These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

269 related articles for article (PubMed ID: 25283634)

  • 1. Do lamin A and lamin C have unique roles?
    Al-Saaidi R; Bross P
    Chromosoma; 2015 Mar; 124(1):1-12. PubMed ID: 25283634
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of novel RNA isoforms of LMNA.
    DeBoy E; Puttaraju M; Jailwala P; Kasoji M; Cam M; Misteli T
    Nucleus; 2017 Sep; 8(5):573-582. PubMed ID: 28857661
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Normal and aberrant splicing of LMNA.
    Luo YB; Mastaglia FL; Wilton SD
    J Med Genet; 2014 Apr; 51(4):215-23. PubMed ID: 24459210
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prelamin A and lamin A appear to be dispensable in the nuclear lamina.
    Fong LG; Ng JK; Lammerding J; Vickers TA; Meta M; Coté N; Gavino B; Qiao X; Chang SY; Young SR; Yang SH; Stewart CL; Lee RT; Bennett CF; Bergo MO; Young SG
    J Clin Invest; 2006 Mar; 116(3):743-52. PubMed ID: 16511604
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Increased expression of the Hutchinson-Gilford progeria syndrome truncated lamin A transcript during cell aging.
    Rodriguez S; Coppedè F; Sagelius H; Eriksson M
    Eur J Hum Genet; 2009 Jul; 17(7):928-37. PubMed ID: 19172989
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [The role of lamins and mutations of LMNA gene in physiological and premature aging].
    Sliwińska MA
    Postepy Biochem; 2007; 53(1):46-52. PubMed ID: 17718387
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Antagonistic functions of LMNA isoforms in energy expenditure and lifespan.
    Lopez-Mejia IC; de Toledo M; Chavey C; Lapasset L; Cavelier P; Lopez-Herrera C; Chebli K; Fort P; Beranger G; Fajas L; Amri EZ; Casas F; Tazi J
    EMBO Rep; 2014 May; 15(5):529-39. PubMed ID: 24639560
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hutchinson-Gilford progeria syndrome.
    Pollex RL; Hegele RA
    Clin Genet; 2004 Nov; 66(5):375-81. PubMed ID: 15479179
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Lamins A and C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophy.
    Motsch I; Kaluarachchi M; Emerson LJ; Brown CA; Brown SC; Dabauvalle MC; Ellis JA
    Eur J Cell Biol; 2005 Sep; 84(9):765-81. PubMed ID: 16218190
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutations in the LMNA gene encoding lamin A/C.
    Genschel J; Schmidt HH
    Hum Mutat; 2000 Dec; 16(6):451-9. PubMed ID: 11102973
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Investigation of age-related changes in LMNA splicing and expression of progerin in human skeletal muscles.
    Luo YB; Mitrpant C; Johnsen RD; Fabian VA; Fletcher S; Mastaglia FL; Wilton SD
    Int J Clin Exp Pathol; 2013; 6(12):2778-86. PubMed ID: 24294364
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The LMNA mutation p.Arg321Ter associated with dilated cardiomyopathy leads to reduced expression and a skewed ratio of lamin A and lamin C proteins.
    Al-Saaidi R; Rasmussen TB; Palmfeldt J; Nissen PH; Beqqali A; Hansen J; Pinto YM; Boesen T; Mogensen J; Bross P
    Exp Cell Res; 2013 Nov; 319(19):3010-9. PubMed ID: 24001739
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [A-type lamins and progeroïd syndromes : persistent farnesylation with dramatic effects].
    Navarro CL; Poitelon Y; Lévy N
    Med Sci (Paris); 2008 Oct; 24(10):833-40. PubMed ID: 18950579
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Nuclear envelope remodelling during human spermiogenesis involves somatic B-type lamins and a spermatid-specific B3 lamin isoform.
    Elkhatib R; Longepied G; Paci M; Achard V; Grillo JM; Levy N; Mitchell MJ; Metzler-Guillemain C
    Mol Hum Reprod; 2015 Mar; 21(3):225-36. PubMed ID: 25477337
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Myopathic lamin mutations cause reductive stress and activate the nrf2/keap-1 pathway.
    Dialynas G; Shrestha OK; Ponce JM; Zwerger M; Thiemann DA; Young GH; Moore SA; Yu L; Lammerding J; Wallrath LL
    PLoS Genet; 2015 May; 11(5):e1005231. PubMed ID: 25996830
    [TBL] [Abstract][Full Text] [Related]  

  • 16. LMNA rs4641 and the muscle lamin A and C isoforms in twins--metabolic implications and transcriptional regulation.
    Wegner L; Anthonsen S; Bork-Jensen J; Dalgaard L; Hansen T; Pedersen O; Poulsen P; Vaag A
    J Clin Endocrinol Metab; 2010 Aug; 95(8):3884-92. PubMed ID: 20501691
    [TBL] [Abstract][Full Text] [Related]  

  • 17. LMNA Mutation c.917T>G (p.L306R) Leads to Deleterious Hyper-Assembly of Lamin A/C and Associates with Severe Right Ventricular Cardiomyopathy and Premature Aging.
    Alastalo TP; West G; Li SP; Keinänen A; Helenius M; Tyni T; Lapatto R; Turanlahti M; Heikkilä P; Kääriäinen H; Laakso M; Mauermann M; Herrmann H; Pihkala J; Taimen P
    Hum Mutat; 2015 Jul; 36(7):694-703. PubMed ID: 25820511
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The muscle dystrophy-causing ΔK32 lamin A/C mutant does not impair the functions of the nucleoplasmic lamin-A/C-LAP2α complex in mice.
    Pilat U; Dechat T; Bertrand AT; Woisetschläger N; Gotic I; Spilka R; Biadasiewicz K; Bonne G; Foisner R
    J Cell Sci; 2013 Apr; 126(Pt 8):1753-62. PubMed ID: 23444379
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Juvenile-onset generalized lipodystrophy due to a novel heterozygous missense LMNA mutation affecting lamin C.
    Patni N; Xing C; Agarwal AK; Garg A
    Am J Med Genet A; 2017 Sep; 173(9):2517-2521. PubMed ID: 28686329
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Altered splicing in prelamin A-associated premature aging phenotypes.
    De Sandre-Giovannoli A; Lévy N
    Prog Mol Subcell Biol; 2006; 44():199-232. PubMed ID: 17076270
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.