Yushiro Yamashita | Semantic Scholar

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Complete nucleotide sequence of Japanese flounder (Paralichthys olivaceus) mitochondrial genome: structural properties and cue for resolving teleostean relationships.

Kenji Saitoh, Ken-ichi Hayashizaki, Yasuhiro Yokoyama, Takashi Asahida, Haruhiko Toyohara, Yushiro Yamashita
The Journal of heredity
2000

We cloned and sequenced the complete mitochondrial genome of Japanese flounder (Paralichthys olivaceus). A circular 17,090 bp mitochondrial genome from the flounder contains 37 structural genes as in… (More)

Retrotransposons of rice as a tool for the functional analysis of genes.

Hirohiko Hirochika, Akio Miyao, +16 authors B. H. Hardy
2001

Five endogenous active retrotransposons have been found in rice. Among them, the most active one, called Tos17, was characterized in detail. Tos17 is silent under normal conditions and becomes active… (More)

Tissue culture–induced mutations and overexpression of full-length cDNAs as a tool for functional analysis of rice genes

Hirohiko Hirochika, Akio Miyao, +8 authors Hiroaki Ichikawa
2007

A collection of 50,000 Tos17-induced mutant rice lines carrying about 250,000 independent insertions was generated. DNA pools derived from 50,000 lines have been produced for polymerase chain… (More)

Tissue culture-induced mutations and overexpression of full-length cDNAs as a tool for functional analysis of rice genes

Hirohiko Hirochika, Mitsue Miyao, +8 authors Hiroaki Ichikawa
2009

P02-130 - Characteristic prefrontal blood volume patterns when imaging body type, high-calorie food, and mother-child attachment in childhood anorexia nervosa: A near infrared spectroscopy study

Introduction The risk for developing and preserving symptoms of anorexia nervosa (AN) in children seems to be multifactorial: individual, familial, socio-cultural, and biological factors interact… (More)

A rice retrotransposon, Tos17, as a tool for gene tagging.

Kazumasa Murata, Akio Miyao, +11 authors Beatriz Betancourt Hardy
2003

A rice retrotransposon, Tos17, possesses unique features: transposition induced by tissue culture, a low copy number (1–4), high frequency of transposition, resulting in 5–30 transposed copies, and… (More)

De novo SHANK3 mutation causes Rett syndrome-like phenotype in a female patient.

Munetsugu Hara, Chihiro Ohba, Yushiro Yamashita, Hirotomo Saitsu, Naomichi Matsumoto, Toyojiro Matsuishi
American journal of medical genetics. Part A
2015

Rett syndrome (RTT) is a neurodevelopmental disorder predominantly affecting females. Females with the MECP2 mutations exhibit a broad spectrum of clinical manifestations ranging from classical Rett… (More)

Contents, Vol. 66, 1994

David S. C. Lee, Adriana Wong, +30 authors Hülya Akhunlar
1994

Subject Index Vol. 66, 1994

David S. C. Lee, Adriana Wong, +30 authors Hülya Akhunlar
1994

Longitudinal study of renal complication among childhood hematology-oncology survivors –Impact of multi-disciplinary therapy–

Keishiro Hojo, Shuichi Ozono, +4 authors Yushiro Yamashita
2019