about
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafnessConsortin, a trans-Golgi network cargo receptor for the plasma membrane targeting and recycling of connexinsChromosomal assignment of the uromodulin gene (UMOD) to 16p13.11Hearing is normal without connexin30Otogelin: a glycoprotein specific to the acellular membranes of the inner earFdp, a new fibrocyte-derived protein related to MIA/CD-RAP, has an in vitro effect on the early differentiation of the inner ear mesenchymeTargeted disruption of otog results in deafness and severe imbalanceConnexin30 deficiency causes instrastrial fluid-blood barrier disruption within the cochlear stria vascularis.Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell deathBmcc1s, a novel brain-isoform of Bmcc1, affects cell morphology by regulating MAP6/STOP functions.Isolation of kidney complementary DNAs down-expressed in Wilms' tumor by a subtractive hybridization approach.The Sarcoglycan complex is expressed in the cerebrovascular system and is specifically regulated by astroglial Cx30 channels.Hearing the messenger: Ins(1,4,5)P3 and deafness.Deletion of astroglial connexins weakens the blood-brain barrier.Translation in astrocyte distal processes sets molecular heterogeneity at the gliovascular interface.Characterization of the promoter of the human KAL gene, responsible for the X-chromosome-linked Kallmann syndrome.Immune quiescence of the brain is set by astroglial connexin 43.Immunoregulation at the gliovascular unit in the healthy brain: A focus on Connexin 43.Purification of Mouse Brain Vessels.Cannabinoids prevent the opposite regulation of astroglial connexin43 hemichannels and gap junction channels induced by pro-inflammatory treatments.[Ins(1,4,5)P3: a messenger for hearing].Connexin 30 is expressed in a subtype of mouse brain pericytes.Expression of the connexin43- and connexin45-encoding genes in the developing and mature mouse inner ear.Cloning and characterization of the mouse collapsin response mediator protein-1, Crmp1.Bmcc1s interacts with the phosphate-activated glutaminase in the brain.Connexin 30 sets synaptic strength by controlling astroglial synapse invasion.Spatiotemporal expression of otogelin in the developing and adult mouse inner ear.Connexin 43 Controls the Astrocyte Immunoregulatory Phenotype.Molecular approach to the pathogenesis of renal anomalies in Kallmann's syndrome and in the branchio-oto-renal syndromeMapping of the otogelin gene (OTGN) to mouse Chromosome 7 and human Chromosome 11p14.3: a candidate for human autosomal recessive nonsyndromic deafness DFNB18Characterization of the Chicken and Quail Homologues of the Human Gene Responsible for the X-Linked Kallmann SyndromeUncoupling of the Astrocyte Syncytium Differentially Affects AQP4 IsoformsAstroglial Connexin 43 Deficiency Protects against LPS-Induced Neuroinflammation: A TSPO Brain µPET Study with [18F]FEPPAAstroDot: a new method for studying the spatial distribution of mRNA in astrocytesPostnatal development of the astrocyte perivascular MLC1/GlialCAM complex defines a temporal window for the gliovascular unit maturation
P50
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Martine Cohen-Salmon
@ast
Martine Cohen-Salmon
@en
Martine Cohen-Salmon
@es
Martine Cohen-Salmon
@nl
Martine Cohen-Salmon
@sl
type
label
Martine Cohen-Salmon
@ast
Martine Cohen-Salmon
@en
Martine Cohen-Salmon
@es
Martine Cohen-Salmon
@nl
Martine Cohen-Salmon
@sl
prefLabel
Martine Cohen-Salmon
@ast
Martine Cohen-Salmon
@en
Martine Cohen-Salmon
@es
Martine Cohen-Salmon
@nl
Martine Cohen-Salmon
@sl
P106
P21
P31
P496
0000-0002-5312-8476