List of works - Martine Cohen-Salmon

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

scientific article

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

scientific article published on 15 October 2020

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

scientific article published on 07 February 2020

Bmcc1s interacts with the phosphate-activated glutaminase in the brain

scientific article published on 12 December 2012

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

scientific article

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

scientific article published in December 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

scientific article

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

scientific article

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

scientific article published in May 1997

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

scientific article published on 16 November 2017

Connexin 30 sets synaptic strength by controlling astroglial synapse invasion

scientific article published on 2 March 2014

Connexin 43 Controls the Astrocyte Immunoregulatory Phenotype.

scientific article

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

scientific article (publication date: 2003)

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

scientific article

Connexins Responsible for Hereditary Deafness — The Tale Unfolds

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

scientific article

Deletion of astroglial connexins weakens the blood-brain barrier.

scientific article

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

scientific article published on 28 November 2020

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

scientific article published on 20 February 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

scientific article

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

scientific article

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

scientific article published on 01 August 2021

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

scientific article published on March 2015

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

scientific article published on 04 December 2020

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

scientific article published on 07 December 2015

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

scientific article published in June 2005

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

scientific article

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

scientific article published on 01 August 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

scientific article published on 29 May 2020

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

scientific article published on 01 January 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

scientific journal article

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

scientific article published on 25 January 2019

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

scientific article published on 01 January 2019

Purification of Mouse Brain Vessels

scientific article published on 10 November 2015

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

scientific article published on 28 December 2020

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

scientific article published in August 2001

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

scientific article published on December 1, 1992

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

scientific article

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.

scientific article

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

scientific article published on 28 March 2017

Uncoupling of the Astrocyte Syncytium Differentially Affects AQP4 Isoforms

scientific article published on 07 February 2020

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

scientific article published on September 1, 1992

List of works by 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 ⬇️