Similar articles for PMID: 30199159

Year	Number of Results
1999	1
2000	2
2002	2
2003	3
2004	5
2005	9
2006	9
2007	3
2008	8
2009	4
2010	1
2011	5
2012	4
2013	6
2014	2
2015	5
2016	5
2017	4
2018	6
2019	4
2020	9
2021	4
2022	1
2023	1
2024	0

1

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.

2

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.

3

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.

4

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. Park YE, et al. Neuromuscul Disord. 2009 Jan;19(1):29-36. doi: 10.1016/j.nmd.2008.09.018. Epub 2008 Dec 12. Neuromuscul Disord. 2009. PMID: 19070492

5

Laminopathies disrupt epigenomic developmental programs and cell fate.

Perovanovic J, Dell'Orso S, Gnochi VF, Jaiswal JK, Sartorelli V, Vigouroux C, Mamchaoui K, Mouly V, Bonne G, Hoffman EP. Perovanovic J, et al. Sci Transl Med. 2016 Apr 20;8(335):335ra58. doi: 10.1126/scitranslmed.aad4991. Sci Transl Med. 2016. PMID: 27099177 Free PMC article.

6

Does satellite cell dysfunction contribute to disease progression in Emery-Dreifuss muscular dystrophy?

Gnocchi VF, Ellis JA, Zammit PS. Gnocchi VF, et al. Biochem Soc Trans. 2008 Dec;36(Pt 6):1344-9. doi: 10.1042/BST0361344. Biochem Soc Trans. 2008. PMID: 19021553 Review.

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

Expression of the myodystrophic R453W mutation of lamin A in C2C12 myoblasts causes promoter-specific and global epigenetic defects.

Håkelien AM, Delbarre E, Gaustad KG, Buendia B, Collas P. Håkelien AM, et al. Exp Cell Res. 2008 May 1;314(8):1869-80. doi: 10.1016/j.yexcr.2008.02.018. Epub 2008 Mar 7. Exp Cell Res. 2008. PMID: 18396274

9

LMNA Mutations G232E and R482L Cause Dysregulation of Skeletal Muscle Differentiation, Bioenergetics, and Metabolic Gene Expression Profile.

Ignatieva EV, Ivanova OA, Komarova MY, Khromova NV, Polev DE, Kostareva AA, Sergushichev A, Dmitrieva RI. Ignatieva EV, et al. Genes (Basel). 2020 Sep 7;11(9):1057. doi: 10.3390/genes11091057. Genes (Basel). 2020. PMID: 32906763 Free PMC article.

10

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. Bonne G, et al. Ann Neurol. 2000 Aug;48(2):170-80. Ann Neurol. 2000. PMID: 10939567

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