Similar articles for PMID: 22065502

Year	Number of Results
2003	3
2004	1
2005	9
2006	6
2007	5
2008	5
2009	9
2010	2
2011	20
2012	9
2013	10
2014	17
2015	7
2016	8
2017	9
2018	8
2019	4
2020	6
2021	7
2022	15
2023	4
2024	1

1

Coronary artery disease in a Werner syndrome-like form of progeria characterized by low levels of progerin, a splice variant of lamin A.

Hisama FM, Lessel D, Leistritz D, Friedrich K, McBride KL, Pastore MT, Gottesman GS, Saha B, Martin GM, Kubisch C, Oshima J. Hisama FM, et al. Am J Med Genet A. 2011 Dec;155A(12):3002-6. doi: 10.1002/ajmg.a.34336. Epub 2011 Nov 7. Am J Med Genet A. 2011. PMID: 22065502 Free PMC article.

2

Increased progerin expression associated with unusual LMNA mutations causes severe progeroid syndromes.

Moulson CL, Fong LG, Gardner JM, Farber EA, Go G, Passariello A, Grange DK, Young SG, Miner JH. Moulson CL, et al. Hum Mutat. 2007 Sep;28(9):882-9. doi: 10.1002/humu.20536. Hum Mutat. 2007. PMID: 17469202

3

LMNA mutations in progeroid syndromes.

Huang S, Kennedy BK, Oshima J. Huang S, et al. Novartis Found Symp. 2005;264:197-202; discussion 202-7, 227-30. Novartis Found Symp. 2005. PMID: 15773755 Review.

4

Differential stem cell aging kinetics in Hutchinson-Gilford progeria syndrome and Werner syndrome.

Wu Z, Zhang W, Song M, Wang W, Wei G, Li W, Lei J, Huang Y, Sang Y, Chan P, Chen C, Qu J, Suzuki K, Belmonte JCI, Liu GH. Wu Z, et al. Protein Cell. 2018 Apr;9(4):333-350. doi: 10.1007/s13238-018-0517-8. Epub 2018 Feb 23. Protein Cell. 2018. PMID: 29476423 Free PMC article.

5

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. Fong LG, et al. Hum Mol Genet. 2009 Jul 1;18(13):2462-71. doi: 10.1093/hmg/ddp184. Epub 2009 Apr 17. Hum Mol Genet. 2009. PMID: 19376814 Free PMC article.

6

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. Lopez-Mejia IC, et al. Hum Mol Genet. 2011 Dec 1;20(23):4540-55. doi: 10.1093/hmg/ddr385. Epub 2011 Aug 29. Hum Mol Genet. 2011. PMID: 21875900

7

An inherited LMNA gene mutation in atypical Progeria syndrome.

Doubaj Y, De Sandre-Giovannoli A, Vera EV, Navarro CL, Elalaoui SC, Tajir M, Lévy N, Sefiani A. Doubaj Y, et al. Am J Med Genet A. 2012 Nov;158A(11):2881-7. doi: 10.1002/ajmg.a.35557. Epub 2012 Sep 18. Am J Med Genet A. 2012. PMID: 22991222

8

Epigenetic involvement in Hutchinson-Gilford progeria syndrome: a mini-review.

Arancio W, Pizzolanti G, Genovese SI, Pitrone M, Giordano C. Arancio W, et al. Gerontology. 2014;60(3):197-203. doi: 10.1159/000357206. Epub 2014 Feb 28. Gerontology. 2014. PMID: 24603298 Free article. Review.

9

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. Reunert J, et al. Eur J Hum Genet. 2012 Sep;20(9):933-7. doi: 10.1038/ejhg.2012.36. Epub 2012 Mar 14. Eur J Hum Genet. 2012. PMID: 22419169 Free PMC article.

10

Cellular stress and AMPK activation as a common mechanism of action linking the effects of metformin and diverse compounds that alleviate accelerated aging defects in Hutchinson-Gilford progeria syndrome.

Finley J. Finley J. Med Hypotheses. 2018 Sep;118:151-162. doi: 10.1016/j.mehy.2018.06.029. Epub 2018 Jun 28. Med Hypotheses. 2018. PMID: 30037605

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