Lista de obras - Martine Cohen-Salmon - Dominio Público Uruguay

A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

artículo científico publicado en 1999

Approche moléculaire de la pathogénie d'un deficit héréditaire de l'olfaction : Le syndrome de Kallmann de Morsier lie au chromosome X

AstroDot: a new method for studying the spatial distribution of mRNA in astrocytes

scientific article published on 25 February 2020

Astrocytes in the regulation of cerebrovascular functions

artículo científico publicado en 2020

Astroglial Connexin 43 Deficiency Protects against LPS-Induced Neuroinflammation: A TSPO Brain µPET Study with [18F]FEPPA

artículo científico publicado en 2020

Bmcc1s interacts with the phosphate-activated glutaminase in the brain

artículo científico publicado en 2012

Bmcc1s, a novel brain-isoform of Bmcc1, affects cell morphology by regulating MAP6/STOP functions

artículo científico publicado en 2012

Cannabinoids prevent the opposite regulation of astroglial connexin43 hemichannels and gap junction channels induced by pro-inflammatory treatments

artículo científico publicado en 2009

Characterization of the Chicken and Quail Homologues of the Human Gene Responsible for the X-Linked Kallmann Syndrome

article

Characterization of the promoter of the human KAL gene, responsible for the X-chromosome-linked Kallmann syndrome

artículo científico publicado en 1995

Chromosomal assignment of the uromodulin gene (UMOD) to 16p13.11

artículo científico publicado en 1993

Cloning and characterization of the mouse collapsin response mediator protein-1, Crmp1.

artículo científico publicado en 1997

Connexin 30 is expressed in a subtype of mouse brain pericytes.

artículo científico publicado en 2017

Connexin 30 sets synaptic strength by controlling astroglial synapse invasion

artículo científico publicado en 2014

Connexin 43 Controls the Astrocyte Immunoregulatory Phenotype.

artículo científico publicado en 2018

Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential

artículo científico publicado en 2003

Connexin30 deficiency causes instrastrial fluid-blood barrier disruption within the cochlear stria vascularis

artículo científico publicado en 2007

Connexins Responsible for Hereditary Deafness — The Tale Unfolds

Consortin, a trans-Golgi network cargo receptor for the plasma membrane targeting and recycling of connexins

artículo científico publicado en 2010

Deletion of astroglial connexins weakens the blood-brain barrier.

artículo científico publicado en 2012

Dp71 contribution to the molecular scaffold anchoring aquaporine-4 channels in brain macroglial cells

artículo científico publicado en 2020

Expression of the connexin43- and connexin45-encoding genes in the developing and mature mouse inner ear.

artículo científico publicado en 2004

Fdp, a new fibrocyte-derived protein related to MIA/CD-RAP, has an in vitro effect on the early differentiation of the inner ear mesenchyme

scientific journal article

Hearing is normal without connexin30

artículo científico publicado en 2013

Hearing the messenger: Ins(1,4,5)P3 and deafness.

artículo científico publicado en 2005

Identification of the GlialCAM interactome: the G protein-coupled receptors GPRC5B and GPR37L1 modulate megalencephalic leukoencephalopathy proteins

artículo científico publicado en 2021

Immune quiescence of the brain is set by astroglial connexin 43.

artículo científico

Immunoprecipitation of Ribosome-Bound mRNAs from Astrocytic Perisynaptic Processes of the Mouse Hippocampus

artículo científico publicado en 2020

Immunoregulation at the gliovascular unit in the healthy brain: A focus on Connexin 43.

artículo científico

Ins(1,4,5)P3: a messenger for hearing

artículo científico publicado en 2005

Isolation of kidney complementary DNAs down-expressed in Wilms' tumor by a subtractive hybridization approach.

artículo científico publicado en 1993

Local Translation in Perisynaptic Astrocytic Processes Is Specific and Changes after Fear Conditioning

artículo científico publicado en 2020

Mapping of the otogelin gene (OTGN) to mouse Chromosome 7 and human Chromosome 11p14.3: a candidate for human autosomal recessive nonsyndromic deafness DFNB18

article

Mitochondrial AIF loss causes metabolic reprogramming, caspase-independent cell death blockade, embryonic lethality, and perinatal hydrocephalus

artículo científico publicado en 2020

Molecular approach to the pathogenesis of renal anomalies in Kallmann's syndrome and in the branchio-oto-renal syndrome

artículo científico publicado en 1998

Neuronal Activity Drives Astroglial Connexin 30 in Perisynaptic Processes and Shapes Its Functions

scientific article published on 01 March 2020

Otogelin: a glycoprotein specific to the acellular membranes of the inner ear

artículo científico publicado en 1997

Postnatal development of the astrocyte perivascular MLC1/GlialCAM complex defines a temporal window for the gliovascular unit maturation

artículo científico publicado en 2019

Preparing the Astrocyte Perivascular Endfeet Transcriptome to Investigate Astrocyte Molecular Regulations at the Brain-Vascular Interface

artículo científico publicado en 2019

Purification of Mouse Brain Vessels

artículo científico publicado en 2015

Role of astroglial Connexin 43 in pneumolysin cytotoxicity and during pneumococcal meningitis

artículo científico publicado en 2020

Spatiotemporal expression of otogelin in the developing and adult mouse inner ear.

