290 related articles for article (PubMed ID: 29893868)
1. Microtubule cytoskeleton regulates Connexin 43 localization and cardiac conduction in cardiomyopathy caused by mutation in A-type lamins gene.
Macquart C; Jüttner R; Morales Rodriguez B; Le Dour C; Lefebvre F; Chatzifrangkeskou M; Schmitt A; Gotthardt M; Bonne G; Muchir A
Hum Mol Genet; 2019 Dec; 28(24):4043-4052. PubMed ID: 29893868
[TBL] [Abstract][Full Text] [Related]
2. Functional Characterization of a Novel Truncating Mutation in Lamin A/C Gene in a Family with a Severe Cardiomyopathy with Conduction Defects.
Gerbino A; Bottillo I; Milano S; Lipari M; Zio R; Morlino S; Mola MG; Procino G; Re F; Zachara E; Grammatico P; Svelto M; Carmosino M
Cell Physiol Biochem; 2017; 44(4):1559-1577. PubMed ID: 29197877
[TBL] [Abstract][Full Text] [Related]
3. Actin-microtubule cytoskeletal interplay mediated by MRTF-A/SRF signaling promotes dilated cardiomyopathy caused by LMNA mutations.
Le Dour C; Chatzifrangkeskou M; Macquart C; Magiera MM; Peccate C; Jouve C; Virtanen L; Heliö T; Aalto-Setälä K; Crasto S; Cadot B; Cardoso D; Mougenot N; Adesse D; Di Pasquale E; Hulot JS; Taimen P; Janke C; Muchir A
Nat Commun; 2022 Dec; 13(1):7886. PubMed ID: 36550158
[TBL] [Abstract][Full Text] [Related]
4. Modulation of cytoskeleton in cardiomyopathy caused by mutations in
Chatzifrangkeskou M; Le Dour C; Muchir A
Am J Physiol Cell Physiol; 2023 Jun; 324(6):C1223-C1235. PubMed ID: 37125775
[TBL] [Abstract][Full Text] [Related]
5. Phosphorylation of connexin43 on S279/282 may contribute to laminopathy-associated conduction defects.
Chen SC; Kennedy BK; Lampe PD
Exp Cell Res; 2013 Apr; 319(6):888-96. PubMed ID: 23261543
[TBL] [Abstract][Full Text] [Related]
6. Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease.
Wolf CM; Wang L; Alcalai R; Pizard A; Burgon PG; Ahmad F; Sherwood M; Branco DM; Wakimoto H; Fishman GI; See V; Stewart CL; Conner DA; Berul CI; Seidman CE; Seidman JG
J Mol Cell Cardiol; 2008 Feb; 44(2):293-303. PubMed ID: 18182166
[TBL] [Abstract][Full Text] [Related]
7. Connexin 43 remodeling induced by LMNA gene mutation Glu82Lys in familial dilated cardiomyopathy with atrial ventricular block.
Sun LP; Wang L; Wang H; Zhang YH; Pu JL
Chin Med J (Engl); 2010 Apr; 123(8):1058-62. PubMed ID: 20497714
[TBL] [Abstract][Full Text] [Related]
8. Prevention of connexin-43 remodeling protects against Duchenne muscular dystrophy cardiomyopathy.
Himelman E; Lillo MA; Nouet J; Gonzalez JP; Zhao Q; Xie LH; Li H; Liu T; Wehrens XH; Lampe PD; Fishman GI; Shirokova N; Contreras JE; Fraidenraich D
J Clin Invest; 2020 Apr; 130(4):1713-1727. PubMed ID: 31910160
[TBL] [Abstract][Full Text] [Related]
9. GJA1-20k Arranges Actin to Guide Cx43 Delivery to Cardiac Intercalated Discs.
Basheer WA; Xiao S; Epifantseva I; Fu Y; Kleber AG; Hong T; Shaw RM
Circ Res; 2017 Oct; 121(9):1069-1080. PubMed ID: 28923791
[TBL] [Abstract][Full Text] [Related]
10. Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy.
Forleo C; Carmosino M; Resta N; Rampazzo A; Valecce R; Sorrentino S; Iacoviello M; Pisani F; Procino G; Gerbino A; Scardapane A; Simone C; Calore M; Torretta S; Svelto M; Favale S
PLoS One; 2015; 10(4):e0121723. PubMed ID: 25837155
[TBL] [Abstract][Full Text] [Related]
11. Amelioration of desmin network defects by αB-crystallin overexpression confers cardioprotection in a mouse model of dilated cardiomyopathy caused by LMNA gene mutation.
