Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism von Shimizu, Nobuyoshi, Kitada, Tohru, Asakawa, Shuichi, Hattori, Nobutaka, Matsumine, Hiroto, Yamamura, Yasuhiro, Minoshima, Shinsei, Yokochi, Masayuki, Mizuno, Yoshikuni

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The Role of G-Protein-Coupled Receptor Kinase 5 in Pathogenesis of Sporadic Parkinson's Disease von Arawaka, Shigeki, Wada, Manabu, Goto, Saori, Karube, Hiroki, Sakamoto, Masahiro, Ren, Chang-Hong, Koyama, Shingo, Nagasawa, Hikaru, Kimura, Hideki, Kawanami, Toru, Kurita, Keiji, Tajima, Katsushi, Daimon, Makoto, Baba, Masanori, Kido, Takashi, Saino, Sachiko, Goto, Kaoru, Asao, Hironobu, Kitanaka, Chihumi, Takashita, Emi, Hongo, Seiji, Nakamura, Takao, Kayama, Takamasa, Suzuki, Yoshihiro, Kobayashi, Kazuo, Katagiri, Tadashi, Kurokawa, Katsuro, Kurimura, Masayuki, Toyoshima, Itaru, Niizato, Kazuhiro, Tsuchiya, Kuniaki, Iwatsubo, Takeshi, Muramatsu, Masaaki, Matsumine, Hiroto, Kato, Takeo

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Immunohistochemical and subcellular localization of parkin protein: Absence of protein in autosomal recessive juvenile parkinsonism patients von Shimura, Hideki, Hattori, Nobutaka, Kubo, Shin-Ichiro, Yoshikawa, Mutsuko, Kitada, Tohru, Matsumine, Hiroto, Asakawa, Shuichi, Minoshima, Shinsei, Yamamura, Yasuhiro, Shimizu, Nobuyoshi, Mizuno, Yoshikuni

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Mitochondrial dysfunction in parkinson's disease von Mizuno, Yoshikuni, Yoshino, Hiroyo, Ikebe, Shin-Ichiro, Hattori, Nobutaka, Kobayashi, Tomonori, Shimoda-Matsubayashi, Satoe, Matsumine, Hiroto, Kondo, Tomoyoshi

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Neurochemical and Neurogenetic Correlates of Parkinson's Disease von Mizuno, Yoshikuni, Hattori, Nobutaka, Matsumine, Hiroto

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Autosomal recessive early-onset parkinsonism with diurnal fluctuation: clinicopathologic characteristics and molecular genetic identification von Yamamura, Yasuhiro, Hattori, Nobutaka, Matsumine, Hiroto, Kuzuhara, Shigeki, Mizuno, Yoshikuni

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Large-scale search of SNPs for type 2 DM susceptibility genes in a Japanese population von Daimon, Makoto, Ji, Guijin, Saitoh, Tamotsu, Oizumi, Toshihide, Tominaga, Makoto, Nakamura, Takahiro, Ishii, Keisuke, Matsuura, Tadashi, Inageda, Kiyoshi, Matsumine, Hiroto, Kido, Takashi, Htay, Lwin, Kamatani, Naoyuki, Muramatsu, Masaaki, Kato, Takeo

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A Microdeletion of D6S305 in a Family of Autosomal Recessive Juvenile Parkinsonism (PARK2) von Matsumine, Hiroto, Yamamura, Yasuhiro, Hattori, Nobutaka, Kobayashi, Tomonori, Kitada, Tohru, Yoritaka, Asako, Mizuno, Yoshikuni

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Structural Dimorphism in the Mitochondrial Targeting Sequence in the Human Manganese Superoxide Dismutase Gene: A Predictive Evidence for Conformational Change to Influence Mitocho... von Shimoda-Matsubayashi, Satoe, Matsumine, Hiroto, Kobayashi, Tomonori, Nakagawa-Hattori, Yuko, Shimizu, Yumiko, Mizuno, Yoshikuni

