PubMed (OMIM) for id: 4000

Year	Number of Results
1886	1
1923	1
1946	1
1949	1
1952	1
1960	2
1961	4
1962	2
1963	1
1964	2
1965	1
1966	1
1967	1
1969	1
1970	2
1971	3
1972	1
1973	1
1974	4
1975	6
1977	1
1978	1
1979	2
1980	3
1981	3
1982	2
1983	1
1984	4
1985	2
1986	10
1987	7
1988	5
1989	4
1990	4
1991	4
1992	3
1993	3
1994	2
1995	3
1996	5
1997	3
1998	3
1999	7
2000	14
2001	8
2002	7
2003	16
2004	13
2005	25
2006	18
2007	16
2008	14
2009	8
2010	7
2011	7
2012	6
2013	7
2014	3
2015	2
2016	2
2017	2
2018	1
2019	2
2022	1
2024	0

1

Abolishing the prelamin A ZMPSTE24 cleavage site leads to progeroid phenotypes with near-normal longevity in mice.

Wang Y, Shilagardi K, Hsu T, Odinammadu KO, Maruyama T, Wu W, Lin CS, Damoci CB, Spear ED, Shin JY, Hsu W, Michaelis S, Worman HJ. Wang Y, et al. Proc Natl Acad Sci U S A. 2022 Mar 1;119(9):e2118695119. doi: 10.1073/pnas.2118695119. Proc Natl Acad Sci U S A. 2022. PMID: 35197292 Free PMC article.

2

Activation of PDGF pathway links LMNA mutation to dilated cardiomyopathy.

Lee J, Termglinchan V, Diecke S, Itzhaki I, Lam CK, Garg P, Lau E, Greenhaw M, Seeger T, Wu H, Zhang JZ, Chen X, Gil IP, Ameen M, Sallam K, Rhee JW, Churko JM, Chaudhary R, Chour T, Wang PJ, Snyder MP, Chang HY, Karakikes I, Wu JC. Lee J, et al. Nature. 2019 Aug;572(7769):335-340. doi: 10.1038/s41586-019-1406-x. Epub 2019 Jul 17. Nature. 2019. PMID: 31316208 Free PMC article.

3

Alteration of performance in a mouse model of Emery-Dreifuss muscular dystrophy caused by A-type lamins gene mutation.

Thomasson R, Vignier N, Peccate C, Mougenot N, Noirez P, Muchir A. Thomasson R, et al. Hum Mol Genet. 2019 Jul 1;28(13):2237-2244. doi: 10.1093/hmg/ddz056. Hum Mol Genet. 2019. PMID: 31220270 Free article.

4

229th ENMC international workshop: Limb girdle muscular dystrophies - Nomenclature and reformed classification Naarden, the Netherlands, 17-19 March 2017.

Straub V, Murphy A, Udd B; LGMD workshop study group. Straub V, et al. Neuromuscul Disord. 2018 Aug;28(8):702-710. doi: 10.1016/j.nmd.2018.05.007. Epub 2018 May 24. Neuromuscul Disord. 2018. PMID: 30055862 No abstract available.

5

A novel somatic mutation achieves partial rescue in a child with Hutchinson-Gilford progeria syndrome.

Bar DZ, Arlt MF, Brazier JF, Norris WE, Campbell SE, Chines P, Larrieu D, Jackson SP, Collins FS, Glover TW, Gordon LB. Bar DZ, et al. J Med Genet. 2017 Mar;54(3):212-216. doi: 10.1136/jmedgenet-2016-104295. Epub 2016 Dec 5. J Med Genet. 2017. PMID: 27920058 Free PMC article.

6

Heart-hand syndrome IV: a second family with LMNA-related cardiomyopathy and brachydactyly.

Zaragoza MV, Hakim SA, Hoang V, Elliott AM. Zaragoza MV, et al. Clin Genet. 2017 Mar;91(3):499-500. doi: 10.1111/cge.12870. Epub 2016 Oct 10. Clin Genet. 2017. PMID: 27723096 Free PMC article.

7

Truncated prelamin A expression in HGPS-like patients: a transcriptional study.

Barthélémy F, Navarro C, Fayek R, Da Silva N, Roll P, Sigaudy S, Oshima J, Bonne G, Papadopoulou-Legbelou K, Evangeliou AE, Spilioti M, Lemerrer M, Wevers RA, Morava E, Robaglia-Schlupp A, Lévy N, Bartoli M, De Sandre-Giovannoli A. Barthélémy F, et al. Eur J Hum Genet. 2015 Aug;23(8):1051-61. doi: 10.1038/ejhg.2014.239. Epub 2015 Feb 4. Eur J Hum Genet. 2015. PMID: 25649378 Free PMC article.

8

The p.R482W substitution in A-type lamins deregulates SREBP1 activity in Dunnigan-type familial partial lipodystrophy.

Vadrot N, Duband-Goulet I, Cabet E, Attanda W, Barateau A, Vicart P, Gerbal F, Briand N, Vigouroux C, Oldenburg AR, Lund EG, Collas P, Buendia B. Vadrot N, et al. Hum Mol Genet. 2015 Apr 1;24(7):2096-109. doi: 10.1093/hmg/ddu728. Epub 2014 Dec 18. Hum Mol Genet. 2015. PMID: 25524705

9

Chemical inhibition of NAT10 corrects defects of laminopathic cells.

Larrieu D, Britton S, Demir M, Rodriguez R, Jackson SP. Larrieu D, et al. Science. 2014 May 2;344(6183):527-32. doi: 10.1126/science.1252651. Science. 2014. PMID: 24786082 Free PMC article.

10

New Lmna knock-in mice provide a molecular mechanism for the 'segmental aging' in Hutchinson-Gilford progeria syndrome.

Jung HJ, Tu Y, Yang SH, Tatar A, Nobumori C, Wu D, Young SG, Fong LG. Jung HJ, et al. Hum Mol Genet. 2014 Mar 15;23(6):1506-15. doi: 10.1093/hmg/ddt537. Epub 2013 Nov 7. Hum Mol Genet. 2014. PMID: 24203701 Free PMC article.

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