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 *

117 related articles for article (PubMed ID: 12473751)

  • 1. Sweetening the pot in muscle: genetic defects of protein glycosylation causing muscle disease.
    Karpati G; Holland P
    Neurology; 2002 Dec; 59(11):1674-6. PubMed ID: 12473751
    [No Abstract]   [Full Text] [Related]  

  • 2. [Childhood reducing body myopathy caused by FHL1 gene variation in a child].
    Wei CJ; Wang ZX; Chang XZ; Lyu JL; Ge L; Fan YB; Zhang YH; Xiong H
    Zhonghua Er Ke Za Zhi; 2020 Feb; 58(2):147-149. PubMed ID: 32102154
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 111th ENMC International Workshop on Multi-minicore Disease. 2nd International MmD Workshop, 9-11 November 2002, Naarden, The Netherlands.
    Jungbluth H; Beggs A; Bönnemann C; Bushby K; Ceuterick-de Groote C; Estournet-Mathiaud B; Goemans N; Guicheney P; Lescure A; Lunardi J; Muntoni F; Quinlivan R; Sewry C; Straub V; Treves S; Ferreiro A
    Neuromuscul Disord; 2004 Nov; 14(11):754-66. PubMed ID: 15482962
    [No Abstract]   [Full Text] [Related]  

  • 4. The sarcoglycan complex in striated and vascular smooth muscle.
    Wheeler MT; Allikian MJ; Heydemann A; McNally EM
    Cold Spring Harb Symp Quant Biol; 2002; 67():389-97. PubMed ID: 12858564
    [No Abstract]   [Full Text] [Related]  

  • 5. 121st ENMC International Workshop on Desmin and Protein Aggregate Myopathies. 7-9 November 2003, Naarden, The Netherlands.
    Goebel H; Fardeau M
    Neuromuscul Disord; 2004 Nov; 14(11):767-73. PubMed ID: 15482963
    [No Abstract]   [Full Text] [Related]  

  • 6. Non-pathogenic protein aggregates in skeletal muscle in MLF1 transgenic mice.
    Li ZF; Wu X; Jiang Y; Liu J; Wu C; Inagaki M; Izawa I; Mizisin AP; Engvall E; Shelton GD
    J Neurol Sci; 2008 Jan; 264(1-2):77-86. PubMed ID: 17854834
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mouse models for thin filament disease.
    Nguyen MA; Hardeman EC
    Adv Exp Med Biol; 2008; 642():66-77. PubMed ID: 19181094
    [TBL] [Abstract][Full Text] [Related]  

  • 8. In vivo characterization of mutant myotilins.
    Keduka E; Hayashi YK; Shalaby S; Mitsuhashi H; Noguchi S; Nonaka I; Nishino I
    Am J Pathol; 2012 Apr; 180(4):1570-80. PubMed ID: 22349301
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The couplonopathies: A comparative approach to a class of diseases of skeletal and cardiac muscle.
    Ríos E; Figueroa L; Manno C; Kraeva N; Riazi S
    J Gen Physiol; 2015 Jun; 145(6):459-74. PubMed ID: 26009541
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Decreased muscle atrophy F-box (MAFbx) expression in regenerating muscle after muscle-damaging exercise.
    Okada A; Ono Y; Nagatomi R; Kishimoto KN; Itoi E
    Muscle Nerve; 2008 Oct; 38(4):1246-53. PubMed ID: 18785187
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular Research on Muscle Protein and Myopathies.
    Karpicheva O
    Int J Mol Sci; 2022 Jun; 23(13):. PubMed ID: 35806104
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Muscle disease: a giant feels the strain.
    Tskhovrebova L; Trinick J
    Nat Med; 2005 May; 11(5):478-9. PubMed ID: 15875052
    [No Abstract]   [Full Text] [Related]  

  • 13. Symptomatic dysferlin gene mutation carriers: characterization of two cases.
    Illa I; De Luna N; Domínguez-Perles R; Rojas-García R; Paradas C; Palmer J; Márquez C; Gallano P; Gallardo E
    Neurology; 2007 Apr; 68(16):1284-9. PubMed ID: 17287450
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel FHL1 mutation in a family with reducing body myopathy.
    Schreckenbach T; Henn W; Kress W; Roos A; Maschke M; Feiden W; Dillmann U; Schulz JB; Weis J; Claeys KG
    Muscle Nerve; 2013 Jan; 47(1):127-34. PubMed ID: 23169582
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ectopic expression of DLK1 protein in skeletal muscle of padumnal heterozygotes causes the callipyge phenotype.
    Davis E; Jensen CH; Schroder HD; Farnir F; Shay-Hadfield T; Kliem A; Cockett N; Georges M; Charlier C
    Curr Biol; 2004 Oct; 14(20):1858-62. PubMed ID: 15498495
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Skeletal muscle channelopathies.
    Jurkat-Rott K; Lerche H; Lehmann-Horn F
    J Neurol; 2002 Nov; 249(11):1493-502. PubMed ID: 12420087
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Tubular aggregates in skeletal muscle: just a special type of protein aggregates?
    Schiaffino S
    Neuromuscul Disord; 2012 Mar; 22(3):199-207. PubMed ID: 22154366
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Can we talk about myoblast fusion?
    Dugdale HF; Ochala J
    Am J Physiol Cell Physiol; 2021 Sep; 321(3):C504-C506. PubMed ID: 34288723
    [No Abstract]   [Full Text] [Related]  

  • 19. Loss of sonic hedgehog gene leads to muscle development disorder and megaesophagus in mice.
    Jia X; Min L; Zhu S; Zhang S; Huang X
    FASEB J; 2018 Oct; 32(10):5703-5715. PubMed ID: 29768039
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The junctophilin family of proteins: from bench to bedside.
    Landstrom AP; Beavers DL; Wehrens XH
    Trends Mol Med; 2014 Jun; 20(6):353-62. PubMed ID: 24636942
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.