1 to 10 of 53 literature results

• The medaka draft genome and insights into vertebrate genome evolution.

  Teleosts comprise more than half of all vertebrate species and have adapted to a variety of marine and freshwater habitats. Their genome evolution and…

  Authors: Masahiro Kasahara, Kiyoshi Naruse, Shin Sasaki, Yoichiro Nakatani, Wei Qu, Budrul Ahsan, Tomoyuki Yamada, Yukinobu Nagayasu, Koichiro Doi, Yasuhiro Kasai,…

  Source: Nature. 2007 Jun 7

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• FAK-mediated extracellular signals are essential for interkinetic nuclear migration and planar divisions in the neuroepithelium.

  During the development of the vertebrate nervous system, mitosis of neural progenitor cells takes place near the lumen, the apical side of the neural …

  Authors: Sachiko Tsuda, Tadao Kitagawa, Shigeo Takashima, Shuichi Asakawa, Nobuyoshi Shimizu, Hiroshi Mitani, Akihiro Shima, Makiko Tsutsumi, Hiroshi Hori, Kiyoshi Naruse,…

  Source: Journal of cell science. 2010 Feb 1

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• DNA sequence and analysis of human chromosome 8.

  The International Human Genome Sequencing Consortium (IHGSC) recently completed a sequence of the human genome. As part of this project, we have focus…

  Authors: Chad Nusbaum, Tarjei S Mikkelsen, Michael C Zody, Shuichi Asakawa, Stefan Taudien, Manuel Garber, Chinnappa D Kodira, Mary G Schueler, Atsushi Shimizu, Charles A Whittaker,…

  Source: Nature. 2006 Jan 19

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• DMY is a Y-specific DM-domain gene required for male development in the medaka fish.

  Although the sex-determining gene Sry has been identified in mammals, no comparable genes have been found in non-mammalian vertebrates. Here, we used …

  Authors: Masaru Matsuda, Yoshitaka Nagahama, Ai Shinomiya, Tadashi Sato, Chika Matsuda, Tohru Kobayashi, Craig E Morrey, Naoki Shibata, Shuichi Asakawa, Nobuyoshi Shimizu,…

  Source: Nature. 2002 May 30

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• Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)n.

  Spinocerebellar ataxia type 31 (SCA31) is an adult-onset autosomal-dominant neurodegenerative disorder showing progressive cerebellar ataxia mainly af…

  Authors: Nozomu Sato, Takeshi Amino, Kazuhiro Kobayashi, Shuichi Asakawa, Taro Ishiguro, Taiji Tsunemi, Makoto Takahashi, Tohru Matsuura, Kevin M Flanigan, Sawa Iwasaki,…

  Source: American journal of human genetics. 2009 Nov

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• Genomic organization of the sex-determining and adjacent regions of the sex chromosomes of medaka.

  Sequencing of the human Y chromosome has uncovered the peculiarities of the genomic organization of a heterogametic sex chromosome of old evolutionary…

  Authors: Mariko Kondo, Ute Hornung, Indrajit Nanda, Shuichiro Imai, Takashi Sasaki, Atsushi Shimizu, Shuichi Asakawa, Hiroshi Hori, Michael Schmid, Nobuyoshi Shimizu,…

  Source: Genome research. 2006 Jul

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• Genome sequence of the ultrasmall unicellular red alga Cyanidioschyzon merolae 10D.

  Small, compact genomes of ultrasmall unicellular algae provide information on the basic and essential genes that support the lives of photosynthetic e…

  Authors: Motomichi Matsuzaki, Osami Misumi, Tadasu Shin-I, Shinichiro Maruyama, Manabu Takahara, Shin-Ya Miyagishima, Toshiyuki Mori, Keiji Nishida, Fumi Yagisawa, Keishin Nishida,…

  Source: Nature. 2004 Apr 8

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• Analysis of eighteen deletion breakpoints in the parkin gene.

  Parkin mutations are responsible for the pathogenesis of autosomal-recessive juvenile parkinsonism (AR-JP). On initial screening of Japanese patients …

  Authors: Shuichi Asakawa, Nobutaka Hattori, Atsushi Shimizu, Yoshiko Shimizu, Shinsei Minoshima, Yoshikuni Mizuno, Nobuyoshi Shimizu

  Source: Biochemical and biophysical research communications. 2009 Nov 6

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• Fast skeletal muscle myosin heavy chain gene cluster of medaka Oryzias latipes enrolled in temperature adaptation.

  To disclose mechanisms involved in temperature acclimation of fish muscle, we subjected eurythermal fish of medaka Oryzias latipes to cloning of myosi…

  Authors: Chun-Shi Liang, Atsushi Kobiyama, Atsushi Shimizu, Takashi Sasaki, Shuichi Asakawa, Nobuyoshi Shimizu, Shugo Watabe

  Source: Physiological genomics. 2007 Apr 24

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• Role of TBX1 in human del22q11.2 syndrome.

  BACKGROUND: Del22q11.2 syndrome is the most frequent known chromosomal microdeletion syndrome, with an incidence of 1 in 4000-5000 livebirths. It is c…

  Authors: Hisato Yagi, Yoshiyuki Furutani, Hiromichi Hamada, Takashi Sasaki, Shuichi Asakawa, Shinsei Minoshima, Fukiko Ichida, Kunitaka Joo, Misa Kimura, Shin-ichiro Imamura,…

  Source: Lancet. 2003 Oct 25

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