Open Access. Powered by Scholars. Published by Universities.®
Biochemistry, Biophysics, and Structural Biology Commons™
Open Access. Powered by Scholars. Published by Universities.®
- Discipline
-
- Biochemistry (104)
- Molecular Biology (102)
- Medicine and Health Sciences (79)
- Cell and Developmental Biology (77)
- Cancer Biology (53)
-
- Cell Biology (42)
- Medical Specialties (35)
- Biology (32)
- Oncology (32)
- Genetics and Genomics (28)
- Physical Sciences and Mathematics (25)
- Medical Sciences (21)
- Chemicals and Drugs (19)
- Chemistry (18)
- Genetics (15)
- Pharmacology, Toxicology and Environmental Health (13)
- Biophysics (12)
- Diseases (12)
- Engineering (11)
- Immunology and Infectious Disease (11)
- Biotechnology (9)
- Laboratory and Basic Science Research (9)
- Amino Acids, Peptides, and Proteins (8)
- Biomedical Engineering and Bioengineering (8)
- Medicinal Chemistry and Pharmaceutics (7)
- Molecular Genetics (7)
- Analytical, Diagnostic and Therapeutic Techniques and Equipment (6)
- Neoplasms (6)
- Institution
-
- The Texas Medical Center Library (16)
- University of Kentucky (13)
- Old Dominion University (10)
- Wayne State University (10)
- City University of New York (CUNY) (9)
-
- Technological University Dublin (8)
- University of South Florida (8)
- Virginia Commonwealth University (7)
- Georgia Southern University (6)
- University of Connecticut (6)
- University of Texas at El Paso (6)
- Western Kentucky University (6)
- Brigham Young University (5)
- Loyola University Chicago (5)
- Purdue University (5)
- University at Albany, State University of New York (5)
- University of Louisville (5)
- Rowan University (4)
- University of Nebraska - Lincoln (4)
- University of Texas Rio Grande Valley (4)
- Wright State University (4)
- Boise State University (3)
- Clemson University (3)
- Marshall University (3)
- St. Mary's University (3)
- University of Arkansas, Fayetteville (3)
- University of Nebraska Medical Center (3)
- Longwood University (2)
- Missouri State University (2)
- Pittsburg State University (2)
- Publication Year
- Publication
-
- Theses and Dissertations (17)
- Dissertations and Theses (Open Access) (8)
- USF Tampa Graduate Theses and Dissertations (8)
- Dissertations, Theses, and Capstone Projects (7)
- Wayne State University Dissertations (7)
-
- Articles (6)
- Electronic Theses and Dissertations (6)
- Faculty, Staff and Students Publications (6)
- Open Access Theses & Dissertations (6)
- Honors College Theses (5)
- Legacy Theses & Dissertations (2009 - 2024) (5)
- Browse all Theses and Dissertations (4)
- Dissertations (4)
- Honors Scholar Theses (4)
- Mahurin Honors College Capstone Experience/Thesis Projects (4)
- Molecular and Cellular Biochemistry Faculty Publications (4)
- Theses and Dissertations--Chemistry (4)
- Biochemistry and Microbiology (3)
- Department of Biochemistry: Faculty Publications (3)
- Graduate Theses and Dissertations (3)
- Honors Theses (3)
- Master's Theses (3)
- Posters - 2026 (3)
- Theses & Dissertations (3)
- Theses and Dissertations in Biomedical Sciences (3)
- Wayne State University Theses (3)
- All Dissertations (2)
- Annual Postdoctoral Science Symposium Abstracts (2)
- Boise State University Theses and Dissertations (2)
- Electrical & Computer Engineering Faculty Publications (2)
- Publication Type
- File Type
Articles 211 - 217 of 217
Full-Text Articles in Biochemistry, Biophysics, and Structural Biology
Tumor Response Tcf-4/Β-Catenin Regulatory Elements For Enhancing Cancer Gene Therapies, Saurabh Kumar Gupta
Tumor Response Tcf-4/Β-Catenin Regulatory Elements For Enhancing Cancer Gene Therapies, Saurabh Kumar Gupta
Theses and Dissertations in Biomedical Sciences
Mutations in the adenomatous polyposis coli gene are frequently associated with progression of colon carcinoma and most other types of epithelial carcinomas. This usually results in stabilization of β-catenin protein levels, followed by transactivation of Tcf-4/β-catenin responsive genes. The effectiveness of a Tcf-4/β-catenin transcriptional enhancer element in combination with a c-fos or carcinoembryonic antigen promoter was tested for its ability to act as a tumor specific regulator of gene expression in a panel of human tumor and normal cell lines. Luciferase reporter assays indicated enhanced activity of the Tcf-4/β-catenin transcriptional element only in tumor cell lines, with minimal activities in …
Identification Of The Rna Cis-Elements That Interact With Srp30a To Regulate The Alternative Splicing Of Caspase 9 Pre-Mrna, Prabhat Mukerjee
Identification Of The Rna Cis-Elements That Interact With Srp30a To Regulate The Alternative Splicing Of Caspase 9 Pre-Mrna, Prabhat Mukerjee
Theses and Dissertations
Studies have shown that the alternative splicing of caspase 9 and the phospho-status of SR proteins, a conserved family of splicing factors, are regulated by chemotherapy and de novo ceramide via the action of protein phosphatase-1 (PP1). Two RNA splice variants are derived from the caspase 9 gene, pro-apoptotic caspase 9a and anti-apoptotic caspase 9b, via alternative splicing by either the inclusion or exclusion of an exon 3, 4, 5, and 6 cassette. In this study, the link between SR proteins and the alternative splicing of caspase 9 was established. Sequence analysis of the exon 3, 4, 5, and 6 …
The Cellular And Molecular Dynamics Of The Queuosine Modification In Transfer Rna: Definition, Modulation, Deficiencies And Effect Of The Queuosine Modification System, Rana C. Morris
Theses and Dissertations in Biomedical Sciences
The presence of the queuosine modification in the wobble position of tRNAasn, tRNasp, tRNAhis, and tRNAtyr is associated with a decrease in cellular growth rate, an increase in the ability to withstand environmental stress, and differentiation of pleuripotent cells into mature phenotypes. The loss of this normal modification is strongly correlated with neoplastic transformation and tumor progression of a wide variety of cancers.
