CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study von Funayama, Manabu, PhD, Ohe, Kenji, MD, Amo, Taku, PhD, Furuya, Norihiko, PhD, Yamaguchi, Junji, MSc, Saiki, Shinji, MD, Li, Yuanzhe, MD, Ogaki, Kotaro, MD, Ando, Maya, MD, Yoshino, Hiroyo, PhD, Tomiyama, Hiroyuki, MD, Nishioka, Kenya, MD, Hasegawa, Kazuko, MD, Saiki, Hidemoto, MD, Satake, Wataru, MD, Mogushi, Kaoru, PhD, Sasaki, Ryogen, MD, Kokubo, Yasumasa, Prof, Kuzuhara, Shigeki, Prof, Toda, Tatsushi, Prof, Mizuno, Yoshikuni, Prof, Uchiyama, Yasuo, Prof, Ohno, Kinji, Prof, Hattori, Nobutaka, Prof

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Reply: PSAP variants in Parkinson's disease: a large cohort study in Chinese mainland population von Oji, Yutaka, Hatano, Taku, Funayama, Manabu, Hattori, Nobutaka

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Loss of Parkinson’s disease-associated protein CHCHD2 affects mitochondrial crista structure and destabilizes cytochrome c von Meng, Hongrui, Yamashita, Chikara, Shiba-Fukushima, Kahori, Inoshita, Tsuyoshi, Funayama, Manabu, Sato, Shigeto, Hatta, Tomohisa, Natsume, Tohru, Umitsu, Masataka, Takagi, Junichi, Imai, Yuzuru, Hattori, Nobutaka

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PINK1 autophosphorylation upon membrane potential dissipation is essential for Parkin recruitment to damaged mitochondria von Okatsu, Kei, Oka, Toshihiko, Iguchi, Masahiro, Imamura, Kenji, Kosako, Hidetaka, Tani, Naoki, Kimura, Mayumi, Go, Etsu, Koyano, Fumika, Funayama, Manabu, Shiba-Fukushima, Kahori, Sato, Shigeto, Shimizu, Hideaki, Fukunaga, Yuko, Taniguchi, Hisaaki, Komatsu, Masaaki, Hattori, Nobutaka, Mihara, Katsuyoshi, Tanaka, Keiji, Matsuda, Noriyuki

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A metabolic profile of polyamines in parkinson disease: A promising biomarker von Saiki, Shinji, Sasazawa, Yukiko, Fujimaki, Motoki, Kamagata, Koji, Kaga, Naoko, Taka, Hikari, Li, Yuanzhe, Souma, Sanae, Hatano, Taku, Imamichi, Yoko, Furuya, Norihiko, Mori, Akio, Oji, Yutaka, Ueno, Shin‐Ichi, Nojiri, Shuko, Miura, Yoshiki, Ueno, Takashi, Funayama, Manabu, Aoki, Shigeki, Hattori, Nobutaka

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Homozygous alpha-synuclein p.A53V in familial Parkinson’s disease von Yoshino, Hiroyo, PhD, Hirano, Makito, MD, PhD, Stoessl, A. Jon, MD, Imamichi, Yoko, BS, Ikeda, Aya, MD, Li, Yuanzhe, MD, PhD, Funayama, Manabu, PhD, Yamada, Ikuko, MD, PhD, Nakamura, Yusaku, MD, PhD, Sossi, Vesna, PhD, Farrer, Matthew J., PhD, Nishioka, Kenya, MD, PhD, Hattori, Nobutaka, MD, PhD

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Variants in saposin D domain of prosaposin gene linked to Parkinson's disease von Oji, Yutaka, Hatano, Taku, Ueno, Shin-Ichi, Funayama, Manabu, Ishikawa, Kei-ichi, Okuzumi, Ayami, Noda, Sachiko, Sato, Shigeto, Satake, Wataru, Toda, Tatsushi, Li, Yuanzhe, Hino-Takai, Tomoko, Kakuta, Soichiro, Tsunemi, Taiji, Yoshino, Hiroyo, Nishioka, Kenya, Hattori, Tatsuya, Mizutani, Yasuaki, Mutoh, Tatsuro, Yokochi, Fusako, Ichinose, Yuta, Koh, Kishin, Shindo, Kazumasa, Takiyama, Yoshihisa, Hamaguchi, Tsuyoshi, Yamada, Masahito, Farrer, Matthew J., Uchiyama, Yasuo, Akamatsu, Wado, Wu, Yih-Ru, Matsuda, Junko, Hattori, Nobutaka

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CHCHD2 and Parkinson's disease—Authors' reply von Funayama, Manabu, Hattori, Nobutaka

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Analysis of LIN28A variants in patients with Parkinson's disease von Peng, Hao, Li, Yuanzhe, Yoshino, Hiroyo, Shimizu, Mai, Nishioka, Kenya, Funayama, Manabu, Hattori, Nobutaka

