Lista de obras -

A modification of the split-tobacco etch virus method for monitoring interactions between membrane proteins in mammalian cells.

artículo científico publicado en 2012

CLCN1 myotonia congenita mutation with a variable pattern of inheritance suggests a novel mechanism of dominant myotonia

artículo científico publicado en 2018

Chloride Channels in Astrocytes: Structure, Roles in Brain Homeostasis and Implications in Disease ⬇️

artículo científico publicado en 2019

Cisplatin activates volume sensitive LRRC8 channel mediated currents in Xenopus oocytes

artículo científico publicado en 2017

Comparison of zebrafish and mice knockouts for Megalencephalic Leukoencephalopathy proteins indicates that GlialCAM/MLC1 forms a functional unit

scientific article published on 21 November 2019

Conservation of chloride channel structure revealed by an inhibitor binding site in ClC-1.

artículo científico publicado en 2003

Cystinuria calls for heteromultimeric amino acid transporters.

artículo científico publicado en 1998

Deficient LRRC8A-dependent volume-regulated anion channel activity is associated with male infertility in mice

article

Depolarization causes the formation of a ternary complex between GlialCAM, MLC1 and ClC-2 in astrocytes: implications in megalencephalic leukoencephalopathy

artículo científico publicado en 2017

Expression of LRRC8/VRAC Currents in Xenopus Oocytes: Advantages and Caveats.

artículo científico publicado en 2018

Expression patterns of MLC1 protein in the central and peripheral nervous systems.

artículo científico publicado en 2007

Functional analyses of mutations in HEPACAM causing megalencephalic leukoencephalopathy

artículo científico publicado en 2014

Functional and structural conservation of CBS domains from CLC chloride channels.

artículo científico publicado en 2004

GlialCAM, a CLC-2 Cl(-) channel subunit, activates the slow gate of CLC chloride channels.

artículo científico publicado en 2014

GlialCAM, a glial cell adhesion molecule implicated in neurological disease.

artículo científico publicado en 2014

GlialCAM/MLC1 modulates LRRC8/VRAC currents in an indirect manner: Implications for megalencephalic leukoencephalopathy

scientific article published on 01 August 2018

Identification and Functional Characterization of CLCN1 Mutations Found in Nondystrophic Myotonia Patients

artículo científico publicado en 2015

Identification and characterization of a membrane protein (y+L amino acid transporter-1) that associates with 4F2hc to encode the amino acid transport activity y+L. A candidate gene for lysinuric protein intolerance

artículo científico publicado en 1998

Identification and characterization of the zebrafish ClC-2 chloride channel orthologs.

artículo científico publicado en 2014

Identification of SLC7A7, encoding y+LAT-1, as the lysinuric protein intolerance gene.

artículo científico publicado en 1999

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

artículo científico publicado en 2021

Insights into MLC pathogenesis: GlialCAM is an MLC1 chaperone required for proper activation of volume-regulated anion currents.

artículo científico publicado en 2013

Investigation of LRRC8-Mediated Volume-Regulated Anion Currents in Xenopus Oocytes

artículo científico publicado en 2016

Knockdown of MLC1 in primary astrocytes causes cell vacuolation: A MLC disease cell model ⬇️

artículo científico publicado el 3 de abril de 2011

Leukoencephalopathy-causing CLCN2 mutations are associated with impaired Cl- channel function and trafficking.

artículo científico publicado en 2017

Localization and functional analyses of the MLC1 protein involved in megalencephalic leukoencephalopathy with subcortical cysts

artículo científico publicado en 2004

Megalencephalic leucoencephalopathy with cysts: defect in chloride currents and cell volume regulation.

artículo científico publicado en 2011

Megalencephalic leukoencephalopathy with subcortical cysts protein 1 regulates glial surface localization of GLIALCAM from fish to humans.

artículo científico publicado en 2014

Megalencephalic leukoencephalopathy with subcortical cysts: A personal biochemical retrospective.

artículo científico publicado en 2017

Megalencephalic leukoencephalopathy with subcortical cysts: chronic white matter oedema due to a defect in brain ion and water homoeostasis ⬇️

artículo científico publicado el 1 de noviembre de 2012

Molecular Biology of Mammalian Plasma Membrane Amino Acid Transporters ⬇️

artículo científico publicado el 1 de octubre de 1998

Molecular mechanisms of MLC1 and GLIALCAM mutations in megalencephalic leukoencephalopathy with subcortical cysts

artículo científico publicado en 2011

Obligatory amino acid exchange via systems bo,+-like and y+L-like. A tertiary active transport mechanism for renal reabsorption of cystine and dibasic amino acids.