artículo científico publicado en 2001

Structure of the X-linked Kallmann syndrome gene and its homologous pseudogene on the Y chromosome

artículo científico publicado el 1 de diciembre de 1992

Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death

artículo científico publicado en 2002

Targeted disruption of otog results in deafness and severe imbalance

scientific journal article

The Sarcoglycan complex is expressed in the cerebrovascular system and is specifically regulated by astroglial Cx30 channels.

artículo científico publicado en 2015

Translation in astrocyte distal processes sets molecular heterogeneity at the gliovascular interface.

artículo científico publicado en 2017

Uncoupling of the Astrocyte Syncytium Differentially Affects AQP4 Isoforms

artículo científico publicado en 2020

X chromosome-linked Kallmann syndrome: stop mutations validate the candidate gene ⬇️

artículo científico publicado el 1 de septiembre de 1992

Lista de obras de Martine Cohen-Salmon

A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

Approche moléculaire de la pathogénie d'un deficit héréditaire de l'olfaction : Le syndrome de Kallmann de Morsier lie au chromosome X

AstroDot: a new method for studying the spatial distribution of mRNA in astrocytes

Astrocytes in the regulation of cerebrovascular functions

Astroglial Connexin 43 Deficiency Protects against LPS-Induced Neuroinflammation: A TSPO Brain µPET Study with [18F]FEPPA

Bmcc1s interacts with the phosphate-activated glutaminase in the brain

Bmcc1s, a novel brain-isoform of Bmcc1, affects cell morphology by regulating MAP6/STOP functions

Cannabinoids prevent the opposite regulation of astroglial connexin43 hemichannels and gap junction channels induced by pro-inflammatory treatments

Characterization of the Chicken and Quail Homologues of the Human Gene Responsible for the X-Linked Kallmann Syndrome

Characterization of the promoter of the human KAL gene, responsible for the X-chromosome-linked Kallmann syndrome

Chromosomal assignment of the uromodulin gene (UMOD) to 16p13.11

Cloning and characterization of the mouse collapsin response mediator protein-1, Crmp1.

Connexin 30 is expressed in a subtype of mouse brain pericytes.

Connexin 30 sets synaptic strength by controlling astroglial synapse invasion

Connexin 43 Controls the Astrocyte Immunoregulatory Phenotype.

Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential

Connexin30 deficiency causes instrastrial fluid-blood barrier disruption within the cochlear stria vascularis

Connexins Responsible for Hereditary Deafness — The Tale Unfolds

Consortin, a trans-Golgi network cargo receptor for the plasma membrane targeting and recycling of connexins

Deletion of astroglial connexins weakens the blood-brain barrier.

Dp71 contribution to the molecular scaffold anchoring aquaporine-4 channels in brain macroglial cells

Expression of the connexin43- and connexin45-encoding genes in the developing and mature mouse inner ear.

Fdp, a new fibrocyte-derived protein related to MIA/CD-RAP, has an in vitro effect on the early differentiation of the inner ear mesenchyme

Hearing is normal without connexin30

Hearing the messenger: Ins(1,4,5)P3 and deafness.

Identification of the GlialCAM interactome: the G protein-coupled receptors GPRC5B and GPR37L1 modulate megalencephalic leukoencephalopathy proteins

Immune quiescence of the brain is set by astroglial connexin 43.

Immunoprecipitation of Ribosome-Bound mRNAs from Astrocytic Perisynaptic Processes of the Mouse Hippocampus

Immunoregulation at the gliovascular unit in the healthy brain: A focus on Connexin 43.

Ins(1,4,5)P3: a messenger for hearing

Isolation of kidney complementary DNAs down-expressed in Wilms' tumor by a subtractive hybridization approach.

Local Translation in Perisynaptic Astrocytic Processes Is Specific and Changes after Fear Conditioning

Mapping of the otogelin gene (OTGN) to mouse Chromosome 7 and human Chromosome 11p14.3: a candidate for human autosomal recessive nonsyndromic deafness DFNB18

Mitochondrial AIF loss causes metabolic reprogramming, caspase-independent cell death blockade, embryonic lethality, and perinatal hydrocephalus

Molecular approach to the pathogenesis of renal anomalies in Kallmann's syndrome and in the branchio-oto-renal syndrome

Neuronal Activity Drives Astroglial Connexin 30 in Perisynaptic Processes and Shapes Its Functions

Otogelin: a glycoprotein specific to the acellular membranes of the inner ear

Postnatal development of the astrocyte perivascular MLC1/GlialCAM complex defines a temporal window for the gliovascular unit maturation

Preparing the Astrocyte Perivascular Endfeet Transcriptome to Investigate Astrocyte Molecular Regulations at the Brain-Vascular Interface

Purification of Mouse Brain Vessels

Role of astroglial Connexin 43 in pneumolysin cytotoxicity and during pneumococcal meningitis

Spatiotemporal expression of otogelin in the developing and adult mouse inner ear.

Structure of the X-linked Kallmann syndrome gene and its homologous pseudogene on the Y chromosome

Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death

Targeted disruption of otog results in deafness and severe imbalance

The Sarcoglycan complex is expressed in the cerebrovascular system and is specifically regulated by astroglial Cx30 channels.

Translation in astrocyte distal processes sets molecular heterogeneity at the gliovascular interface.

Uncoupling of the Astrocyte Syncytium Differentially Affects AQP4 Isoforms

X chromosome-linked Kallmann syndrome: stop mutations validate the candidate gene ⬇️