T
T Yamada
Researcher at University of Michigan
Publications - 17
Citations - 2295
T Yamada is an academic researcher from University of Michigan. The author has contributed to research in topics: Gastrin & Somatostatin. The author has an hindex of 12, co-authored 17 publications receiving 2227 citations. Previous affiliations of T Yamada include Kobe University.
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Journal ArticleDOI
Molecular cloning, expression, and gene localization of a fourth melanocortin receptor
Ira Gantz,Hiroto Miwa,Yoshitaka Konda,Yoshimasa Shimoto,Takao Tashiro,Stanley J. Watson,John DelValle,T Yamada +7 more
TL;DR: The cloning, expression, and gene localization of a fourth human melanocortin receptor, the melanocortex-4 receptor, is reported, which is expressed primarily in the brain, but its expression is notably absent in the adrenal cortex, melanocytes, and placenta.
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Molecular cloning of a novel melanocortin receptor.
Ira Gantz,Yoshitaka Konda,Takao Tashiro,Yoshimasa Shimoto,Hiroto Miwa,Gerd Munzert,Stanley J. Watson,John DelValle,T Yamada +8 more
TL;DR: The molecular cloning and pharmacologic characterization of a third member of this receptor family is reported, which characterizes it as an MSH receptor specific to the heptapeptide core common to adrenocorticotropic hormone and alpha-, beta-, and gamma-MSH.
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Molecular cloning of the human histamine H2 receptor
TL;DR: The technique of polymerase chain reaction with oligonucleotide primers based upon the nucleotide sequence of the canine H2 histamine receptor gene, which was recently isolated to clone its human homologue, confirms that it has successfully cloned a novel gene encoding the human H2 Histamine receptor.
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Molecular basis for the interaction of histamine with the histamine H2 receptor.
Ira Gantz,John DelValle,Lidong Wang,Takao Tashiro,Gerd Munzert,Yi-Jun Guo,Yoshitaka Konda,T Yamada +7 more
TL;DR: A model for Histamine binding is proposed in which Asp98 is essential for histamine binding and action, Asp186 defines H2 selectivity, and Thr190 is important in establishing the kinetics of histaminebinding, but is not essential for H2Selectivity.
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Mechanisms for direct inhibition of canine gastric parietal cells by somatostatin
TL;DR: The data indicate that somatostatin directly inhibits parietal cell activity via mechanisms both dependent on and independent of the pertussis toxin-sensitive inhibitory guanine nucleotide-binding protein.