324 related articles for article (PubMed ID: 11792809)
1. Properties of lamin A mutants found in Emery-Dreifuss muscular dystrophy, cardiomyopathy and Dunnigan-type partial lipodystrophy.
Ostlund C; Bonne G; Schwartz K; Worman HJ
J Cell Sci; 2001 Dec; 114(Pt 24):4435-45. PubMed ID: 11792809
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Expression of lamin A mutated in the carboxyl-terminal tail generates an aberrant nuclear phenotype similar to that observed in cells from patients with Dunnigan-type partial lipodystrophy and Emery-Dreifuss muscular dystrophy.
Favreau C; Dubosclard E; Ostlund C; Vigouroux C; Capeau J; Wehnert M; Higuet D; Worman HJ; Courvalin JC; Buendia B
Exp Cell Res; 2003 Jan; 282(1):14-23. PubMed ID: 12490190
[TBL] [Abstract][Full Text] [Related]
4. Effects of expressing lamin A mutant protein causing Emery-Dreifuss muscular dystrophy and familial partial lipodystrophy in HeLa cells.
Bechert K; Lagos-Quintana M; Harborth J; Weber K; Osborn M
Exp Cell Res; 2003 May; 286(1):75-86. PubMed ID: 12729796
[TBL] [Abstract][Full Text] [Related]
5. Effect of pathogenic mis-sense mutations in lamin A on its interaction with emerin in vivo.
Holt I; Ostlund C; Stewart CL; Man Nt; Worman HJ; Morris GE
J Cell Sci; 2003 Jul; 116(Pt 14):3027-35. PubMed ID: 12783988
[TBL] [Abstract][Full Text] [Related]
6. Both lamin A and lamin C mutations cause lamina instability as well as loss of internal nuclear lamin organization.
Broers JL; Kuijpers HJ; Ostlund C; Worman HJ; Endert J; Ramaekers FC
Exp Cell Res; 2005 Apr; 304(2):582-92. PubMed ID: 15748902
[TBL] [Abstract][Full Text] [Related]
7. Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery-Dreifuss muscular dystrophy.
Wang Y; Herron AJ; Worman HJ
Hum Mol Genet; 2006 Aug; 15(16):2479-89. PubMed ID: 16825283
[TBL] [Abstract][Full Text] [Related]
8. The R482Q lamin A/C mutation that causes lipodystrophy does not prevent nuclear targeting of lamin A in adipocytes or its interaction with emerin.
Holt I; Clements L; Manilal S; Brown SC; Morris GE
Eur J Hum Genet; 2001 Mar; 9(3):204-8. PubMed ID: 11313760
[TBL] [Abstract][Full Text] [Related]
9. Mutations in the LMNA gene encoding lamin A/C.
Genschel J; Schmidt HH
Hum Mutat; 2000 Dec; 16(6):451-9. PubMed ID: 11102973
[TBL] [Abstract][Full Text] [Related]
10. Identification of lamin A/C ( LMNA) gene mutations in Korean patients with autosomal dominant Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy 1B.
Ki CS; Hong JS; Jeong GY; Ahn KJ; Choi KM; Kim DK; Kim JW
J Hum Genet; 2002; 47(5):225-8. PubMed ID: 12032588
[TBL] [Abstract][Full Text] [Related]
11. Nuclear envelope proteins and associated diseases.
Nagano A; Arahata K
Curr Opin Neurol; 2000 Oct; 13(5):533-9. PubMed ID: 11073359
[TBL] [Abstract][Full Text] [Related]
12. Expression and localization of nuclear proteins in autosomal-dominant Emery-Dreifuss muscular dystrophy with LMNA R377H mutation.
Reichart B; Klafke R; Dreger C; Krüger E; Motsch I; Ewald A; Schäfer J; Reichmann H; Müller CR; Dabauvalle MC
BMC Cell Biol; 2004 Mar; 5():12. PubMed ID: 15053843
[TBL] [Abstract][Full Text] [Related]
13. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease.
Fatkin D; MacRae C; Sasaki T; Wolff MR; Porcu M; Frenneaux M; Atherton J; Vidaillet HJ; Spudich S; De Girolami U; Seidman JG; Seidman C; Muntoni F; Müehle G; Johnson W; McDonough B
N Engl J Med; 1999 Dec; 341(23):1715-24. PubMed ID: 10580070
[TBL] [Abstract][Full Text] [Related]
14. The cell cycle dependent mislocalisation of emerin may contribute to the Emery-Dreifuss muscular dystrophy phenotype.
Fairley EA; Riddell A; Ellis JA; Kendrick-Jones J
J Cell Sci; 2002 Jan; 115(Pt 2):341-54. PubMed ID: 11839786
[TBL] [Abstract][Full Text] [Related]
15. The role of the nuclear envelope in Emery-Dreifuss muscular dystrophy.
Morris GE
Trends Mol Med; 2001 Dec; 7(12):572-7. PubMed ID: 11733221
[TBL] [Abstract][Full Text] [Related]
16. Multisystem dystrophy syndrome due to novel missense mutations in the amino-terminal head and alpha-helical rod domains of the lamin A/C gene.
Garg A; Speckman RA; Bowcock AM
Am J Med; 2002 May; 112(7):549-55. PubMed ID: 12015247
[TBL] [Abstract][Full Text] [Related]
17. Emery-Dreifuss Muscular Dystrophy-Associated Mutant Forms of Lamin A Recruit the Stress Responsive Protein Ankrd2 into the Nucleus, Affecting the Cellular Response to Oxidative Stress.
Angori S; Capanni C; Faulkner G; Bean C; Boriani G; Lattanzi G; Cenni V
Cell Physiol Biochem; 2017; 42(1):169-184. PubMed ID: 28531892
[TBL] [Abstract][Full Text] [Related]
18. Lamins A and C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophy.
Motsch I; Kaluarachchi M; Emerson LJ; Brown CA; Brown SC; Dabauvalle MC; Ellis JA
Eur J Cell Biol; 2005 Sep; 84(9):765-81. PubMed ID: 16218190
[TBL] [Abstract][Full Text] [Related]
19. FHL1B Interacts with Lamin A/C and Emerin at the Nuclear Lamina and is Misregulated in Emery-Dreifuss Muscular Dystrophy.
Ziat E; Mamchaoui K; Beuvin M; Nelson I; Azibani F; Spuler S; Bonne G; Bertrand AT
J Neuromuscul Dis; 2016 Nov; 3(4):497-510. PubMed ID: 27911330
[TBL] [Abstract][Full Text] [Related]
20. Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease.
Jakobs PM; Hanson EL; Crispell KA; Toy W; Keegan H; Schilling K; Icenogle TB; Litt M; Hershberger RE
J Card Fail; 2001 Sep; 7(3):249-56. PubMed ID: 11561226
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]