Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Masanori, Takaiwa"'
Autor:
Masataka Hisano, Motoshi Hattori, Kiyonobu Ishizuka, Kazuhide Suyama, Takaya Iida, Yoko Shirai, Masanori Takaiwa, Atsutoshi Shiratori, Naoto Kaneko, Hideki Ban, Sho Ishiwa, Kenichiro Miura, Tomoo Yabuuchi, Taro Ando
Publikováno v:
Clinical and Experimental Nephrology. 25:531-536
There are two approaches for treating cytomegalovirus (CMV) infection occurring after kidney transplantation (KTx). One is preemptive therapy in which treatment is started after confirming positive CMV antigenemia using periodic antigenemia assay. Th
Autor:
Susumu Kanzaki, Kaori Nikaido, Yoshiki Seino, Masanori Takaiwa, Katsumi Nagata, Masako Kawakami, Toshihide Kubo, Tadashi Moriwake
Publikováno v:
Clinical Pediatric Endocrinology. 9:19-24
Autor:
Takayuki, Miyai, Kunihiko, Aya, Masanori, Takaiwa, Kunimasa, Yan, Yoshikazu, Sado, Hiroyuki, Tanaka, Tsuneo, Morishima
Publikováno v:
Histology and histopathology. 29(2)
Many mutations in the NPHS1 gene were detected among patients with congenital nephrotic syndrome. Functional analysis of those mutations was done with a stable-expression cell line. Nevertheless, establishing such a cell line is time-consuming.We est
Autor:
Nobuyuki Kodani, Kosei Hasegawa, Kunihiko Aya, Motofumi Yokoyama, Hiroyuki Tanaka, Takayuki Miyai, Masanori Takaiwa, Youichi Kondo, Yoshiki Seino, Tsuneo Morishima
Publikováno v:
ResearcherID
Fibroblast growth factor 23 (FGF23) is a potent regulator of Pi and 1,25-(OH)(2)D homeostasis. Early postpartum infants show intriguing changes in serum levels of Ca, Pi, PTH and 1,25-(OH)(2)D. However, the role of FGF23 in the early neonatal mineral
Autor:
Yixia Xie, Rajesh Kumar, Baozhi Yuan, Peter S. N. Rowe, Thomas L. Clemens, Jian Q. Feng, Masanori Takaiwa, Marc K. Drezner
Publikováno v:
Journal of Clinical Investigation.
Patients with X-linked hypophosphatemia (XLH) and the hyp-mouse, a model of XLH characterized by a deletion in the Phex gene, manifest hypophosphatemia, renal phosphate wasting, and rickets/osteomalacia. Cloning of the PHEX/Phex gene and mutations in