Similar articles for PMID: 29618840

Year	Number of Results
1999	2
2000	2
2001	3
2002	2
2003	3
2004	4
2005	10
2006	9
2007	3
2008	8
2009	7
2010	2
2011	7
2012	8
2013	7
2014	3
2015	6
2016	4
2017	9
2018	10
2019	9
2020	20
2021	14
2022	7
2023	4
2024	0

1

SMAD6 overexpression leads to accelerated myogenic differentiation of LMNA mutated cells.

Janin A, Bauer D, Ratti F, Valla C, Bertrand A, Christin E, Chopin E, Streichenberger N, Bonne G, Gache V, Cohen T, Méjat A. Janin A, et al. Sci Rep. 2018 Apr 4;8(1):5618. doi: 10.1038/s41598-018-23918-x. Sci Rep. 2018. PMID: 29618840 Free PMC article.

2

Lamin A/C Assembly Defects in LMNA-Congenital Muscular Dystrophy Is Responsible for the Increased Severity of the Disease Compared with Emery-Dreifuss Muscular Dystrophy.

Bertrand AT, Brull A, Azibani F, Benarroch L, Chikhaoui K, Stewart CL, Medalia O, Ben Yaou R, Bonne G. Bertrand AT, et al. Cells. 2020 Mar 31;9(4):844. doi: 10.3390/cells9040844. Cells. 2020. PMID: 32244403 Free PMC article.

3

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. Cenni V, et al. J Med Genet. 2005 Mar;42(3):214-20. doi: 10.1136/jmg.2004.026112. J Med Genet. 2005. PMID: 15744034 Free PMC article.

4

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. Reichart B, et al. BMC Cell Biol. 2004 Mar 30;5:12. doi: 10.1186/1471-2121-5-12. BMC Cell Biol. 2004. PMID: 15053843 Free PMC article.

5

Elevated TGF β2 serum levels in Emery-Dreifuss Muscular Dystrophy: Implications for myocyte and tenocyte differentiation and fibrogenic processes.

Bernasconi P, Carboni N, Ricci G, Siciliano G, Politano L, Maggi L, Mongini T, Vercelli L, Rodolico C, Biagini E, Boriani G, Ruggiero L, Santoro L, Schena E, Prencipe S, Evangelisti C, Pegoraro E, Morandi L, Columbaro M, Lanzuolo C, Sabatelli P, Cavalcante P, Cappelletti C, Bonne G, Muchir A, Lattanzi G. Bernasconi P, et al. Nucleus. 2018 Jan 1;9(1):292-304. doi: 10.1080/19491034.2018.1467722. Nucleus. 2018. PMID: 29693488 Free PMC article.

6

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. Ziat E, et al. J Neuromuscul Dis. 2016 Nov 29;3(4):497-510. doi: 10.3233/JND-160169. J Neuromuscul Dis. 2016. PMID: 27911330

7

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. Cohen TV, et al. Hum Mol Genet. 2013 Jul 15;22(14):2852-69. doi: 10.1093/hmg/ddt135. Epub 2013 Mar 27. Hum Mol Genet. 2013. PMID: 23535822 Free PMC article.

8

THE ROLE OF LMNA MUTATIONS IN MYOGENIC DIFFERENTIATION OF PRIMARY SATELLITE CELLS AND C2C12 CELLS.

Perepelina KI, Smolina NA, Zabirnik AS, Dmitrieva RI, Malashicheva AB, Kostareva AA. Perepelina KI, et al. Tsitologiia. 2017;59(2):117-24. Tsitologiia. 2017. PMID: 30199159 English, Russian.

9

Impaired nuclear functions lead to increased senescence and inefficient differentiation in human myoblasts with a dominant p.R545C mutation in the LMNA gene.

Kandert S, Wehnert M, Müller CR, Buendia B, Dabauvalle MC. Kandert S, et al. Eur J Cell Biol. 2009 Oct;88(10):593-608. doi: 10.1016/j.ejcb.2009.06.002. Epub 2009 Jul 8. Eur J Cell Biol. 2009. PMID: 19589617

10

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. Favreau C, et al. Exp Cell Res. 2003 Jan 1;282(1):14-23. doi: 10.1006/excr.2002.5669. Exp Cell Res. 2003. PMID: 12490190

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