Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Kunihiko, Aya"'
Autor:
Yuko Hamasaki, Riku Hamada, Masaki Muramatsu, Shinsuke Matsumoto, Kunihiko Aya, Kenji Ishikura, Tetsuji Kaneko, Kazumoto Iijima
Publikováno v:
BMC Nephrology, Vol 21, Iss 1, Pp 1-8 (2020)
Abstract Background Congenital nephrotic syndrome (CNS) and infantile nephrotic syndrome (INS) cause substantial morbidity and mortality. In Japan, there is a lack of knowledge regarding the characteristics of CNS and INS. This study aimed to clarify
Externí odkaz:
https://doaj.org/article/a28695e98d3745aa99a9966deea06489
Autor:
Yukie Okabe, Kunihiko Aya, Kohei Tokioka, Masaya Hattori, Mikita Yamamoto, Mariko Sawada, Kaori Uchino, Nobuyoshi Mimaki, Nobuaki Takeda, Kenji Waki, Yoshio Arakaki
Publikováno v:
Japanese journal of pediatric nephrology. 35:101-108
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::609ca8706b2d363721ef90fd3049ea3e
https://doi.org/10.3165/jjpn.cr.2021.0199
https://doi.org/10.3165/jjpn.cr.2021.0199
Autor:
Shinsuke Matsumoto, Kazumoto Iijima, Masaki Muramatsu, Yuko Hamasaki, Kenji Ishikura, Riku Hamada, Kunihiko Aya, Tetsuji Kaneko
Publikováno v:
BMC Nephrology, Vol 21, Iss 1, Pp 1-8 (2020)
BMC Nephrology
BMC Nephrology
Background Congenital nephrotic syndrome (CNS) and infantile nephrotic syndrome (INS) cause substantial morbidity and mortality. In Japan, there is a lack of knowledge regarding the characteristics of CNS and INS. This study aimed to clarify the char
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0d296a2d007ad7ca46a1d0255d7a10c
https://doi.org/10.21203/rs.3.rs-22986/v1
https://doi.org/10.21203/rs.3.rs-22986/v1
Autor:
Kosei Hasegawa, Yoshiharu Nagaoka, Hidehiko Maruyama, Hiroyuki Tanaka, Tsuneo Morishima, Kunihiko Aya
Publikováno v:
Clinical Pediatric Endocrinology
Noonan syndrome is characterized by facial dysmorphology, congenital heart disease and growth failure. Although it is also accompanied by deranged lymph-vessel formation, protein-losing enteropathy (PLE) with Noonan syndrome is rarely reported. We re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c974a7abf653534a98623e806235c6dd
https://doi.org/10.1297/cpe.18.87
https://doi.org/10.1297/cpe.18.87
Autor:
Deborah V. Novack, Osami Kanagawa, Kunihiko Aya, Muhammad Alhawagri, Hideki Kitaura, Amanda Hagen-Stapleton
Publikováno v:
Journal of Clinical Investigation. 115:1848-1854
NF-(kappa)B is an important component of both autoimmunity and bone destruction in RA. NF-(kappa)B-inducing kinase (NIK) is a key mediator of the alternative arm of the NF-(kappa)B pathway, which is characterized by the nuclear translocation of RelB/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a2dfff7ea8a320cd0546a7975c83134
https://doi.org/10.1172/jci23763
https://doi.org/10.1172/jci23763
Publikováno v:
American Journal of Kidney Diseases. 40:697-703
Background: NPHS1, which encodes nephrin, recently has been identified as the gene in which mutations cause congenital nephrotic syndrome of the Finnish type (CNF). We previously reported novel missense mutations of NPHS1 in a Japanese patient with C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7c03ffdca4c3a9ea9aacecbbf2d8935
https://doi.org/10.1053/ajkd.2002.35676
https://doi.org/10.1053/ajkd.2002.35676
Autor:
Xu Feng, Deborah V. Novack, F. Patrick Ross, Kunihiko Aya, Roberta Faccio, Steven L. Teitelbaum, Daniel S. Ory, Kevin P. McHugh, Martin I. Boyer
Publikováno v:
Journal of Clinical Investigation. 107:1137-1144
Osteoclastic bone resorption requires cell-matrix contact, an event mediated by the alpha v beta 3 integrin. The structural components of the integrin that mediate osteoclast function are, however, not in hand. To address this issue, we generated mic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c45247608c867ba6b2ddf7925c6b0fc
https://doi.org/10.1172/jci12040
https://doi.org/10.1172/jci12040
Publikováno v:
Kidney International. 55:1696-1703
Expression of parathyroid hormone-related peptide messenger ribonucleic acid in developing kidney. Background Parathyroid hormone (PTH)-related peptide (PTHrP), originally identified as a causative agent of hypercalcemia of malignancy, has been impli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70581b8d4edada345ab8e2ec8fd51365
https://doi.org/10.1046/j.1523-1755.1999.00417.x
https://doi.org/10.1046/j.1523-1755.1999.00417.x
Autor:
Youjirou Ichinose, Kunihiko Aya, Megumi Kobayashi, Hiroshi Igaki, Naho Nishioka, Masumi Tsuyuki, Yoshiki Seino, Kazuo Tsuzuki, Hiroyuki Tanaka
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 82:2716-2719
Familial hypocalciuric hypercalcemia (FHH) is characterized by lifelong asymptomatic hypercalcemia without PTH hypersecretion and is inherited as an autosomal dominant trait with near 100% penetrance. In contrast, neonatal severe hyperparathyroidism
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9242e5b1c27b331a161745e2e8e3711
https://doi.org/10.1210/jcem.82.8.4135
https://doi.org/10.1210/jcem.82.8.4135
Publikováno v:
Nihon Shoni Jinzobyo Gakkai Zasshi. 10:173-177
腎臓における副甲状腺ホルモン関連ペプチド (PTHrP) mRNAの発現量をRT-PCRにより，局在をin situ hybridizationにより検討した。マウス腎の発達段階における検討では，PTHrPmRNAは0日齢，1週齢で最
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76d2a2691907f7c3e4edb44dd9d5a629
https://doi.org/10.3165/jjpn.10.173
https://doi.org/10.3165/jjpn.10.173