|1.||Sipponen, Pentti: 4 articles (01/2008 - 01/2002)|
|2.||Yuan, Yuan: 3 articles (06/2015 - 05/2007)|
|3.||Sipponen, P: 3 articles (06/2007 - 07/2002)|
|4.||Gong, Yuehua: 2 articles (06/2015 - 03/2014)|
|5.||Aoki, Kazuo: 2 articles (09/2014 - 01/2012)|
|6.||Chen, Tie-Hui: 2 articles (09/2014 - 01/2012)|
|7.||Zheng, Kui-Cheng: 2 articles (09/2014 - 01/2012)|
|8.||Wu, Bing-Shan: 2 articles (09/2014 - 01/2012)|
|9.||Reshetnikov, O V: 2 articles (01/2012 - 11/2007)|
|10.||Kurilovich, S A: 2 articles (01/2012 - 11/2007)|
02/01/2007 - "The PGI, PGR and G-17 values were related significantly with the grades and/or sites of atrophic gastritis (P<0.01). "
01/01/2011 - "An algorithm (GastroPanel) for the non-invasive diagnosis of atrophic gastritis has been previously proposed, based on serum pepsinogen-I, gastrin-17, and Helicobacter pylori (H. "
01/01/2007 - "None of the markers of pepsinogen (PG) I, PGII, and gastrin 17 (G17) indicated atrophic gastritis. "
10/01/2004 - "The test panel composed of pepsinogen I and protein stimulated gastrin-17 may be used as the "serological gastric biopsy" detecting multifocal atrophic gastritis. "
07/01/2002 - "We investigated whether atrophic gastritis can be diagnosed and typed non-endoscopically if the serum levels of pepsinogen I (S-PGI) and gastrin-17 (S-G-17) are assayed in connection with H. "
08/01/2007 - "Moreover, tumor perfusion measurements corroborated the MR results, indicating a significant reduction in tissue perfusion after VTA treatment (mean tissue fluorescence, 570.4 arbitrary units [au] per gram +/- 27 vs 161.7 au/g +/- 17; P < .05). "
03/01/2008 - "Gastrin-17 dose dependently increased c-fos induction in both cancer cell lines. "
04/07/2006 - "The P64K-polypeptide cross-linked immunogen immunized rabbit and achieved a higher titer antibody against gastrin 17 than the G17P64K fusion protein immunogen, which could inhibit the growth of the tumor cell SW480."
07/01/1995 - "Tumor weight evaluation represented a good parameter of neoplasm evolution: of 19 cases weighing less than 250 g, 17 had no evidence of disease after surgery, and 2 had an unfavorable prognosis. "
11/01/1986 - "These data demonstrate that physiological concentrations of gastrin-17 can stimulate the growth of a human cancer cell line and that some degree of synchronization may be necessary to demonstrate similar effects in other cell lines. "
|3.||Duodenal Ulcer (Curling's Ulcer)
02/01/1984 - "A dose response study of the effect on gastric acid secretion of synthetic human gastrin-17 in doses of 50,200, and 500 ng/kg/h was performed in eight healthy volunteers and in eight patients with duodenal ulcer. "
07/31/1987 - "NH2-terminal of gastrin-17 in duodenal ulcer disease: identification of progastrin-17."
09/01/1986 - "Comparison of acid secretory responsiveness to gastrin heptadecapeptide and of gastrin heptadecapeptide pharmacokinetics in duodenal ulcer patients and normal subjects."
01/01/1985 - "The ratio G-17/G-34 was similar in placebo-treated normal subjects and placebo-treated patients with gastric or duodenal ulcers. "
01/01/1984 - "In contrast to healthy subjects, duodenal ulcer patients in the active phase contain large amounts of a peptide in serum and antrum which react with antiserum specific for the N-terminus, but not the C-terminus of gastrin-17. "
02/01/2008 - "The sensitivity and specificity of the PG I:II ratio (< or =3) and gastrin 17 (>17 pmol/mL) together were 9.4% and 99% for screening corpus-predominant gastritis and 14.8% and 97.8%, respectively, for screening intestinal metaplasia in the corpus. "
07/01/1983 - "The results suggest that gastrin cells process gastrin-17 abnormally during the acute phase of duodenal ulcer and gastritis."
07/01/1983 - "Increased concentrations of the NH2-terminal fragment of gastrin-17 in acute duodenal ulcer and acute gastritis."
03/01/2014 - "pylori IgG titer was associated positively with grade of histological gastritis, mucosal bacterial density and concentrations of serum PGI, PGII and gastrin-17, and negatively with PGI/II ratio."
02/01/2008 - "With the extension of gastritis, PGII was increased up to 2.5 times (6.6 +/- 2.8 microg/mL in normal mucosa, 9.5 +/- 6.7 microg/mL in antral gastritis, and 16.9 +/- 12.4 microg/mL in corpus-predominant gastritis; P < .01), PGI increased slightly (88.3 +/- 29.4 microg/mL in normal mucosa and 111.2 +/- 71.4 microg/mL in corpus-predominant gastritis), and gastrin 17 was increased substantially in corpus-predominant gastritis (15.3 +/- 19.5 pmol/mL vs 3.8 +/- 5.7 pmol/mL in normal mucosa). "
10/01/2011 - "We evaluated the diagnostic utility of serum PG-I, PG-II, PG-I/PG-II ratio and gastrin-17 (G-17) to detect IM and atrophy. "
01/01/2011 - "A serum G-17<2.6 pmol/l or G-17>40 pmol/l was 81% sensitive and 73.3% specific for diagnosing fundic atrophy. "
11/01/2009 - "The objective of the current study was to validate a biomarker method (pepsinogen I/II ratio and gastrin-17) for indirect detection of atrophy of the stomach mucosa versus standard histopathology in Caucasian and Asian populations. "
10/01/2004 - "Low serum level of stimulated gastrin-17 (< 5 pmol/l) and/or pepsinogen I (< 50 microg/l), were found in 16 of 19 patients (84.2%) with and in 7 of 36 patients (19.4%) without atrophy in the histological study. "
03/01/2013 - "The degree of atrophy was determined by the levels of serum pepsinogen1, and gastrin-17 and the presence of Helicobacter pylori antibodies detected by an enzyme immunoassay. "
|2.||Pepsinogen A (Pepsinogen)
|5.||Glycine (Aminoacetic Acid)
|8.||Biological Markers (Surrogate Marker)
|10.||Cholecystokinin B Receptor
|2.||Proximal Gastric Vagotomy