BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 10908904)

  • 21. [Mutation analysis of a Chinese family with autosomal dominant Emery-Dreifuss muscular dystrophy].
    Yuan JH; Hu J; Zhao Z; Shen HR; Li N; Bing Q
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Apr; 27(2):136-9. PubMed ID: 20376791
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. 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]  

  • 24. 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]  

  • 25. Frequent low penetrance mutations in the Lamin A/C gene, causing Emery Dreifuss muscular dystrophy.
    Vytopil M; Ricci E; Dello Russo A; Hanisch F; Neudecker S; Zierz S; Ricotti R; Demay L; Richard P; Wehnert M; Bonne G; Merlini L; Toniolo D
    Neuromuscul Disord; 2002 Dec; 12(10):958-63. PubMed ID: 12467752
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1B.
    Park YE; Hayashi YK; Goto K; Komaki H; Hayashi Y; Inuzuka T; Noguchi S; Nonaka I; Nishino I
    Neuromuscul Disord; 2009 Jan; 19(1):29-36. PubMed ID: 19070492
    [TBL] [Abstract][Full Text] [Related]  

  • 28. TMEM43 mutations in Emery-Dreifuss muscular dystrophy-related myopathy.
    Liang WC; Mitsuhashi H; Keduka E; Nonaka I; Noguchi S; Nishino I; Hayashi YK
    Ann Neurol; 2011 Jun; 69(6):1005-13. PubMed ID: 21391237
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Clinical, genealogical and molecular genetic study of Emery-Dreifuss muscular dystrophy].
    Rudenskaia GE; Tverskaia SM; Chukhrova AL; Zakliaz'minskaia EV; Kuropatkina IuV; Dadali EL; Perminov VS; Poliakov AV
    Zh Nevrol Psikhiatr Im S S Korsakova; 2006; 106(10):58-65. PubMed ID: 17117676
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Emery dreifuss muscular dystrophy: a clinico-pathological study.
    Gayathri N; Taly AB; Sinha S; Suresh TG; Gorai D
    Neurol India; 2006 Jun; 54(2):197-9. PubMed ID: 16804269
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Multisystem dystrophy syndrome due to novel missense mutations in the amino-terminal head and alpha-helical rod domains of the lamin A/C gene.
    Garg A; Speckman RA; Bowcock AM
    Am J Med; 2002 May; 112(7):549-55. PubMed ID: 12015247
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Myofiber degeneration in autosomal dominant Emery-Dreifuss muscular dystrophy (AD-EDMD) (LGMD1B).
    Mittelbronn M; Hanisch F; Gleichmann M; Stötter M; Korinthenberg R; Wehnert M; Bonne G; Rudnik-Schöneborn S; Bornemann A
    Brain Pathol; 2006 Oct; 16(4):266-72. PubMed ID: 17107595
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy.
    Gueneau L; Bertrand AT; Jais JP; Salih MA; Stojkovic T; Wehnert M; Hoeltzenbein M; Spuler S; Saitoh S; Verschueren A; Tranchant C; Beuvin M; Lacene E; Romero NB; Heath S; Zelenika D; Voit T; Eymard B; Ben Yaou R; Bonne G
    Am J Hum Genet; 2009 Sep; 85(3):338-53. PubMed ID: 19716112
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Skeletal muscle pathology in autosomal dominant Emery-Dreifuss muscular dystrophy with lamin A/C mutations.
    Sewry CA; Brown SC; Mercuri E; Bonne G; Feng L; Camici G; Morris GE; Muntoni F
    Neuropathol Appl Neurobiol; 2001 Aug; 27(4):281-90. PubMed ID: 11532159
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A novel SYNE2 mutation identified by whole exome sequencing in a Korean family with Emery-Dreifuss muscular dystrophy.
    Lee SJ; Lee S; Choi E; Shin S; Park J
    Clin Chim Acta; 2020 Jul; 506():50-54. PubMed ID: 32184094
    [TBL] [Abstract][Full Text] [Related]  

  • 38. FHL1B Interacts with Lamin A/C and Emerin at the Nuclear Lamina and is Misregulated in Emery-Dreifuss Muscular Dystrophy.
    Ziat E; Mamchaoui K; Beuvin M; Nelson I; Azibani F; Spuler S; Bonne G; Bertrand AT
    J Neuromuscul Dis; 2016 Nov; 3(4):497-510. PubMed ID: 27911330
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Effect of pathogenic mis-sense mutations in lamin A on its interaction with emerin in vivo.
    Holt I; Ostlund C; Stewart CL; Man Nt; Worman HJ; Morris GE
    J Cell Sci; 2003 Jul; 116(Pt 14):3027-35. PubMed ID: 12783988
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Clinical and genetic characteristics of Emery-Dreifuss muscular dystrophy patients from Turkey: 30 years longitudinal follow-up study.
    Yunisova G; Ceylaner S; Oflazer P; Deymeer F; Parman YG; Durmus H
    Neuromuscul Disord; 2022 Sep; 32(9):718-727. PubMed ID: 35922275
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.