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Results: 1 to 20 of 118

1.

Primary laminopathy fibroblasts display altered genome organization and apoptosis.

Meaburn KJ, Cabuy E, Bonne G, Levy N, Morris GE, Novelli G, Kill IR, Bridger JM.

Aging Cell. 2007 Apr;6(2):139-53. Epub 2007 Feb 5.

PMID:
17274801
[PubMed - indexed for MEDLINE]
Free Article
2.

Chromosome positioning is largely unaffected in lymphoblastoid cell lines containing emerin or A-type lamin mutations.

Meaburn KJ, Levy N, Toniolo D, Bridger JM.

Biochem Soc Trans. 2005 Dec;33(Pt 6):1438-40.

PMID:
16246140
[PubMed - indexed for MEDLINE]
3.

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.

PMID:
11792810
[PubMed - indexed for MEDLINE]
Free Article
4.

Nuclear envelope proteins and chromatin arrangement: a pathogenic mechanism for laminopathies.

Maraldi NM, Lattanzi G, Capanni C, Columbaro M, Merlini L, Mattioli E, Sabatelli P, Squarzoni S, Manzoli FA.

Eur J Histochem. 2006 Jan-Mar;50(1):1-8. Review.

PMID:
16584978
[PubMed - indexed for MEDLINE]
5.

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 1;282(1):14-23.

PMID:
12490190
[PubMed - indexed for MEDLINE]
6.

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 29;68(22):1883-94.

PMID:
17536044
[PubMed - indexed for MEDLINE]
7.

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 30;5:12.

PMID:
15053843
[PubMed - indexed for MEDLINE]
Free PMC Article
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.

PMID:
11792809
[PubMed - indexed for MEDLINE]
Free Article
9.

Emery-Dreifuss muscular dystrophy.

Muchir A, Worman HJ.

Curr Neurol Neurosci Rep. 2007 Jan;7(1):78-83. Review.

PMID:
17217858
[PubMed - indexed for MEDLINE]
10.

Nesprin-1 and -2 are involved in the pathogenesis of Emery Dreifuss muscular dystrophy and are critical for nuclear envelope integrity.

Zhang Q, Bethmann C, Worth NF, Davies JD, Wasner C, Feuer A, Ragnauth CD, Yi Q, Mellad JA, Warren DT, Wheeler MA, Ellis JA, Skepper JN, Vorgerd M, Schlotter-Weigel B, Weissberg PL, Roberts RG, Wehnert M, Shanahan CM.

Hum Mol Genet. 2007 Dec 1;16(23):2816-33. Epub 2007 Aug 29.

PMID:
17761684
[PubMed - indexed for MEDLINE]
Free Article
11.

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. Epub 2006 Feb 14.

PMID:
16478798
[PubMed - indexed for MEDLINE]
Free Article
12.

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 15;115(Pt 2):341-54.

PMID:
11839786
[PubMed - indexed for MEDLINE]
Free Article
13.

[Structural organization and function of nuclear envelope].

Gubanova NV, Kiseleva EV.

Tsitologiia. 2007;49(4):257-69. Review. Russian.

PMID:
17657938
[PubMed - indexed for MEDLINE]
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. doi: 10.1016/j.bbadis.2012.01.014. Epub 2012 Feb 3.

PMID:
22326558
[PubMed - indexed for MEDLINE]
Free Article
15.

Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations.

Muchir A, Medioni J, Laluc M, Massart C, Arimura T, van der Kooi AJ, Desguerre I, Mayer M, Ferrer X, Briault S, Hirano M, Worman HJ, Mallet A, Wehnert M, Schwartz K, Bonne G.

Muscle Nerve. 2004 Oct;30(4):444-50.

PMID:
15372542
[PubMed - indexed for MEDLINE]
16.

The role of the nuclear envelope in Emery-Dreifuss muscular dystrophy.

Morris GE.

Trends Mol Med. 2001 Dec;7(12):572-7.

PMID:
11733221
[PubMed - indexed for MEDLINE]
17.

Heart to heart: from nuclear proteins to Emery-Dreifuss muscular dystrophy.

Morris GE, Manilal S.

Hum Mol Genet. 1999;8(10):1847-51. Review.

PMID:
10469836
[PubMed - indexed for MEDLINE]
Free Article
18.

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 15;286(1):75-86.

PMID:
12729796
[PubMed - indexed for MEDLINE]
19.

Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in Japan.

Astejada MN, Goto K, Nagano A, Ura S, Noguchi S, Nonaka I, Nishino I, Hayashi YK.

Acta Myol. 2007 Dec;26(3):159-64. Review.

PMID:
18646565
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Emerin and the nuclear lamina in muscle and cardiac disease.

Holaska JM.

Circ Res. 2008 Jul 3;103(1):16-23. doi: 10.1161/CIRCRESAHA.108.172197. Review.

PMID:
18596264
[PubMed - indexed for MEDLINE]
Free Article
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