BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

179 related articles for article (PubMed ID: 32200007)

  • 1. A muscle-specific calpain, CAPN3, forms a homotrimer.
    Hata S; Doi N; Shinkai-Ouchi F; Ono Y
    Biochim Biophys Acta Proteins Proteom; 2020 Jul; 1868(7):140411. PubMed ID: 32200007
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Muscle-specific calpain-3 is phosphorylated in its unique insertion region for enrichment in a myofibril fraction.
    Ojima K; Ono Y; Hata S; Noguchi S; Nishino I; Sorimachi H
    Genes Cells; 2014 Nov; 19(11):830-41. PubMed ID: 25252031
    [TBL] [Abstract][Full Text] [Related]  

  • 3. CAPN3-mediated processing of C-terminal titin replaced by pathological cleavage in titinopathy.
    Charton K; Sarparanta J; Vihola A; Milic A; Jonson PH; Suel L; Luque H; Boumela I; Richard I; Udd B
    Hum Mol Genet; 2015 Jul; 24(13):3718-31. PubMed ID: 25877298
    [TBL] [Abstract][Full Text] [Related]  

  • 4. An eccentric calpain, CAPN3/p94/calpain-3.
    Ono Y; Ojima K; Shinkai-Ouchi F; Hata S; Sorimachi H
    Biochimie; 2016 Mar; 122():169-87. PubMed ID: 26363099
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mdm muscular dystrophy: interactions with calpain 3 and a novel functional role for titin's N2A domain.
    Huebsch KA; Kudryashova E; Wooley CM; Sher RB; Seburn KL; Spencer MJ; Cox GA
    Hum Mol Genet; 2005 Oct; 14(19):2801-11. PubMed ID: 16115818
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 7(1):27. PubMed ID: 29241457
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The N- and C-terminal autolytic fragments of CAPN3/p94/calpain-3 restore proteolytic activity by intermolecular complementation.
    Ono Y; Shindo M; Doi N; Kitamura F; Gregorio CC; Sorimachi H
    Proc Natl Acad Sci U S A; 2014 Dec; 111(51):E5527-36. PubMed ID: 25512505
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Calpain 3, the "gatekeeper" of proper sarcomere assembly, turnover and maintenance.
    Beckmann JS; Spencer M
    Neuromuscul Disord; 2008 Dec; 18(12):913-21. PubMed ID: 18974005
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Calpain 3 is a modulator of the dysferlin protein complex in skeletal muscle.
    Huang Y; de Morrée A; van Remoortere A; Bushby K; Frants RR; den Dunnen JT; van der Maarel SM
    Hum Mol Genet; 2008 Jun; 17(12):1855-66. PubMed ID: 18334579
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Non-proteolytic functions of calpain-3 in sarcoplasmic reticulum in skeletal muscles.
    Ojima K; Ono Y; Ottenheijm C; Hata S; Suzuki H; Granzier H; Sorimachi H
    J Mol Biol; 2011 Apr; 407(3):439-49. PubMed ID: 21295580
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Crystal structure of calpain-3 penta-EF-hand (PEF) domain - a homodimerized PEF family member with calcium bound at the fifth EF-hand.
    Partha SK; Ravulapalli R; Allingham JS; Campbell RL; Davies PL
    FEBS J; 2014 Jul; 281(14):3138-49. PubMed ID: 24846670
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Autolytic activation of calpain 3 proteinase is facilitated by calmodulin protein.
    Ermolova N; Kramerova I; Spencer MJ
    J Biol Chem; 2015 Jan; 290(2):996-1004. PubMed ID: 25389288
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Compound heterozygous
    Zhang C; Zheng X; Lu D; Xu L; Che F; Liu S
    Mol Med Rep; 2021 Jun; 23(6):. PubMed ID: 33899113
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 44(1):38-43. PubMed ID: 16971480
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 18():e7. PubMed ID: 27055500
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Impaired calcium calmodulin kinase signaling and muscle adaptation response in the absence of calpain 3.
    Kramerova I; Kudryashova E; Ermolova N; Saenz A; Jaka O; López de Munain A; Spencer MJ
    Hum Mol Genet; 2012 Jul; 21(14):3193-204. PubMed ID: 22505582
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Limb girdle muscular dystrophy in a sibling pair with a homozygous Ser606Leu mutation in the alternatively spliced IS2 region of calpain 3.
    Jenne DE; Kley RA; Vorgerd M; Schröder JM; Weis J; Reimann H; Albrecht B; Nürnberg P; Thiele H; Müller CR; Meng G; Witt CC; Labeit S
    Biol Chem; 2005 Jan; 386(1):61-7. PubMed ID: 15843148
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Interactions with M-band titin and calpain 3 link myospryn (CMYA5) to tibial and limb-girdle muscular dystrophies.
    Sarparanta J; Blandin G; Charton K; Vihola A; Marchand S; Milic A; Hackman P; Ehler E; Richard I; Udd B
    J Biol Chem; 2010 Sep; 285(39):30304-15. PubMed ID: 20634290
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 69(4):563-569. PubMed ID: 31410652
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.