Search Results - "Tadokoro, Keiko" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Transdifferentiation of the retinal pigment epithelia to the neural retina by transfer of the Pax6 transcriptional factor

Transdifferentiation of the retinal pigment epithelia to the neural retina by transfer of the Pax6 transcriptional factor

by Azuma, Noriyuki, Tadokoro, Keiko, Asaka, Astuko, Yamada, Masao, Yamaguchi, Yuki, Handa, Hiroshi, Matsushima, Satsuki, Watanabe, Takashi, Kida, Yasuyuki, Ogura, Toshihiko, Torii, Masaaki, Shimamura, Kenji, Nakafuku, Masato
Published in Human molecular genetics (15.04.2005)

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The Pax6 isoform bearing an alternative spliced exon promotes the development of the neural retinal structure

The Pax6 isoform bearing an alternative spliced exon promotes the development of the neural retinal structure

by Azuma, Noriyuki, Tadokoro, Keiko, Asaka, Astuko, Yamada, Masao, Yamaguchi, Yuki, Handa, Hiroshi, Matsushima, Satsuki, Watanabe, Takashi, Kohsaka, Shinichi, Kida, Yasuyuki, Shiraishi, Tomoki, Ogura, Toshihiko, Shimamura, Kenji, Nakafuku, Masato
Published in Human molecular genetics (15.03.2005)

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Frequent occurrence of protein isoforms with or without a single amino acid residue by subtle alternative splicing: the case of Gln in DRPLA affects subcellular localization of the products

Frequent occurrence of protein isoforms with or without a single amino acid residue by subtle alternative splicing: the case of Gln in DRPLA affects subcellular localization of the products

by Tadokoro, Keiko, Yamazaki-Inoue, Mayu, Tachibana, Maki, Fujishiro, Mina, Nagao, Kazuaki, Toyoda, Masashi, Ozaki, Miwako, Ono, Masami, Miki, Nobuhiro, Miyashita, Toshiyuki, Yamada, Masao
Published in Journal of human genetics (01.09.2005)

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Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA)

Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA)

by Nagafuchi, Shigeo, Yanagisawa, Hiroko, Ohsaki, Emiko, Shirayama, Takefumi, Tadokoro, Keiko, Inoue, Tadashi, Yamada, Masao
Published in Nature genetics (01.10.1994)

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Exon 9 mutations in the WT1 gene, without influencing KTS splice isoforms, are also responsible for Frasier syndrome

Exon 9 mutations in the WT1 gene, without influencing KTS splice isoforms, are also responsible for Frasier syndrome

by Kohsaka, Takao, Tagawa, Manabu, Takekoshi, Yasuro, Yanagisawa, Hiroko, Tadokoro, Keiko, Yamada, Masao
Published in Human mutation (01.12.1999)

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Molecular cloning and characterization of six novel isoforms of human Bim, a member of the proapoptotic Bcl‐2 family1

Molecular cloning and characterization of six novel isoforms of human Bim, a member of the proapoptotic Bcl‐2 family1

by U, Mami, Miyashita, Toshiyuki, Shikama, Yoshiaki, Tadokoro, Keiko, Yamada, Masao
Published in FEBS letters (30.11.2001)

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Gene amplification and overexpression of epidermal growth factor receptor in squamous cell carcinoma of the head and neck

Gene amplification and overexpression of epidermal growth factor receptor in squamous cell carcinoma of the head and neck

by Rikimaru, K, Tadokoro, K, Yamamoto, T, Enomoto, S, Tsuchida, N
Published in Head & neck (01.01.1992)

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Mutations of the PAX6 Gene Detected in Patients with a Variety of Optic-Nerve Malformations

Mutations of the PAX6 Gene Detected in Patients with a Variety of Optic-Nerve Malformations

by Azuma, Noriyuki, Yamaguchi, Yuki, Handa, Hiroshi, Tadokoro, Keiko, Asaka, Atsuko, Kawase, Eriko, Yamada, Masao
Published in American journal of human genetics (01.06.2003)

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Molecular cloning and characterization of six novel isoforms of human Bim, a member of the proapoptotic Bcl-2 family

Molecular cloning and characterization of six novel isoforms of human Bim, a member of the proapoptotic Bcl-2 family

by U, Mami, Miyashita, Toshiyuki, Shikama, Yoshiaki, Tadokoro, Keiko, Yamada, Masao
Published in FEBS letters (30.11.2001)

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Protein binding of a DRPLA family through arginine-glutamic acid dipeptide repeats is enhanced by extended polyglutamine

