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Journal Abstract Search

294 related items for PubMed ID: 22443334

  • 1. Calpain 3 is important for muscle regeneration: evidence from patients with limb girdle muscular dystrophies.
    Hauerslev S, Sveen ML, Duno M, Angelini C, Vissing J, Krag TO.
    BMC Musculoskelet Disord; 2012 Mar 23; 13():43. PubMed ID: 22443334
    [Abstract] [Full Text] [Related]

  • 2. 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 23; 139(Pt 8):2154-63. PubMed ID: 27259757
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  • 3. Limb girdle muscular dystrophy type 2A in India: a study based on semi-quantitative protein analysis, with clinical and histopathological correlation.
    Pathak P, Sharma MC, Sarkar C, Jha P, Suri V, Mohd H, Singh S, Bhatia R, Gulati S.
    Neurol India; 2010 Aug 23; 58(4):549-54. PubMed ID: 20739790
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  • 4. Muscle pathology in 31 patients with calpain 3 gene mutations.
    Nadaj-Pakleza AA, Dorobek M, Nestorowicz K, Ryniewicz B, Szmidt-Sałkowska E, Kamińska AM.
    Neurol Neurochir Pol; 2013 Aug 23; 47(3):214-22. PubMed ID: 23821418
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  • 5. Analysis of the UK diagnostic strategy for limb girdle muscular dystrophy 2A.
    Groen EJ, Charlton R, Barresi R, Anderson LV, Eagle M, Hudson J, Koref MS, Straub V, Bushby KM.
    Brain; 2007 Dec 23; 130(Pt 12):3237-49. PubMed ID: 18055493
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  • 6. Calpain 3 deficiency affects SERCA expression and function in the skeletal muscle.
    Toral-Ojeda I, Aldanondo G, Lasa-Elgarresta J, Lasa-Fernández H, Fernández-Torrón R, López de Munain A, Vallejo-Illarramendi A.
    Expert Rev Mol Med; 2016 Apr 08; 18():e7. PubMed ID: 27055500
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  • 7. Muscle MRI findings in patients with limb girdle muscular dystrophy with calpain 3 deficiency (LGMD2A) and early contractures.
    Mercuri E, Bushby K, Ricci E, Birchall D, Pane M, Kinali M, Allsop J, Nigro V, Sáenz A, Nascimbeni A, Fulizio L, Angelini C, Muntoni F.
    Neuromuscul Disord; 2005 Feb 08; 15(2):164-71. PubMed ID: 15694138
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  • 8. Impaired regeneration in calpain-3 null muscle is associated with perturbations in mTORC1 signaling and defective mitochondrial biogenesis.
    Yalvac ME, Amornvit J, Braganza C, Chen L, Hussain SA, Shontz KM, Montgomery CL, Flanigan KM, Lewis S, Sahenk Z.
    Skelet Muscle; 2017 Dec 14; 7(1):27. PubMed ID: 29241457
    [Abstract] [Full Text] [Related]

  • 9. Novel Missense CAPN3 Mutation Responsible for Adult-Onset Limb Girdle Muscular Dystrophy with Calves Hypertrophy.
    Rekik S, Sakka S, Ben Romdhan S, Farhat N, Baba Amer Y, Lehkim L, Authier FJ, Mhiri C.
    J Mol Neurosci; 2019 Dec 14; 69(4):563-569. PubMed ID: 31410652
    [Abstract] [Full Text] [Related]

  • 10. Analysis of calpain-3 protein in muscle biopsies of different muscular dystrophies from India.
    Renjini R, Gayathri N, Nalini A, Srinivas Bharath MM.
    Indian J Med Res; 2012 Jun 14; 135(6):878-86. PubMed ID: 22825607
    [Abstract] [Full Text] [Related]

  • 11. Screening of calpain-3 autolytic activity in LGMD muscle: a functional map of CAPN3 gene mutations.
    Fanin M, Nascimbeni AC, Angelini C.
    J Med Genet; 2007 Jan 14; 44(1):38-43. PubMed ID: 16971480
    [Abstract] [Full Text] [Related]

  • 12. Mutational Spectrum of CAPN3 with Genotype-Phenotype Correlations in Limb Girdle Muscular Dystrophy Type 2A/R1 (LGMD2A/LGMDR1) Patients in India.
    Pathak P, Sharma MC, Jha P, Sarkar C, Faruq M, Jha P, Suri V, Bhatia R, Singh S, Gulati S, Husain M.
    J Neuromuscul Dis; 2021 Jan 14; 8(1):125-136. PubMed ID: 33337384
    [Abstract] [Full Text] [Related]

  • 13. cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in Denmark.
    Duno M, Sveen ML, Schwartz M, Vissing J.
    Eur J Hum Genet; 2008 Aug 14; 16(8):935-40. PubMed ID: 18337726
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  • 15. Attenuated Ca(2+) release in a mouse model of limb girdle muscular dystrophy 2A.
    DiFranco M, Kramerova I, Vergara JL, Spencer MJ.
    Skelet Muscle; 2016 Aug 14; 6():11. PubMed ID: 26913171
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