Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 98

1.

Differential temporal and spatial progerin expression during closure of the ductus arteriosus in neonates.

Bökenkamp R, Raz V, Venema A, DeRuiter MC, van Munsteren C, Olive M, Nabel EG, Gittenberger-de Groot AC.

PLoS One. 2011;6(9):e23975. doi: 10.1371/journal.pone.0023975. Epub 2011 Sep 6. Erratum in: PLoS One. 2011;6(9). doi: 10.1371/annotation/c0198e87-d087-444c-8be9-780adb1582be.

2.

Investigation of age-related changes in LMNA splicing and expression of progerin in human skeletal muscles.

Luo YB, Mitrpant C, Johnsen RD, Fabian VA, Fletcher S, Mastaglia FL, Wilton SD.

Int J Clin Exp Pathol. 2013 Nov 15;6(12):2778-86. eCollection 2013.

3.

Blocking farnesylation of the prelamin A variant in Hutchinson-Gilford progeria syndrome alters the distribution of A-type lamins.

Wang Y, Ostlund C, Choi JC, Swayne TC, Gundersen GG, Worman HJ.

Nucleus. 2012 Sep-Oct;3(5):452-62. doi: 10.4161/nucl.21675. Epub 2012 Aug 16.

4.

Investigation of splicing changes and post-translational processing of LMNA in sporadic inclusion body myositis.

Luo YB, Mitrpant C, Johnsen R, Fabian V, Needham M, Fletcher S, Wilton SD, Mastaglia FL.

Int J Clin Exp Pathol. 2013 Aug 15;6(9):1723-33. eCollection 2013.

5.

Absence of progeria-like disease phenotypes in knock-in mice expressing a non-farnesylated version of progerin.

Yang SH, Chang SY, Ren S, Wang Y, Andres DA, Spielmann HP, Fong LG, Young SG.

Hum Mol Genet. 2011 Feb 1;20(3):436-44. doi: 10.1093/hmg/ddq490. Epub 2010 Nov 18.

6.

Neonatal progeria: increased ratio of progerin to lamin A leads to progeria of the newborn.

Reunert J, Wentzell R, Walter M, Jakubiczka S, Zenker M, Brune T, Rust S, Marquardt T.

Eur J Hum Genet. 2012 Sep;20(9):933-7. doi: 10.1038/ejhg.2012.36. Epub 2012 Mar 14.

7.

Eliminating the synthesis of mature lamin A reduces disease phenotypes in mice carrying a Hutchinson-Gilford progeria syndrome allele.

Yang SH, Qiao X, Farber E, Chang SY, Fong LG, Young SG.

J Biol Chem. 2008 Mar 14;283(11):7094-9. doi: 10.1074/jbc.M708138200. Epub 2008 Jan 4.

8.

The truncated prelamin A in Hutchinson-Gilford progeria syndrome alters segregation of A-type and B-type lamin homopolymers.

Delbarre E, Tramier M, Coppey-Moisan M, Gaillard C, Courvalin JC, Buendia B.

Hum Mol Genet. 2006 Apr 1;15(7):1113-22. Epub 2006 Feb 15.

PMID:
16481358
9.
10.

Cytokeratin expression in human arteries pertinent to intimal thickening formation in the ductus arteriosus.

Slomp J, Gittenberger-de Groot AC, Koteliansky VE, Glukhova MA, Bogers AJ, Poelmann RE.

Differentiation. 1997 Aug;61(5):305-11.

PMID:
9342841
11.

Increasing the length of progerin's isoprenyl anchor does not worsen bone disease or survival in mice with Hutchinson-Gilford progeria syndrome.

Davies BS, Yang SH, Farber E, Lee R, Buck SB, Andres DA, Spielmann HP, Agnew BJ, Tamanoi F, Fong LG, Young SG.

J Lipid Res. 2009 Jan;50(1):126-34. doi: 10.1194/jlr.M800424-JLR200. Epub 2008 Aug 29.

12.

Identification of differential protein interactors of lamin A and progerin.

Kubben N, Voncken JW, Demmers J, Calis C, van Almen G, Pinto Y, Misteli T.

Nucleus. 2010 Nov-Dec;1(6):513-25. doi: 10.4161/nucl.1.6.13512. Epub 2010 Sep 3.

13.

Regulation of vascular tone and remodeling of the ductus arteriosus.

Yokoyama U, Minamisawa S, Ishikawa Y.

J Smooth Muscle Res. 2010;46(2):77-87. Review.

14.

Differentiation, dedifferentiation, and apoptosis of smooth muscle cells during the development of the human ductus arteriosus.

Slomp J, Gittenberger-de Groot AC, Glukhova MA, Conny van Munsteren J, Kockx MM, Schwartz SM, Koteliansky VE.

Arterioscler Thromb Vasc Biol. 1997 May;17(5):1003-9.

15.

Activating the synthesis of progerin, the mutant prelamin A in Hutchinson-Gilford progeria syndrome, with antisense oligonucleotides.

Fong LG, Vickers TA, Farber EA, Choi C, Yun UJ, Hu Y, Yang SH, Coffinier C, Lee R, Yin L, Davies BS, Andres DA, Spielmann HP, Bennett CF, Young SG.

Hum Mol Genet. 2009 Jul 1;18(13):2462-71. doi: 10.1093/hmg/ddp184. Epub 2009 Apr 17.

16.

A-type lamins and Hutchinson-Gilford progeria syndrome: pathogenesis and therapy.

Gonzalez JM, Pla D, Perez-Sala D, Andres V.

Front Biosci (Schol Ed). 2011 Jun 1;3:1133-46. Review.

PMID:
21622261
17.

Mapping of lamin A- and progerin-interacting genome regions.

Kubben N, Adriaens M, Meuleman W, Voncken JW, van Steensel B, Misteli T.

Chromosoma. 2012 Oct;121(5):447-64. doi: 10.1007/s00412-012-0376-7. Epub 2012 May 19.

18.

Nuclear localization signal deletion mutants of lamin A and progerin reveal insights into lamin A processing and emerin targeting.

Wu D, Flannery AR, Cai H, Ko E, Cao K.

Nucleus. 2014 Jan-Feb;5(1):66-74. doi: 10.4161/nucl.28068. Epub 2014 Feb 4.

19.

Defective extracellular pyrophosphate metabolism promotes vascular calcification in a mouse model of Hutchinson-Gilford progeria syndrome that is ameliorated on pyrophosphate treatment.

Villa-Bellosta R, Rivera-Torres J, Osorio FG, Acín-Pérez R, Enriquez JA, López-Otín C, Andrés V.

Circulation. 2013 Jun 18;127(24):2442-51. doi: 10.1161/CIRCULATIONAHA.112.000571. Epub 2013 May 20.

20.

A conserved splicing mechanism of the LMNA gene controls premature aging.

Lopez-Mejia IC, Vautrot V, De Toledo M, Behm-Ansmant I, Bourgeois CF, Navarro CL, Osorio FG, Freije JM, Stévenin J, De Sandre-Giovannoli A, Lopez-Otin C, Lévy N, Branlant C, Tazi J.

Hum Mol Genet. 2011 Dec 1;20(23):4540-55. doi: 10.1093/hmg/ddr385. Epub 2011 Aug 29.

PMID:
21875900

Supplemental Content

Support Center