Zobrazeno 1 - 10
of 123
pro vyhledávání: '"Michio Inoue"'
Autor:
Han Ba Bui, Satoshi Watanabe, Norimichi Nomura, Kehong Liu, Tomoko Uemura, Michio Inoue, Akihisa Tsutsumi, Hiroyuki Fujita, Kengo Kinoshita, Yukinari Kato, So Iwata, Masahide Kikkawa, Kenji Inaba
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-16 (2023)
Abstract Zinc ions (Zn2+) are vital to most cells, with the intracellular concentrations of Zn2+ being tightly regulated by multiple zinc transporters located at the plasma and organelle membranes. We herein present the 2.2-3.1 Å-resolution cryo-EM
Externí odkaz:
https://doaj.org/article/9f73ce98b94448a691a914cd33c09204
Autor:
Kaiku Uegaki, Yuji Tokunaga, Michio Inoue, Seiji Takashima, Kenji Inaba, Koh Takeuchi, Ryo Ushioda, Kazuhiro Nagata
Publikováno v:
Cell Reports, Vol 42, Iss 7, Pp 112742- (2023)
Summary: The endoplasmic reticulum (ER) maintains an oxidative redox environment that is advantageous for the oxidative folding of nascent polypeptides entering the ER. Reductive reactions within the ER are also crucial for maintaining ER homeostasis
Externí odkaz:
https://doaj.org/article/c8656a4d782e41afb0fd6a0599406302
Autor:
Michio Inoue, Yoshihiko Saito, Takahiro Yonekawa, Megumu Ogawa, Aritoshi Iida, Ichizo Nishino, Satoru Noguchi
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-13 (2021)
Abstract Background Collagen VI-related dystrophy spans a clinical continuum from severe Ullrich congenital muscular dystrophy to milder Bethlem myopathy. This disease is caused by causative variants in COL6A1, COL6A2, or COL6A3. Most reported causat
Externí odkaz:
https://doaj.org/article/6cd731b60cf04dc1bd0ec25cfc1495ca
Autor:
Pascal Laforêt, Michio Inoue, Evelyne Goillot, Claire Lefeuvre, Umut Cagin, Nathalie Streichenberger, Sarah Leonard-Louis, Guy Brochier, Angeline Madelaine, Clemence Labasse, Carola Hedberg-Oldfors, Thomas Krag, Louisa Jauze, Julien Fabregue, Philippe Labrune, Jose Milisenda, Aleksandra Nadaj-Pakleza, Sabrina Sacconi, Federico Mingozzi, Giuseppe Ronzitti, François Petit, Benedikt Schoser, Anders Oldfors, John Vissing, Norma B. Romero, Ichizo Nishino, Edoardo Malfatti
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-16 (2019)
Abstract Glycogen storage disorder type III (GSDIII), or debranching enzyme (GDE) deficiency, is a rare metabolic disorder characterized by variable liver, cardiac, and skeletal muscle involvement. GSDIII manifests with liver symptoms in infancy and
Externí odkaz:
https://doaj.org/article/93fd2c97c0914ab89cce0bad8ec56750
Autor:
Munenori Oyama, Yuko Ohnuki, Michio Inoue, Akinori Uruha, Satoshi Yamashita, Sachiko Yutani, Jantima Tanboon, Jin Nakahara, Shingo Suzuki, Takashi Shiina, Ichizo Nishino, Shigeaki Suzuki
Publikováno v:
PLoS ONE, Vol 15, Iss 8, p e0237890 (2020)
IntroductionInclusion body myositis (IBM) is an idiopathic inflammatory myopathy, characterized by unique clinical features including finger flexor and quadriceps muscle weakness and a lack of any reliable treatment. The human leukocyte antigen (HLA)
Externí odkaz:
https://doaj.org/article/4584950c1b8d4f82915daf532d995b72
Publikováno v:
Case Reports in Pediatrics, Vol 2016 (2016)
Background. The outcome of neonates with congenital cutaneous Langerhans cell histiocytosis (LCH) is variable. Observations. We report a case of LCH in a female premature neonate born at 33-week gestation. She had disseminated cutaneous lesions, whic
Externí odkaz:
https://doaj.org/article/6d2fc9cce330404bbfa4739f021e856f
Autor:
Yuka Hama, Madoka Mori-Yoshimura, Kazutaka Aizawa, Yasushi Oya, Hisayoshi Nakamura, Michio Inoue, Aritoshi Iida, Noriko Sato, Ikuya Nonaka, Ichizo Nishino, Yuji Takahashi
Publikováno v:
Neuromuscular Disorders. 32:516-520
Autor:
Jantima Tanboon, Michio Inoue, Shinya Hirakawa, Hisateru Tachimori, Shinichiro Hayashi, Satoru Noguchi, Naoko Okiyama, Manabu Fujimoto, Shigeaki Suzuki, Ichizo Nishino
Publikováno v:
Brain Pathology.
Antisynthetase syndrome is recently recognized as one of the major entities of autoimmune myositis. The prototype of antisynthetase syndrome is anti-Jo-1 antibody associated syndrome while the syndromes associated with non-Jo-1 antisynthetase antibod
Autor:
Zhenghao Chen, Satoshi Watanabe, Hironori Hashida, Michio Inoue, Yasukazu Daigaku, Masahide Kikkawa, Kenji Inaba
Publikováno v:
Science Advances. 9
Secretory pathway Ca 2+ /Mn 2+ ATPase 1 (SPCA1) actively transports cytosolic Ca 2+ and Mn 2+ into the Golgi lumen, playing a crucial role in cellular calcium and manganese homeostasis. Detrimental mutations of the ATP2C1 gene encoding SPCA1 cause Ha
Autor:
Schiava, Marianela, Ikenaga, Chiseko, Topf, Ana, Caballero-´Avila, Marta, Tsui-Fen Chou, Shan Li, Feng Wang, Daw, Jil, Stojkovic, Tanya, Villar-Quiles, Rocio, Ichizo Nishino, Michio Inoue, Yukako Nishimori, Yoshihiko Saito, Masahisa Katsuno, Noda, Seiya, Chihiro Ito, Mieko Otsuka, Nahir, Sruthi, Manousakis, Georgios
Publikováno v:
Neurology: Genetics; Oct2023, Vol. 9 Issue 5, p1-12, 12p