Protein binding of a DRPLA family through arginine-glutamic acid dipeptide repeats is enhanced by extended polyglutamine

by Yanagisawa, H, Bundo, M, Miyashita, T, Okamura-Oho, Y, Tadokoro, K, Tokunaga, K, Yamada, M
Published in Human molecular genetics (22.05.2000)

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Molecular cloning and characterization of six novel isoforms of human Bim, a member of the proapoptotic Bcl‐2 family 1

Molecular cloning and characterization of six novel isoforms of human Bim, a member of the proapoptotic Bcl‐2 family 1

by U, Mami, Miyashita, Toshiyuki, Shikama, Yoshiaki, Tadokoro, Keiko, Yamada, Masao
Published in FEBS letters (30.11.2001)

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Protein binding of a DRPLA family through arginine-glutamic acid dipeptide repeats is enhanced by extended polyglutamine

Protein binding of a DRPLA family through arginine-glutamic acid dipeptide repeats is enhanced by extended polyglutamine

by Yanagisawa, Hiroko, Bundo, Miki, Miyashita, Toshiyuki, Okamura-Oho, Yuko, Tadokoro, Keiko, Tokunaga, Katsushi, Yamada, Masao
Published in Human molecular genetics (22.05.2000)

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A Unique Origin and Multistep Process for the Generation of Expanded DRPLA Triplet Repeats

A Unique Origin and Multistep Process for the Generation of Expanded DRPLA Triplet Repeats

by Yanagisawa, Hiroko, Fujii, Katsura, Nagafuchi, Shigeo, Nakahori, Yutaka, Nakagome, Yasuo, Akane, Atsushi, Nakamura, Masataka, Sano, Akira, Komure, Osamu, Kondo, Ikuko, Kyu Jin, Dong, Sørensen, Sven A., Potter, Nicholas T., Robert Young, S., Nakamura, Koichiro, Nukina, Nobuyuki, Nagao, Yoshiro, Tadokoro, Keiko, Okuyama, Torayuki, Miyashita, Toshiyuki, Inoue, Tadashi, Kanazawa, Ichiro, Yamada, Masao
Published in Human molecular genetics (01.03.1996)

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Megabase-scale analysis of the origin of N-myc amplicons in human neuroblastomas

Megabase-scale analysis of the origin of N-myc amplicons in human neuroblastomas

by Akiyama, Kiyotaka, Kanda, Naotoshi, Yamada, Masao, Tadokoro, Keiko, Matsunaga, Tadashi, Nishi, Yoshisuke
Published in Nucleic acids research (25.01.1994)

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Intragenic homozygous deletion of the WT1 gene in Wilms' tumor

Intragenic homozygous deletion of the WT1 gene in Wilms' tumor

by Tadokoro, K, Fujii, H, Ohshima, A, Kakizawa, Y, Shimizu, K, Sakai, A, Sumiyoshi, K, Inoue, T, Hayashi, Y, Yamada, M
Published in Oncogene (01.06.1992)

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PCR detection of 9 polymorphisms in the WT1 gene

PCR detection of 9 polymorphisms in the WT1 gene

by Tadokoro, K, Oki, N, Sakai, A, Fujii, H, Ohshima, A, Nagafuchi, S, Inoue, T, Yamada, M
Published in Human molecular genetics (01.12.1993)

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Taql RFLPs at the Wilms' tumor gene (WT1)

Taql RFLPs at the Wilms' tumor gene (WT1)

by Tadokoro, Keiko, Kato, Mieko, Yokota, Shin-ichi, Yamada, Masao
Published in Nucleic acids research (11.05.1991)

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Genomic Organization of the Human WT1 Gene

Genomic Organization of the Human WT1 Gene

by Tadokoro, Keiko, Oki, Noriko, Fujii, Hanako, Ohshima, Akira, Inoue, Tadashi, Yamada, Masao
Published in Cancer science (01.11.1992)

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Transcriptional Regulation of PDGF-A and TGF-β by +KTS WT1 Deletion Mutants and a Mutant Mimicking Denys-Drash Syndrome

Transcriptional Regulation of PDGF-A and TGF-β by +KTS WT1 Deletion Mutants and a Mutant Mimicking Denys-Drash Syndrome

by Jin, Dong Kyu, Kang, Soon Ja, Kim, Sung Jin, Bang, Eun Hee, Hwang, Hye Zin, Tadokoro, Keiko, Yamada, Masao, Kohsaka, Takao
Published in Renal failure (01.01.1999)

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TaqI RFLPs at the Wilm's tumor gene (WT1)

TaqI RFLPs at the Wilm's tumor gene (WT1)

by TADOKORO, K, KATO, M, YOKOTA, S.-I, YAMADA, M
Published in Nucleic acids research (11.05.1991)

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