These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
201 related articles for article (PubMed ID: 31220270)
1. Alteration of performance in a mouse model of Emery-Dreifuss muscular dystrophy caused by A-type lamins gene mutation. Thomasson R; Vignier N; Peccate C; Mougenot N; Noirez P; Muchir A Hum Mol Genet; 2019 Jul; 28(13):2237-2244. PubMed ID: 31220270 [TBL] [Abstract][Full Text] [Related]
2. Inhibition of extracellular signal-regulated kinase 1/2 signaling has beneficial effects on skeletal muscle in a mouse model of Emery-Dreifuss muscular dystrophy caused by lamin A/C gene mutation. Muchir A; Kim YJ; Reilly SA; Wu W; Choi JC; Worman HJ Skelet Muscle; 2013 Jul; 3(1):17. PubMed ID: 23815988 [TBL] [Abstract][Full Text] [Related]
3. Emerin deficiency does not exacerbate cardiomyopathy in a murine model of Emery-Dreifuss muscular dystrophy caused by an LMNA gene mutation. Wada E; Matsumoto K; Susumu N; Kato M; Hayashi YK J Physiol Sci; 2023 Nov; 73(1):27. PubMed ID: 37940872 [TBL] [Abstract][Full Text] [Related]
4. Activation of MAPK in hearts of EMD null mice: similarities between mouse models of X-linked and autosomal dominant Emery Dreifuss muscular dystrophy. Muchir A; Pavlidis P; Bonne G; Hayashi YK; Worman HJ Hum Mol Genet; 2007 Aug; 16(15):1884-95. PubMed ID: 17567779 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Clinical aspects of Emery-Dreifuss muscular dystrophy. Madej-Pilarczyk A Nucleus; 2018 Jan; 9(1):268-274. PubMed ID: 29633897 [TBL] [Abstract][Full Text] [Related]
8. Inhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins. Muchir A; Shan J; Bonne G; Lehnart SE; Worman HJ Hum Mol Genet; 2009 Jan; 18(2):241-7. PubMed ID: 18927124 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Cardiac effects of the c.1583 C→G LMNA mutation in two families with Emery-Dreifuss muscular dystrophy. Zhang L; Shen H; Zhao Z; Bing Q; Hu J Mol Med Rep; 2015 Oct; 12(4):5065-71. PubMed ID: 26165385 [TBL] [Abstract][Full Text] [Related]
14. [The first Japanese case of autosomal dominant Emery-Dreifuss muscular dystrophy with a novel mutation in the lamin A/C gene]. Onishi Y; Higuchi J; Ogawa T; Namekawa A; Hayashi H; Odakura H; Goto K; Hayashi YK Rinsho Shinkeigaku; 2002 Feb; 42(2):140-4. PubMed ID: 12424964 [TBL] [Abstract][Full Text] [Related]