The distribution and functional properties of Pelizaeus–Merzbacher-like disease-linked Cx47 mutations on Cx47/Cx47 homotypic and Cx47/Cx43 heterotypic gap junctions
Published 2013 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
The distribution and functional properties of Pelizaeus–Merzbacher-like disease-linked Cx47 mutations on Cx47/Cx47 homotypic and Cx47/Cx43 heterotypic gap junctions
Authors
Keywords
-
Journal
BIOCHEMICAL JOURNAL
Volume 452, Issue 2, Pages 249-258
Publisher
Portland Press Ltd.
Online
2013-04-03
DOI
10.1042/bj20121821
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Aspartic Acid Residue D3 Critically Determines Cx50 Gap Junction Channel Transjunctional Voltage-Dependent Gating and Unitary Conductance
- (2012) Li Xin et al. BIOPHYSICAL JOURNAL
- How do mutations in GJB1 cause X-linked Charcot–Marie–Tooth disease?
- (2012) Kleopas A. Kleopa et al. BRAIN RESEARCH
- Expanded spectrum of Pelizaeus–Merzbacher-like disease: literature revision and description of a novel GJC2 mutation in an unusually severe form
- (2012) Roberta Biancheri et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Genome-wide search for novel human uORFs and N-terminal protein extensions using ribosomal footprinting
- (2012) C. Fritsch et al. GENOME RESEARCH
- Structural organization of intercellular channels II. Amino terminal domain of the connexins: sequence, functional roles, and structure
- (2011) Eric C. Beyer et al. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES
- Asparagine 175 of Connexin32 Is a Critical Residue for Docking and Forming Functional Heterotypic Gap Junction Channels with Connexin26
- (2011) So Nakagawa et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Cx32 and Cx47 mediate oligodendrocyte:astrocyte and oligodendrocyte:oligodendrocyte gap junction coupling
- (2011) Sameh K. Wasseff et al. NEUROBIOLOGY OF DISEASE
- Pathologic and Phenotypic Alterations in a Mouse Expressing a Connexin47 Missense Mutation That Causes Pelizaeus-Merzbacher–Like Disease in Humans
- (2011) Oliver Tress et al. PLoS Genetics
- Structure of the gap junction channel and its implications for its biological functions
- (2010) Shoji Maeda et al. CELLULAR AND MOLECULAR LIFE SCIENCES
- Pelizaeus–Merzbacher-like disease is caused not only by a loss of connexin47 function but also by a hemichannel dysfunction
- (2010) Simone Diekmann et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Functional heterotypic interactions between astrocyte and oligodendrocyte connexins
- (2010) Laura M. Magnotti et al. GLIA
- Oligodendrocytes in mouse corpus callosum are coupled via gap junction channels formed by connexin47 and connexin32
- (2010) Marta Maglione et al. GLIA
- Two novel gap junction protein alpha 12 gene mutations in two Chinese patients with Pelizaeus–Merzbacher-like disease
- (2009) Jingmin Wang et al. BRAIN & DEVELOPMENT
- Connexin-26 mutations in deafness and skin disease
- (2009) Jack R. Lee et al. EXPERT REVIEWS IN MOLECULAR MEDICINE
- Structure of the connexin 26 gap junction channel at 3.5 Å resolution
- (2009) Shoji Maeda et al. NATURE
- 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
- (2009) J.E. Rash NEUROSCIENCE
- Gap Junctions
- (2009) D. A. Goodenough et al. Cold Spring Harbor Perspectives in Biology
- Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations
- (2008) Jennifer L. Orthmann-Murphy et al. BRAIN
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now