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Pediatric Research|July 4, 2008
Cardiac ion channel gene mutations in sudden infant death syndromeTesshu Otagiri, Kazuki Kijima, Motoki Osawa, et al.
Legal Medicine (Tokyo, Japan)|March 7, 2006
Parentally imprinted allele typing at a short tandem repeat locus in intron 1a of imprinted gene KCNQ1Hong-De Xu, Emiko Naito, Koji Dewa, et al.
American Journal of Physical Anthropology|September 29, 2011
Mitochondrial DNA analysis of Hokkaido Jomon skeletons: remnants of archaic maternal lineages at the southwestern edge of former BeringiaNoboru Adachi, Ken-ichi Shinoda, Kazuo Umetsu, et al.
American Journal of Physical Anthropology|May 16, 2002
Extreme mtDNA homogeneity in continental Asian populationsHiroki Oota, Takashi Kitano, Feng Jin, et al.
Molecular Phylogenetics and Evolution|February 24, 2024
Integrating mitochondrial and nuclear genomic data to decipher the evolutionary history of Eubranchipus species in JapanTakashi Kitano, Mitsutoshi Tabata, Norihito Takahashi, et al.
Natural Product Research|July 12, 2017
Anti-steatosis compounds from leaves of Mallotus furetianusXuedan Huang, Mingzhu Xu, Tatsuya Shirahata, et al.
Electrophoresis|June 22, 2011
Global genetic analysis of all single nucleotide polymorphisms in exons of the human deoxyribonuclease I-like 3 gene and their effect on its catalytic activityMisuzu Ueki, Junko Fujihara, Haruo Takeshita, et al.
Legal Medicine (Tokyo, Japan)|May 16, 2009
Allele frequencies and haplotypes for 28 Y-STRs in Ovambo populationJunko Fujihara, Isao Yuasa, Tomonori Muro, et al.
Legal Medicine (Tokyo, Japan)|September 15, 2004
A novel 56-bp variable tandem repeat polymorphism in the human deoxyribonuclease I gene and its population dataToshihiro Yasuda, Reiko Iida, Misuzu Ueki, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|March 18, 2005
Neonatal hyperbilirubinemia and the bilirubin uridine diphosphate-glucuronosyltransferase gene: the common -3263T > G mutation of phenobarbital response enhancer module is not associated with the neonatal hyperbilirubinemia in JapaneseMasayo Kanai, Kazuki Kijima, Emi Shirahata, et al.
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