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Items: 1 to 20 of 57

1.

An in vitro enzymatic assay coupled to proteomics analysis reveals a new DNA processing activity for Ewing sarcoma and TAF(II)68 proteins.

Guipaud O, Guillonneau F, Labas V, Praseuth D, Rossier J, Lopez B, Bertrand P.

Proteomics. 2006 Nov;6(22):5962-72.

PMID:
17106916
2.

Oncoprotein EWS-FLI1 activity is enhanced by RNA helicase A.

Toretsky JA, Erkizan V, Levenson A, Abaan OD, Parvin JD, Cripe TP, Rice AM, Lee SB, Uren A.

Cancer Res. 2006 Jun 1;66(11):5574-81.

3.

Lamin A-dependent nuclear defects in human aging.

Scaffidi P, Misteli T.

Science. 2006 May 19;312(5776):1059-63. Epub 2006 Apr 27.

4.

EWS-ETS oncoproteins: the linchpins of Ewing tumors.

Janknecht R.

Gene. 2005 Dec 19;363:1-14. Epub 2005 Oct 3. Review.

PMID:
16202544
5.

SPO11 is required for sex-body formation, and Spo11 heterozygosity rescues the prophase arrest of Atm-/- spermatocytes.

Bellani MA, Romanienko PJ, Cairatti DA, Camerini-Otero RD.

J Cell Sci. 2005 Aug 1;118(Pt 15):3233-45. Epub 2005 Jul 5.

6.

Stimulation of Oct-4 activity by Ewing's sarcoma protein.

Lee J, Rhee BK, Bae GY, Han YM, Kim J.

Stem Cells. 2005 Jun-Jul;23(6):738-51.

7.
8.

DNA repair, genome stability, and aging.

Lombard DB, Chua KF, Mostoslavsky R, Franco S, Gostissa M, Alt FW.

Cell. 2005 Feb 25;120(4):497-512. Review.

9.

Aging and nuclear organization: lamins and progeria.

Mounkes LC, Stewart CL.

Curr Opin Cell Biol. 2004 Jun;16(3):322-7. Review.

PMID:
15145358
10.
11.

Disruption of spermatogenesis in mice lacking A-type lamins.

Alsheimer M, Liebe B, Sewell L, Stewart CL, Scherthan H, Benavente R.

J Cell Sci. 2004 Mar 1;117(Pt 7):1173-8.

12.

LMNA mutations in atypical Werner's syndrome.

Bonne G, Levy N.

Lancet. 2003 Nov 8;362(9395):1585-6; author reply 1586. No abstract available.

PMID:
14615129
13.

LMNA mutations in atypical Werner's syndrome.

Vigouroux C, Caux F, Capeau J, Christin-Maitre S, Cohen A.

Lancet. 2003 Nov 8;362(9395):1585; author reply 1586. No abstract available.

PMID:
14615128
14.

LMNA mutations in atypical Werner's syndrome.

Chen L, Lee L, Kudlow BA, Dos Santos HG, Sletvold O, Shafeghati Y, Botha EG, Garg A, Hanson NB, Martin GM, Mian IS, Kennedy BK, Oshima J.

Lancet. 2003 Aug 9;362(9382):440-5.

PMID:
12927431
15.

Acute mutation of retinoblastoma gene function is sufficient for cell cycle re-entry.

Sage J, Miller AL, Pérez-Mancera PA, Wysocki JM, Jacks T.

Nature. 2003 Jul 10;424(6945):223-8.

PMID:
12853964
16.

A progeroid syndrome in mice is caused by defects in A-type lamins.

Mounkes LC, Kozlov S, Hernandez L, Sullivan T, Stewart CL.

Nature. 2003 May 15;423(6937):298-301.

PMID:
12748643
17.

Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome.

Eriksson M, Brown WT, Gordon LB, Glynn MW, Singer J, Scott L, Erdos MR, Robbins CM, Moses TY, Berglund P, Dutra A, Pak E, Durkin S, Csoka AB, Boehnke M, Glover TW, Collins FS.

Nature. 2003 May 15;423(6937):293-8. Epub 2003 Apr 25.

18.

Lamin a truncation in Hutchinson-Gilford progeria.

De Sandre-Giovannoli A, Bernard R, Cau P, Navarro C, Amiel J, Boccaccio I, Lyonnet S, Stewart CL, Munnich A, Le Merrer M, Lévy N.

Science. 2003 Jun 27;300(5628):2055. Epub 2003 Apr 17. No abstract available.

19.

Proto-oncoprotein TLS/FUS is associated to the nuclear matrix and complexed with splicing factors PTB, SRm160, and SR proteins.

Meissner M, Lopato S, Gotzmann J, Sauermann G, Barta A.

Exp Cell Res. 2003 Feb 15;283(2):184-95.

PMID:
12581738
20.

Cooperative interaction of EWS with CREB-binding protein selectively activates hepatocyte nuclear factor 4-mediated transcription.

Araya N, Hirota K, Shimamoto Y, Miyagishi M, Yoshida E, Ishida J, Kaneko S, Kaneko M, Nakajima T, Fukamizu A.

J Biol Chem. 2003 Feb 14;278(7):5427-32. Epub 2002 Nov 28.

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