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Functional significance of gastrin gene expression in human cancer cells
Jill P. Smith
, Michael F. Verderame
, Elizabeth N. Ballard
,
Ian S. Zagon
The Pennsylvania State University
College of Medicine (University Park Curriculum)
Department of Medicine
Penn State Cancer Institute
Cancer Institute, Experimental Therapeutics
Penn State Neuroscience Institute
Department of Neuroscience and Experimental Therapeutics
Research output
:
Contribution to journal
›
Article
›
peer-review
17
Link opens in a new tab
Scopus citations
Overview
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Keyphrases
Gene Expression
100%
Functional Significance
100%
Cancer Cells
100%
Gastrin
100%
Cholecystokinin
50%
Complementary DNA (cDNA)
25%
Tumor
16%
Transfected Cells
16%
Tumor Size
16%
Human Pancreatic Cancer
16%
Cell number
8%
Stable Transfection
8%
Cell Growth
8%
Effects on Growth
8%
Binding Assay
8%
Receptor Gene
8%
COS Cells
8%
Tumor Incidence
8%
Monkey
8%
BxPC-3
8%
Pancreatic Cancer Cells
8%
Antisense
8%
Splice Variant
8%
Gastrointestinal Hormones
8%
Latency Time
8%
Periampullary Cancer
8%
Reduced Latency
8%
Medicine and Dentistry
Gene Expression
100%
Cancer Cell
100%
Gastrin
100%
Receptor
50%
Cholecystokinin
50%
Neoplasm
33%
Pancreas Cancer
25%
Complementary DNA
25%
Genetic Transfection
16%
In Vitro
8%
Antisense
8%
Cancer Incidence
8%
Cell Growth
8%
Receptor Gene
8%
Cholecystokinin B Receptor
8%
Binding Assay
8%
COS-1
8%
Pharmacology, Toxicology and Pharmaceutical Science
Malignant Neoplasm
100%
Gastrin
100%
Receptor
58%
Cholecystokinin
50%
Neoplasm
33%
Pancreas Cancer
25%
Complementary DNA
25%
Cancer Incidence
8%
Haplorhini
8%
Cholecystokinin B Receptor
8%
Gastrointestinal Polypeptide
8%