Gorlin syndrome (nevoid basal cell carcinoma syndrome): Update and literature review von Fujii, Katsunori, Miyashita, Toshiyuki

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Confocal Microscopy for Intracellular Co-localization of Proteins von Miyashita, Toshiyuki

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Establishment of a Gorlin syndrome model from induced neural progenitor cells exhibiting constitutive GLI1 expression and high sensitivity to inhibition by smoothened (SMO) von Ikehara, Hajime, Fujii, Katsunori, Miyashita, Toshiyuki, Ikemoto, Yu, Nagamine, Marina, Shimojo, Naoki, Umezawa, Akihiro

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MicroRNAs profiling in fibroblasts derived from patients with Gorlin syndrome von Shiohama, Tadashi, Fujii, Katsunori, Miyashita, Toshiyuki, Takatani, Tomozumi, Ikehara, Hajime, Uchikawa, Hideki, Motojima, Toshino, Uchida, Tomoko, Shimojo, Naoki

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PTCH1-null induced pluripotent stem cells exclusively differentiate into immature ectodermal cells with large areas of medulloblastoma-like tissue von Nagao, Kazuaki, Kato, Chise, Ikemoto, Yu, Motojima, Toshino, Fujii, Katsunori, Umezawa, Akihiro, Miyashita, Toshiyuki

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Spatiotemporal dynamics of OCT4 protein localization during preimplantation development in mice von Fukuda, Atsushi, Mitani, Atsushi, Miyashita, Toshiyuki, Kobayashi, Hisato, Umezawa, Akihiro, Akutsu, Hidenori

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Chromatin condensation of Xist genomic loci during oogenesis in mice von Fukuda, Atsushi, Mitani, Atsushi, Miyashita, Toshiyuki, Umezawa, Akihiro, Akutsu, Hidenori

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Specific temperament in patients with nevoid basal cell carcinoma syndrome von Uchikawa, Hideki, Fujii, Katsunori, Shiohama, Tadashi, Nakazato, Michiko, Shimizu, Eiji, Miyashita, Toshiyuki, Shimojo, Naoki

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Maintenance of Xist Imprinting Depends on Chromatin Condensation State and Rnf12 Dosage in Mice von Fukuda, Atsushi, Mitani, Atsushi, Miyashita, Toshiyuki, Sado, Takashi, Umezawa, Akihiro, Akutsu, Hidenori

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Patched1 Haploinsufficiency Increases Adult Bone Mass and Modulates Gli3 Repressor Activity von Ohba, Shinsuke, Kawaguchi, Hiroshi, Kugimiya, Fumitaka, Ogasawara, Toru, Kawamura, Naohiro, Saito, Taku, Ikeda, Toshiyuki, Fujii, Katsunori, Miyajima, Tsuyoshi, Kuramochi, Akira, Miyashita, Toshiyuki, Oda, Hiromi, Nakamura, Kozo, Takato, Tsuyoshi, Chung, Ung-il

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Nationwide survey of nevoid basal cell carcinoma syndrome in Japan revealing the low frequency of basal cell carcinoma von Endo, Mamiko, Fujii, Katsunori, Sugita, Katsuo, Saito, Kayoko, Kohno, Yoichi, Miyashita, Toshiyuki

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RCAN1 is an important mediator of glucocorticoid-induced apoptosis in human leukemic cells von Nagao, Kazuaki, Iwai, Yujiro, Miyashita, Toshiyuki

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L-leucine and SPNS1 coordinately ameliorate dysfunction of autophagy in mouse and human Niemann-Pick type C disease von Yanagisawa, Hiroko, Ishii, Tomohiro, Endo, Kentaro, Kawakami, Emiko, Nagao, Kazuaki, Miyashita, Toshiyuki, Akiyama, Keiko, Watabe, Kazuhiko, Komatsu, Masaaki, Yamamoto, Daisuke, Eto, Yoshikatsu

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Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome von Fujii, Katsunori, Ohashi, Hirofumi, Suzuki, Maiko, Hatsuse, Hiromi, Shiohama, Tadashi, Uchikawa, Hideki, Miyashita, Toshiyuki

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A familial case of overgrowth syndrome caused by a 9q22.3 microdeletion in a mother and daughter von Yamada, Hikari, Shimura, Masaru, Takahashi, Hidekuni, Nara, Shonosuke, Morishima, Yasuyuki, Go, Soken, Miyashita, Toshiyuki, Numabe, Hironao, Kawashima, Hisashi

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Tumor suppressor p53 is a direct transcriptional activator of the human bax gene von Toshiyuki, Miyashita, Reed, John C

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The serine 106 residue within the N-terminal transactivation domain is crucial for Oct4 function in mice von Mitani, Atsushi, Fukuda, Atsushi, Miyashita, Toshiyuki, Umezawa, Akihiro, Akutsu, Hidenori

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Selective haploinsufficiency of longer isoforms of PTCH1 protein can cause nevoid basal cell carcinoma syndrome von Suzuki, Maiko, Hatsuse, Hiromi, Nagao, Kazuaki, Takayama, Yoshinaga, Kameyama, Kohzoh, Kabasawa, Yuji, Omura, Ken, Yoshida, Masayuki, Fujii, Katsunori, Miyashita, Toshiyuki

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A novel PTCH1 mutation in basal cell nevus syndrome with rare craniofacial features von Murata, Yuka, Kurosaka, Hiroshi, Ohata, Yasuhisa, Aikawa, Tomonao, Takahata, Sosuke, Fujii, Katsunori, Miyashita, Toshiyuki, Morita, Chisato, Inubushi, Toshihiro, Kubota, Takuo, Sakai, Norio, Ozono, Keiichi, Kogo, Mikihiko, Yamashiro, Takashi

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Mirror syndrome associated with fetal transient abnormal myelopoiesis in Down syndrome von Kobayashi, Yoshinari, Miyoshi, Takekazu, Matsuyama, Taka-aki, Miyauchi, Jun, Miyashita, Toshiyuki, Ishibashi-Ueda, Hatsue, Yoshimatsu, Jun

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