Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Noboru Kitayama"'
Publikováno v:
Regulatory Peptides. 52:195-203
Chromogranin A (CGA) is thought to be a precursor of pancreastatin (PST). Carbachol (Cch) stimulated the secretion of CGA and PST from QGP-1N cells derived from a human pancreatic islet cell tumor. Atropine inhibited the secretion of both. Sodium flu
Autor:
Akira Kono, Kyoko Miyasaka, Noboru Kitayama, Iwamoto N, Kayoko Tateishi, Yuji Matsuoka, Takao Shimazoe, Akihiro Funakoshi
Publikováno v:
Life Sciences. 54:1571-1578
Circulating molecular forms with pancreastatin (PST)-like immunoreactivity in plasma from normal subjects were examined. An immunoreactive form corresponding to a human PST-like sequence [human chromogranin-A-(250–301)] (hPST-52) and a larger form
Publikováno v:
Pancreas. 8:375-382
In this investigation we studied pancreastatin (PST) secretion from a human PST producing cell line (QGP-1N) in response to various secretagogues. Immunocytochemical study revealed the immunoreactivity of PST and somatostatin (SMT) in the same cells
Publikováno v:
Biochemical and Biophysical Research Communications. 185:1041-1047
It is found that secretion of pancreastatin and somatostatin from QGP-1N cells is regulated through muscarinic receptor-mediated activation of phosphatidylinositide hydrolysis system. In this report, whether the cAMP pathway interacts with the phosph
Publikováno v:
Life sciences. 57(9)
The plasma levels of chromogranin A (CGA) in patients with islet cell tumor and plasma CGA responses to administration of a somatostatin analogue (Octreotide) in two of these patients were examined in comparison with plasma pancreastatin (PST) levels
Publikováno v:
Regulatory peptides. 49(2)
Effects of various secretagogues on secretion of neurotensin from a pancreatic islet cell carcinoma cell line (QGP-1N) were examined. Carbachol stimulated secretion of neurotensin concentration-dependently in the range of 10 −6 –10 −4 M. The ne
Publikováno v:
Life sciences. 50(9)
We examined the in vitro degradation of human pancreastatin-52 (hPST-52) and a larger molecular form (approximate 15 kDa) of human PST by an enzyme extract from human kidney. The PST-degrading activity was determined from the amount of immunoreactive
Publikováno v:
The Proceedings of Conference of Hokuriku-Shinetsu Branch. :205-206
Publikováno v:
Regulatory Peptides. 40:260
Akademický článek
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