Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Kie Ito"'
Autor:
Zhenyong Wu, Grant F Kusick, Manon MM Berns, Sumana Raychaudhuri, Kie Itoh, Alexander M Walter, Edwin R Chapman, Shigeki Watanabe
Publikováno v:
eLife, Vol 12 (2024)
Despite decades of intense study, the molecular basis of asynchronous neurotransmitter release remains enigmatic. Synaptotagmin (syt) 7 and Doc2 have both been proposed as Ca2+ sensors that trigger this mode of exocytosis, but conflicting findings ha
Externí odkaz:
https://doaj.org/article/a941dafebeac4bb681369387d5e79f94
Autor:
Tyler H. Ogunmowo, Haoyuan Jing, Sumana Raychaudhuri, Grant F. Kusick, Yuuta Imoto, Shuo Li, Kie Itoh, Ye Ma, Haani Jafri, Matthew B. Dalva, Edwin R. Chapman, Taekjip Ha, Shigeki Watanabe, Jian Liu
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-16 (2023)
Abstract Compensatory endocytosis keeps the membrane surface area of secretory cells constant following exocytosis. At chemical synapses, clathrin-independent ultrafast endocytosis maintains such homeostasis. This endocytic pathway is temporally and
Externí odkaz:
https://doaj.org/article/5cf401e46fe64d69884a9f4db7edc244
Autor:
Satoshi Watanabe, Yuta Nihongaki, Kie Itoh, Toru Uyama, Satoshi Toda, Shigeki Watanabe, Takanari Inoue
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-15 (2022)
Approaches for manipulating individual organelles are important for learning more about their functions. Here the authors report a tool utilising phospholipase A/acyltransferases (PLAATs) for rapid defunctionalisation of organelles through remodellin
Externí odkaz:
https://doaj.org/article/fb70ab7254af4f4dabcd7ae96323f9d0
Autor:
Kie, Ito, Taku, Obara, Takayoshi, Ohkubo, Kenta, Gonokami, Takahiro, Shinki, Taku, Shibamiya, Manami, Nakashita, Mitsuru, Kobayashi, Jin, Funahashi, Azusa, Hara, Hirohito, Metoki, Kei, Asayama, Ryusuke, Inoue, Masahiro, Kikuya, Nariyasu, Mano, Yutaka, Imai, Kazuhito, Totsune
Publikováno v:
Blood Pressure Monitoring. 14:160-165
The objective of this study was to clarify the factors affecting the morning-evening home systolic blood pressure (BP) difference (home systolic ME dif) in treated hypertensive patients, including evening home BP measuring conditions, based on the da
Autor:
Kie Ito, Masayuki Hata, Kiyoshi Kita, Takashi Ueda, Narie Sasaki, Akihiko Nakano, Shigeharu Sato, Ryoko Yui, Katsura Maeda-Sano, Kimiko Murakami-Murofushi
Publikováno v:
CYTOLOGIA. 74:449-455
Organellar DNA in mitochondria and plastids are organized with proteins into a compact structure known as the nucleoid. As the nucleoid is supposed to be the unit of inheritance for the organellar genome, it is important to understand its cytological
Autor:
Taku, Obara, Kie, Ito, Takayoshi, Ohkubo, Taku, Shibamiya, Takahiro, Shinki, Manami, Nakashita, Azusa, Hara, Hirohito, Metoki, Ryusuke, Inoue, Kei, Asayama, Masahiro, Kikuya, Nariyasu, Mano, Yutaka, Imai, Kazuhito, Totsune
Publikováno v:
Hypertension research : official journal of the Japanese Society of Hypertension. 32(12)
We evaluated the control condition of morning and evening home blood pressure (BP) and compared patients who had isolated uncontrolled morning hypertension and those who had sustained uncontrolled (morning and evening) hypertension using data from th
