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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2000 1
2001 2
2002 3
2003 7
2004 14
2005 18
2006 18
2007 19
2008 23
2009 14
2010 26
2011 16
2012 17
2013 19
2014 10
2015 13
2016 14
2017 17
2018 27
2019 20
2020 16
2021 18
2022 16
2023 7
2024 0

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Similar articles for PMID: 16061563

310 results

Results by year

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Page 1
High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics.
van Tintelen JP, Hofstra RM, Katerberg H, Rossenbacker T, Wiesfeld AC, du Marchie Sarvaas GJ, Wilde AA, van Langen IM, Nannenberg EA, van der Kooi AJ, Kraak M, van Gelder IC, van Veldhuisen DJ, Vos Y, van den Berg MP; Working Group on Inherited Cardiac Disorders, line 27/50, Interuniversity Cardiology Institute of The Netherlands. van Tintelen JP, et al. Am Heart J. 2007 Dec;154(6):1130-9. doi: 10.1016/j.ahj.2007.07.038. Epub 2007 Sep 14. Am Heart J. 2007. PMID: 18035086
Thymopoietin (lamina-associated polypeptide 2) gene mutation associated with dilated cardiomyopathy.
Taylor MR, Slavov D, Gajewski A, Vlcek S, Ku L, Fain PR, Carniel E, Di Lenarda A, Sinagra G, Boucek MM, Cavanaugh J, Graw SL, Ruegg P, Feiger J, Zhu X, Ferguson DA, Bristow MR, Gotzmann J, Foisner R, Mestroni L; Familial Cardiomyopathy Registry Research Group. Taylor MR, et al. Hum Mutat. 2005 Dec;26(6):566-74. doi: 10.1002/humu.20250. Hum Mutat. 2005. PMID: 16247757
Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption.
Gupta P, Bilinska ZT, Sylvius N, Boudreau E, Veinot JP, Labib S, Bolongo PM, Hamza A, Jackson T, Ploski R, Walski M, Grzybowski J, Walczak E, Religa G, Fidzianska A, Tesson F. Gupta P, et al. Basic Res Cardiol. 2010 May;105(3):365-77. doi: 10.1007/s00395-010-0085-4. Epub 2010 Feb 3. Basic Res Cardiol. 2010. PMID: 20127487 Free PMC article.
Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicity.
Cattin ME, Bertrand AT, Schlossarek S, Le Bihan MC, Skov Jensen S, Neuber C, Crocini C, Maron S, Lainé J, Mougenot N, Varnous S, Fromes Y, Hansen A, Eschenhagen T, Decostre V, Carrier L, Bonne G. Cattin ME, et al. Hum Mol Genet. 2013 Aug 1;22(15):3152-64. doi: 10.1093/hmg/ddt172. Epub 2013 Apr 10. Hum Mol Genet. 2013. PMID: 23575224 Free article.
310 results