M
Masayuki Tanemoto
Researcher at Tohoku University
Publications - 94
Citations - 2983
Masayuki Tanemoto is an academic researcher from Tohoku University. The author has contributed to research in topics: Internal medicine & Renal artery. The author has an hindex of 27, co-authored 83 publications receiving 2757 citations. Previous affiliations of Masayuki Tanemoto include Teikyo University & Osaka University.
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Journal ArticleDOI
An inwardly rectifying K(+) channel, Kir4.1, expressed in astrocytes surrounds synapses and blood vessels in brain.
Kayoko Higashi,Akikazu Fujita,Atsushi Inanobe,Masayuki Tanemoto,Katsumi Doi,Takeshi Kubo,Yoshihisa Kurachi +6 more
TL;DR: Data suggest that Kir4.1 is expressed in a limited population of brain astrocytes and may play a specific role in the glial K(+)-buffering action.
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Isolation and characterization of a digoxin transporter and its rat homologue expressed in the kidney.
Tsuyoshi Mikkaichi,Takehiro Suzuki,Tohru Onogawa,Tohru Onogawa,Masayuki Tanemoto,Hiroya Mizutamari,Masahiro Okada,Tatsuji Chaki,Satohiro Masuda,Taro Tokui,Nobuaki Eto,Michiaki Abe,Fumitoshi Satoh,Michiaki Unno,Takanori Hishinuma,Ken-ichi Inui,Sadayoshi Ito,Junichi Goto,Takaaki Abe +18 more
TL;DR: Human OATP4C1/rat Oatp4c1 might be a first step of the transport pathway of digoxin and various compounds into urine in the kidney, which is one of the most commonly prescribed drugs for the treatment of heart failure.
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The organic anion transporter (OATP) family.
TL;DR: The recently identified organic anion transporter family OATP/LST (liver-specific transporter) family, transport bile acids, hormones as well as eicosanoids, various compounds and substrate specificity is reviewed.
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An inward rectifier K+ channel at the basolateral membrane of the mouse distal convoluted tubule: similarities with Kir4‐Kir5.1 heteromeric channels
Stéphane Lourdel,Marc Paulais,Françoise Cluzeaud,Marcelle Bens,Masayuki Tanemoto,Yoshihisa Kurachi,Alain Vandewalle,Jacques Teulon +7 more
TL;DR: The DCT K+ channel differs from other functionally identified renal K+ channels with regard to its inhibition by spermine and insensitivity to internal ATP and Ca2+, and at the current state of knowledge, the channel is similar to Kir4.1‐Kir5.1 heteromeric channels.
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In vivo formation of a proton-sensitive K+ channel by heteromeric subunit assembly of Kir5.1 with Kir4.1.
TL;DR: The results indicate that the co‐assembly of Kir5.1 with Kir4.1 occurs in vivo, at least in kidney, and may therefore sense intracellular pH in renal epithelium and be involved in the regulation of acid‐base homeostasis.