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Items: 1 to 20 of 59

1.

A ceRNA analysis on LMNA gene focusing on the Hutchinson-Gilford progeria syndrome.

Arancio W, Giordano C, Pizzolanti G.

J Clin Bioinforma. 2013 Jan 14;3(1):2. doi: 10.1186/2043-9113-3-2.

2.

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.

3.

Hutchinson-Gilford progeria syndrome.

Pollex RL, Hegele RA.

Clin Genet. 2004 Nov;66(5):375-81. Review.

PMID:
15479179
5.
6.

Identification of novel RNA isoforms of LMNA.

DeBoy E, Puttaraju M, Jailwala P, Kasoji M, Cam M, Misteli T.

Nucleus. 2017 Sep 3;8(5):573-582. doi: 10.1080/19491034.2017.1348449. Epub 2017 Aug 31.

PMID:
28857661
7.

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
8.
9.
10.

Hutchinson-Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literature.

Mazereeuw-Hautier J, Wilson LC, Mohammed S, Smallwood D, Shackleton S, Atherton DJ, Harper JI.

Br J Dermatol. 2007 Jun;156(6):1308-14. Epub 2007 Apr 25. Review.

PMID:
17459035
11.
12.

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.

13.

Progeroid syndrome with scleroderma-like skin changes associated with homozygous R435C LMNA mutation.

Madej-Pilarczyk A, Rosińska-Borkowska D, Rekawek J, Marchel M, Szaluś E, Jabłońska S, Hausmanowa-Petrusewicz I.

Am J Med Genet A. 2009 Nov;149A(11):2387-92. doi: 10.1002/ajmg.a.33018.

PMID:
19842191
14.
15.

Low and high expressing alleles of the LMNA gene: implications for laminopathy disease development.

Rodríguez S, Eriksson M.

PLoS One. 2011;6(9):e25472. doi: 10.1371/journal.pone.0025472. Epub 2011 Sep 29.

16.

Hutchinson-Gilford progeria syndrome: review of the phenotype.

Hennekam RC.

Am J Med Genet A. 2006 Dec 1;140(23):2603-24. Review.

PMID:
16838330
17.
18.

[The role of lamins and mutations of LMNA gene in physiological and premature aging].

Sliwińska MA.

Postepy Biochem. 2007;53(1):46-52. Review. Polish.

PMID:
17718387
19.

Progeria: a new kind of Laminopathy-- report of the First European Symposium on Progeria and creation of EURO-Progeria, a European Consortium on Progeria and related disorders.

Brune T, Bonne G, Denecke J, Elcioglu N, Hennekam RC, Marquardt T, Ozgen H, Stamsnijder M, Steichen E, Steinmann B, Wehnert M, Levy N.

Pediatr Endocrinol Rev. 2004 Sep;2(1):39-45.

PMID:
16429102
20.

Mutations in the mouse Lmna gene causing progeria, muscular dystrophy and cardiomyopathy.

Kozlov S, Mounkes L, Cutler D, Sullivan T, Hernandez L, Levy N, Rottman J, Stewart CL.

Novartis Found Symp. 2005;264:246-58; discussion 258-63. Review.

PMID:
15773758

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