BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

279 related articles for article (PubMed ID: 25343322)

  • 41. Multitissular involvement in a family with LMNA and EMD mutations: Role of digenic mechanism?
    Ben Yaou R; Toutain A; Arimura T; Demay L; Massart C; Peccate C; Muchir A; Llense S; Deburgrave N; Leturcq F; Litim KE; Rahmoun-Chiali N; Richard P; Babuty D; Récan-Budiartha D; Bonne G
    Neurology; 2007 May; 68(22):1883-94. PubMed ID: 17536044
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Abnormal nuclear shape and impaired mechanotransduction in emerin-deficient cells.
    Lammerding J; Hsiao J; Schulze PC; Kozlov S; Stewart CL; Lee RT
    J Cell Biol; 2005 Aug; 170(5):781-91. PubMed ID: 16115958
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifuss muscular dystrophy.
    Brown CA; Lanning RW; McKinney KQ; Salvino AR; Cherniske E; Crowe CA; Darras BT; Gominak S; Greenberg CR; Grosmann C; Heydemann P; Mendell JR; Pober BR; Sasaki T; Shapiro F; Simpson DA; Suchowersky O; Spence JE
    Am J Med Genet; 2001 Sep; 102(4):359-67. PubMed ID: 11503164
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Dysfunctional lamins as mediators of oxidative stress in Emery-Dreifuss muscular dystrophy.
    Niebroj-Dobosz I; Sokołowska B; Madej-Pilarczyk A; Marchel M; Hausmanowa-Petrusewicz I
    Folia Neuropathol; 2017; 55(3):193-198. PubMed ID: 28984111
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery-Dreifuss muscular dystrophy.
    Wang Y; Herron AJ; Worman HJ
    Hum Mol Genet; 2006 Aug; 15(16):2479-89. PubMed ID: 16825283
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Impaired nuclear functions lead to increased senescence and inefficient differentiation in human myoblasts with a dominant p.R545C mutation in the LMNA gene.
    Kandert S; Wehnert M; Müller CR; Buendia B; Dabauvalle MC
    Eur J Cell Biol; 2009 Oct; 88(10):593-608. PubMed ID: 19589617
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Emerin in health and disease.
    Koch AJ; Holaska JM
    Semin Cell Dev Biol; 2014 May; 29():95-106. PubMed ID: 24365856
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Distribution of emerin and lamins in the heart and implications for Emery-Dreifuss muscular dystrophy.
    Manilal S; Sewry CA; Pereboev A; Man N; Gobbi P; Hawkes S; Love DR; Morris GE
    Hum Mol Genet; 1999 Feb; 8(2):353-9. PubMed ID: 9949197
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Impaired mechanical response of an EDMD mutation leads to motility phenotypes that are repaired by loss of prenylation.
    Zuela N; Zwerger M; Levin T; Medalia O; Gruenbaum Y
    J Cell Sci; 2016 May; 129(9):1781-91. PubMed ID: 27034135
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophy.
    Mercuri E; Counsell S; Allsop J; Jungbluth H; Kinali M; Bonne G; Schwartz K; Bydder G; Dubowitz V; Muntoni F
    Neuropediatrics; 2002 Feb; 33(1):10-4. PubMed ID: 11930270
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Mapping disease-related missense mutations in the immunoglobulin-like fold domain of lamin A/C reveals novel genotype-phenotype associations for laminopathies.
    Scharner J; Lu HC; Fraternali F; Ellis JA; Zammit PS
    Proteins; 2014 Jun; 82(6):904-15. PubMed ID: 24375749
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Expression of a mutant lamin A that causes Emery-Dreifuss muscular dystrophy inhibits in vitro differentiation of C2C12 myoblasts.
    Favreau C; Higuet D; Courvalin JC; Buendia B
    Mol Cell Biol; 2004 Feb; 24(4):1481-92. PubMed ID: 14749366
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Significance of 1B and 2B domains in modulating elastic properties of lamin A.
    Bera M; Ainavarapu SR; Sengupta K
    Sci Rep; 2016 Jun; 6():27879. PubMed ID: 27301336
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Lamin A/C-mediated neuromuscular junction defects in Emery-Dreifuss muscular dystrophy.
    Méjat A; Decostre V; Li J; Renou L; Kesari A; Hantaï D; Stewart CL; Xiao X; Hoffman E; Bonne G; Misteli T
    J Cell Biol; 2009 Jan; 184(1):31-44. PubMed ID: 19124654
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Emerin self-assembly and nucleoskeletal coupling regulate nuclear envelope mechanics against stress.
    Fernandez A; Bautista M; Wu L; Pinaud F
    J Cell Sci; 2022 Mar; 135(6):. PubMed ID: 35178558
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Immunocytochemistry of nuclear domains and Emery-Dreifuss muscular dystrophy pathophysiology.
    Maraldi NM; Lattanzi G; Sabatelli P; Ognibene A; Columbaro M; Capanni C; Rutigliano C; Mattioli E; Squarzoni S
    Eur J Histochem; 2003; 47(1):3-16. PubMed ID: 12685553
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Emerin Is Required for Proper Nucleus Reassembly after Mitosis: Implications for New Pathogenetic Mechanisms for Laminopathies Detected in EDMD1 Patients.
    Dubińska-Magiera M; Kozioł K; Machowska M; Piekarowicz K; Filipczak D; Rzepecki R
    Cells; 2019 Mar; 8(3):. PubMed ID: 30871242
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Differentiation of C2C12 myoblasts expressing lamin A mutated at a site responsible for Emery-Dreifuss muscular dystrophy is improved by inhibition of the MEK-ERK pathway and stimulation of the PI3-kinase pathway.
    Favreau C; Delbarre E; Courvalin JC; Buendia B
    Exp Cell Res; 2008 Apr; 314(6):1392-405. PubMed ID: 18294630
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Lmo7 is an emerin-binding protein that regulates the transcription of emerin and many other muscle-relevant genes.
    Holaska JM; Rais-Bahrami S; Wilson KL
    Hum Mol Genet; 2006 Dec; 15(23):3459-72. PubMed ID: 17067998
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Structural alterations of Lamin A protein in dilated cardiomyopathy.
    Bhattacharjee P; Banerjee A; Banerjee A; Dasgupta D; Sengupta K
    Biochemistry; 2013 Jun; 52(24):4229-41. PubMed ID: 23701190
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.