254 related articles for article (PubMed ID: 11709282)
1. The A-type lamins: nuclear structural proteins as a focus for muscular dystrophy and cardiovascular diseases.
Mounkes LC; Burke B; Stewart CL
Trends Cardiovasc Med; 2001 Oct; 11(7):280-5. PubMed ID: 11709282
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifuss muscular dystrophy.
Brown CA; Lanning RW; McKinney KQ; Salvino AR; Cherniske E; Crowe CA; Darras BT; Gominak S; Greenberg CR; Grosmann C; Heydemann P; Mendell JR; Pober BR; Sasaki T; Shapiro F; Simpson DA; Suchowersky O; Spence JE
Am J Med Genet; 2001 Sep; 102(4):359-67. PubMed ID: 11503164
[TBL] [Abstract][Full Text] [Related]
5. The nuclear envelope in muscular dystrophy and cardiovascular diseases.
Burke B; Mounkes LC; Stewart CL
Traffic; 2001 Oct; 2(10):675-83. PubMed ID: 11576443
[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. The nuclear muscular dystrophies.
Wehnert MS; Bonne G
Semin Pediatr Neurol; 2002 Jun; 9(2):100-7. PubMed ID: 12138994
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophy.
van der Kooi AJ; Bonne G; Eymard B; Duboc D; Talim B; Van der Valk M; Reiss P; Richard P; Demay L; Merlini L; Schwartz K; Busch HF; de Visser M
Neurology; 2002 Aug; 59(4):620-3. PubMed ID: 12196663
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy.
Sullivan T; Escalante-Alcalde D; Bhatt H; Anver M; Bhat N; Nagashima K; Stewart CL; Burke B
J Cell Biol; 1999 Nov; 147(5):913-20. PubMed ID: 10579712
[TBL] [Abstract][Full Text] [Related]
12. Characterization of adiposity and metabolism in Lmna-deficient mice.
Cutler DA; Sullivan T; Marcus-Samuels B; Stewart CL; Reitman ML
Biochem Biophys Res Commun; 2002 Mar; 291(3):522-7. PubMed ID: 11855819
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy.
Bonne G; Di Barletta MR; Varnous S; Bécane HM; Hammouda EH; Merlini L; Muntoni F; Greenberg CR; Gary F; Urtizberea JA; Duboc D; Fardeau M; Toniolo D; Schwartz K
Nat Genet; 1999 Mar; 21(3):285-8. PubMed ID: 10080180
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Lamin A/C and emerin are critical for skeletal muscle satellite cell differentiation.
Frock RL; Kudlow BA; Evans AM; Jameson SA; Hauschka SD; Kennedy BK
Genes Dev; 2006 Feb; 20(4):486-500. PubMed ID: 16481476
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene.
Bonne G; Mercuri E; Muchir A; Urtizberea A; Bécane HM; Recan D; Merlini L; Wehnert M; Boor R; Reuner U; Vorgerd M; Wicklein EM; Eymard B; Duboc D; Penisson-Besnier I; Cuisset JM; Ferrer X; Desguerre I; Lacombe D; Bushby K; Pollitt C; Toniolo D; Fardeau M; Schwartz K; Muntoni F
Ann Neurol; 2000 Aug; 48(2):170-80. PubMed ID: 10939567
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
