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ß-arrestin signaling and regulation of transcription
ß-arrestin signaling and regulation of transcription

- Wiley Online Library
- Wiley Online Library

development. A G-protein beta-subunit is essential for Dictyostelium
development. A G-protein beta-subunit is essential for Dictyostelium

Signal Transduction by the Receptors for Thrombopoietin (c
Signal Transduction by the Receptors for Thrombopoietin (c

Nuclear hormone receptors (contd)
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... Regulating transcription factor activity (contd) ...
The Extracellular Matrix
The Extracellular Matrix

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PDF

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No Slide Title

6-ch05-proteins -Lec 6 [Compatibility Mode]
6-ch05-proteins -Lec 6 [Compatibility Mode]

Identification of the Sites of Asparagine
Identification of the Sites of Asparagine

... We also demonstrated that all six potential N-linked glycosylation sites on TSHR ectodomain are actually glycosylated in CHO-Lec8 cells. However, it is uncertain that TSHR endogenously expressed in thyroid cells also contains six N-linked carbohydrates. It has been reported that the number of the ac ...
Adenovirus RIDα regulates endosome maturation by mimicking GTP
Adenovirus RIDα regulates endosome maturation by mimicking GTP

Protein traffic in polarized epithelial cells: the polymeric
Protein traffic in polarized epithelial cells: the polymeric

... In these fibroblasts, when the plg-R reaches the cell sur­ face it is not immediately cleaved to SC. This results in a pool of uncleaved receptor on the surface where it is capable of internalizing bound ligand. About 35% of the bound ligand can be internalized. This endocytosed ligand is rapidly re ...
1. Introduction 2. Fundamentals 3. Glycosylation 4
1. Introduction 2. Fundamentals 3. Glycosylation 4

Issues in predicting protein function from sequence
Issues in predicting protein function from sequence

... accurate for genes found in completely sequenced genomes. Even for such genomes, past lineage-speci®c deletions of paralogous genes can result in paralogues falsely being predicted as orthologues. Additional complexities in assignment arise from complete genome, or largescale gene, duplications that ...
How Do Plant Mitochondria Avoid Importing Chloroplast Proteins
How Do Plant Mitochondria Avoid Importing Chloroplast Proteins

... known sizes of subunits in the yeast complex. In particular, no homologs of Tom37 or Tom22 were apparent and there was an additional protein of around 9 kD. The absence of Tom37 from the plant complex was not so surprising, since this subunit is also missing from the N. crassa complex, and the Tom37 ...
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Cell Communication

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receptors. properties of ROR alpha, a novel

... Cloning of RORal, RORa2, and RORa3 ROR was isolated as part of a screen to identify RAR- and RXR-related genes that might play a direct or even an indirect role in vitamin A physiology. The DNA-binding domain of the human RARa was used as a probe to screen recombinant DNA libraries to search for unr ...
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The Structure of MYB Proteins

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Patrick_Chapter_5

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5.3 G Protein-Coupled Receptors

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Regulated appearance of NMDA receptor subunits and channel

Pegvisomant, a Growth Hormone-Specific Antagonist, Undergoes
Pegvisomant, a Growth Hormone-Specific Antagonist, Undergoes

... tensity of fluorescence between ligands, because the affinity of the detection antibody differed between the ligands. However, in the calculation of percent internalization, we are comparing the same ligand at the cell surface with that internalized under identical experimental conditions. Therefore ...
Gene repression by nuclear hormone receptors
Gene repression by nuclear hormone receptors

... roughly divided into receptors that bind to steroids, receptors that bind to non-steroids and orphan receptors for which no ligand is yet known. Interestingly, hormone-bound NHRs can have both activation and repression functions. When bound to their response element they activate target genes; howev ...
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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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