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 *

205 related articles for article (PubMed ID: 21063730)

  • 41. Uncoordinated transcription and compromised muscle function in the lmna-null mouse model of Emery- Emery-Dreyfuss muscular dystrophy.
    Gnocchi VF; Scharner J; Huang Z; Brady K; Lee JS; White RB; Morgan JE; Sun YB; Ellis JA; Zammit PS
    PLoS One; 2011 Feb; 6(2):e16651. PubMed ID: 21364987
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Does satellite cell dysfunction contribute to disease progression in Emery-Dreifuss muscular dystrophy?
    Gnocchi VF; Ellis JA; Zammit PS
    Biochem Soc Trans; 2008 Dec; 36(Pt 6):1344-9. PubMed ID: 19021553
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Emery-Dreifuss muscular dystrophy.
    Heller SA; Shih R; Kalra R; Kang PB
    Muscle Nerve; 2020 Apr; 61(4):436-448. PubMed ID: 31840275
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Emery-Dreifuss muscular dystrophy: the most recognizable laminopathy.
    Madej-Pilarczyk A; Kochański A
    Folia Neuropathol; 2016; 54(1):1-8. PubMed ID: 27179216
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Cardiac dysrhythmias,cardiomyopathy and muscular dystrophy in patients with Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy type 1B.
    Hong JS; Ki CS; Kim JW; Suh YL; Kim JS; Baek KK; Kim BJ; Ahn KJ; Kim DK
    J Korean Med Sci; 2005 Apr; 20(2):283-90. PubMed ID: 15832002
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Emery-Dreifuss muscular dystrophy.
    Muchir A; Worman HJ
    Curr Neurol Neurosci Rep; 2007 Jan; 7(1):78-83. PubMed ID: 17217858
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Activation of MAPK in hearts of EMD null mice: similarities between mouse models of X-linked and autosomal dominant Emery Dreifuss muscular dystrophy.
    Muchir A; Pavlidis P; Bonne G; Hayashi YK; Worman HJ
    Hum Mol Genet; 2007 Aug; 16(15):1884-95. PubMed ID: 17567779
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Clinical and Genetic Heterogeneity of Nuclear Envelopathy Related Muscular Dystrophies in an Indian Cohort.
    Baskar D; Preethish-Kumar V; Polavarapu K; Vengalil S; Nashi S; Menon D; Ganaraja VH; Girija MS; Nandeesh BN; Arunachal G; Nalini A
    J Neuromuscul Dis; 2024; 11(5):969-979. PubMed ID: 39058449
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Autosomal recessive Emery-Dreifuss muscular dystrophy caused by a novel mutation (R225Q) in the lamin A/C gene identified by exome sequencing.
    Jimenez-Escrig A; Gobernado I; Garcia-Villanueva M; Sanchez-Herranz A
    Muscle Nerve; 2012 Apr; 45(4):605-10. PubMed ID: 22431096
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Genetics of laminopathies.
    Ben Yaou R; Muchir A; Arimura T; Massart C; Demay L; Richard P; Bonne G
    Novartis Found Symp; 2005; 264():81-90; discussion 90-97, 227-30. PubMed ID: 15773749
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Disease severity in dominant Emery Dreifuss is increased by mutations in both emerin and desmin proteins.
    Muntoni F; Bonne G; Goldfarb LG; Mercuri E; Piercy RJ; Burke M; Yaou RB; Richard P; Récan D; Shatunov A; Sewry CA; Brown SC
    Brain; 2006 May; 129(Pt 5):1260-8. PubMed ID: 16585054
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Emery-Dreifuss muscular dystrophy.
    Helbling-Leclerc A; Bonne G; Schwartz K
    Eur J Hum Genet; 2002 Mar; 10(3):157-61. PubMed ID: 11973618
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Phenotype-Genotype Analysis of Chinese Patients with Early-Onset LMNA-Related Muscular Dystrophy.
    Tan D; Yang H; Yuan Y; Bonnemann C; Chang X; Wang S; Wu Y; Wu X; Xiong H
    PLoS One; 2015; 10(6):e0129699. PubMed ID: 26098624
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Nuclear alterations in autosomal-dominant Emery-Dreifuss muscular dystrophy.
    Sabatelli P; Lattanzi G; Ognibene A; Columbaro M; Capanni C; Merlini L; Maraldi NM; Squarzoni S
    Muscle Nerve; 2001 Jun; 24(6):826-9. PubMed ID: 11360268
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Expression and localization of nuclear proteins in autosomal-dominant Emery-Dreifuss muscular dystrophy with LMNA R377H mutation.
    Reichart B; Klafke R; Dreger C; Krüger E; Motsch I; Ewald A; Schäfer J; Reichmann H; Müller CR; Dabauvalle MC
    BMC Cell Biol; 2004 Mar; 5():12. PubMed ID: 15053843
    [TBL] [Abstract][Full Text] [Related]  

  • 56. The role of the nuclear envelope in Emery-Dreifuss muscular dystrophy.
    Morris GE
    Trends Mol Med; 2001 Dec; 7(12):572-7. PubMed ID: 11733221
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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]  

  • 58. Dysregulation of FHL1 spliceforms due to an indel mutation produces an Emery-Dreifuss muscular dystrophy plus phenotype.
    Tiffin HR; Jenkins ZA; Gray MJ; Cameron-Christie SR; Eaton J; Aftimos S; Markie D; Robertson SP
    Neurogenetics; 2013 May; 14(2):113-21. PubMed ID: 23456229
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Investigating the pathology of Emery-Dreifuss muscular dystrophy.
    Brown SC; Piercy RJ; Muntoni F; Sewry CA
    Biochem Soc Trans; 2008 Dec; 36(Pt 6):1335-8. PubMed ID: 19021551
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Heart to heart: from nuclear proteins to Emery-Dreifuss muscular dystrophy.
    Morris GE; Manilal S
    Hum Mol Genet; 1999; 8(10):1847-51. PubMed ID: 10469836
    [TBL] [Abstract][Full Text] [Related]  

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