Plasma membrane channels formed by connexins: their regulation and functions

JC Sáez, VM Berthoud, MC Branes… - Physiological …, 2003 - journals.physiology.org
Sáez, Juan C., Viviana M. Berthoud, María C. Brañes, Agustín D. Martínez, and Eric C.
Beyer. Plasma Membrane Channels Formed by Connexins: Their Regulation and Functions …

Gap junctions: structure and function

WH Evans, PEM Martin - Molecular membrane biology, 2002 - Taylor & Francis
Gap junctions are plasma membrane spatial microdomains constructed of assemblies of
channel proteins called connexins in vertebrates and innexins in invertebrates. The …

[图书][B] Ion channels and disease

FM Ashcroft - 1999 - books.google.com
Ion channels are membrane proteins that act as gated pathways for the movement of ions
across cell membranes. They play essential roles in the physiology of all cells. In recent …

[HTML][HTML] Defective gap junctional intercellular communication in the carcinogenic process

M Mesnil, S Crespin, JL Avanzo… - Biochimica et Biophysica …, 2005 - Elsevier
Gap junctions are membrane structures made of intercellular channels which permit the
diffusion from cytoplasm to cytoplasm of small hydrophilic molecules. Nearly 40 years ago …

Emerging therapies for Charcot-Marie-Tooth inherited neuropathies

M Stavrou, I Sargiannidou, E Georgiou… - International Journal of …, 2021 - mdpi.com
Inherited neuropathies known as Charcot-Marie-Tooth (CMT) disease are genetically
heterogeneous disorders affecting the peripheral nerves, causing significant and slowly …

Genetic diseases and gene knockouts reveal diverse connexin functions

TW White, DL Paul - Annual review of physiology, 1999 - annualreviews.org
▪ Abstract Intercellular channels present in gap junctions allow cells to share small
molecules and thus coordinate a wide range of behaviors. Remarkably, although junctions …

Biology of Schwann cells

GJ Kidd, N Ohno, BD Trapp - Handbook of clinical neurology, 2013 - Elsevier
The fundamental roles of Schwann cells during peripheral nerve formation and regeneration
have been recognized for more than 100 years, but the cellular and molecular mechanisms …

Connexin32‐null mice develop demyelinating peripheral neuropathy

SS Scherer, YT Xu, E Nelles, K Fischbeck, K Willecke… - Glia, 1998 - Wiley Online Library
Mutations in the gene encoding the gap junction protein connexin32 (Cx32) cause X‐linked
Charcot‐Marie‐Tooth disease (CMTX), a common form of inherited demyelinating …

Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32

P Anzini, DHH Neuberg, M Schachner… - Journal of …, 1997 - Soc Neuroscience
Mutations affecting the connexin 32 (Cx32) gene are associated with the X-linked form of the
hereditary peripheral neuropathy Charcot–Marie–Tooth disease (CMTX). We show that …

Charcot‐Marie‐Tooth disease and related neuropathies: mutation distribution and genotype‐phenotype correlation

CF Boerkoel, H Takashima, CA Garcia… - Annals of Neurology …, 2002 - Wiley Online Library
Abstract Charcot‐Marie‐Tooth disease (CMT) is a genetically heterogeneous disorder that
has been associated with alterations of several proteins: peripheral myelin protein 22 …