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Experimental gene therapy of human colon cancer
R. J. Bold
, R. E. Warren
, J. Ishizuka
, Y. S. Cho-Chung
,
C. M. Townsend
, J. C. Thompson
, R. J. Joehl
, E. D. Whitman
Surgery
Research output
:
Contribution to journal
›
Article
›
peer-review
13
Scopus citations
Overview
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Keyphrases
Antisense Oligonucleotides
100%
Gene Therapy
100%
Cyclic Adenosine Monophosphate (cAMP)
100%
Human Colon Cancer
100%
Protein Kinase
50%
HCT116 Cells
50%
Human Colon Cancer Cells
37%
LoVo Cells
37%
Protein Level
25%
Gastrin
25%
Mediated Growth
25%
Regulatory Subunit
25%
Cancer Cells
12%
Growth Inhibition
12%
Western Blotting
12%
Signal Transduction Pathway
12%
Cell number
12%
MRNA Level
12%
Cellular Proteins
12%
New Therapeutic Strategies
12%
Relative Amount
12%
Target mRNA
12%
Northern Blotting
12%
LoVo
12%
Tritiated Thymidine
12%
Effects on Growth
12%
HCT116
12%
Protein Translation
12%
Membrane Permeable
12%
Sequence-specific Binding
12%
Thymidine Incorporation
12%
Basal Growth
12%
Dual Effect
12%
Biochemistry, Genetics and Molecular Biology
Cyclic Adenosine Monophosphate
100%
Antisense
100%
Colon
100%
Gene Therapy
100%
Cancer Cell
50%
Protein Kinase A
50%
Messenger RNA
25%
Gastrin
25%
DNA Synthesis
12%
Signal Transduction
12%
Northern Blotting
12%
Translation (Protein Synthesis)
12%
Cell Count
12%
Pharmacology, Toxicology and Pharmaceutical Science
Cyclic AMP
100%
Antisense Oligodeoxynucleotide
100%
Colon Carcinoma
100%
Cyclic AMP Dependent Protein Kinase
50%
Gastrin
25%
Messenger RNA
25%
Malignant Neoplasm
12%
Cell Protein
12%
Thymidine
12%
Immunology and Microbiology
Antisense
100%
Colon
100%
Cancer Cell
50%
Kinase A
50%
Gastrin
25%
Signal Transduction
12%
DNA Synthesis
12%
Northern Blotting
12%
Cell Count
12%
Translation (Protein Synthesis)
12%