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Kazuo Moriwaki

Researcher at National Institute of Genetics

Publications -  18
Citations -  1216

Kazuo Moriwaki is an academic researcher from National Institute of Genetics. The author has contributed to research in topics: Antigen & Subspecies. The author has an hindex of 14, co-authored 18 publications receiving 1195 citations. Previous affiliations of Kazuo Moriwaki include Kobe University.

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Biochemical diversity and evolution in the genus Mus.

TL;DR: Thirteen biochemical groups of wild mice from Europe, Asia, and Africa belonging to the genus Mus are analyzed at 22–42 protein loci and Phylogenetic trees are proposed and patterns of biochemical evolution are discussed.
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Origins of Laboratory Mice Deduced from Restriction Patterns of Mitochondrial DNA

TL;DR: The findings suggest that the strains NZB and NZC stemmed from a European founder stock which differed from the ancestral stocks of other laboratory strains and that the ancestral mice of the RR strain had been transported from China to Japan.
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Evolutionary Relationships among Five Subspecies of MUS MUSCULUS Based on Restriction Enzyme Cleavage Patterns of Mitochondrial DNA

TL;DR: Estimates of genetic distances between the various races and subspecies were obtained by comparing cleavage maps of the mtDNAs with various restriction enzymes and suggest that M. molossinus is situated in a unique evolutionary position among Asian subspecies.
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Dominant expression of a distinctive V14+ T-cell antigen receptor α chain in mice

TL;DR: Observations, such as the expression of homogeneous Valpha 14-J alpha 281 in athymic mice, suggest that the positive selection of V alpha 14+ T cells occurs extrathymically.
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Genetic control of sex-dependent meiotic recombination in the major histocompatibility complex of the mouse.

TL;DR: Original recombinants whose breakpoints were defined by direct sequencing of PCR‐amplified DNAs were tested for the rate of secondary recombination in the crosses with laboratory strains in order to determine the location of such a genetic element and demonstrated that the chromosomal segment proximal to the hotspot is essential for enhancement of recombination.