Autor:
Emmanuelle C. Genin, Sylvie Bannwarth, Françoise Lespinasse, Bernardo Ortega-Vila, Konstantina Fragaki, Kie Itoh, Elodie Villa, Sandra Lacas-Gervais, Manu Jokela, Mari Auranen, Emil Ylikallio, Alessandra Mauri-Crouzet, Henna Tyynismaa, Anna Vihola, Gaelle Augé, Charlotte Cochaud, Hiromi Sesaki, Jean-Ehrland Ricci, Bjarne Udd, Cristofol Vives-Bauza, Véronique Paquis-Flucklinger
Publikováno v:
Neurobiology of Disease, Vol 119, Iss , Pp 159-171 (2018)
Following the involvement of CHCHD10 in FrontoTemporal-Dementia-Amyotrophic Lateral Sclerosis (FTD-ALS) clinical spectrum, a founder mutation (p.Gly66Val) in the same gene was identified in Finnish families with late-onset spinal motor neuronopathy (
Externí odkaz:
https://doaj.org/article/4dd012f21baf4cd2b4f522f52e36c6f3
Autor:
Neeharika Nemani, Edmund Carvalho, Dhanendra Tomar, Zhiwei Dong, Andrea Ketschek, Sarah L. Breves, Fabián Jaña, Alison M. Worth, Julie Heffler, Palaniappan Palaniappan, Aparna Tripathi, Ramasamy Subbiah, Massimo F. Riitano, Ajay Seelam, Thomas Manfred, Kie Itoh, Shuxia Meng, Hiromi Sesaki, William J. Craigen, Sudarsan Rajan, Santhanam Shanmughapriya, Jeffrey Caplan, Benjamin L. Prosser, Donald L. Gill, Peter B. Stathopulos, Gianluca Gallo, David C. Chan, Prashant Mishra, Muniswamy Madesh
Publikováno v:
Cell Reports, Vol 23, Iss 4, Pp 1005-1019 (2018)
Summary: Mitochondria shape cytosolic calcium ([Ca2+]c) transients and utilize the mitochondrial Ca2+ ([Ca2+]m) in exchange for bioenergetics output. Conversely, dysregulated [Ca2+]c causes [Ca2+]m overload and induces permeability transition pore an
Externí odkaz:
https://doaj.org/article/d8a52722cb5c491eaab6dfcbe01c7e01
Autor:
Kie Itoh, Daisuke Murata, Takashi Kato, Tatsuya Yamada, Yoichi Araki, Atsushi Saito, Yoshihiro Adachi, Atsushi Igarashi, Shuo Li, Mikhail Pletnikov, Richard L Huganir, Shigeki Watanabe, Atsushi Kamiya, Miho Iijima, Hiromi Sesaki
Publikováno v:
eLife, Vol 8 (2019)
Dynamin-related protein 1 (Drp1) divides mitochondria as a mechano-chemical GTPase. However, the function of Drp1 beyond mitochondrial division is largely unknown. Multiple Drp1 isoforms are produced through mRNA splicing. One such isoform, Drp1ABCD,
Externí odkaz:
https://doaj.org/article/d127a1b7a9bc4de8a744e7a0583a8eba
Autor:
Emmanuelle C Genin, Morgane Plutino, Sylvie Bannwarth, Elodie Villa, Eugenia Cisneros‐Barroso, Madhuparna Roy, Bernardo Ortega‐Vila, Konstantina Fragaki, Françoise Lespinasse, Estefania Pinero‐Martos, Gaëlle Augé, David Moore, Florence Burté, Sandra Lacas‐Gervais, Yusuke Kageyama, Kie Itoh, Patrick Yu‐Wai‐Man, Hiromi Sesaki, Jean‐Ehrland Ricci, Cristofol Vives‐Bauza, Véronique Paquis‐Flucklinger
Publikováno v:
EMBO Molecular Medicine, Vol 8, Iss 1, Pp 58-72 (2015)
Abstract CHCHD10‐related diseases include mitochondrial DNA instability disorder, frontotemporal dementia‐amyotrophic lateral sclerosis (FTD‐ALS) clinical spectrum, late‐onset spinal motor neuropathy (SMAJ), and Charcot–Marie–Tooth diseas
Externí odkaz:
https://doaj.org/article/a6eda45384124c2da28b788438fcf63d