Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Etsuko Keduka"'
Autor:
Etsuko Keduka, Hiroaki Mitsuhashi, Satoru Noguchi, Ichizo Nishino, Yukiko K. Hayashi, Wen-Chen Liang, Ikuya Nonaka
Publikováno v:
Annals of Neurology. 69:1005-1013
Objective: Emery-Dreifuss muscular dystrophy (EDMD) is a genetically heterogeneous muscular disease that presents with muscular dystrophy, joint contractures, and cardiomyopathy with conduction defects. Mutations in several nuclear envelope protein g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::751bc43a73ee065942ef69f93fc1b24a
https://doi.org/10.1002/ana.22338
https://doi.org/10.1002/ana.22338
Publikováno v:
Experimental Cell Research. 316:477-490
The small GTPase M-Ras is highly expressed in the central nervous system and plays essential roles in neuronal differentiation. However, its other cellular and physiological functions remain to be elucidated. Here, we clarify the novel functions of M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58707698eedf1d7d5edfd4e813e78314
https://doi.org/10.1016/j.yexcr.2009.09.028
https://doi.org/10.1016/j.yexcr.2009.09.028
Autor:
Haruko Watanabe-Takano, Yutaka Satou, Ai Kaiho, Michio Ogasawara, Nori Satoh, Mayuko Hamada, Kazunori Takano, Etsuko Keduka, Takeshi Endo
Publikováno v:
Gene. 429:49-58
The Ras family small GTPases play a variety of essential roles in eukaryotes. Among them, classical Ras (H-Ras, K-Ras, and N-Ras) and its orthologues are conserved from yeast to human. In ascidians, which phylogenetically exist between invertebrates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d52e8f3f164f2344492d0d2b287427fb
https://doi.org/10.1016/j.gene.2008.10.001
https://doi.org/10.1016/j.gene.2008.10.001
Autor:
Etsuko Keduka, Toru Imamura, Yukiko K. Hayashi, Nobukazu Araki, Hiroshi Takeshima, Ichizo Nishino, Chie Matsuda, Katsuya Miyake, Kimihiko Kameyama
Publikováno v:
PLoS Currents
In skeletal muscle, Mitsugumin 53 (MG53), also known as muscle-specific tripartite motif 72, reportedly interacts with dysferlin to regulate membrane repair. To better understand the interactions between dysferlin and MG53, we conducted immunoprecipi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::793925f11263e15e583b9130e5e0e0ba
http://europepmc.org/articles/PMC3493068
http://europepmc.org/articles/PMC3493068
Autor:
Yukiko K. Hayashi, S. Shalaby, Etsuko Keduka, Ikuya Nonaka, Hiroaki Mitsuhashi, Ichizo Nishino, Satoru Noguchi
Publikováno v:
The American journal of pathology. 180(4)
Myofibrillar myopathy (MFM) is a group of disorders that are pathologically defined by the disorganization of the myofibrillar alignment associated with the intracellular accumulation of Z-disk–associated proteins. MFM is caused by mutations in gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf2264b1073eedf4a58c5e55c42f6dde
https://pubmed.ncbi.nlm.nih.gov/22349301
https://pubmed.ncbi.nlm.nih.gov/22349301
Autor:
Chie Matsuda, Katsuya Miyake, Kimihiko Kameyama, Etsuko Keduka, Hiroshi Takeshima, Toru Imamura, Nobukazu Araki, Ichizo Nishino, Yukiko Hayashi
Publikováno v:
PLoS Currents; 2012, p538-546, 9p