The "normal" system for formation of the queuosine modification in tRNA was studied in human fibroblast cell cultures and in mouse, rat and human liver tissues. The queuosine modification system …
Development Of An In Vitro Assay To Predict Patient Response To Radiotheraphy, Mary Sheridan
Development Of An In Vitro Assay To Predict Patient Response To Radiotheraphy, Mary Sheridan
Doctoral
At the present time, the treatment plan for a patient with cancer is usually based on parameters such as tumour site, histological type, and tumour stage and performance status. However, it is well know that the radiosensitivity of human cancers varies widely from one patient to another (Fertil et al., 1981), and that even within these broad categories some tumours will show greater response to radiotherapy than others. If those patients unlikely to be cured by radiotherapy could be identified prior to commencement of treatment, alternative or more aggressive therapies might be selected which may give a better chance of …
Identification And Characterization Of Genes Associated With V-Jun Induced Cell Transformation, Martin Toralballa Hadman
Identification And Characterization Of Genes Associated With V-Jun Induced Cell Transformation, Martin Toralballa Hadman
Biological Sciences Theses & Dissertations
The v-jun oncogene was initially identified as the causative agent for fibrosarcomas in chickens. Studies show that overexpression of v-Jun proteins transforms chicken embryo fibroblasts (CEF) in vitro, and forms tumors in chickens in vivo. The mechanisms for this are not clearly defined. Conceivably, overexpression of an unregulated transcription factor would cause cell transfonnation by illicit regulation of its target genes. In support of this, we show that in vivo v-Jun complexes exhibit differential binding to in vitro generated AP-1 and 'AP-1 like' target sequences, suggesting that the pattern of target gene expression is altered during cell transformation. …
The Role Of Small Peptides In Cancer Physiology And Chemotherapy, Bao-Ling Tsay
The Role Of Small Peptides In Cancer Physiology And Chemotherapy, Bao-Ling Tsay
Theses and Dissertations in Biomedical Sciences
The targeting of proven anticancer drugs specifically to cancer cells would provide a unique opportunity to restrict neoplasms without damaging the cancer patient. The present research utilizes the phenomenon of illicit transport, i.e. the coupling of normally impermeant metabolites to permeant metabolites, in targeting the drug melphalan to mouse Ehrlich ascites tumor cells. The dipeptide beta-alanyl-melphalan was synthesized and tested in vitro for toxicity towards mouse Ehrlich ascites tumor cells, mouse liver cells, and mouse 3T3 embryonic cells. The parent compound, melphalan, was used as a control treatment. In addition, both melphalan and beta-alanyl-melphalan were utilized in in vivo chemotherapeutic …
Studies Of N⁵, N¹⁰-Methylene Tetrahydrofolate Reductase From Porcine Kidney And Mouse L1210-Induced Tumor Tissues, Purification And Interaction With Antifolates, David W. Jayme
Theses and Dissertations
Methylene tetrahydrofolate reductase has been purified 1000-fold from porcine kidney and 400-fold from mouse L1210-induced tumor tissue by classical methods. The enzyme preparations have been demonstrated to be essentially free of contaminating methionine synthetase and serine transhydroxymethylase activity. Studies of the kinetic properties of the kidney and tumor enzymes, with respect to the reverse reaction using N5-methyl tetrahydrofolate as the variable substrate, have indicated Km values of 2.0 and 2.4 x 10-4 M, respectively. Inhibition of this key branch point enzyme in folate metabolism by a number of antimetabolites indicates that several of these antifolate compounds exhibit enzyme inhibition superior …