436 related articles for article (PubMed ID: 33396724)
1. 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]
2. 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]
3. Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1B.
Park YE; Hayashi YK; Goto K; Komaki H; Hayashi Y; Inuzuka T; Noguchi S; Nonaka I; Nishino I
Neuromuscul Disord; 2009 Jan; 19(1):29-36. PubMed ID: 19070492
[TBL] [Abstract][Full Text] [Related]
4. Clinical spectrum and genetic variations of
Fan Y; Tan D; Song D; Zhang X; Chang X; Wang Z; Zhang C; Chan SH; Wu Q; Wu L; Wang S; Yan H; Ge L; Yang H; Mao B; Bönnemann C; Liu J; Wang S; Yuan Y; Wu X; Zhang H; Xiong H
J Med Genet; 2021 May; 58(5):326-333. PubMed ID: 32571898
[TBL] [Abstract][Full Text] [Related]
5. Lamin A/C-mediated neuromuscular junction defects in Emery-Dreifuss muscular dystrophy.
Méjat A; Decostre V; Li J; Renou L; Kesari A; Hantaï D; Stewart CL; Xiao X; Hoffman E; Bonne G; Misteli T
J Cell Biol; 2009 Jan; 184(1):31-44. PubMed ID: 19124654
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery-Dreifuss muscular dystrophy.
Cenni V; Sabatelli P; Mattioli E; Marmiroli S; Capanni C; Ognibene A; Squarzoni S; Maraldi NM; Bonne G; Columbaro M; Merlini L; Lattanzi G
J Med Genet; 2005 Mar; 42(3):214-20. PubMed ID: 15744034
[TBL] [Abstract][Full Text] [Related]
8. Importance and challenge of making an early diagnosis in LMNA-related muscular dystrophy.
Menezes MP; Waddell LB; Evesson FJ; Cooper S; Webster R; Jones K; Mowat D; Kiernan MC; Johnston HM; Corbett A; Harbord M; North KN; Clarke NF
Neurology; 2012 Apr; 78(16):1258-63. PubMed ID: 22491857
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Novel LMNA mutations in patients with Emery-Dreifuss muscular dystrophy and functional characterization of four LMNA mutations.
Scharner J; Brown CA; Bower M; Iannaccone ST; Khatri IA; Escolar D; Gordon E; Felice K; Crowe CA; Grosmann C; Meriggioli MN; Asamoah A; Gordon O; Gnocchi VF; Ellis JA; Mendell JR; Zammit PS
Hum Mutat; 2011 Feb; 32(2):152-67. PubMed ID: 20848652
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Multitissular involvement in a family with LMNA and EMD mutations: Role of digenic mechanism?
Ben Yaou R; Toutain A; Arimura T; Demay L; Massart C; Peccate C; Muchir A; Llense S; Deburgrave N; Leturcq F; Litim KE; Rahmoun-Chiali N; Richard P; Babuty D; Récan-Budiartha D; Bonne G
Neurology; 2007 May; 68(22):1883-94. PubMed ID: 17536044
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Lamin Mutations Cause Increased YAP Nuclear Entry in Muscle Stem Cells.
Owens DJ; Fischer M; Jabre S; Moog S; Mamchaoui K; Butler-Browne G; Coirault C
Cells; 2020 Mar; 9(4):. PubMed ID: 32231000
[TBL] [Abstract][Full Text] [Related]
16. Muscle Magnetic Resonance Imaging in Patients with Various Clinical Subtypes of
Lin HT; Liu X; Zhang W; Liu J; Zuo YH; Xiao JX; Zhu Y; Yuan Y; Wang ZX
Chin Med J (Engl); 2018 Jun; 131(12):1472-1479. PubMed ID: 29893365
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Muscle imaging analogies in a cohort of patients with different clinical phenotypes caused by LMNA gene mutations.
Carboni N; Mura M; Marrosu G; Cocco E; Marini S; Solla E; Mateddu A; Maioli MA; Piras R; Mallarini G; Mercuro G; Porcu M; Marrosu MG
Muscle Nerve; 2010 Apr; 41(4):458-63. PubMed ID: 19882644
[TBL] [Abstract][Full Text] [Related]
20. Phenotype-Genotype Analysis of Chinese Patients with Early-Onset LMNA-Related Muscular Dystrophy.
Tan D; Yang H; Yuan Y; Bonnemann C; Chang X; Wang S; Wu Y; Wu X; Xiong H
PLoS One; 2015; 10(6):e0129699. PubMed ID: 26098624
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
