Zobrazeno 1 - 10
of 1 907
pro vyhledávání: '"F, Marumo"'
Autor:
Wataru Ogawa, Yoshio Terada, Sei Sasaki, Masato Kasuga, Satoko Hanada, F Marumo, Haruko Shimamura, Seiji Inoshita, Michio Kuwahara
Publikováno v:
Kidney International. 60(2):553-567
Hyperosmolality activates Akt and regulates apoptosis in renal tubular cells . Background The novel serine-threonine kinase Akt is a critical enzyme in cell survival. We investigated the roles of the Akt pathway and apoptotic signals in ( 1 ) Madin-D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e5d198a6b8cc1d6767b9f64fbe8a5d3
Publikováno v:
Mycotoxins. 50:45-51
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9b7fd580c43d44be0e0ed44dec19d45
https://doi.org/10.2520/myco1975.50.45
https://doi.org/10.2520/myco1975.50.45
Publikováno v:
Annual Review of Physiology. 60:199-220
▪ Abstract Since the molecular identification of the first aquaporin in 1992, the number of proteins known to belong to this family has been rapidly increasing. These members may be separated into two subgroups based on gene structure, sequence hom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dea962305770976d03dd43f899b43f8
https://doi.org/10.1146/annurev.physiol.60.1.199
https://doi.org/10.1146/annurev.physiol.60.1.199
Autor:
H Sakamoto, M Fukui, Y Tomino, Sei Sasaki, Shinichi Uchida, T Morimoto, N Nagano, Yoshiaki Kondo, F Marumo, H Hanamizu
Publikováno v:
Journal of the American Society of Nephrology. 9:811-818
Mutations in the CLCN5 gene have been demonstrated in three disorders of hypercalciuric nephrolithiasis, i.e., Dent's disease, X-linked recessive nephrolithiasis, and X-linked recessive hypophosphatemic rickets. Recently, a number of Japanese childre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7893cfdaa50c3b697635bd25c79131b5
https://doi.org/10.1681/asn.v95811
https://doi.org/10.1681/asn.v95811
Autor:
Takashi Akiba, R. Sasaki, Kiyoshi Kurokawa, Kei-ichiro Maeda, Toshio Shinoda, Kazuo Kubo, F Marumo, Takashi Sato, T. Kitaoka, Toru Shinzato, Shigeru Nakai, C. Yamazaki
Publikováno v:
Nephrology Dialysis Transplantation. 12:889-898
Beginning in 1966, the Patient Registration Committee of the Japanese Society for Dialysis Therapy has conducted a survey once a year on renal replacement therapy in Japan. As of 1983, the survey covered the life/death of patients in the survey years
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6329e71b2e4ccfecc09dee8b8c70bb8b
https://doi.org/10.1093/ndt/12.5.889
https://doi.org/10.1093/ndt/12.5.889
Publikováno v:
American Journal of Physiology-Renal Physiology. 272:F235-F241
Aquaporin-3 (AQP3) is unique in its structure (lowest homology with other aquaporins) and in its function (significantly conductive to both small nonelectrolytes and water). However, there is a controversy among researchers on its water transport and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a441615948e2417065d930f991cb69c6
https://doi.org/10.1152/ajprenal.1997.272.2.f235
https://doi.org/10.1152/ajprenal.1997.272.2.f235
Autor:
Kazuo Kubo, Kiyoshi Kurokawa, C. Yamazaki, Kei-ichiro Maeda, Takashi Akiba, R. Sasaki, Toshio Shinoda, Takashi Sato, Toru Shinzato, F Marumo, Shigeru Nakai, T. Kitaoka
Publikováno v:
Nephrology Dialysis Transplantation. 11:2139-2142
The prognosis for haemodialysis patients is reported to be more favourable in Japan than in Europe or North America. Consequently, evaluation of the death predictors for haemodialysis patients in Japan is of considerable interest outside Japan. The P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::645c5d1e16e363c53d5ad979345048af
https://doi.org/10.1093/oxfordjournals.ndt.a027127
https://doi.org/10.1093/oxfordjournals.ndt.a027127
Publikováno v:
Journal of Clinical Investigation. 97:1780-1784
Mutations in beta or gamma subunit of the epithelial sodium channel (ENaC) have been found to cause a hereditary form of human hypertension, Liddle syndrome. Most of the mutations reported are either nonsense mutations or frame shift mutations which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8f97e34bf1c58759e671fb850bb4c3f
https://doi.org/10.1172/jci118606
https://doi.org/10.1172/jci118606
Endothelin-3 induces hypertrophy of cardiomyocytes by the endogenous endothelin-1-mediated mechanism
Publikováno v:
Journal of Clinical Investigation. 97:366-372
We have recently reported that endothelin-1 (ET-1) mediates angiotensin II-induced hypertrophy of cardiomyocytes as an autocrine/paracrine factor. In the present study, we examined whether endothelin-3 (ET-3) induces hypertrophy of cultured neonatal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d73793c0b09a3ccadce3c3aaad5a317
https://doi.org/10.1172/jci118424
https://doi.org/10.1172/jci118424
Autor:
Sei Sasaki, Kiyohide Fushimi, N. Fujita, San-e Ishikawa, G. Fujisawa, F Marumo, Toshikazu Saito
Publikováno v:
American Journal of Physiology-Renal Physiology. 269:F926-F931
We determined whether aquaporin of collecting duct (AQP-CD) is involved in pathogenesis of water retention in rats with experimental models of syndrome of inappropriate secretion of antidiuretic hormone (SIADH) and liver cirrhosis. SIADH rats were ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a6c63d576872b708369691bc566d684
https://doi.org/10.1152/ajprenal.1995.269.6.f926
https://doi.org/10.1152/ajprenal.1995.269.6.f926