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WWOX, a Novel WW Domain-containing Protein
WWOX, a Novel WW Domain-containing Protein

... Interestingly, the NH2 terminus of the putative WWOX protein showed homology to ubiquitin ligases such as NEDD4, YES-associated protein YAP65, and other WW domain-containing proteins (data not shown). Further amino acid sequence analysis using the PROSITE database identified two regions within the p ...
L'adrenoleucodistròfia lligada a l'X (X-ALD) és un desordre metabòlic d'origen... caracteritzat per una desmielinització progressiva del sistema nerviós central o...
L'adrenoleucodistròfia lligada a l'X (X-ALD) és un desordre metabòlic d'origen... caracteritzat per una desmielinització progressiva del sistema nerviós central o...

Inhibition of signal transduction pathways involved in inflammation G. Haegeman
Inhibition of signal transduction pathways involved in inflammation G. Haegeman

... pathway and the concomitant production of inflammatory cytokines. In order to understand the inflammatory process at the "molecular" level and thus devise more specific molecular targets for the development of novel anti-inflammatory drugs, the author9s group has studied signal transduction pathways ...
Provisional PDF - BioMed Central
Provisional PDF - BioMed Central

Gene expression
Gene expression

Diacylglycerol kinase θ couples farnesoid X receptor
Diacylglycerol kinase θ couples farnesoid X receptor

as a PDF
as a PDF

... AF-1 domain (28), has been identified as a major site of ligand-stimulated phosphorylation (18, 26) and has also been shown to be phosphorylated by mitogenactivated protein kinase in response to EGF stimulation of cells (19, 20). Conversion of this residue to a nonphosphorylatable alanine (HE457) ab ...
Repression of human cytomegalovirus gene expression asscoiated
Repression of human cytomegalovirus gene expression asscoiated

11_Lecture_picture version
11_Lecture_picture version

... 1. Signaling recognition: chemical messenger (ligand) binds to receptor protein. – Chemical messenger can be a peptide, small inorganic molecule, or lipid hormone ...
A novel isoform of the smooth muscle cell
A novel isoform of the smooth muscle cell

Molecular mechanisms of glucocorticoid action
Molecular mechanisms of glucocorticoid action

fibulins: a versatile family of extracellular matrix proteins
fibulins: a versatile family of extracellular matrix proteins

Gene Section MIER1 (mesoderm induction early response 1 homolog (Xenopus laevis))
Gene Section MIER1 (mesoderm induction early response 1 homolog (Xenopus laevis))

intracellular accumulations
intracellular accumulations

4-Lipoprotein Metabolism2017-04-19 04:103.5 MB
4-Lipoprotein Metabolism2017-04-19 04:103.5 MB

Gene Section PTCH2 (patched homolog 2 (Drosophila)) Atlas of Genetics and Cytogenetics
Gene Section PTCH2 (patched homolog 2 (Drosophila)) Atlas of Genetics and Cytogenetics

Epithelial Integrin O/6~4: Complete Primary Structure of and Variant
Epithelial Integrin O/6~4: Complete Primary Structure of and Variant

Expression of Human 21-Hydroxylase (P450c21) in Bacterial and
Expression of Human 21-Hydroxylase (P450c21) in Bacterial and

Mutation of a Highly Conserved Aspartic Acid in the Adrenergic
Mutation of a Highly Conserved Aspartic Acid in the Adrenergic

mHDA1/HDAC5 Histone Deacetylase Interacts with and
mHDA1/HDAC5 Histone Deacetylase Interacts with and

Document
Document

Gene Section CLTCL1 (clathrin heavy polypeptide-like 1) Atlas of Genetics and Cytogenetics
Gene Section CLTCL1 (clathrin heavy polypeptide-like 1) Atlas of Genetics and Cytogenetics

Up to the minute project summary:
Up to the minute project summary:

REFLECTIONS
REFLECTIONS

Introduction:
Introduction:

< 1 ... 17 18 19 20 21 22 23 24 25 ... 34 >

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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