PMC Links for Nucleotide (Select 365906263) - PMC

Select item 20923901.

The Mutant Form of Lamin A that Causes Hutchinson-Gilford Progeria Is a Biomarker of Cellular Aging in Human Skin

Dayle McClintock, Desiree Ratner, Meepa Lokuge, David M. Owens, Leslie B. Gordon, Francis S. Collins, Karima Djabali

PLoS One. 2007; 2(12): e1269. Published online 2007 Dec 5. doi: 10.1371/journal.pone.0001269

PMCID:: PMC2092390

Abstract Article PDF–804K

Select item 18552502.

Lamin A-Dependent Nuclear Defects in Human Aging

Paola Scaffidi, Tom Misteli

Science. Author manuscript; available in PMC 2007 Apr 24.

Published in final edited form as: Science. 2006 May 19; 312(5776): 1059–1063. Published online 2006 Apr 27. doi: 10.1126/science.1127168

PMCID:: PMC1855250

Abstract Article PDF–1.2M

Select item 64605653.

Assessment of fibroblast nuclear morphology aids interpretation of LMNA variants

Florence H. J. van Tienen, Patrick J. Lindsey, Miriam A. F. Kamps, Ingrid P. Krapels, Frans C. S. Ramaekers, Han G. Brunner, Arthur van den Wijngaard, Jos L. V. Broers

Eur J Hum Genet. 2019 Mar; 27(3): 389–399. Published online 2018 Nov 12. doi: 10.1038/s41431-018-0294-0

PMCID:: PMC6460565

Abstract Article PDF–1.0M

Select item 42875744.

Mandibuloacral dysplasia type A-associated progeria caused by homozygous LMNA mutation in a family from Southern China

Di-Qing Luo, Xiao-Zhu Wang, Yan Meng, Ding-Yang He, Ying-Ming Chen, Zhi-Yong Ke, Ming Yan, Yu Huang, Da-Fang Chen

BMC Pediatr. 2014; 14: 256. Published online 2014 Oct 7. doi: 10.1186/1471-2431-14-256

PMCID:: PMC4287574

Abstract Article PDF–1.7M

Select item 42446135.

Importance of genetic evaluation and testing in pediatric cardiomyopathy

Muhammad Tariq, Stephanie M Ware

World J Cardiol. 2014 Nov 26; 6(11): 1156–1165. Published online 2014 Nov 26. doi: 10.4330/wjc.v6.i11.1156

PMCID:: PMC4244613

Abstract Article PDF–899K

Select item 34933366.

Influenza A H3N2 subtype virus NS1 protein targets into the nucleus and binds primarily via its C-terminal NLS2/NoLS to nucleolin and fibrillarin

Krister Melén, Janne Tynell, Riku Fagerlund, Pascal Roussel, Danièle Hernandez-Verdun, Ilkka Julkunen

Virol J. 2012; 9: 167. Published online 2012 Aug 21. doi: 10.1186/1743-422X-9-167

PMCID:: PMC3493336

Abstract Article PDF–2.9M

Select item 27813007.

Automated DNA mutation detection using universal conditions direct sequencing: application to ten muscular dystrophy genes

Richard R Bennett, Hal E Schneider, Elicia Estrella, Stephanie Burgess, Andrew S Cheng, Caitlin Barrett, Va Lip, Poh San Lai, Yiping Shen, Bai-Lin Wu, Basil T Darras, Alan H Beggs, Louis M Kunkel

BMC Genet. 2009; 10: 66. Published online 2009 Oct 18. doi: 10.1186/1471-2156-10-66

PMCID:: PMC2781300

Abstract Article PDF–698K

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