Open Access. Powered by Scholars. Published by Universities.®
Cellular and Molecular Physiology Commons™
Open Access. Powered by Scholars. Published by Universities.®
- Discipline
-
- Medicine and Health Sciences (20)
- Biochemistry, Biophysics, and Structural Biology (13)
- Amino Acids, Peptides, and Proteins (11)
- Biochemistry (11)
- Chemicals and Drugs (11)
-
- Molecular Biology (11)
- Nucleic Acids, Nucleotides, and Nucleosides (10)
- Other Biochemistry, Biophysics, and Structural Biology (10)
- Medical Sciences (6)
- Medical Physiology (5)
- Systems and Integrative Physiology (5)
- Biology (3)
- Cardiovascular Diseases (3)
- Diseases (3)
- Biotechnology (2)
- Endocrinology (2)
- Analytical, Diagnostic and Therapeutic Techniques and Equipment (1)
- Anatomy (1)
- Animal Sciences (1)
- Aquaculture and Fisheries (1)
- Bioimaging and Biomedical Optics (1)
- Biological Engineering (1)
- Biomedical Engineering and Bioengineering (1)
- Cancer Biology (1)
- Cardiovascular System (1)
- Cell and Developmental Biology (1)
- Comparative and Evolutionary Physiology (1)
- Institution
-
- Chapman University (11)
- University of Nebraska Medical Center (4)
- University of Kentucky (3)
- Eastern Illinois University (2)
- Virginia Commonwealth University (2)
-
- Boise State University (1)
- California Polytechnic State University, San Luis Obispo (1)
- East Tennessee State University (1)
- Georgia Southern University (1)
- Old Dominion University (1)
- The Texas Medical Center Library (1)
- The University of San Francisco (1)
- The University of Southern Mississippi (1)
- Thomas Jefferson University (1)
- University of Arkansas, Fayetteville (1)
- University of Louisville (1)
- University of San Diego (1)
- Keyword
-
- Translation (3)
- Adherent cell monolayer (2)
- Angiotensin II (2)
- DMSO (2)
- Heart failure (2)
-
- Manganese superoxide dismutase (2)
- MnSOD (2)
- Osmotic stress (2)
- Oxidative stress (2)
- Reactive oxygen species (2)
- Respiration (OXPHOS) (2)
- 1α-OH-B (1)
- 4-hydroxynonenal (1)
- AT1R (1)
- ATP Synthase (1)
- Acidophilic (1)
- Adenoviridae (1)
- Amino acid (1)
- Aminoacyl tRNA Synthesis (1)
- Aminoacyl tRNA Synthetase (1)
- Aminoacyl-tRNA (1)
- AngII (1)
- Angiotensin type 1 receptor (1)
- Animals (1)
- Anti-oxidant (1)
- Atlantic stingray (1)
- Bacterial Pathogenesis (1)
- Bile acids (1)
- Biomarker (1)
- Blood Pressure (1)
- Publication
-
- Biology, Chemistry, and Environmental Sciences Faculty Articles and Research (10)
- Journal Articles: Cellular & Integrative Physiology (4)
- Undergraduate Honors Theses (3)
- Theses and Dissertations (2)
- Theses and Dissertations--Physiology (2)
-
- Biomedical Engineering (1)
- Boise State University Theses and Dissertations (1)
- Center for Translational Medicine Faculty Papers (1)
- Dissertations and Theses (Open Access) (1)
- Faculty Research & Creative Activity (1)
- Faculty and Staff Scholarship (1)
- Graduate Theses and Dissertations (1)
- Honors College Theses (1)
- Master's Theses (1)
- School of Medical Diagnostics & Translational Sciences Publications (1)
- Student Scholar Symposium Abstracts and Posters (1)
- Surgery Faculty Publications (1)
- Theses (1)
- Publication Type
Articles 31 - 34 of 34
Full-Text Articles in Cellular and Molecular Physiology
Trpa1 Channels In Cochlear Supporting Cells Regulate Hearing Sensitivity After Noise Exposure, Alejandra C. Velez-Ortega
Trpa1 Channels In Cochlear Supporting Cells Regulate Hearing Sensitivity After Noise Exposure, Alejandra C. Velez-Ortega
Theses and Dissertations--Physiology
TRPA1 channels are sensors for noxious stimuli in a subset of nociceptive neurons. TRPA1 channels are also expressed in cells of the mammalian inner ear, but their function in this tissue remains unknown given that Trpa1–/– mice exhibit normal hearing, balance and sensory mechanotransduction. Here we show that non-sensory (supporting) cells of the hearing organ in the cochlea detect tissue damage via the activation of TRPA1 channels and subsequently modulate cochlear amplification through active cellshape changes.
We found that cochlear supporting cells of wild type but not Trpa1–/– mice generate inward currents and robust long-lasting Ca2+ responses …
Transmural Heterogeneity Of Cellular Level Cardiac Contractile Properties In Aging And Heart Failure, Premi Haynes
Transmural Heterogeneity Of Cellular Level Cardiac Contractile Properties In Aging And Heart Failure, Premi Haynes
Theses and Dissertations--Physiology
The left ventricle of the heart relaxes when it fills with blood and contracts to eject blood into circulation to meet the body’s metabolic demands. Dysfunction in either relaxation or contraction of the left ventricle can lead to heart failure. Transmural heterogeneity is thought to contribute to normal ventricular wall motion but it is not well understood how transmural modifications affect the failing left ventricle. The overall hypothesis of this dissertation is that normal left ventricles exhibit transmural heterogeneity in cellular level contractile properties and with aging and heart failure there are region-specific changes in cellular level contractile mechanisms.
Age …
Comparison Of Two Different Sprint Interval Training Work-To-Rest Ratios On Acute Metabolic And Inflammatory Responses, Christopher R. Harnish
Comparison Of Two Different Sprint Interval Training Work-To-Rest Ratios On Acute Metabolic And Inflammatory Responses, Christopher R. Harnish
Theses and Dissertations
High intensity exercise is believed to yield greater results on health and human performance than moderate intensity exercise. Extensive research indicates that not only do high-intensity interval training (HIT) and sprint interval training (SIT) produce significant improvements in cardiovascular fitness and disease, they may be more effective at improving long-term metabolic function, including insulin sensitivity (Si), by producing more mitochondria. Moreover, compliance rates for HIT and SIT participation are reported to be the same or better than traditional moderate intensity exercise. Because lack of time is often cited as major hindrance to exercise participation, SIT is also seen as a …
Regulation Of Pancreatic Α And Β Cell Function By The Bile Acid Receptor Tgr5, Divya Prasanna Kumar
Regulation Of Pancreatic Α And Β Cell Function By The Bile Acid Receptor Tgr5, Divya Prasanna Kumar
Theses and Dissertations
The discovery that bile acids act as endogenous ligands of the membrane receptor TGR5 and the nuclear receptor FXR increased their significance as regulators of cholesterol, glucose and energy metabolism. Activation of TGR5, expressed on enteroendocrine L cells, by bile acids caused secretion of GLP-1, which stimulates insulin secretion from pancreatic β cells. Expression of TGR5 on pancreatic islet cells and the direct effect of bile acids on the endocrine functions of pancreas, however, are not fully understood. The aim of this study was to identify expression of TGR5 in pancreatic islet cells and determine the effect of bile acids …