BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 24386194)

  • 21. Laminopathies; Mutations on single gene and various human genetic diseases.
    Kang SM; Yoon MH; Park BJ
    BMB Rep; 2018 Jul; 51(7):327-337. PubMed ID: 29764566
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Expression of an LMNA-N195K variant of A-type lamins results in cardiac conduction defects and death in mice.
    Mounkes LC; Kozlov SV; Rottman JN; Stewart CL
    Hum Mol Genet; 2005 Aug; 14(15):2167-80. PubMed ID: 15972724
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Generation of induced pluripotent stem cell lines from 3 distinct laminopathies bearing heterogeneous mutations in lamin A/C.
    Ho JC; Zhou T; Lai WH; Huang Y; Chan YC; Li X; Wong NL; Li Y; Au KW; Guo D; Xu J; Siu CW; Pei D; Tse HF; Esteban MA
    Aging (Albany NY); 2011 Apr; 3(4):380-90. PubMed ID: 21483033
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Altered protein dynamics of disease-associated lamin A mutants.
    Gilchrist S; Gilbert N; Perry P; Ostlund C; Worman HJ; Bickmore WA
    BMC Cell Biol; 2004 Dec; 5(1):46. PubMed ID: 15596010
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Incomplete nonsense-mediated decay of mutant lamin A/C mRNA provokes dilated cardiomyopathy and ventricular tachycardia.
    Geiger SK; Bär H; Ehlermann P; Wälde S; Rutschow D; Zeller R; Ivandic BT; Zentgraf H; Katus HA; Herrmann H; Weichenhan D
    J Mol Med (Berl); 2008 Mar; 86(3):281-9. PubMed ID: 17987279
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease.
    Fatkin D; MacRae C; Sasaki T; Wolff MR; Porcu M; Frenneaux M; Atherton J; Vidaillet HJ; Spudich S; De Girolami U; Seidman JG; Seidman C; Muntoni F; Müehle G; Johnson W; McDonough B
    N Engl J Med; 1999 Dec; 341(23):1715-24. PubMed ID: 10580070
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The effect of the lamin A and its mutants on nuclear structure, cell proliferation, protein stability, and mobility in embryonic cells.
    Piekarowicz K; Machowska M; Dratkiewicz E; Lorek D; Madej-Pilarczyk A; Rzepecki R
    Chromosoma; 2017 Aug; 126(4):501-517. PubMed ID: 27534416
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Phosphorylation of lamins determine their structural properties and signaling functions.
    Torvaldson E; Kochin V; Eriksson JE
    Nucleus; 2015; 6(3):166-71. PubMed ID: 25793944
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Morphological analysis of 13 LMNA variants identified in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.
    Cowan J; Li D; Gonzalez-Quintana J; Morales A; Hershberger RE
    Circ Cardiovasc Genet; 2010 Feb; 3(1):6-14. PubMed ID: 20160190
    [TBL] [Abstract][Full Text] [Related]  

  • 30. In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patients.
    Sylvius N; Bilinska ZT; Veinot JP; Fidzianska A; Bolongo PM; Poon S; McKeown P; Davies RA; Chan KL; Tang AS; Dyack S; Grzybowski J; Ruzyllo W; McBride H; Tesson F
    J Med Genet; 2005 Aug; 42(8):639-47. PubMed ID: 16061563
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease.
    Wolf CM; Wang L; Alcalai R; Pizard A; Burgon PG; Ahmad F; Sherwood M; Branco DM; Wakimoto H; Fishman GI; See V; Stewart CL; Conner DA; Berul CI; Seidman CE; Seidman JG
    J Mol Cell Cardiol; 2008 Feb; 44(2):293-303. PubMed ID: 18182166
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations.
    Arimura T; Onoue K; Takahashi-Tanaka Y; Ishikawa T; Kuwahara M; Setou M; Shigenobu S; Yamaguchi K; Bertrand AT; Machida N; Takayama K; Fukusato M; Tanaka R; Somekawa S; Nakano T; Yamane Y; Kuba K; Imai Y; Saito Y; Bonne G; Kimura A
    Cardiovasc Res; 2013 Aug; 99(3):382-94. PubMed ID: 23631840
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Long-term expression of the lamin A mutant associated with dilated cardiomyopathy induces senescence.
    Moriuchi T; Muraoka T; Mio K; Osumi T; Hirose F
    Genes Cells; 2014 Dec; 19(12):901-18. PubMed ID: 25319090
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mechanics in human fibroblasts and progeria: Lamin A mutation E145K results in stiffening of nuclei.
    Apte K; Stick R; Radmacher M
    J Mol Recognit; 2017 Feb; 30(2):. PubMed ID: 27677907
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Cardiac manifestations of laminopathies].
    Brette S; Penisson-Besnier I; Dupuis JM; Bonne G; Victor J
    Arch Mal Coeur Vaiss; 2004 Oct; 97(10):973-7. PubMed ID: 16008174
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Structures of the lamin A/C R335W and E347K mutants: implications for dilated cardiolaminopathies.
    Bollati M; Barbiroli A; Favalli V; Arbustini E; Charron P; Bolognesi M
    Biochem Biophys Res Commun; 2012 Feb; 418(2):217-21. PubMed ID: 22266370
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Lamin A/C mutations in dilated cardiomyopathy.
    Tesson F; Saj M; Uvaize MM; Nicolas H; Płoski R; Bilińska Z
    Cardiol J; 2014; 21(4):331-42. PubMed ID: 24846508
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice.
    Nikolova V; Leimena C; McMahon AC; Tan JC; Chandar S; Jogia D; Kesteven SH; Michalicek J; Otway R; Verheyen F; Rainer S; Stewart CL; Martin D; Feneley MP; Fatkin D
    J Clin Invest; 2004 Feb; 113(3):357-69. PubMed ID: 14755333
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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
    Basic Res Cardiol; 2010 May; 105(3):365-77. PubMed ID: 20127487
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.