Galata Z; Kloukina I; Kostavasili I; Varela A; Davos CH; Makridakis M; Bonne G; Capetanaki Y
J Mol Cell Cardiol; 2018 Dec; 125():73-86. PubMed ID: 30342008
[TBL] [Abstract][Full Text] [Related]
12. Decreased WNT/β-catenin signalling contributes to the pathogenesis of dilated cardiomyopathy caused by mutations in the lamin a/C gene.
Le Dour C; Macquart C; Sera F; Homma S; Bonne G; Morrow JP; Worman HJ; Muchir A
Hum Mol Genet; 2017 Jan; 26(2):333-343. PubMed ID: 28069793
[TBL] [Abstract][Full Text] [Related]
13. Trafficking highways to the intercalated disc: new insights unlocking the specificity of connexin 43 localization.
Zhang SS; Shaw RM
Cell Commun Adhes; 2014 Feb; 21(1):43-54. PubMed ID: 24460200
[TBL] [Abstract][Full Text] [Related]
14. Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicity.
Cattin ME; Bertrand AT; Schlossarek S; Le Bihan MC; Skov Jensen S; Neuber C; Crocini C; Maron S; Lainé J; Mougenot N; Varnous S; Fromes Y; Hansen A; Eschenhagen T; Decostre V; Carrier L; Bonne G
Hum Mol Genet; 2013 Aug; 22(15):3152-64. PubMed ID: 23575224
[TBL] [Abstract][Full Text] [Related]
15. Cardiomyopathy-Associated Gene 1-Sensitive PKC-Dependent Connexin 43 Expression and Phosphorylation in Left Ventricular Noncompaction Cardiomyopathy.
Xie Y; Liu S; Hu S; Wei Y
Cell Physiol Biochem; 2017; 44(2):828-842. PubMed ID: 29176328
[TBL] [Abstract][Full Text] [Related]
16. Role of an alternatively spliced form of alphaII-spectrin in localization of connexin 43 in cardiomyocytes and regulation by stress-activated protein kinase.
Ursitti JA; Petrich BG; Lee PC; Resneck WG; Ye X; Yang J; Randall WR; Bloch RJ; Wang Y
J Mol Cell Cardiol; 2007 Mar; 42(3):572-81. PubMed ID: 17276456
[TBL] [Abstract][Full Text] [Related]
17. Nε-lysine acetylation determines dissociation from GAP junctions and lateralization of connexin 43 in normal and dystrophic heart.
Colussi C; Rosati J; Straino S; Spallotta F; Berni R; Stilli D; Rossi S; Musso E; Macchi E; Mai A; Sbardella G; Castellano S; Chimenti C; Frustaci A; Nebbioso A; Altucci L; Capogrossi MC; Gaetano C
Proc Natl Acad Sci U S A; 2011 Feb; 108(7):2795-800. PubMed ID: 21282606
[TBL] [Abstract][Full Text] [Related]
18. Skeletal and Cardiac Muscle Disorders Caused by Mutations in Genes Encoding Intermediate Filament Proteins.
Maggi L; Mavroidis M; Psarras S; Capetanaki Y; Lattanzi G
Int J Mol Sci; 2021 Apr; 22(8):. PubMed ID: 33923914
[TBL] [Abstract][Full Text] [Related]
19. Cardiomyocyte-specific overexpression of the ubiquitin ligase Wwp1 contributes to reduction in Connexin 43 and arrhythmogenesis.
Basheer WA; Harris BS; Mentrup HL; Abreha M; Thames EL; Lea JB; Swing DA; Copeland NG; Jenkins NA; Price RL; Matesic LE
J Mol Cell Cardiol; 2015 Nov; 88():1-13. PubMed ID: 26386426
[TBL] [Abstract][Full Text] [Related]
20. Remodeled connexin 43 hemichannels alter cardiac excitability and promote arrhythmias.
Lillo MA; Muñoz M; Rhana P; Gaul-Muller K; Quan J; Shirokova N; Xie LH; Santana LF; Fraidenraich D; Contreras JE
J Gen Physiol; 2023 Jul; 155(7):. PubMed ID: 37191672
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
