Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 175

1.

Emerin binding to Btf, a death-promoting transcriptional repressor, is disrupted by a missense mutation that causes Emery-Dreifuss muscular dystrophy.

Haraguchi T, Holaska JM, Yamane M, Koujin T, Hashiguchi N, Mori C, Wilson KL, Hiraoka Y.

Eur J Biochem. 2004 Mar;271(5):1035-45.

PMID:
15009215
2.

Distinct functional domains in emerin bind lamin A and DNA-bridging protein BAF.

Lee KK, Haraguchi T, Lee RS, Koujin T, Hiraoka Y, Wilson KL.

J Cell Sci. 2001 Dec;114(Pt 24):4567-73.

3.
4.

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.

5.

Transcriptional repressor germ cell-less (GCL) and barrier to autointegration factor (BAF) compete for binding to emerin in vitro.

Holaska JM, Lee KK, Kowalski AK, Wilson KL.

J Biol Chem. 2003 Feb 28;278(9):6969-75. Epub 2002 Dec 18.

6.

The Emery-Dreifuss muscular dystrophy phenotype arises from aberrant targeting and binding of emerin at the inner nuclear membrane.

Fairley EA, Kendrick-Jones J, Ellis JA.

J Cell Sci. 1999 Aug;112 ( Pt 15):2571-82. Erratum in: J Cell Sci 1999 Dec;112(Pt 24):following 4800.

7.

BAF is required for emerin assembly into the reforming nuclear envelope.

Haraguchi T, Koujin T, Segura-Totten M, Lee KK, Matsuoka Y, Yoneda Y, Wilson KL, Hiraoka Y.

J Cell Sci. 2001 Dec;114(Pt 24):4575-85.

8.

How does a g993t mutation in the emerin gene cause Emery-Dreifuss muscular dystrophy?

Holt I, Clements L, Manilal S, Morris GE.

Biochem Biophys Res Commun. 2001 Oct 12;287(5):1129-33.

PMID:
11587540
9.

Unusual expression of emerin in a patient with X-linked Emery-Dreifuss muscular dystrophy.

Di Blasi C, Morandi L, Raffaele di Barletta M, Bione S, Bernasconi P, Cerletti M, Bono R, Blasevich F, Toniolo D, Mora M.

Neuromuscul Disord. 2000 Dec;10(8):567-71.

PMID:
11053683
10.

Lmo7 is an emerin-binding protein that regulates the transcription of emerin and many other muscle-relevant genes.

Holaska JM, Rais-Bahrami S, Wilson KL.

Hum Mol Genet. 2006 Dec 1;15(23):3459-72. Epub 2006 Oct 26.

PMID:
17067998
11.

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. Epub 2007 Mar 30.

PMID:
17462627
12.

Effect of pathogenic mis-sense mutations in lamin A on its interaction with emerin in vivo.

Holt I, Ostlund C, Stewart CL, Man Nt, Worman HJ, Morris GE.

J Cell Sci. 2003 Jul 15;116(Pt 14):3027-35. Epub 2003 Jun 3.

13.

Distinct regions specify the nuclear membrane targeting of emerin, the responsible protein for Emery-Dreifuss muscular dystrophy.

Tsuchiya Y, Hase A, Ogawa M, Yorifuji H, Arahata K.

Eur J Biochem. 1999 Feb;259(3):859-65.

14.

Changes at P183 of emerin weaken its protein-protein interactions resulting in X-linked Emery-Dreifuss muscular dystrophy.

Ellis JA, Yates JR, Kendrick-Jones J, Brown CA.

Hum Genet. 1999 Mar;104(3):262-8.

PMID:
10323252
15.

MAN1 and emerin have overlapping function(s) essential for chromosome segregation and cell division in Caenorhabditis elegans.

Liu J, Lee KK, Segura-Totten M, Neufeld E, Wilson KL, Gruenbaum Y.

Proc Natl Acad Sci U S A. 2003 Apr 15;100(8):4598-603. Epub 2003 Apr 8.

16.

Structural analysis of emerin, an inner nuclear membrane protein mutated in X-linked Emery-Dreifuss muscular dystrophy.

Wolff N, Gilquin B, Courchay K, Callebaut I, Worman HJ, Zinn-Justin S.

FEBS Lett. 2001 Jul 20;501(2-3):171-6.

17.

Immunocytochemistry of nuclear domains and Emery-Dreifuss muscular dystrophy pathophysiology.

Maraldi NM, Lattanzi G, Sabatelli P, Ognibene A, Columbaro M, Capanni C, Rutigliano C, Mattioli E, Squarzoni S.

Eur J Histochem. 2003;47(1):3-16. Review.

PMID:
12685553
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.

PMID:
10469836
19.

Emerin interacts in vitro with the splicing-associated factor, YT521-B.

Wilkinson FL, Holaska JM, Zhang Z, Sharma A, Manilal S, Holt I, Stamm S, Wilson KL, Morris GE.

Eur J Biochem. 2003 Jun;270(11):2459-66.

20.

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

Supplemental Content

Support Center