Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Kiyoko Inui"'
Autor:
Yoshinori Sato, Hiroyasu Tsukaguchi, Koichiro Higasa, Naoto Kawata, Kiyoko Inui, Tran Nguyen Truc Linh, Tran Thuy Huong Quynh, Inoue Yoshihiko, Fumihiko Koiwa, Ashio Yoshimura
Publikováno v:
BMC Nephrology, Vol 22, Iss 1, Pp 1-10 (2021)
Abstract Background IgA nephropathy (IgAN) is the most common primary glomerulonephritis worldwide. Although most IgAN cases are sporadic, few show a familial aggregation. However, the prevalence and prognosis of IgAN individuals with positive famili
Externí odkaz:
https://doaj.org/article/4d51439a482d4421a2539bb4365973b0
Autor:
Naoto Kawata, Fumihiko Koiwa, Tran Thuy Huong Quynh, Tran Nguyen Truc Linh, Yoshinori Sato, Koichiro Higasa, Hiroyasu Tsukaguchi, Ashio Yoshimura, Inoue Yoshihiko, Kiyoko Inui
Publikováno v:
BMC Nephrology, Vol 22, Iss 1, Pp 1-10 (2021)
BMC Nephrology
BMC Nephrology
Background IgA nephropathy (IgAN) is the most common primary glomerulonephritis worldwide. Although most IgAN cases are sporadic, few show a familial aggregation. However, the prevalence and prognosis of IgAN individuals with positive familial histor
Autor:
Hiroyasu Tsukaguchi, Izumi Yamaguchi, Toshiaki Usui, Ashio Yoshimura, Hiroyuki Morita, Takao Hayashi, Naoki Morito, Mai Thi Nhu Tran, Hiroshi Sato, Huan Thanh Nguyen, Yoshinori Sato, Yuichi Maruta, Fumihiko Koiwa, Masayo Harada, Fumihiko Matsuda, Junko Takagi, Satoru Takahashi, Shinya Ayabe, Yoshihiko Inoue, Seiya Mizuno, Michito Hamada, Koichiro Higasa, Shoichiro Horita, Kiyoko Inui, Fumihiro Sugiyama
Publikováno v:
Kidney International. 94:396-407
Focal segmental glomerulosclerosis (FSGS) is a leading cause of end-stage renal disease in children and adults. Genetic factors significantly contribute to early-onset FSGS, but the etiologies of most adult cases remain unknown. Genetic studies of mo
Autor:
Fumihiko Koiwa, Yoshihiko Inoue, Kazuo Otake, Kiyoko Inui, Hiroyuki Morita, Yoshihiro Wakayama, Masahiko Ayaki, Yoshinori Sato, Ashio Yoshimura, Junko Takagi, Sho Hirase
Publikováno v:
Biomedical Journal of Scientific & Technical Research. 22
Bardet-Biedl syndrome (BBS; OMIM #209900) is a pleiotropic genetic disorder, or ciliopathy, with autosomal recessive inheritance [1].
Autor:
Yuko Yamano, Yoshihiko Inoue, Eri Kawashima, Tomoaki Miyazaki, Kiyoko Inui, Nobuharu Kaneshima, Ashio Yoshimura, Shinya Omiya, Toshio Nakadate, Sakura Nagumo
Publikováno v:
The Showa University Journal of Medical Sciences. 27:167-174
Autor:
Takeshi Hasegawa, Hironori Tayama, Yoshihiko Inoue, Daisuke Komukai, Yoshikuni Nagayama, Ashio Yoshimura, Hiroki Nishiwaki, Mamiko Takayasu, Eri Kawashima, Kiyoko Inui
Publikováno v:
Clinical and Experimental Nephrology. 19:646-652
In 2011, the Japanese Society of Nephrology (JSN) published new clinical guidelines for IgA nephropathy (IgAN) with a new risk stratification based on clinical and histological severity. For classification, patients are divided into four groups (low,
Publikováno v:
Nephron. 137(3)
Background/Aims: Although microangiopathic hemolysis (MAH) is a well-known complication of malignant phase hypertension (MPH), only less data on whether MAH in MPH predicts renal outcome exist. Therefore, we evaluated whether MAH was associated with
Autor:
Kiyoko Inui, Nobuhiko Ohno, Shinichi Ohno, Ashio Yoshimura, Eri Kawashima, Yurika Saitoh, Nobuo Terada
Publikováno v:
In Vivo Cryotechnique in Biomedical Research and Application for Bioimaging of Living Animal Organs ISBN: 9784431557227
In vivo cryotechnique (IVCT) has been useful to examine native immunolocalizations of soluble proteins in animal kidneys, reflecting their living states. By using them, we have examined some immunolocalized proteins in nephrons of rat kidneys under e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e470f1b59e03408fa57ff956e06b41b
https://doi.org/10.1007/978-4-431-55723-4_24
https://doi.org/10.1007/978-4-431-55723-4_24
Autor:
Mutsushi Matsuyama, Kiyoko Nakano, Kiyotaka Akiyama, Shiro Suetsugu, Noriko Wakisaka, Hiroyuki Morita, Seiko Kuraba, Yasuharu Numata, Kiyoko Inui, Hiroaki Oniki, Ashio Yoshimura, Terukuni Ideura, Yoshihisa Yamamoto, Tadaomi Takenawa
Publikováno v:
Mammalian Genome. 19:41-50
The BUF/Mna strain of rat is a model of focal and segmental glomerulosclerosis (FSGS) in which a quantitative trait locus (QTL) for proteinuria, Pur1, has been identified. The aim of the present study was to identify candidates for the Pur1 gene. To
Autor:
K Yoshitome, Takafumi Morisaki, Akinobu Hamada, Kimio Tomita, Yukimasa Kohda, Hiroshi Watanabe, Hideyuki Saito, Takanobu Matsuzaki, Hiroshi Nonoguchi, Kiyoko Inui
Publikováno v:
Kidney International. 71(6):539-547
The effect of acute renal failure (ARF) induced by ischemia/reperfusion (I/R) of rat kidney on the expression of organic anion transporters (OATs) was examined. The level of serum indoxyl sulfate (IS), a uremic toxin and substrate of OATs in renal tu