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Showing 1 to 20 of 26 for “"pharmacological target"”.

  1. IGF1R as a pharmacological target in allergic asthma and cancer-promoting factor in the lung tumor microenvironment

    IGF1R (receptor del factor de crecimiento similar a la insulina tipo 1) es una tirosina quinasa ubicua que modula múltiples funciones celulares, como la proliferación, el crecimiento, la diferenciación y la supervivencia. El asma es una enfermedad pulmonar crónica caracterizada por obstrucción …

    dialnet Repository record for IGF1R as a pharmacological target in allergic asthma and cancer-promoting factor in the lung tumor microenvironment (opens in a new tab)

  2. Mitochondrial permeability transition following calcium overload. - Its role in neuronal cell death and potential as a pharmacological target.

    There is currently no clinically available drug with neuroprotective properties to limit the evolving cell death following e.g. stroke or traumatic brain injury. The mitochondrial permeability transition (mPT) is a potential pathological mechanism causing cell death in the CNS. As the name implies, …

    lund Repository record for Mitochondrial permeability transition following calcium overload. - Its role in neuronal cell death and potential as a pharmacological target. (opens in a new tab)

  3. Functional Characterization of CRIP1a Knockout Mice

    … amygdala. Thus, CRIP1a might serve as a future pharmacological target for studying and treating anxiety disorders.

    vcu Repository record for Functional Characterization of CRIP1a Knockout Mice (opens in a new tab)

  4. Regulation of IGFBP-5 and Osteoblast Functions by Nuclear Factor I

    … Growth Factor (IGF) system is a major target of GC inhibition in bone. We found that GCs inhibit expression of IGF binding protein-5 (IGFBP5) which binds IGFs and stimulates osteoblast activity by IGF dependent and independent mechanisms. GC-induced inhibition of IGFPB5 promoter …

    loma-linda Repository record for Regulation of IGFBP-5 and Osteoblast Functions by Nuclear Factor I (opens in a new tab)

  5. Novel approaches towards pharmacological enhancement of motivation

    This work explores novel approaches towards pharmacological enhancement of motivated behaviour. A loss of motivation remains a severe unmet clinical need in a number of neuropsychiatric and neurodegenerative disorders. The work described in this thesis, can be divided into two sections. Initially, …

    cambridge Repository record for Novel approaches towards pharmacological enhancement of motivation (opens in a new tab)

  6. Aldehyde dehydrogenases (ALDH) expression in cancer tissues as potential pharmacological targets for therapeutic intervention. Probing ALDH expression and function in 2D- and 3D-cultured cancer cell lines

    … was found not to be involved in inhibiting the pharmacological effect or causing resistance to different cytotoxic and molecularly targeted anticancer drugs. To unravel the functional role of ALDH7A1, 9 compounds obtained from a virtual screening of 24,000 compounds from the Maybridge collection …

    bradford Repository record for Aldehyde dehydrogenases (ALDH) expression in cancer tissues as potential pharmacological targets for therapeutic intervention. Probing ALDH expression and function in 2D- and 3D-cultured cancer cell lines (opens in a new tab)

  7. Aldehyde dehydrogenases (ALDH) expression in cancer tissues as potential pharmacological targets for therapeutic intervention. Probing ALDH expression and function in 2D- and 3D-cultured cancer cell lines

    … was found not to be involved in inhibiting the pharmacological effect or causing resistance to different cytotoxic and molecularly targeted anticancer drugs. To unravel the functional role of ALDH7A1, 9 compounds obtained from a virtual screening of 24,000 compounds from the Maybridge collection …

    bradford Repository record for Aldehyde dehydrogenases (ALDH) expression in cancer tissues as potential pharmacological targets for therapeutic intervention. Probing ALDH expression and function in 2D- and 3D-cultured cancer cell lines (opens in a new tab)

  8. Aldehyde dehydrogenases (ALDH) expression in cancer tissues as potential pharmacological targets for therapeutic intervention. Probing ALDH expression and function in 2D- and 3D-cultured cancer cell lines

    … was found not to be involved in inhibiting the pharmacological effect or causing resistance to different cytotoxic and molecularly targeted anticancer drugs. To unravel the functional role of ALDH7A1, 9 compounds obtained from a virtual screening of 24,000 compounds from the Maybridge collection …

    bradford Repository record for Aldehyde dehydrogenases (ALDH) expression in cancer tissues as potential pharmacological targets for therapeutic intervention. Probing ALDH expression and function in 2D- and 3D-cultured cancer cell lines (opens in a new tab)

  9. Internally Translated Cx43 Isoform GJA1-20k Affects Epithelial to Mesenchymal Transition and Metastatic Cancer Cell Behavior

    … remodeling could be promising as a potential pharmacological target process independent of transcriptional or post-translational pathways. Ultimately, by adding novel information in the expanding and compelling field of translational control, this work could aid in developing the future of …

    vt Repository record for Internally Translated Cx43 Isoform GJA1-20k Affects Epithelial to Mesenchymal Transition and Metastatic Cancer Cell Behavior (opens in a new tab)

