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Chemical Messengers
Chemical Messengers

Introduction to Neuropharmacology
Introduction to Neuropharmacology

... Receptor types and Selectivity • Drug Selectivity: selectivity of drug for effected receptor – Does drug bind to only α1 receptors or does it also bind to β1 and β2 receptors? ...
48x36 Poster Template
48x36 Poster Template

gWIZ GFP Mammalian Expression Vector
gWIZ GFP Mammalian Expression Vector

Gene Section EPHA3 (EPH receptor A3) Atlas of Genetics and Cytogenetics
Gene Section EPHA3 (EPH receptor A3) Atlas of Genetics and Cytogenetics

Gene Section MERTK (c-mer proto-oncogene tyrosine kinase) Atlas of Genetics and Cytogenetics
Gene Section MERTK (c-mer proto-oncogene tyrosine kinase) Atlas of Genetics and Cytogenetics

... Y754) within the activation loop of the kinase domain have been identified as the primary sites of autophosphorylation (Ling et al., 1996). These three residues are also conserved in the same sequence context in Axl and Tyro-3. Another residue within the kinase domain, Y872, is part of consensus GRB ...
Cell Signalling Pathways
Cell Signalling Pathways

Supplemental Figure Legends
Supplemental Figure Legends

Team Publications
Team Publications

The Endocrine System
The Endocrine System

... mechanism ...
U1-snRNA–mediated rescue of mRNA processing in
U1-snRNA–mediated rescue of mRNA processing in

... Modified small nuclear RNAs (snRNAs) have been shown to promote changes in mRNA splicing in cellular and animal models of human diseases. However, these approaches were mainly aimed at inducing skipping of defective exons,10,11 an approach that would not produce functional coagulation proteins, or m ...
Gene Section FUBP1 (far upstream element (FUSE) binding protein 1)
Gene Section FUBP1 (far upstream element (FUSE) binding protein 1)

No Slide Title
No Slide Title

... An example of an intracellular, ligand-gated channel Alberts et al., Molecular Biology of the Cell, © Garland Science ...
Brown and Goldstein: The Cholesterol Chronicles
Brown and Goldstein: The Cholesterol Chronicles

Catalytic Aza-Wittig Cyclisations for Heterocyclic Synthesis
Catalytic Aza-Wittig Cyclisations for Heterocyclic Synthesis

LIPOPROTEIN LIPASE DEFICIENCY, HYPERTRIGLYCERIDEMIA
LIPOPROTEIN LIPASE DEFICIENCY, HYPERTRIGLYCERIDEMIA

... The metabolic syndrome is comprised of a cluster of metabolic disorders, of which many promote the development of atherosclerosis, increase the risk of cardiovascular disease and diabetes. Insulin resistance is at the heart of the metabolic syndrome. Elevated serum triglycerides commonly associate w ...
Principles of Biochemistry
Principles of Biochemistry

... Turn off of the signal (cont.): 3. Hormone Receptor desensitization occurs. This process varies with the hormone.   Some receptors are phosphorylated via Gprotein-coupled receptor kinases.   The phosphorylated receptor may then bind to a protein arrestin that blocks receptor-Gprotein activation & ...
邵吉民_Signaling_and_diseases
邵吉民_Signaling_and_diseases

How does inflammation contribute to pathogenesis of atherosclerosis.
How does inflammation contribute to pathogenesis of atherosclerosis.

Metabolism of lipids digestion, absorption, resynthesis in
Metabolism of lipids digestion, absorption, resynthesis in

G-protein-mediated pathway
G-protein-mediated pathway

... Activated MEK then phosphorylates another protein kinase called MAPK causing its activation. This series of phosphylating activations is called a kinase cascade. It results in amplification of the signal ...
Ch 11 PP - medmood.com
Ch 11 PP - medmood.com

... chemical messengers, which can be peptides, small chemicals or proteins, in a specific one-to-one relationship. ...
No Slide Title
No Slide Title

Abstract Ferullo
Abstract Ferullo

... levels of cheY were observed in both wild type and mutant cells that contained a deletion plasmid ??? for other chemotactic gene products. Specifically, overproduction and endogenous levels of CheY in both wild type and mutant cells exhibited either a shift from a counter-clockwise rotation to a clo ...
Arrestin - Psychiatry Training
Arrestin - Psychiatry Training

... •Review aspects of chemical transmission and intracellular signalling in the brain •Role of neurotransmitter/signal transduction abnormalities in selected neurological/psychiatric disorders –Rational pharmacology for nervous system disorders –Prediction of side-effect profile ...
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VLDL receptor



The very-low-density-lipoprotein receptor (VLDLR) is a transmembrane lipoprotein receptor of the low-density-lipoprotein (LDL) receptor family. VLDLR shows considerable homology with the members of this lineage. Discovered in 1992 by T. Yamamoto, VLDLR is widely distributed throughout the tissues of the body, including the heart, skeletal muscle, adipose tissue, and the brain, but is absent from the liver. This receptor has an important role in cholesterol uptake, metabolism of apoprotein-E-containing triacylglycerol-rich lipoproteins, and neuronal migration in the developing brain. In humans, VLDLR is encoded by the VLDLR gene. Mutations of this gene may lead to a variety of symptoms and diseases, which include type I lissencephaly, cerebellar hypoplasia, and atherosclerosis.
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