Search Results - "Takitoh, Takako"

Activation of Aurora-A is essential for neuronal migration via modulation of microtubule organization by Takitoh, Takako, Kumamoto, Kanako, Wang, Chen-Chi, Sato, Makoto, Toba, Shiori, Wynshaw-Boris, Anthony, Hirotsune, Shinji

“…Neuronal migration is a critical feature to ensure proper location and wiring of neurons during cortical development. Postmitotic neurons migrate from the…”
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Gamma-cross-linked nonfibrillar collagen gel as a scaffold for osteogenic differentiation of mesenchymal stem cells by Takitoh, Takako, Bessho, Masahiko, Hirose, Motohiro, Ohgushi, Hajime, Mori, Hideki, Hara, Masayuki

“…We fabricated a transparent nonfibrillar collagen gel using gamma irradiation (5 kGy) and cultured rat mesenchymal stem cells (MSCs) on both the…”
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Inhibition of calpain increases LIS1 expression and partially rescues in vivo phenotypes in a mouse model of lissencephaly by Umeshima, Hiroki, Wynshaw-Boris, Anthony, Yamada, Masami, Sorimachi, Hiroyuki, Takao, Keizo, Yoshida, Yuko, Mori, Daisuke, Hirotsune, Shinji, Sato, Makoto, Kengaku, Mineko, Miyakawa, Tsuyoshi, Takitoh, Takako

“…Lissencephaly is a developmental brain disorder caused by mutations in LIS1 and characterized by impaired neuronal migration. Inhibiting calpain prevents LIS1…”
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mNUDC is required for plus-end-directed transport of cytoplasmic dynein and dynactins by kinesin-1 by Yamada, Masami, Toba, Shiori, Takitoh, Takako, Yoshida, Yuko, Mori, Daisuke, Nakamura, Takeshi, Iwane, Atsuko H, Yanagida, Toshio, Imai, Hiroshi, Yu-Lee, Li-yuan, Schroer, Trina, Wynshaw-Boris, Anthony, Hirotsune, Shinji

“…Lissencephaly is a devastating neurological disorder caused by defective neuronal migration. The LIS1 (or PAFAH1B1 ) gene was identified as the gene mutated in…”
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In vitro osteogenic differentiation of HOS cells on two types of collagen gels by Takitoh, Takako, Kato, Yoichi, Nakasu, Asako, Tadokoro, Mika, Bessho, Masahiko, Hirose, Motohiro, Ohgushi, Hajime, Mori, Hideki, Hara, Masayuki

“…HOS cell is a model strain of human osteoblasts derived from human osteosarcoma. We cultured the HOS cells on both the conventional collagen gel (neutral gel),…”
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Inhibition of calpain increases LIS1(PAFAH1B1) and partially rescues in vivo phenotypes in a mouse model of lissencephaly by Yamada, Masami, Yoshida, Yuko, Mori, Daisuke, Takitoh, Takako, Kengaku, Mineko, Umeshima, Hiroki, Takao, Keizo, Miyakawa, Tsuyoshi, Sato, Makoto, Sorimachi, Hiroyuki, Wynshaw-Boris, Anthony, Hirotsune, Shinji

“…Lissencephaly is a devastating neurological disorder due to defective neuronal migration. LIS1 (or PAFAH1B1 ) was identified as the gene mutated in…”
Get full text