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。Expanded spectrum of Pelizaeus-Merzbacher-like disease: literature revision and description of a novel GJC2 mutation in an unusually severe form
Roberta Biancheri et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2013)
Structural organization of intercellular channels II. Amino terminal domain of the connexins: sequence, functional roles, and structure
Eric C. Beyer et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES (2012)
Aspartic Acid Residue D3 Critically Determines Cx50 Gap Junction Channel Transjunctional Voltage-Dependent Gating and Unitary Conductance
Li Xin et al.
BIOPHYSICAL JOURNAL (2012)
How do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease?
Kleopas A. Kleopa et al.
BRAIN RESEARCH (2012)
Genome-wide search for novel human uORFs and N-terminal protein extensions using ribosomal footprinting
Claudia Fritsch et al.
GENOME RESEARCH (2012)
Structure of the gap junction channel and its implications for its biological functions
Shoji Maeda et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2011)
Functional Heterotypic Interactions Between Astrocyte and Oligodendrocyte Connexins
Laura M. Magnotti et al.
GLIA (2011)
Asparagine 175 of Connexin32 Is a Critical Residue for Docking and Forming Functional Heterotypic Gap Junction Channels with Connexin26
So Nakagawa et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2011)
Cx32 and Cx47 mediate oligodendrocyte:astrocyte and oligodendrocyte:oligodendrocyte gap junction coupling
Sameh K. Wasseff et al.
NEUROBIOLOGY OF DISEASE (2011)
Pathologic and Phenotypic Alterations in a Mouse Expressing a Connexin47 Missense Mutation That Causes Pelizaeus-Merzbacher-Like Disease in Humans
Oliver Tress et al.
PLOS GENETICS (2011)
Two novel gap junction protein alpha 12 gene mutations in two Chinese patients with Pelizaeus-Merzbacher-like disease
Jingmin Wang et al.
BRAIN & DEVELOPMENT (2010)
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)
Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations
Jennifer L. Orthmann-Murphy et al.
BRAIN (2009)
Connexin-26 mutations in deafness and skin disease
Jack R. Lee et al.
EXPERT REVIEWS IN MOLECULAR MEDICINE (2009)
Structure of the connexin 26 gap junction channel at 3.5 Å resolution
Shoji Maeda et al.
NATURE (2009)
Gap Junctions
Daniel A. Goodenough et al.
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2009)
GJA12 mutations are a rare cause of Pelizaeus-Merzbacher-like disease
M. Henneke et al.
NEUROLOGY (2008)
Diversity of preferred nucleotide sequences around the translation initiation codon in eukaryote genomes
So Nakagawa et al.
NUCLEIC ACIDS RESEARCH (2008)
Two distinct heterotypic channels mediate gap junction coupling between astrocyte and oligodendrocyte connexins
Jennifer L. Orthmann-Murphy et al.
JOURNAL OF NEUROSCIENCE (2007)
Differential potency of dominant negative connexin43 mutants in oculodentodigital dysplasia
Xiang-Qun Gong et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus-Merzbacher-like disease
Jennifer L. Orthmann-Murphy et al.
MOLECULAR AND CELLULAR NEUROSCIENCE (2007)
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)
GJA12 mutations in children with recessive hypomyelinating leukoencephalopathy
M. Bugiani et al.
NEUROLOGY (2006)
Non-syndromic, autosomal-recessive deafness
MB Petersen et al.
CLINICAL GENETICS (2006)
Astrocytes, from brain glue to communication elements: The revolution continues
A Volterra et al.
NATURE REVIEWS NEUROSCIENCE (2005)
Distribution and intensity of constraint in mammalian genomic sequence
GM Cooper et al.
GENOME RESEARCH (2005)
Oculodentodigital dysplasia-causing connexin43 mutants are non-functional and exhibit dominant effects on wild-type connexin43
W Roscoe et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (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)
Gap junction channel gating
FF Bukauskas et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES (2004)
Unique distributions of the gap junction proteins Connexin29, Connexin32, and Connexin47 in oligodendrocytes
KA Kleopa et al.
GLIA (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)
Update on connexins and gap junctions in neurons and glia in the mammalian nervous system
JI Nagy et al.
BRAIN RESEARCH REVIEWS (2004)
Amino terminal glutamate residues confer spermine sensitivity and affect voltage gating and channel conductance of rat connexin40 gap junctions
H Musa et al.
JOURNAL OF PHYSIOLOGY-LONDON (2004)
Connexin47, connexin29 and connexin32 co-expression in oligodendrocytes and Cx47 association with zonula occludens-1 (Zo-1) in mouse brain
X Li et al.
NEUROSCIENCE (2004)
Four classes of intercellular channels between glial cells in the CNS
BM Altevogt et al.
JOURNAL OF NEUROSCIENCE (2004)
Gap junctions and the connexin protein family
G Söhl et al.
CARDIOVASCULAR RESEARCH (2004)
A monomeric red fluorescent protein
RE Campbell et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
Connexin26 in adult rodent central nervous system: Demonstration at astrocytic gap junctions and colocalization with connexin30 and connexin43
JI Nagy et al.
JOURNAL OF COMPARATIVE NEUROLOGY (2001)
分享论文