  10. Alpha Synuclein Oligomers in Human Pathology: Significance of Nitrative Alpha Synuclein Modifications

    … αSyn in humans and may thus constitute a viable pharmacological target. These data also suggest that nitrative modifications of small amounts of αSyn, although not particularly toxic per se, may seed unmodified local αSyn to form stable oligomers that possess increased neurotoxicity. This …

    utmb Repository record for Alpha Synuclein Oligomers in Human Pathology: Significance of Nitrative Alpha Synuclein Modifications (opens in a new tab)

  11. Pharmacological regulation and function of store-operated calcium channels

    … to allow Ca²⁺ influx. In this thesis, the pharmacological aspects andregulatory mechanisms of SOCE were investigated using HEK293 cells overexpressing STIM1, ORAI or TRPC genes. The expression and function of TRPC channels and their spliced variants in native cells were also examined.Using …

    hull Repository record for Pharmacological regulation and function of store-operated calcium channels (opens in a new tab)

  12. In vitro and in vivo studies on the activating platelet collagen receptor glycoprotein VI in mice

    … to evaluate its potential as an antithrombotic target. The first mAb against (mouse) GPVI, JAQ1, was generated and used to demonstrate that GPVI requires the FcRgamma-chain for its expression and function and that this receptor is the central molecule in collagen-induced platelet activation. …

    wurz-thes Repository record for In vitro and in vivo studies on the activating platelet collagen receptor glycoprotein VI in mice (opens in a new tab)

  13. Neuropharmacological Mechanisms Underlying Incentive Salience and Stress

    … behavior. Using a combination of genetic and pharmacological tools, the role of individual opioid receptors in restoring approach behavior suppressed by stress in the NIH test was next dissected. These studies identified the mu opioid receptor as a critical mediator of approach behavior and a …

    penn Repository record for Neuropharmacological Mechanisms Underlying Incentive Salience and Stress (opens in a new tab)

  14. PORPHYRIN DERIVATIVES AS VERSATILE PROTEASOME MODULATORS

    … For this reason the proteasome has become a pharmacological target for cancer and neurodegenerative diseases where opposite effects are desirable, inhibition and activation respectively. Interestingly, accumulation of the ubiquitin-conjugated proteins, which have been tagged for degradation, …

    catania Repository record for PORPHYRIN DERIVATIVES AS VERSATILE PROTEASOME MODULATORS (opens in a new tab)

  15. Modulation of heme oxygenase-1 activity by novel synthetic compounds for pharmacological applications

    … oxygenase (HO) has been regarded as a potential pharmacological target, especially the inducible isoform, heme oxygenase-1 (HO-1). HO catalyzes the rate-limiting step of endogenous heme degradation, releasing carbon monoxide (CO), free iron (Fe2+), and biliverdin (BV), then reduced to bilirubin …

    catania Repository record for Modulation of heme oxygenase-1 activity by novel synthetic compounds for pharmacological applications (opens in a new tab)

  16. ROLE OF ASGR1 IN METABOLIC SYNDROME, OBESITY, AND ATHEROSCLEROSIS

    … Furthermore, total plasma N-glycome and untargeted liver proteomics were carried out for functional analysis. Second, to evaluate the lipid metabolism and atherosclerosis, we backcrossed ASGR1-/- with LDL-R-/- and ApoE-/- mice, generating DKO mice lacking ASGR1-/-/LDL-R-/- or …

    milano Repository record for ROLE OF ASGR1 IN METABOLIC SYNDROME, OBESITY, AND ATHEROSCLEROSIS (opens in a new tab)

  17. Resistance to Apoptosis in Smooth Muscle Cells and Stent-Induced Stenosis in Coronary and Peripheral Arteries

    … restenosis in one artery may serve as a pharmacological target in another artery that does not express the same characteristic.

    creighton Repository record for Resistance to Apoptosis in Smooth Muscle Cells and Stent-Induced Stenosis in Coronary and Peripheral Arteries (opens in a new tab)

  18. Investigations into the cellular and molecular changes in the amygdala in models of temporal lobe epilepsy and maternal immune activation

    … in epilepsy with GAT-1 being an attractive pharmacological target. Electron microscopy was used to examine the distribution, expression and morphology of GAT-1 expressing structures in the amygdala of the TLE model. Results suggest that GAT-1 was preferentially expressed on putative axon …

    cork Repository record for Investigations into the cellular and molecular changes in the amygdala in models of temporal lobe epilepsy and maternal immune activation (opens in a new tab)

  19. Identification and Characterization of the Mechanisms of Action of Novel Antiviral Compounds Targeting the Minimal Replication-Transcription Complex of SARS-CoV-2

    … the RNA polymerase RNA dependent (RdRp) is the pharmacological target of two of the three drugs currently in clinical use for the treatment of COVID-19, namely remdesivir and molnupiravir. However, the absence of strong evidence of in vivo efficacy and safety still calls for the development of …

    cagliari Repository record for Identification and Characterization of the Mechanisms of Action of Novel Antiviral Compounds Targeting the Minimal Replication-Transcription Complex of SARS-CoV-2 (opens in a new tab)

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