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Items: 1 to 20 of 125

1.

Structural alterations of Lamin A protein in dilated cardiomyopathy.

Bhattacharjee P, Banerjee A, Banerjee A, Dasgupta D, Sengupta K.

Biochemistry. 2013 Jun 18;52(24):4229-41. doi: 10.1021/bi400337t. Epub 2013 Jun 5.

PMID:
23701190
2.

Viscoelastic behavior of human lamin A proteins in the context of dilated cardiomyopathy.

Banerjee A, Rathee V, Krishnaswamy R, Bhattacharjee P, Ray P, Sood AK, Sengupta K.

PLoS One. 2013 Dec 30;8(12):e83410. doi: 10.1371/journal.pone.0083410. eCollection 2013.

3.

Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicity.

Cattin ME, Bertrand AT, Schlossarek S, Le Bihan MC, Skov Jensen S, Neuber C, Crocini C, Maron S, Lainé J, Mougenot N, Varnous S, Fromes Y, Hansen A, Eschenhagen T, Decostre V, Carrier L, Bonne G.

Hum Mol Genet. 2013 Aug 1;22(15):3152-64. doi: 10.1093/hmg/ddt172. Epub 2013 Apr 10.

4.
5.

The LMNA mutation p.Arg321Ter associated with dilated cardiomyopathy leads to reduced expression and a skewed ratio of lamin A and lamin C proteins.

Al-Saaidi R, Rasmussen TB, Palmfeldt J, Nissen PH, Beqqali A, Hansen J, Pinto YM, Boesen T, Mogensen J, Bross P.

Exp Cell Res. 2013 Nov 15;319(19):3010-9. doi: 10.1016/j.yexcr.2013.08.024. Epub 2013 Aug 31.

PMID:
24001739
6.

A comparative study of Drosophila and human A-type lamins.

Schulze SR, Curio-Penny B, Speese S, Dialynas G, Cryderman DE, McDonough CW, Nalbant D, Petersen M, Budnik V, Geyer PK, Wallrath LL.

PLoS One. 2009 Oct 26;4(10):e7564. doi: 10.1371/journal.pone.0007564.

7.

Mutation Glu82Lys in lamin A/C gene is associated with cardiomyopathy and conduction defect.

Wang H, Wang J, Zheng W, Wang X, Wang S, Song L, Zou Y, Yao Y, Hui R.

Biochem Biophys Res Commun. 2006 May 26;344(1):17-24.

PMID:
16630578
8.

Thymopoietin (lamina-associated polypeptide 2) gene mutation associated with dilated cardiomyopathy.

Taylor MR, Slavov D, Gajewski A, Vlcek S, Ku L, Fain PR, Carniel E, Di Lenarda A, Sinagra G, Boucek MM, Cavanaugh J, Graw SL, Ruegg P, Feiger J, Zhu X, Ferguson DA, Bristow MR, Gotzmann J, Foisner R, Mestroni L; Familial Cardiomyopathy Registry Research Group.

Hum Mutat. 2005 Dec;26(6):566-74.

PMID:
16247757
9.

Laminopathy-inducing lamin A mutants can induce redistribution of lamin binding proteins into nuclear aggregates.

Hübner S, Eam JE, Hübner A, Jans DA.

Exp Cell Res. 2006 Jan 15;312(2):171-83. Epub 2005 Nov 14.

PMID:
16289535
10.

Incomplete nonsense-mediated decay of mutant lamin A/C mRNA provokes dilated cardiomyopathy and ventricular tachycardia.

Geiger SK, Bär H, Ehlermann P, Wälde S, Rutschow D, Zeller R, Ivandic BT, Zentgraf H, Katus HA, Herrmann H, Weichenhan D.

J Mol Med (Berl). 2008 Mar;86(3):281-9. Epub 2007 Nov 7.

PMID:
17987279
11.

Myopathic lamin mutations impair nuclear stability in cells and tissue and disrupt nucleo-cytoskeletal coupling.

Zwerger M, Jaalouk DE, Lombardi ML, Isermann P, Mauermann M, Dialynas G, Herrmann H, Wallrath LL, Lammerding J.

Hum Mol Genet. 2013 Jun 15;22(12):2335-49. doi: 10.1093/hmg/ddt079. Epub 2013 Feb 19.

12.

The lamin CxxM motif promotes nuclear membrane growth.

Prüfert K, Vogel A, Krohne G.

J Cell Sci. 2004 Dec 1;117(Pt 25):6105-16. Epub 2004 Nov 16.

13.

Crystal structure of the human lamin A coil 2B dimer: implications for the head-to-tail association of nuclear lamins.

Strelkov SV, Schumacher J, Burkhard P, Aebi U, Herrmann H.

J Mol Biol. 2004 Oct 29;343(4):1067-80.

PMID:
15476822
14.

In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patients.

Sylvius N, Bilinska ZT, Veinot JP, Fidzianska A, Bolongo PM, Poon S, McKeown P, Davies RA, Chan KL, Tang AS, Dyack S, Grzybowski J, Ruzyllo W, McBride H, Tesson F.

J Med Genet. 2005 Aug;42(8):639-47.

15.

Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice.

Nikolova V, Leimena C, McMahon AC, Tan JC, Chandar S, Jogia D, Kesteven SH, Michalicek J, Otway R, Verheyen F, Rainer S, Stewart CL, Martin D, Feneley MP, Fatkin D.

J Clin Invest. 2004 Feb;113(3):357-69.

16.

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.

17.
18.

Nesprin-1 and actin contribute to nuclear and cytoskeletal defects in lamin A/C-deficient cardiomyopathy.

Nikolova-Krstevski V, Leimena C, Xiao XH, Kesteven S, Tan JC, Yeo LS, Yu ZY, Zhang Q, Carlton A, Head S, Shanahan C, Feneley MP, Fatkin D.

J Mol Cell Cardiol. 2011 Mar;50(3):479-86. doi: 10.1016/j.yjmcc.2010.12.001. Epub 2010 Dec 13.

PMID:
21156181
19.

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
20.

Both lamin A and lamin C mutations cause lamina instability as well as loss of internal nuclear lamin organization.

Broers JL, Kuijpers HJ, Ostlund C, Worman HJ, Endert J, Ramaekers FC.

Exp Cell Res. 2005 Apr 1;304(2):582-92. Epub 2004 Dec 20.

PMID:
15748902
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