Closing the gap on autosomal dominant connexin-26 and connexin-43 mutants linked to human disease.
about
Ubiquitin-independent proteasomal degradation of endoplasmic reticulum-localized connexin43 mediated by CIP75Bidirectional communication between oocytes and follicle cells: ensuring oocyte developmental competenceConnexin hemichannel and pannexin channel electrophysiology: how do they differ?Premature osteoblast clustering by enamel matrix proteins induces osteoblast differentiation through up-regulation of connexin 43 and N-cadherinStructure and functional studies of N-terminal Cx43 mutants linked to oculodentodigital dysplasia.Syndromic and non-syndromic disease-linked Cx43 mutations.The transcription factor GCF2 is an upstream repressor of the small GTPAse RhoA, regulating membrane protein trafficking, sensitivity to doxorubicin, and resistance to cisplatin.Connexin 47 mutations increase risk for secondary lymphedema following breast cancer treatmentEffects of phosphorylation on the structure and backbone dynamics of the intrinsically disordered connexin43 C-terminal domainConnexins, pannexins, innexins: novel roles of "hemi-channels"ERp29 restricts Connexin43 oligomerization in the endoplasmic reticulum.Neurological manifestations of oculodentodigital dysplasia: a Cx43 channelopathy of the central nervous system?Protein-mediated interactions of pancreatic islet cellsConnexins: mechanisms regulating protein levels and intercellular communicationConnexins: key mediators of endocrine function.Degradation of connexins through the proteasomal, endolysosomal and phagolysosomal pathways.Overview of skin diseases linked to connexin gene mutations.Gap junction regulation by calmodulin.The "connexin" between bone cells and skeletal functions.Connexin30.3 is expressed in mouse embryonic stem cells and is responsive to leukemia inhibitory factor.Tyrosine-dependent basolateral targeting of human connexin43-eYFP in Madin-Darby canine kidney cells can be disrupted by the oculodentodigital dysplasia mutation L90VCx40.8, a Cx43-like protein, forms gap junction channels inefficiently and may require Cx43 for its association at the plasma membrane.Connexin 43 and hearing: possible implications for retrocochlear auditory processing.Connexins in Cardiovascular and Neurovascular Health and Disease: Pharmacological Implications.Connexin43 Mutant Patient-Derived Induced Pluripotent Stem Cells Exhibit Altered Differentiation Potential.From the Clinical Problem to the Basic Research-Co-Culture Models of Osteoblasts and Osteoclasts
P2860
Q24302500-65BD2A93-463F-4F22-B86E-C596675FD7B9Q24634160-DE69A9F8-F13B-40D5-8F62-751363A2CBF0Q26824824-DA0441B8-D8E0-4EFE-B25E-1A2042712149Q28741433-432748CE-0564-4F43-B599-E612C65FBF9EQ30419343-6EE2C437-879F-4D9B-A630-900B1A5CDA25Q34398416-FF49D6EB-A07C-401B-B058-ED94FD6A6332Q36008522-58E5DB13-9767-4500-9447-34D9C5F4E4EEQ36763693-4F69D337-44A9-4674-9828-26F4692C05D0Q37112753-86FD0038-462B-4532-B99C-F1F53326753AQ37130086-506E9FAE-BB3E-4BBE-A6D9-EE5BE1A47A32Q37193492-47D4E330-0B3E-48F5-B8DB-39D72FDC917EQ37199244-FB8924D5-C0CA-44D2-9215-78C8887B6AEFQ37287798-E2352AB9-2597-46CC-A16F-CA32205E1853Q37707115-1466B677-BA05-4EF9-826A-AEEBCF4B88F4Q37947566-2D06EDDD-4EB6-47E2-9C4D-95F83AECA4E1Q38024660-41B4AAB5-EFBD-466F-89AB-77C059A45782Q38107003-FD046AA7-EFA5-48A5-A446-D26208D7B29BQ38179727-D46025EA-B2FA-44FD-8849-554F2AA74C6FQ38211108-0E4CFBEC-87B3-433D-9B6E-7CBBB89E14F8Q38716198-8A9DD3BF-CE6D-4791-81AE-71957996FB3AQ39782970-D9AF8A56-3957-49F6-A6C4-71CF8C66D015Q41906790-E12D7A77-845E-41AE-B91A-2296A2E450FAQ45871099-6AE773FC-29E9-4815-9DCE-D6608E61106AQ47770967-138137FF-88F6-4427-8327-3CA7BF974CBCQ48263130-0D1A4DD7-884A-4FEC-9DE7-7DA124162CA5Q58800954-AB1C0EB9-F984-4F33-AF99-8495611B90DD
P2860
Closing the gap on autosomal dominant connexin-26 and connexin-43 mutants linked to human disease.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 18 December 2007
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Closing the gap on autosomal d ...... tants linked to human disease.
@en
Closing the gap on autosomal d ...... tants linked to human disease.
@nl
type
label
Closing the gap on autosomal d ...... tants linked to human disease.
@en
Closing the gap on autosomal d ...... tants linked to human disease.
@nl
prefLabel
Closing the gap on autosomal d ...... tants linked to human disease.
@en
Closing the gap on autosomal d ...... tants linked to human disease.
@nl
P2860
P356
P1476
Closing the gap on autosomal d ...... tants linked to human disease.
@en
P2860
P304
P356
10.1074/JBC.R700041200
P407
P50
P577
2007-12-18T00:00:00Z