artículo científico publicado en 1996

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

artículo científico publicado en 2019

Role of zebrafish ClC-K/barttin channels in apical kidney chloride reabsorption

scientific article published on 03 July 2019

Sequential amino acid exchange across b(0,+)-like system in chicken brush border jejunum.

artículo científico publicado en 2001

Structural determinants of interaction, trafficking and function in the ClC-2/MLC1 subunit GlialCAM involved in leukodystrophy.

artículo científico publicado en 2015

The amino acid transport system y+L/4F2hc is a heteromultimeric complex.

artículo científico publicado en 1998

Lista de obras de

A modification of the split-tobacco etch virus method for monitoring interactions between membrane proteins in mammalian cells.

CLCN1 myotonia congenita mutation with a variable pattern of inheritance suggests a novel mechanism of dominant myotonia

Chloride Channels in Astrocytes: Structure, Roles in Brain Homeostasis and Implications in Disease ⬇️

Cisplatin activates volume sensitive LRRC8 channel mediated currents in Xenopus oocytes

Comparison of zebrafish and mice knockouts for Megalencephalic Leukoencephalopathy proteins indicates that GlialCAM/MLC1 forms a functional unit

Conservation of chloride channel structure revealed by an inhibitor binding site in ClC-1.

Cystinuria calls for heteromultimeric amino acid transporters.

Deficient LRRC8A-dependent volume-regulated anion channel activity is associated with male infertility in mice

Depolarization causes the formation of a ternary complex between GlialCAM, MLC1 and ClC-2 in astrocytes: implications in megalencephalic leukoencephalopathy

Expression of LRRC8/VRAC Currents in Xenopus Oocytes: Advantages and Caveats.

Expression patterns of MLC1 protein in the central and peripheral nervous systems.

Functional analyses of mutations in HEPACAM causing megalencephalic leukoencephalopathy

Functional and structural conservation of CBS domains from CLC chloride channels.

GlialCAM, a CLC-2 Cl(-) channel subunit, activates the slow gate of CLC chloride channels.

GlialCAM, a glial cell adhesion molecule implicated in neurological disease.

GlialCAM/MLC1 modulates LRRC8/VRAC currents in an indirect manner: Implications for megalencephalic leukoencephalopathy

Identification and Functional Characterization of CLCN1 Mutations Found in Nondystrophic Myotonia Patients

Identification and characterization of a membrane protein (y+L amino acid transporter-1) that associates with 4F2hc to encode the amino acid transport activity y+L. A candidate gene for lysinuric protein intolerance

Identification and characterization of the zebrafish ClC-2 chloride channel orthologs.

Identification of SLC7A7, encoding y+LAT-1, as the lysinuric protein intolerance gene.

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

Insights into MLC pathogenesis: GlialCAM is an MLC1 chaperone required for proper activation of volume-regulated anion currents.

Investigation of LRRC8-Mediated Volume-Regulated Anion Currents in Xenopus Oocytes

Knockdown of MLC1 in primary astrocytes causes cell vacuolation: A MLC disease cell model ⬇️

Leukoencephalopathy-causing CLCN2 mutations are associated with impaired Cl- channel function and trafficking.

Localization and functional analyses of the MLC1 protein involved in megalencephalic leukoencephalopathy with subcortical cysts

Megalencephalic leucoencephalopathy with cysts: defect in chloride currents and cell volume regulation.

Megalencephalic leukoencephalopathy with subcortical cysts protein 1 regulates glial surface localization of GLIALCAM from fish to humans.

Megalencephalic leukoencephalopathy with subcortical cysts: A personal biochemical retrospective.

Megalencephalic leukoencephalopathy with subcortical cysts: chronic white matter oedema due to a defect in brain ion and water homoeostasis ⬇️

Molecular Biology of Mammalian Plasma Membrane Amino Acid Transporters ⬇️

Molecular mechanisms of MLC1 and GLIALCAM mutations in megalencephalic leukoencephalopathy with subcortical cysts

Obligatory amino acid exchange via systems bo,+-like and y+L-like. A tertiary active transport mechanism for renal reabsorption of cystine and dibasic amino acids.

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

Role of zebrafish ClC-K/barttin channels in apical kidney chloride reabsorption

Sequential amino acid exchange across b(0,+)-like system in chicken brush border jejunum.

Structural determinants of interaction, trafficking and function in the ClC-2/MLC1 subunit GlialCAM involved in leukodystrophy.

The amino acid transport system y+L/4F2hc is a heteromultimeric complex.