299 related articles for article (PubMed ID: 31844279)
1. Mutant lamins cause nuclear envelope rupture and DNA damage in skeletal muscle cells.
Earle AJ; Kirby TJ; Fedorchak GR; Isermann P; Patel J; Iruvanti S; Moore SA; Bonne G; Wallrath LL; Lammerding J
Nat Mater; 2020 Apr; 19(4):464-473. PubMed ID: 31844279
[TBL] [Abstract][Full Text] [Related]
2. In Silico and In Vivo Analysis of Amino Acid Substitutions That Cause Laminopathies.
Hinz BE; Walker SG; Xiong A; Gogal RA; Schnieders MJ; Wallrath LL
Int J Mol Sci; 2021 Oct; 22(20):. PubMed ID: 34681887
[TBL] [Abstract][Full Text] [Related]
3. Lamin A/C Assembly Defects in
Bertrand AT; Brull A; Azibani F; Benarroch L; Chikhaoui K; Stewart CL; Medalia O; Ben Yaou R; Bonne G
Cells; 2020 Mar; 9(4):. PubMed ID: 32244403
[No Abstract] [Full Text] [Related]
4. Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth.
Owens DJ; Messéant J; Moog S; Viggars M; Ferry A; Mamchaoui K; Lacène E; Roméro N; Brull A; Bonne G; Butler-Browne G; Coirault C
Int J Mol Sci; 2020 Dec; 22(1):. PubMed ID: 33396724
[TBL] [Abstract][Full Text] [Related]
5. Emery-Dreifuss muscular dystrophy: focal point nuclear envelope.
Muchir A; Worman HJ
Curr Opin Neurol; 2019 Oct; 32(5):728-734. PubMed ID: 31460960
[TBL] [Abstract][Full Text] [Related]
6. Nuclear envelope defects associated with LMNA mutations cause dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy.
Raharjo WH; Enarson P; Sullivan T; Stewart CL; Burke B
J Cell Sci; 2001 Dec; 114(Pt 24):4447-57. PubMed ID: 11792810
[TBL] [Abstract][Full Text] [Related]
7. Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies.
Arimura T; Helbling-Leclerc A; Massart C; Varnous S; Niel F; Lacène E; Fromes Y; Toussaint M; Mura AM; Keller DI; Amthor H; Isnard R; Malissen M; Schwartz K; Bonne G
Hum Mol Genet; 2005 Jan; 14(1):155-69. PubMed ID: 15548545
[TBL] [Abstract][Full Text] [Related]
8. Lamin A/C and emerin regulate MKL1-SRF activity by modulating actin dynamics.
Ho CY; Jaalouk DE; Vartiainen MK; Lammerding J
Nature; 2013 May; 497(7450):507-11. PubMed ID: 23644458
[TBL] [Abstract][Full Text] [Related]
9. Uncoordinated transcription and compromised muscle function in the lmna-null mouse model of Emery- Emery-Dreyfuss muscular dystrophy.
Gnocchi VF; Scharner J; Huang Z; Brady K; Lee JS; White RB; Morgan JE; Sun YB; Ellis JA; Zammit PS
PLoS One; 2011 Feb; 6(2):e16651. PubMed ID: 21364987
[TBL] [Abstract][Full Text] [Related]
10. Drosophila Models Reveal Properties of Mutant Lamins That Give Rise to Distinct Diseases.
Walker SG; Langland CJ; Viles J; Hecker LA; Wallrath LL
Cells; 2023 Apr; 12(8):. PubMed ID: 37190051
[TBL] [Abstract][Full Text] [Related]
11. Emery-Dreifuss muscular dystrophy, laminopathies, and other nuclear envelopathies.
Bonne G; Quijano-Roy S
Handb Clin Neurol; 2013; 113():1367-76. PubMed ID: 23622360
[TBL] [Abstract][Full Text] [Related]
12. Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regeneration.
Bakay M; Wang Z; Melcon G; Schiltz L; Xuan J; Zhao P; Sartorelli V; Seo J; Pegoraro E; Angelini C; Shneiderman B; Escolar D; Chen YW; Winokur ST; Pachman LM; Fan C; Mandler R; Nevo Y; Gordon E; Zhu Y; Dong Y; Wang Y; Hoffman EP
Brain; 2006 Apr; 129(Pt 4):996-1013. PubMed ID: 16478798
[TBL] [Abstract][Full Text] [Related]
13. Laminopathies affecting skeletal and cardiac muscles: clinical and pathophysiological aspects.
Decostre V; Ben Yaou R; Bonne G
Acta Myol; 2005 Oct; 24(2):104-9. PubMed ID: 16550926
[TBL] [Abstract][Full Text] [Related]
14. Protein profiling reveals energy metabolism and cytoskeletal protein alterations in LMNA mutation carriers.
Magagnotti C; Bachi A; Zerbini G; Fattore E; Fermo I; Riba M; Previtali SC; Ferrari M; Andolfo A; Benedetti S
Biochim Biophys Acta; 2012 Jun; 1822(6):970-9. PubMed ID: 22326558
[TBL] [Abstract][Full Text] [Related]
15. Myopathic lamin mutations impair nuclear stability in cells and tissue and disrupt nucleo-cytoskeletal coupling.
Zwerger M; Jaalouk DE; Lombardi ML; Isermann P; Mauermann M; Dialynas G; Herrmann H; Wallrath LL; Lammerding J
Hum Mol Genet; 2013 Jun; 22(12):2335-49. PubMed ID: 23427149
[TBL] [Abstract][Full Text] [Related]
16. The muscle dystrophy-causing ΔK32 lamin A/C mutant does not impair the functions of the nucleoplasmic lamin-A/C-LAP2α complex in mice.
Pilat U; Dechat T; Bertrand AT; Woisetschläger N; Gotic I; Spilka R; Biadasiewicz K; Bonne G; Foisner R
J Cell Sci; 2013 Apr; 126(Pt 8):1753-62. PubMed ID: 23444379
[TBL] [Abstract][Full Text] [Related]
17. A CRISPR/Cas9 zebrafish lamin A/C mutant model of muscular laminopathy.
Nicolas HA; Hua K; Quigley H; Ivare J; Tesson F; Akimenko MA
Dev Dyn; 2022 Apr; 251(4):645-661. PubMed ID: 34599606
[TBL] [Abstract][Full Text] [Related]
18. Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2α.
Cohen TV; Gnocchi VF; Cohen JE; Phadke A; Liu H; Ellis JA; Foisner R; Stewart CL; Zammit PS; Partridge TA
Hum Mol Genet; 2013 Jul; 22(14):2852-69. PubMed ID: 23535822
[TBL] [Abstract][Full Text] [Related]
19. Nuclear envelope proteins and neuromuscular diseases.
Ostlund C; Worman HJ
Muscle Nerve; 2003 Apr; 27(4):393-406. PubMed ID: 12661041
[TBL] [Abstract][Full Text] [Related]
20. Decreased mechanical stiffness in LMNA-/- cells is caused by defective nucleo-cytoskeletal integrity: implications for the development of laminopathies.
Broers JL; Peeters EA; Kuijpers HJ; Endert J; Bouten CV; Oomens CW; Baaijens FP; Ramaekers FC
Hum Mol Genet; 2004 Nov; 13(21):2567-80. PubMed ID: 15367494
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
