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 *

141 related articles for article (PubMed ID: 8661728)

  • 21. Limb-girdle muscular dystrophy type 2A can result from accelerated autoproteolytic inactivation of calpain 3.
    Garnham CP; Hanna RA; Chou JS; Low KE; Gourlay K; Campbell RL; Beckmann JS; Davies PL
    Biochemistry; 2009 Apr; 48(15):3457-67. PubMed ID: 19226146
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Dystrophinopathies, congenital muscular dystrophy, limb-girdle dystrophies: updated classification].
    Teijeira-Bautista S; García-García D; Teijeiro-Ferreira A; Fernández-Hojas R; Fernández-Rodríguez JM; Navarro-Fernández-Balbuena C
    Rev Neurol; 1998 Jun; 26(154):1021-6. PubMed ID: 9658487
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A foundation for limb-girdle muscular dystrophy.
    van Ommen GJ
    Nat Med; 1995 May; 1(5):412-4. PubMed ID: 7585084
    [No Abstract]   [Full Text] [Related]  

  • 24. Calpainopathy-a survey of mutations and polymorphisms.
    Richard I; Roudaut C; Saenz A; Pogue R; Grimbergen JE; Anderson LV; Beley C; Cobo AM; de Diego C; Eymard B; Gallano P; Ginjaar HB; Lasa A; Pollitt C; Topaloglu H; Urtizberea JA; de Visser M; van der Kooi A; Bushby K; Bakker E; Lopez de Munain A; Fardeau M; Beckmann JS
    Am J Hum Genet; 1999 Jun; 64(6):1524-40. PubMed ID: 10330340
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) gene.
    Chiannilkulchai N; Pasturaud P; Richard I; Auffray C; Beckmann JS
    Hum Mol Genet; 1995 Apr; 4(4):717-25. PubMed ID: 7633422
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A small in-frame deletion within the protease domain of muscle-specific calpain, p94 causes early-onset limb-girdle muscular dystrophy 2A.
    Häffner K; Speer A; Hübner C; Voit T; Oexle K
    Hum Mutat; 1998; Suppl 1():S298-300. PubMed ID: 9452114
    [No Abstract]   [Full Text] [Related]  

  • 27. Calpain 3 deficiency presenting as fibre type disproportion.
    Vattemi G; Tonin P; Neri M; Marini M; Gualandi F; Guglielmi V; Ferlini A; Tomelleri G
    Neuropathol Appl Neurobiol; 2009 Dec; 35(6):614-7. PubMed ID: 19490426
    [No Abstract]   [Full Text] [Related]  

  • 28. [LGMD2A(calpain 3 deficiency)].
    Kawai H
    Ryoikibetsu Shokogun Shirizu; 2001; (35):79-83. PubMed ID: 11555997
    [No Abstract]   [Full Text] [Related]  

  • 29. Understanding the heterogeneity of the limb-girdle muscular dystrophies.
    Bushby K
    Biochem Soc Trans; 1996 May; 24(2):489-96. PubMed ID: 8736790
    [No Abstract]   [Full Text] [Related]  

  • 30. Selective pseudohypertrophy of vastus medialis muscles associated with calpain 3 deficiency.
    Vattemi G; Neri M; Marini M; Gualandi F; Tonin P; Bertolasi L; Guglielmi V; Catalli C; Novelli G; Ferlini A; Tomelleri G
    Neurologist; 2012 Sep; 18(5):306-9. PubMed ID: 22931740
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The third human FER-1-like protein is highly similar to dysferlin.
    Britton S; Freeman T; Vafiadaki E; Keers S; Harrison R; Bushby K; Bashir R
    Genomics; 2000 Sep; 68(3):313-21. PubMed ID: 10995573
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mutations of CAPN3 in Korean patients with limb-girdle muscular dystrophy.
    Shin JH; Kim HS; Lee CH; Kim CM; Park KH; Kim DS
    J Korean Med Sci; 2007 Jun; 22(3):463-9. PubMed ID: 17596655
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Making sense of the limb-girdle muscular dystrophies.
    Bushby KM
    Brain; 1999 Aug; 122 ( Pt 8)():1403-20. PubMed ID: 10430828
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Safety and efficacy of AAV-mediated calpain 3 gene transfer in a mouse model of limb-girdle muscular dystrophy type 2A.
    Bartoli M; Roudaut C; Martin S; Fougerousse F; Suel L; Poupiot J; Gicquel E; Noulet F; Danos O; Richard I
    Mol Ther; 2006 Feb; 13(2):250-9. PubMed ID: 16290124
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Limb girdle muscular dystrophy type 2A (CAPN3): mapping using allelic association.
    Lonjou C; Collins A; Beckmann J; Allamand V; Morton N
    Hum Hered; 1998; 48(6):333-7. PubMed ID: 9813455
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Loss of calpain 3 proteolytic activity leads to muscular dystrophy and to apoptosis-associated IkappaBalpha/nuclear factor kappaB pathway perturbation in mice.
    Richard I; Roudaut C; Marchand S; Baghdiguian S; Herasse M; Stockholm D; Ono Y; Suel L; Bourg N; Sorimachi H; Lefranc G; Fardeau M; Sébille A; Beckmann JS
    J Cell Biol; 2000 Dec; 151(7):1583-90. PubMed ID: 11134085
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Prenatal diagnosis of limb-girdle muscular dystrophy type 2A.
    Restagno G; Romero N; Richard I; Beckmann JS; Pagliano M; Ferrone M; Carbonara A; Merlini L
    Neuromuscul Disord; 1996 May; 6(3):173-6. PubMed ID: 8784805
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Calpain and pathology in view of structure-function relationships].
    Sorimachi H; Kawabata Y
    Nihon Yakurigaku Zasshi; 2003 Jul; 122(1):21-9. PubMed ID: 12843569
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families.
    Passos-Bueno MR; Moreira ES; Marie SK; Bashir R; Vasquez L; Love DR; Vainzof M; Iughetti P; Oliveira JR; Bakker E; Strachan T; Bushby K; Zatz M
    J Med Genet; 1996 Feb; 33(2):97-102. PubMed ID: 8929943
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A heterozygous 21-bp deletion in CAPN3 causes dominantly inherited limb girdle muscular dystrophy.
    Vissing J; Barresi R; Witting N; Van Ghelue M; Gammelgaard L; Bindoff LA; Straub V; Lochmüller H; Hudson J; Wahl CM; Arnardottir S; Dahlbom K; Jonsrud C; Duno M
    Brain; 2016 Aug; 139(Pt 8):2154-63. PubMed ID: 27259757
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.