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Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in the Parkin gene... von Hattori, Nobutaka, Kitada, Tohru, Matsumine, Hiroto, Asakawa, Shuichi, Yamamura, Yasuhiro, Yoshino, Hiroyo, Kobayashi, Tomonori, Yokochi, Masayuki, Wang, Mei, Yoritaka, Asako, Kondo, Tomoyoshi, Kuzuhara, Shigeki, Nakamura, Shigenobu, Shimizu, Nobuyoshi, Mizuno, Yoshikuni

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Localization of a gene for an autosomal recessive form of juvenile parkinsonism to chromosome 6q25.2-27 von MATSUMINE, H, SAITO, M, SANPEI, K, KOIKE, R, MORI, H, KONDO, T, MIZUTANI, Y, SCHÄFFER, A. A, YAMAMURA, Y, NAKAMURA, S, KUZUHARA, S, TSUJI, S, SHIMODA-MATSUBAYASHI, S, MIZUNO, Y, TANAKA, H, ISHIKAWA, A, NAKAGAWA-HATTORI, Y, YOKOCHI, M, KOBAYASHI, T, IGARASHI, S, TAKANO, H

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Point mutations (Thr240Arg and Gln311Stop) [correction of Thr240Arg and Ala311Stop] in the Parkin gene von Hattori, N, Matsumine, H, Asakawa, S, Kitada, T, Yoshino, H, Elibol, B, Brookes, A J, Yamamura, Y, Kobayashi, T, Wang, M, Yoritaka, A, Minoshima, S, Shimizu, N, Mizuno, Y

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A loss-of-function mechanism of nigral neuron death without Lewy body formation: autosomal recessive juvenile parkinsonism (AR-JP) von Matsumine, H

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Polymorphism in theparkin gene in sporadic Parkinson's disease von Wang, Mei, Hattori, Nobutaka, Matsumine, Hiroto, Kobayashi, Tomonori, Yoshino, Hiroyo, Morioka, Akiko, Kitada, Tohru, Asakawa, Shuichi, Minoshima, Shinsei, Shimizu, Nobuyoshi, Mizuno, Yoshikuni

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Structural Dimorphism in the Mitochondrial Targeting Sequence in the Human Manganese Superoxide Dismutase Gene von Shimoda-Matsubayashi, Satoe, Matsumine, Hiroto, Kobayashi, Tomonori, Nakagawa-Hattori, Yuko, Shimizu, Yumiko, Mizuno, Yoshikuni

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Point Mutations (Thr240Arg and Ala311Stop) in theParkinGene von Hattori, Nobutaka, Matsumine, Hiroto, Asakawa, Shuichi, Kitada, Tohru, Yoshino, Hiroyo, Elibol, Blüent, Brookes, Anthony J., Yamamura, Yasuhiro, Kobayashi, Tomonori, Wang, Mei, Yoritaka, Asako, Minoshima, Shinsei, Shimizu, Nobuyoshi, Mizuno, Yoshikuni

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Refinement of the gene locus for autosomal recessive juvenile parkinsonism (AR-JP) on chromosome 6q25.2-27 and identification of markers exhibiting linkage disequilibrium von Saito, Masaaki, Matsumine, Hiroto, Tanaka, Hajime, Ishikawa, Atsushi, Shimoda-Matsubayashi, Satoe, Schäffer, Alejandro A., Mizuno, Yoshikuni, Tsuji, S.

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Polymorphism in the parkin gene in sporadic Parkinson's disease von Wang, Mei, Hattori, Nobutaka, Matsumine, Hiroto, Kobayashi, Tomonori, Yoshino, Hiroyo, Morioka, Akiko, Kitada, Tohru, Asakawa, Shuichi, Minoshima, Shinsei, Shimizu, Nobuyoshi, Mizuno, Yoshikuni

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Association between the gene encoding the E2 subunit of the α-ketoglutarate dehydrogenase complex and Parkinson's disease von Kobayashi, Tomonori, Matsumine, Hiroto, Matuda, Sadayuki, Mizuno, Yoshikuni

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Early onset parkinsonism with diurnal fluctuation maps to a locus for juvenile parkinsonism von MATSUMINE, H, YAMAMURA, Y, KOBAYASHI, T, NAKAMURA, S, KUZUHARA, S, MIZUNO, Y

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