BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

438 related articles for article (PubMed ID: 15773755)

  • 1. LMNA mutations in progeroid syndromes.
    Huang S; Kennedy BK; Oshima J
    Novartis Found Symp; 2005; 264():197-202; discussion 202-7, 227-30. PubMed ID: 15773755
    [TBL] [Abstract][Full Text] [Related]  

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

  • 3. A homozygous ZMPSTE24 null mutation in combination with a heterozygous mutation in the LMNA gene causes Hutchinson-Gilford progeria syndrome (HGPS): insights into the pathophysiology of HGPS.
    Denecke J; Brune T; Feldhaus T; Robenek H; Kranz C; Auchus RJ; Agarwal AK; Marquardt T
    Hum Mutat; 2006 Jun; 27(6):524-31. PubMed ID: 16671095
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hutchinson-Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literature.
    Mazereeuw-Hautier J; Wilson LC; Mohammed S; Smallwood D; Shackleton S; Atherton DJ; Harper JI
    Br J Dermatol; 2007 Jun; 156(6):1308-14. PubMed ID: 17459035
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Incomplete processing of mutant lamin A in Hutchinson-Gilford progeria leads to nuclear abnormalities, which are reversed by farnesyltransferase inhibition.
    Glynn MW; Glover TW
    Hum Mol Genet; 2005 Oct; 14(20):2959-69. PubMed ID: 16126733
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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
    Protein Cell; 2018 Apr; 9(4):333-350. PubMed ID: 29476423
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Nuclear deformation characterizes Werner syndrome cells.
    Adelfalk C; Scherthan H; Hirsch-Kauffmann M; Schweiger M
    Cell Biol Int; 2005 Dec; 29(12):1032-7. PubMed ID: 16314120
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease.
    Sagelius H; Rosengardten Y; Hanif M; Erdos MR; Rozell B; Collins FS; Eriksson M
    J Cell Sci; 2008 Apr; 121(Pt 7):969-78. PubMed ID: 18334552
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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
    Am J Med Genet A; 2011 Dec; 155A(12):3002-6. PubMed ID: 22065502
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Search and insights into novel genetic alterations leading to classical and atypical Werner syndrome.
    Oshima J; Hisama FM
    Gerontology; 2014; 60(3):239-46. PubMed ID: 24401204
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Reversible phenotype in a mouse model of Hutchinson-Gilford progeria syndrome.
    Sagelius H; Rosengardten Y; Schmidt E; Sonnabend C; Rozell B; Eriksson M
    J Med Genet; 2008 Dec; 45(12):794-801. PubMed ID: 18708427
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genome-scale expression profiling of Hutchinson-Gilford progeria syndrome reveals widespread transcriptional misregulation leading to mesodermal/mesenchymal defects and accelerated atherosclerosis.
    Csoka AB; English SB; Simkevich CP; Ginzinger DG; Butte AJ; Schatten GP; Rothman FG; Sedivy JM
    Aging Cell; 2004 Aug; 3(4):235-43. PubMed ID: 15268757
    [TBL] [Abstract][Full Text] [Related]  

  • 13. p.S143F mutation in lamin A/C: a new phenotype combining myopathy and progeria.
    Kirschner J; Brune T; Wehnert M; Denecke J; Wasner C; Feuer A; Marquardt T; Ketelsen UP; Wieacker P; Bönnemann CG; Korinthenberg R
    Ann Neurol; 2005 Jan; 57(1):148-51. PubMed ID: 15622532
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic alterations in accelerated ageing syndromes. Do they play a role in natural ageing?
    Puzianowska-Kuznicka M; Kuznicki J
    Int J Biochem Cell Biol; 2005 May; 37(5):947-60. PubMed ID: 15743670
    [TBL] [Abstract][Full Text] [Related]  

  • 15. HGPS and related premature aging disorders: from genomic identification to the first therapeutic approaches.
    Pereira S; Bourgeois P; Navarro C; Esteves-Vieira V; Cau P; De Sandre-Giovannoli A; Lévy N
    Mech Ageing Dev; 2008; 129(7-8):449-59. PubMed ID: 18513784
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Telomere length in Hutchinson-Gilford progeria syndrome.
    Decker ML; Chavez E; Vulto I; Lansdorp PM
    Mech Ageing Dev; 2009 Jun; 130(6):377-83. PubMed ID: 19428457
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Aging and nuclear organization: lamins and progeria.
    Mounkes LC; Stewart CL
    Curr Opin Cell Biol; 2004 Jun; 16(3):322-7. PubMed ID: 15145358
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [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]  

  • 19. A progeroid syndrome in mice is caused by defects in A-type lamins.
    Mounkes LC; Kozlov S; Hernandez L; Sullivan T; Stewart CL
    Nature; 2003 May; 423(6937):298-301. PubMed ID: 12748643
    [TBL] [Abstract][Full Text] [Related]  

  • 20. LMNA mutation in progeroid syndrome in association with strokes.
    Gonzalez-Quereda L; Delgadillo V; Juan-Mateu J; Verdura E; Rodriguez MJ; Baiget M; Pineda M; Gallano P
    Eur J Med Genet; 2011; 54(6):e576-9. PubMed ID: 21791255
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.