Publications by authors named "Isao Yuasa"

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Anti-steatosis compounds from leaves of Mallotus furetianus.
Xuedan Huang, Mingzhu Xu, Tatsuya Shirahata, Wei Li, Kazuo Koike, Akiko Kojima-Yuasa, Isao Yuasa

Nat Prod Res· June 2018

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Disruption of the Responsible Gene in a Phosphoglucomutase 1 Deficiency Patient by Homozygous Chromosomal Inversion.
Katsuyuki Yokoi, Yoko Nakajima, Tamae Ohye, Hidehito Inagaki, Yoshinao Wada, Isao Yuasa

JIMD Rep· May 2018

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Japaneseplex: A forensic SNP assay for identification of Japanese people using Japanese-specific alleles.
Isao Yuasa, Atsushi Akane, Toshimichi Yamamoto, Aya Matsusue, Minoru Endoh

Leg Med (Tokyo)· April 2018

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Epileptic phenotype of FGFR3-related bilateral medial temporal lobe dysgenesis.
Tetsuya Okazaki, Yoshiaki Saito, Riyo Ueda, Takeya Awashima, Yoko Nishimura, Isao Yuasa

Brain Dev· January 2017

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Genotyping of the c.1423C>T (p.P475S) polymorphism in the ADAMTS13 gene by APLP and HRM assays: Northeastern Asian origin of the mutant.
Mayumi Nakagawa, Aya Matsusue, Kazuo Umetsu, Morio Iino, Takaki Ishikawa, Isao Yuasa

Leg Med (Tokyo)· July 2016

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The global distribution of the p.R1193Q polymorphism in the SCN5A gene.
Aya Matsusue, Isao Yuasa, Kazuo Umetsu, Nori Nakayashiki, Koji Dewa

Leg Med (Tokyo)· March 2016

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The art of traditional native PAGE: The APLP 48-ID assay for human identification.
Kazuo Umetsu, Isao Yuasa, Masaki Hashiyada, Noboru Adachi, Gotaro Watanabe

Leg Med (Tokyo)· March 2016

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Investigation of Japanese-specific alleles: most are of Jomon lineage.
Isao Yuasa, Kazuo Umetsu, Noboru Adachi, Aya Matsusue, Nori Nakayashiki

Leg Med (Tokyo)· January 2015

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De novo mutations in SLC35A2 encoding a UDP-galactose transporter cause early-onset epileptic encephalopathy.
Hirofumi Kodera, Kazuyuki Nakamura, Hitoshi Osaka, Yoshihiro Maegaki, Kazuhiro Haginoya, Isao Yuasa

Hum Mutat· December 2013

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Near fixation of 374l allele frequencies of the skin pigmentation gene SLC45A2 in Africa.
Gérard Lucotte, Isao Yuasa

Biochem Genet· October 2013

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A hypervariable STR polymorphism in the CFI gene: southern origin of East Asian-specific group H alleles.
Isao Yuasa, Feng Jin, Shinji Harihara, Aya Matsusue, Junko Fujihara

Leg Med (Tokyo)· September 2013

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A hypervariable STR polymorphism in the CFI gene: mutation rate and no linkage disequilibrium with FGA.
Isao Yuasa, Nori Nakayashiki, Kazuo Umetsu, Hiroaki Nishimukai, Aya Matsusue

Leg Med (Tokyo)· May 2013

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A commentary on assignment of Y-chromosomal SNPs found in Japanese population to Y-chromosomal haplogroup tree.
Isao Yuasa

J Hum Genet· April 2013

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Three Japanese Patients with Beta-Ketothiolase Deficiency Who Share a Mutation, c.431A>C (H144P) in ACAT1 : Subtle Abnormality in Urinary Organic Acid Analysis and Blood Acylcarnitine Analysis Using Tandem Mass Spectrometry.
Toshiyuki Fukao, Shinsuke Maruyama, Toshihiro Ohura, Yuki Hasegawa, Mitsuo Toyoshima, Isao Yuasa

JIMD Rep· February 2013

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Replication study of the association of SNPs in the LHX3-QSOX2 and IGF1 loci with adult height in the Japanese population; wide-ranging comparison of each SNP genotype distribution.
Junko Fujihara, Haruo Takeshita, Kaori Kimura-Kataoka, Isao Yuasa, Reiko Iida

Leg Med (Tokyo)· July 2012

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Nonsynonymous single-nucleotide polymorphisms of the human apoptosis-related endonuclease--DNA fragmentation factor beta polypeptide, endonuclease G, and Flap endonuclease-1--genes show a low degree of genetic heterogeneity.
Haruo Takeshita, Junko Fujihara, Misuzu Ueki, Reiko Iida, Yoshiro Koda, Isao Yuasa

DNA Cell Biol· January 2012

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Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I.
Mailys Guillard, Yoshinao Wada, Hana Hansikova, Isao Yuasa, Katerina Vesela

J Inherit Metab Dis· August 2011

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Distribution of OCA2∗481Thr and OCA2∗615Arg, associated with hypopigmentation, in several additional populations.
Isao Yuasa, Shinji Harihara, Feng Jin, Hiroaki Nishimukai, Junko Fujihara

Leg Med (Tokyo)· July 2011

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Confirmation that SNPs in the high mobility group-A2 gene (HMGA2) are associated with adult height in the Japanese population; wide-ranging population survey of height-related SNPs in HMGA2.
Haruo Takeshita, Junko Fujihara, Mikiko Soejima, Yoshiro Koda, Kaori Kimura-Kataoka, Isao Yuasa

Electrophoresis· July 2011

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Global genetic analysis of all single nucleotide polymorphisms in exons of the human deoxyribonuclease I-like 3 gene and their effect on its catalytic activity.
Misuzu Ueki, Junko Fujihara, Haruo Takeshita, Kaori Kimura-Kataoka, Reiko Iida, Isao Yuasa

Electrophoresis· June 2011

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Simultaneous determination of seven informative Y chromosome SNPs to differentiate East Asian, European, and African populations.
Tomonori Muro, Reiko Iida, Junko Fujihara, Toshihiro Yasuda, Yukina Watanabe, Isao Yuasa

Leg Med (Tokyo)· May 2011

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Genetic variants associated with arsenic metabolism within human arsenic (+3 oxidation state) methyltransferase show wide variation across multiple populations.
Junko Fujihara, Toshihiro Yasuda, Hideaki Kato, Isao Yuasa, Arturo Panduro

Arch Toxicol· February 2011

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Global analysis of single nucleotide polymorphisms in the exons of human deoxyribonuclease I-like 1 and 2 genes.
Junko Fujihara, Toshihiro Yasuda, Reiko Iida, Kaori Kimura-Kataoka, Mikiko Soejima, Isao Yuasa

Electrophoresis· October 2010

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A Japanese-specific allele in the GALNT11 gene.
Isao Yuasa, Kazuo Umetsu, Aya Matsusue, Hiroaki Nishimukai, Shinji Harihara

Leg Med (Tokyo)· July 2010

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