Syndromic and non-syndromic disease-linked Cx43 mutations.
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Recent advances in understanding ichthyosis pathogenesisGap junction connexins in female reproductive organs: implications for women's reproductive healthMitotic cells form actin-based bridges with adjacent cells to provide intercellular communication during rounding.Mutations in cardiovascular connexin genes.Up-regulation of BMP2/4 signaling increases both osteoblast-specific marker expression and bone marrow adipogenesis in Gja1Jrt/+ stromal cell cultures.Dominant De Novo Mutations in GJA1 Cause Erythrokeratodermia Variabilis et Progressiva, without Features of Oculodentodigital Dysplasia.Connexins and pannexins in the skeleton: gap junctions, hemichannels and moreConnexinopathies: a structural and functional glimpseConnexins: substrates and regulators of autophagyMolecular mechanisms regulating formation, trafficking and processing of annular gap junctions.Role of connexins and pannexins during ontogeny, regeneration, and pathologies of boneProteomic Analysis of Connexin 43 Reveals Novel Interactors Related to Osteoarthritis.A new high-throughput screening-compatible gap junctional intercellular communication assayCardiomyocyte-specific overexpression of the ubiquitin ligase Wwp1 contributes to reduction in Connexin 43 and arrhythmogenesis.Dominant de novo DSP mutations cause erythrokeratodermia-cardiomyopathy syndrome.Connexins in the skeletonDegradation of gap junction connexins is regulated by the interaction with Cx43-interacting protein of 75 kDa (CIP75).A Germline Variant in the PANX1 Gene Has Reduced Channel Function and Is Associated with Multisystem DysfunctionTwo Different Functions of Connexin43 Confer Two Different Bone Phenotypes in Zebrafish.The C-terminal domain of connexin43 modulates cartilage structure via chondrocyte phenotypic changes.Mix and match: investigating heteromeric and heterotypic gap junction channels in model systems and native tissues.Connexins: sensors of epidermal integrity that are therapeutic targets.Mechanisms linking connexin mutations to human diseases.Connexins and skin disease: insights into the role of beta connexins in skin homeostasis.Connexins and pannexins in the integumentary system: the skin and appendages.Connexin channels in congenital skin disorders.Erythrokeratodermia variabilis et progressiva.Specific functional pathologies of Cx43 mutations associated with oculodentodigital dysplasiaDefective signaling, osteoblastogenesis and bone remodeling in a mouse model of connexin 43 C-terminal truncation.Human diseases associated with connexin mutations.Intracellular trafficking pathways of Cx43 gap junction channels.Connexins and Pannexins in Bone and Skeletal Muscle.A known mutation in GJB6 in a large Chinese family with hidrotic ectodermal dysplasia.Anchored PKA as a gatekeeper for gap junctions.Atomic structure of the innexin-6 gap junction channel determined by cryo-EM.Gap junctional communication in health and disease.Joint diseases: from connexins to gap junctions.Connexin43 intercellular communication drives the early differentiation of human bone marrow stromal cells into osteoblasts.Spatiotemporal expression pattern of Connexin 43 during early chick embryogenesis.Role of connexin 43 in different forms of intercellular communication - gap junctions, extracellular vesicles and tunnelling nanotubes.
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P2860
Syndromic and non-syndromic disease-linked Cx43 mutations.
description
2014 nî lūn-bûn
@nan
2014 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Syndromic and non-syndromic disease-linked Cx43 mutations.
@ast
Syndromic and non-syndromic disease-linked Cx43 mutations.
@en
Syndromic and non-syndromic disease-linked Cx43 mutations.
@nl
type
label
Syndromic and non-syndromic disease-linked Cx43 mutations.
@ast
Syndromic and non-syndromic disease-linked Cx43 mutations.
@en
Syndromic and non-syndromic disease-linked Cx43 mutations.
@nl
prefLabel
Syndromic and non-syndromic disease-linked Cx43 mutations.
@ast
Syndromic and non-syndromic disease-linked Cx43 mutations.
@en
Syndromic and non-syndromic disease-linked Cx43 mutations.
@nl
P2860
P1433
P1476
Syndromic and non-syndromic disease-linked Cx43 mutations.
@en
P2860
P304
P356
10.1016/J.FEBSLET.2013.12.022
P407
P50
P577
2014-01-14T00:00:00Z