WorldCat Identities

Thompson, Craig (Craig B.)

Works: 7 works in 19 publications in 1 language and 499 library holdings
Genres: Criticism, interpretation, etc 
Roles: Editor, Author
Classifications: RC268.5, 616.994071
Publication Timeline
Most widely held works by Craig Thompson
The molecular basis of cancer by John Mendelsohn( Book )

10 editions published between 2008 and 2015 in English and held by 102 WorldCat member libraries worldwide

Stay current with the latest discoveries in molecular and genomic research. Sweeping revisions throughout include eight brand-new chapters on: Tumor Suppressor Genes; Inflammation and Cancer; Cancer Systems Biology: The Future; Biomarkers Assessing Risk of Cancer; Understanding and Using Information About Cancer Genomes; The Technology of Analyzing Nucleic Acids in Cancer; Molecular Abnormalities in Kidney Cancer; and Molecular Pathology
Speaking of identities : the presentation of American Indian experience by Craig Thompson( )

4 editions published in 1993 in English and Undetermined and held by 6 WorldCat member libraries worldwide

The right direction by Craig Thompson( )

1 edition published in 1992 in English and held by 1 WorldCat member library worldwide

DNA damage, deamidation, and death by Craig Thompson( )

1 edition published in 2002 in English and held by 1 WorldCat member library worldwide

Untitled by Craig Thompson( )

1 edition published in 1986 in English and held by 1 WorldCat member library worldwide

Sedimentation Behavior of Activated Human Granulocytes: Aggregation and Volume Effects( )

1 edition published in 1983 in English and held by 0 WorldCat member libraries worldwide

Human peripheral blood granulocytes (PMN's) obtained from normal adults were studied by an analytical gravity sedimentation system. Exposure of PMN's to endotoxin-activated serum (EAS) in a Ficoll density gradient containing Hank's balanced salt solution with calcium and magnesium produced significantly different sedimentation patterns compared to the granulocytes exposed to normal serum under the same conditions. Experiments were performed to determine whether changes in granulocyte density, volume, shape, or aggregation were responsible for the sedimentation pattern of granulocytes exposed to EAS. Granulocyte aggregation was inhibited by the absence of calcium and magnesium in the medium during granulocyte stimulation, whereas the changes in granulocyte shape and volume associated with granulocyte stimulation were not affected. The data indicate that the altered granulocyte sedimentation pattern in the presence of EAS and calcium and magnesium was produced by granulocyte aggregation and not by changes in granulocyte volume, or shape
An Inducible Cytoplasmic Factor (AU-B) Binds Selectively to AUUUA multimers in the 3' Untranslated Region of Lymphokine mRNA( )

1 edition published in 1991 in English and held by 0 WorldCat member libraries worldwide

Although the primary control of eukaryotic gene expression occurs at the transcriptional level, it has become clear that posttranscriptional mechanisms also play important roles in gene regulation. For instance, the efficiency of nuclear RNA splicing and processing has been suggested to play a regulatory role in the expression of some genes (21). Within the cytoplasm, selective mRNA compartmentalization, translation, and degradation, can each influence the final level of gene expression. In order for gene expression to be regulated selectively at any level, the cell must have a means to discriminate between genes or their products. For example, selective gene expression is regulated at the transcriptional level in part by interactions between sequence- specific nuclear DNA-binding proteins (transcription factors) and sequence motifs within promoter/enhancer regions. This study was undertaken to determine whether similar sequence-specific cytoplasmic RNA-binding factors are involved in regulating cytoplasmic mRNA metabolism
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Audience Level
  Kids General Special  
Audience level: 0.54 (from 0.52 for The molecu ... to 1.00 for Sedimentat ...)

The molecular basis of cancer
English (18)