Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 202

1.

Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice.

Puckelwartz MJ, Kessler E, Zhang Y, Hodzic D, Randles KN, Morris G, Earley JU, Hadhazy M, Holaska JM, Mewborn SK, Pytel P, McNally EM.

Hum Mol Genet. 2009 Feb 15;18(4):607-20. doi: 10.1093/hmg/ddn386.

2.

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.

3.

Distinct functional domains in nesprin-1alpha and nesprin-2beta bind directly to emerin and both interactions are disrupted in X-linked Emery-Dreifuss muscular dystrophy.

Wheeler MA, Davies JD, Zhang Q, Emerson LJ, Hunt J, Shanahan CM, Ellis JA.

Exp Cell Res. 2007 Aug 1;313(13):2845-57.

PMID:
17462627
4.

Nesprin 1 is critical for nuclear positioning and anchorage.

Zhang J, Felder A, Liu Y, Guo LT, Lange S, Dalton ND, Gu Y, Peterson KL, Mizisin AP, Shelton GD, Lieber RL, Chen J.

Hum Mol Genet. 2010 Jan 15;19(2):329-41. doi: 10.1093/hmg/ddp499.

5.

LINC complex alterations in DMD and EDMD/CMT fibroblasts.

Taranum S, Vaylann E, Meinke P, Abraham S, Yang L, Neumann S, Karakesisoglou I, Wehnert M, Noegel AA.

Eur J Cell Biol. 2012 Aug;91(8):614-28. doi: 10.1016/j.ejcb.2012.03.003.

6.

Nesprin-2 is a multi-isomeric protein that binds lamin and emerin at the nuclear envelope and forms a subcellular network in skeletal muscle.

Zhang Q, Ragnauth CD, Skepper JN, Worth NF, Warren DT, Roberts RG, Weissberg PL, Ellis JA, Shanahan CM.

J Cell Sci. 2005 Feb 15;118(Pt 4):673-87.

7.

Nesprins: tissue-specific expression of epsilon and other short isoforms.

Duong NT, Morris GE, Lam le T, Zhang Q, Sewry CA, Shanahan CM, Holt I.

PLoS One. 2014 Apr 9;9(4):e94380. doi: 10.1371/journal.pone.0094380.

8.

LINC complexes in health and disease.

Méjat A, Misteli T.

Nucleus. 2010 Jan-Feb;1(1):40-52. doi: 10.4161/nucl.1.1.10530. Review.

9.

Dynamics and molecular interactions of linker of nucleoskeleton and cytoskeleton (LINC) complex proteins.

Ostlund C, Folker ES, Choi JC, Gomes ER, Gundersen GG, Worman HJ.

J Cell Sci. 2009 Nov 15;122(Pt 22):4099-108. doi: 10.1242/jcs.057075.

10.

Mutations in LMNA modulate the lamin A--Nesprin-2 interaction and cause LINC complex alterations.

Yang L, Munck M, Swaminathan K, Kapinos LE, Noegel AA, Neumann S.

PLoS One. 2013 Aug 20;8(8):e71850. doi: 10.1371/journal.pone.0071850.

11.

Reinforcing the LINC complex connection to actin filaments: the role of FHOD1 in TAN line formation and nuclear movement.

Antoku S, Zhu R, Kutscheidt S, Fackler OT, Gundersen GG.

Cell Cycle. 2015;14(14):2200-5. doi: 10.1080/15384101.2015.1053665.

12.

Emery-Dreifuss muscular dystrophy at the nuclear envelope: 10 years on.

Ellis JA.

Cell Mol Life Sci. 2006 Dec;63(23):2702-9. Review.

PMID:
17013557
13.

Mammalian SUN protein interaction networks at the inner nuclear membrane and their role in laminopathy disease processes.

Haque F, Mazzeo D, Patel JT, Smallwood DT, Ellis JA, Shanahan CM, Shackleton S.

J Biol Chem. 2010 Jan 29;285(5):3487-98. doi: 10.1074/jbc.M109.071910.

14.

Linker of nucleoskeleton and cytoskeleton (LINC) complex-mediated actin-dependent nuclear positioning orients centrosomes in migrating myoblasts.

Chang W, Antoku S, Östlund C, Worman HJ, Gundersen GG.

Nucleus. 2015;6(1):77-88. doi: 10.1080/19491034.2015.1004947.

15.

Nesprin-2 Giant (NUANCE) maintains nuclear envelope architecture and composition in skin.

Lüke Y, Zaim H, Karakesisoglou I, Jaeger VM, Sellin L, Lu W, Schneider M, Neumann S, Beijer A, Munck M, Padmakumar VC, Gloy J, Walz G, Noegel AA.

J Cell Sci. 2008 Jun 1;121(11):1887-98. doi: 10.1242/jcs.019075.

16.

Contribution of SUN1 mutations to the pathomechanism in muscular dystrophies.

Li P, Meinke P, Huong le TT, Wehnert M, Noegel AA.

Hum Mutat. 2014 Apr;35(4):452-61. doi: 10.1002/humu.22504.

PMID:
24375709
17.

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.

18.

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

Morris GE, Manilal S.

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

19.

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.

20.

The nuclear envelope, muscular dystrophy and gene expression.

Wilson KL.

Trends Cell Biol. 2000 Apr;10(4):125-9. Review.

PMID:
10740265
Items per page

Supplemental Content

Support Center