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Generation of a control iPS cell line (JUCGRMi006-A) with no abnormalities in Parkinson's disease-related genes von Ishikawa, Kei-ichi, Shiga, Takahiro, Funayama, Manabu, Hattori, Nobutaka, Akamatsu, Wado

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Generation of a control iPS cell line (JUCGRMi005-A) with no abnormalities in Parkinson's disease-related genes von Ishikawa, Kei-ichi, Shiga, Takahiro, Funayama, Manabu, Hattori, Nobutaka, Akamatsu, Wado

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Loss of Atg2b and Gskip Impairs the Maintenance of the Hematopoietic Stem Cell Pool Size von Sakai, Shun-suke, Hasegawa, Atsushi, Ishimura, Ryosuke, Tamura, Naoki, Kageyama, Shun, Komatsu-Hirota, Satoko, Abe, Manabu, Ling, Yiwei, Okuda, Shujiro, Funayama, Manabu, Kikkawa, Mika, Miura, Yoshiki, Sakimura, Kenji, Narita, Ichiei, Waguri, Satoshi, Shimizu, Ritsuko, Komatsu, Masaaki

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Clinical characterization of patients with leucine-rich repeat kinase 2 genetic variants in Japan von Li, Yuanzhe, Ikeda, Aya, Yoshino, Hiroyo, Oyama, Genko, Kitani, Mitsuhiro, Daida, Kensuke, Hayashida, Arisa, Ogaki, Kotaro, Yoshida, Kousuke, Kimura, Takashi, Nakayama, Yoshiaki, Ito, Hidefumi, Sugeno, Naoto, Aoki, Masashi, Miyajima, Hiroaki, Kimura, Katsuo, Ueda, Naohisa, Watanabe, Masao, Urabe, Takao, Takanashi, Masashi, Funayama, Manabu, Nishioka, Kenya, Hattori, Nobutaka

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Identifying Therapeutic Agents for Amelioration of Mitochondrial Clearance Disorder in Neurons of Familial Parkinson Disease von Yamaguchi, Akihiro, Ishikawa, Kei-ichi, Inoshita, Tsuyoshi, Shiba-Fukushima, Kahori, Saiki, Shinji, Hatano, Taku, Mori, Akio, Oji, Yutaka, Okuzumi, Ayami, Li, Yuanzhe, Funayama, Manabu, Imai, Yuzuru, Hattori, Nobutaka, Akamatsu, Wado

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Lysosomal Storage of Subunit c of Mitochondrial ATP Synthase in Brain-Specific Atp13a2-Deficient Mice von Sato, Shigeto, Koike, Masato, Funayama, Manabu, Ezaki, Junji, Fukuda, Takahiro, Ueno, Takashi, Uchiyama, Yasuo, Hattori, Nobutaka

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Clinical Manifestations and Molecular Backgrounds of Parkinson's Disease Regarding Genes Identified From Familial and Population Studies von Nishioka, Kenya, Imai, Yuzuru, Yoshino, Hiroyo, Li, Yuanzhe, Funayama, Manabu, Hattori, Nobutaka

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Clinical heterogeneity of frontotemporal dementia and Parkinsonism linked to chromosome 17 caused by MAPT N279K mutation in relation to tau positron emission tomography features von Ikeda, Aya, Shimada, Hitoshi, Nishioka, Kenya, Takanashi, Masashi, Hayashida, Arisa, Li, Yuanzhe, Yoshino, Hiroyo, Funayama, Manabu, Ueno, Yuji, Hatano, Taku, Sahara, Naruhiko, Suhara, Tetsuya, Higuchi, Makoto, Hattori, Nobutaka

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ATP13A2 deficiency induces a decrease in cathepsin D activity, fingerprint-like inclusion body formation, and selective degeneration of dopaminergic neurons von Matsui, Hideaki, Sato, Fumiaki, Sato, Shigeto, Koike, Masato, Taruno, Yosuke, Saiki, Shinji, Funayama, Manabu, Ito, Hidefumi, Taniguchi, Yoshihito, Uemura, Norihito, Toyoda, Atsushi, Sakaki, Yoshiyuki, Takeda, Shunichi, Uchiyama, Yasuo, Hattori, Nobutaka, Takahashi, Ryosuke

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Isolated nigral degeneration without pathological protein aggregation in autopsied brains with LRRK2 p.R1441H homozygous and heterozygous mutations von Takanashi, Masashi, Funayama, Manabu, Matsuura, Eiji, Yoshino, Hiroyo, Li, Yuanzhe, Tsuyama, Sho, Takashima, Hiroshi, Nishioka, Kenya, Hattori, Nobutaka

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An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family von Funayama, Manabu, Hasegawa, Kazuko, Ohta, Etsuro, Kawashima, Noriko, Komiyama, Masaru, Kowa, Hisayuki, Tsuji, Shoji, Obata, Fumiya

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