相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Characterization of Panglial Gap Junction Networks in the Thalamus, Neocortex, and Hippocampus Reveals a Unique Population of Glial Cells
Stephanie Griemsmann et al.
CEREBRAL CORTEX (2015)
Adapting Brain Metabolism to Myelination and Long-Range Signal Transduction
Johannes Hirrlinger et al.
GLIA (2014)
The distribution and functional properties of Pelizaeus-Merzbacher-like disease-linked Cx47 mutations on Cx47/Cx47 homotypic and Cx47/Cx43 heterotypic gap junctions
Mi Seong Kim et al.
BIOCHEMICAL JOURNAL (2013)
Brain white matter oedema due to ClC-2 chloride channel deficiency: an observational analytical study
Christel Depienne et al.
LANCET NEUROLOGY (2013)
Regulation of connexin hemichannel activity by membrane potential and the extracellular calcium in health and disease
Ilaria Fasciani et al.
NEUROPHARMACOLOGY (2013)
Analysis Tool Web Services from the EMBL-EBI
Hamish McWilliam et al.
NUCLEIC ACIDS RESEARCH (2013)
Panglial Gap Junctional Communication is Essential for Maintenance of Myelin in the CNS
Oliver Tress et al.
JOURNAL OF NEUROSCIENCE (2012)
Megalencephalic leukoencephalopathy with subcortical cysts: chronic white matter oedema due to a defect in brain ion and water homoeostasis
Marjo S. van der Knaap et al.
LANCET NEUROLOGY (2012)
Gap junction permeability: selectivity for anionic and cationic probes
G. Kanaporis et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2011)
Functional Heterotypic Interactions Between Astrocyte and Oligodendrocyte Connexins
Laura M. Magnotti et al.
GLIA (2011)
Cx32 and Cx47 mediate oligodendrocyte:astrocyte and oligodendrocyte:oligodendrocyte gap junction coupling
Sameh K. Wasseff et al.
NEUROBIOLOGY OF DISEASE (2011)
Pelizaeus-Merzbacher-like disease is caused not only by a loss of connexin47 function but also by a hemichannel dysfunction
Simone Diekmann et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2010)
Oligodendrocytes in Mouse Corpus Callosum are Coupled Via Gap Junction Channels Formed by Connexin47 and Connexin32
Marta Maglione et al.
GLIA (2010)
MOLECULAR DISRUPTIONS OF THE PANGLIAL SYNCYTIUM BLOCK POTASSIUM SIPHONING AND AXONAL SALTATORY CONDUCTION: PERTINENCE TO NEUROMYELITIS OPTICA AND OTHER DEMYELINATING DISEASES OF THE CENTRAL NERVOUS SYSTEM
J. E. Rash
NEUROSCIENCE (2010)
CPHmodels-3.0-remote homology modeling using structure-guided sequence profiles
Morten Nielsen et al.
NUCLEIC ACIDS RESEARCH (2010)
Structure of the connexin 26 gap junction channel at 3.5 Å resolution
Shoji Maeda et al.
NATURE (2009)
Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10
Ute I. Scholl et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Charges dispersed over the permeation pathway determine the charge selectivity and conductance of a Cx32 chimeric hemichannel
Seunghoon Oh et al.
JOURNAL OF PHYSIOLOGY-LONDON (2008)
Two distinct heterotypic channels mediate gap junction coupling between astrocyte and oligodendrocyte connexins
Jennifer L. Orthmann-Murphy et al.
JOURNAL OF NEUROSCIENCE (2007)
An evaluation of automated homology modelling methods at low target-template sequence similarity
James A. R. Dalton et al.
BIOINFORMATICS (2007)
Three-dimensional structure of a human connexin26 gap junction channel reveals a plug in the vestibule
Atsunori Oshima et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus-Merzbacher-like disease
Jennifer L. Orthmann-Murphy et al.
MOLECULAR AND CELLULAR NEUROSCIENCE (2007)
The spectrum of neuromyelitis optica
Dean M. Wingerchuk et al.
LANCET NEUROLOGY (2007)
Species specificity of mammalian connexin-26 to form open voltage-gated hemichannels
Daniel Gonzalez et al.
FASEB JOURNAL (2006)
Genetic and physiological evidence that oligodendrocyte gap junctions contribute to spatial buffering of potassium released during neuronal activity
Daniela M. Menichella et al.
JOURNAL OF NEUROSCIENCE (2006)
Scalable molecular dynamics with NAMD
JC Phillips et al.
JOURNAL OF COMPUTATIONAL CHEMISTRY (2005)
A 2-bp deletion in the GJA1 gene is associated with oculo-dento-digital dysplasia with palmoplantar keratoderma
MAM van Steensel et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2005)
Connexin-47 and connexin-32 in gap junctions of oligodendrocyte somata, myelin sheaths, paranodal loops and Schmidt-Lanterman incisures: Implications for ionic homeostasis and potassium siphoning
N Kamasawa et al.
NEUROSCIENCE (2005)
The permeability of gap junction channels to probes of different size is dependent on connexin composition and permeant-pore affinities
PA Weber et al.
BIOPHYSICAL JOURNAL (2004)
Mutations in the gene encoding gap junction protein α12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease
B Uhlenberg et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
PDB2PQR: an automated pipeline for the setup of Poisson-Boltzmann electrostatics calculations
TJ Dolinsky et al.
NUCLEIC ACIDS RESEARCH (2004)
Four classes of intercellular channels between glial cells in the CNS
BM Altevogt et al.
JOURNAL OF NEUROSCIENCE (2004)
Coupling of astrocyte connexins Cx26, Cx30, Cx43 to oligodendrocyte Cx29, Cx32, Cx47: Implications from normal and connexin32 knockout mice
JI Nagy et al.
GLIA (2003)
Electrostatics of nanosystems: Application to microtubules and the ribosome
NA Baker et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)
The first extracellular loop domain is a major determinant of charge selectivity in connexin46 channels
EB Trexler et al.
BIOPHYSICAL JOURNAL (2000)
分享论文
