Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Kayo Ikuta"'
Publikováno v:
Frontiers in Nutrition, Vol 10 (2023)
The relationship between intestinal microbiota and cognitive function has been investigated as one of the major topics within the intestinal microbiota–gut–brain axis. Although an increasing number of studies have demonstrated an improvement in l
Externí odkaz:
https://doaj.org/article/e874e7b2091e42b396e660b93024f264
Autor:
Hazuki Tamada, Kayo Ikuta, Yusuke Makino, Daisuke Joho, Takeru Suzuki, Masaki Kakeyama, Mitsuharu Matsumoto
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2022)
Cognitive flexibility is the ability to rapidly adapt to a constantly changing environment. It is impaired by aging as well as in various neurological diseases, including dementia and mild cognitive impairment. In rodents, although many behavioral te
Externí odkaz:
https://doaj.org/article/088b2c572c4d4db8bfa80b15d1a499b1
Autor:
Ai Hanazaki, Kayo Ikuta, Shohei Sasaki, Sumire Sasaki, Megumi Koike, Kazuya Tanifuji, Yuki Arima, Ichiro Kaneko, Yuji Shiozaki, Sawako Tatsumi, Tomoka Hasegawa, Norio Amizuka, Ken‐ichi Miyamoto, Hiroko Segawa
Publikováno v:
Physiological Reports, Vol 8, Iss 3, Pp n/a-n/a (2020)
Abstract SLC34A3/NPT2c/NaPi‐2c/Npt2c is a growth‐related NaPi cotransporter that mediates the uptake of renal sodium‐dependent phosphate (Pi). Mutation of human NPT2c causes hereditary hypophosphatemic rickets with hypercalciuria. Mice with Npt
Externí odkaz:
https://doaj.org/article/5c073f670fde43a4b70470221bc3277b
Autor:
Shohei Sasaki, Hiroko Segawa, Ai Hanazaki, Ruri Kirino, Toru Fujii, Kayo Ikuta, Miwa Noguchi, Sumire Sasaki, Megumi Koike, Kazuya Tanifuji, Yuji Shiozaki, Ichiro Kaneko, Sawako Tatsumi, Takaaki Shimohata, Yoshichika Kawai, Sonoko Narisawa, José Luis Millán, Ken-ichi Miyamoto
Publikováno v:
Kidney & Blood Pressure Research, Vol 43, Iss 5, Pp 1409-1424 (2018)
Background/Aims: Hyperphosphatemia is a serious complication of late-stage chronic kidney disease (CKD). Intestinal inorganic phosphate (Pi) handling plays an important role in Pi homeostasis in CKD. We investigated whether intestinal alkaline phosph
Externí odkaz:
https://doaj.org/article/36c57e898e644c9e9d8a52246f8a75e4
Autor:
Osamu Fujii, Sawako Tatsumi, Mao Ogata, Tomohiro Arakaki, Haruna Sakaguchi, Kengo Nomura, Atsumi Miyagawa, Kayo Ikuta, Ai Hanazaki, Ichiro Kaneko, Hiroko Segawa, Ken-ichi Miyamoto
Publikováno v:
Frontiers in Endocrinology, Vol 8 (2017)
In response to kidney damage, osteocytes increase the production of several hormones critically involved in mineral metabolism. Recent studies suggest that osteocyte function is altered very early in the course of chronic kidney disease. In the prese
Externí odkaz:
https://doaj.org/article/19c6f3960c8a4d25b79a5b66fe38b401
Autor:
Daisuke Joho, Masahira Takahashi, Takeru Suzuki, Kayo Ikuta, Mitsuharu Matsumoto, Masaki Kakeyama
Publikováno v:
Brain Communications; 2023, Vol. 5 Issue 6, p1-9, 9p
Autor:
Hiroko Segawa, Yasuko Ishikawa, Toru Fujii, Sawako Tatsumi, Yuji Shiozaki, Ai Hanazaki, Kayo Ikuta, Ken-ichi Miyamoto, Ichiro Kaneko
Publikováno v:
Pflügers Archiv - European Journal of Physiology. 471:123-136
Inorganic phosphate (Pi) secretion from the salivary glands and dietary Pi are key Pi sources. The regulatory mechanisms of Pi homeostasis in the salivary glands are unknown. We investigated how salivary Pi concentrations are regulated by dietary Pi
Autor:
Hiroko Segawa, Ichiro Kaneko, Sumire Sasaki, Yuki Arima, Tomoka Hasegawa, Ai Hanazaki, Kayo Ikuta, Yuji Shiozaki, Shohei Sasaki, Ken-ichi Miyamoto, Sawako Tatsumi, Kazuya Tanifuji, Norio Amizuka, Megumi Koike
Publikováno v:
Physiological Reports, Vol 8, Iss 3, Pp n/a-n/a (2020)
Physiological Reports
Physiological Reports
SLC34A3/NPT2c/NaPi‐2c/Npt2c is a growth‐related NaPi cotransporter that mediates the uptake of renal sodium‐dependent phosphate (Pi). Mutation of human NPT2c causes hereditary hypophosphatemic rickets with hypercalciuria. Mice with Npt2c knocko
Autor:
Shinsuke Kido, Ken-ichi Miyamoto, Ichiro Kaneko, Hitoshi Saito, Hiroko Segawa, Toru Fujii, Ai Hanazaki, Norio Amizuka, Tomoka Hasegawa, Sawako Tatsumi, Kayo Ikuta
Publikováno v:
Endocrinology. 159:2741-2758
X-linked hypophosphatemia (XLH), the most common form of inheritable rickets, is caused by inactivation of phosphate-regulating gene with homologies to endopeptidases on the X chromosome (PHEX) and leads to fibroblast growth factor (FGF) 23-dependent
Autor:
Takaaki Shimohata, José Luis Millán, Shohei Sasaki, Ai Hanazaki, Ruri Kirino, Toru Fujii, Kayo Ikuta, Yuji Shiozaki, Ichiro Kaneko, Sumire Sasaki, Hiroko Segawa, Miwa Noguchi, Sonoko Narisawa, Sawako Tatsumi, Ken-ichi Miyamoto, Megumi Koike, Yoshichika Kawai, Kazuya Tanifuji
Publikováno v:
Kidney Blood Press Res
Kidney & Blood Pressure Research, Vol 43, Iss 5, Pp 1409-1424 (2018)
Kidney & Blood Pressure Research, Vol 43, Iss 5, Pp 1409-1424 (2018)
Background/Aims: Hyperphosphatemia is a serious complication of late-stage chronic kidney disease (CKD). Intestinal inorganic phosphate (Pi) handling plays an important role in Pi homeostasis in CKD. We investigated whether intestinal alkaline phosph