevens-Johnson syndrome with severe ocular surface complicationsMayumi Ueta, Katsushi Tokunaga, Chie Sotozono, et al.
Journal of Neurology|October 28, 2003
Toward identification of susceptibility genes for sporadic Parkinson's diseaseTatsushi Toda, Yoshio Momose, Miho Murata, et al.
Biochemical and Biophysical Research Communications|October 10, 2002
Identification of the hRDH-E2 gene, a novel member of the SDR family, and its increased expression in psoriatic lesionYasunari Matsuzaka, Koichi Okamoto, Hitomi Tsuji, et al.
Gene|December 9, 2003
Identification of NAD+-dependent isocitrate dehydrogenase 3 gamma-like (IDH3GL) gene and its genetic polymorphismsKoichi Okamoto, Yasunari Matsuzaka, Yoko Yoshikawa, et al.
Molecular Genetics and Metabolism|March 27, 2019
The prevalence of GALM mutations that cause galactosemia: A database of functionally evaluated variantsShinya Iwasawa, Atsuo Kikuchi, Yoichi Wada, et al.
Platelets|May 24, 2014
Whole-exome sequencing confirmation of a novel heterozygous mutation in RUNX1 in a pregnant woman with platelet disorderMiyuki Obata, Seiji Tsutsumi, Satoshi Makino, et al.
Pageof 17

Showing results (11-20 of 169) with videos related to

Sort By:
Pageof 17
Scientific Reports|January 14, 2021
Facial UV photo imaging for skin pigmentation assessment using conditional generative adversarial networksKaname Kojima, Kosuke Shido, Gen Tamiya, et al.
Plos Computational Biology|October 1, 2020
A genotype imputation method for de-identified haplotype reference information by using recurrent neural networkKaname Kojima, Shu Tadaka, Fumiki Katsuoka, et al.
Genomics|February 8, 2003
SLURP-2, a novel member of the human Ly-6 superfamily that is up-regulated in psoriasis vulgarisHitomi Tsuji, Koichi Okamoto, Yasunari Matsuzaka, et al.
The Journal of Medical Investigation : JMI|December 22, 2005
Molecular dissection and anatomical basis of dystonia: X-linked recessive dystonia-parkinsonism (DYT3)Ryuji Kaji, Satoshi Goto, Gen Tamiya, et al.
Plos One|August 23, 2012
HLA-A*0206 with TLR3 polymorphisms exerts more than additive effects in Stevens-Johnson syndrome with severe ocular surface complicationsMayumi Ueta, Katsushi Tokunaga, Chie Sotozono, et al.
Journal of Neurology|October 28, 2003
Toward identification of susceptibility genes for sporadic Parkinson's diseaseTatsushi Toda, Yoshio Momose, Miho Murata, et al.
Biochemical and Biophysical Research Communications|October 10, 2002
Identification of the hRDH-E2 gene, a novel member of the SDR family, and its increased expression in psoriatic lesionYasunari Matsuzaka, Koichi Okamoto, Hitomi Tsuji, et al.
Gene|December 9, 2003
Identification of NAD+-dependent isocitrate dehydrogenase 3 gamma-like (IDH3GL) gene and its genetic polymorphismsKoichi Okamoto, Yasunari Matsuzaka, Yoko Yoshikawa, et al.
Molecular Genetics and Metabolism|March 27, 2019
The prevalence of GALM mutations that cause galactosemia: A database of functionally evaluated variantsShinya Iwasawa, Atsuo Kikuchi, Yoichi Wada, et al.
Platelets|May 24, 2014
Whole-exome sequencing confirmation of a novel heterozygous mutation in RUNX1 in a pregnant woman with platelet disorderMiyuki Obata, Seiji Tsutsumi, Satoshi Makino, et al.
Pageof 17