BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

237 related articles for article (PubMed ID: 31586140)

  • 1. Early skeletal muscle pathology and disease progress in the dy
    Gawlik KI; Körner Z; Oliveira BM; Durbeej M
    Sci Rep; 2019 Oct; 9(1):14324. PubMed ID: 31586140
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Laminin α1 reduces muscular dystrophy in dy
    Gawlik KI; Harandi VM; Cheong RY; Petersén Å; Durbeej M
    Matrix Biol; 2018 Sep; 70():36-49. PubMed ID: 29544677
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exon Skipping Using Antisense Oligonucleotides for Laminin-Alpha2-Deficient Muscular Dystrophy.
    Hara Y; Mizobe Y; Miyatake S; Takizawa H; Nagata T; Yokota T; Takeda S; Aoki Y
    Methods Mol Biol; 2018; 1828():553-564. PubMed ID: 30171567
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Laminin alpha2 deficiency and muscular dystrophy; genotype-phenotype correlation in mutant mice.
    Guo LT; Zhang XU; Kuang W; Xu H; Liu LA; Vilquin JT; Miyagoe-Suzuki Y; Takeda S; Ruegg MA; Wewer UM; Engvall E
    Neuromuscul Disord; 2003 Mar; 13(3):207-15. PubMed ID: 12609502
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Potent pro-inflammatory and pro-fibrotic molecules, osteopontin and galectin-3, are not major disease modulators of laminin α2 chain-deficient muscular dystrophy.
    Gawlik KI; Holmberg J; Svensson M; Einerborg M; Oliveira BM; Deierborg T; Durbeej M
    Sci Rep; 2017 Mar; 7():44059. PubMed ID: 28281577
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Proteasome inhibition improves the muscle of laminin α2 chain-deficient mice.
    Carmignac V; Quéré R; Durbeej M
    Hum Mol Genet; 2011 Feb; 20(3):541-52. PubMed ID: 21084425
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Loss of dystrophin and β-sarcoglycan significantly exacerbates the phenotype of laminin α2 chain-deficient animals.
    Gawlik KI; Holmberg J; Durbeej M
    Am J Pathol; 2014 Mar; 184(3):740-52. PubMed ID: 24393714
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Bortezomib partially improves laminin α2 chain-deficient muscular dystrophy.
    Körner Z; Fontes-Oliveira CC; Holmberg J; Carmignac V; Durbeej M
    Am J Pathol; 2014 May; 184(5):1518-28. PubMed ID: 24631023
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Autophagy is increased in laminin α2 chain-deficient muscle and its inhibition improves muscle morphology in a mouse model of MDC1A.
    Carmignac V; Svensson M; Körner Z; Elowsson L; Matsumura C; Gawlik KI; Allamand V; Durbeej M
    Hum Mol Genet; 2011 Dec; 20(24):4891-902. PubMed ID: 21920942
    [TBL] [Abstract][Full Text] [Related]  

  • 10. CD90-positive cells, an additional cell population, produce laminin alpha2 upon transplantation to dy(3k)/dy(3k) mice.
    Fukada S; Yamamoto Y; Segawa M; Sakamoto K; Nakajima M; Sato M; Morikawa D; Uezumi A; Miyagoe-Suzuki Y; Takeda S; Tsujikawa K; Yamamoto H
    Exp Cell Res; 2008 Jan; 314(1):193-203. PubMed ID: 17963748
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Elimination of myostatin does not combat muscular dystrophy in dy mice but increases postnatal lethality.
    Li ZF; Shelton GD; Engvall E
    Am J Pathol; 2005 Feb; 166(2):491-7. PubMed ID: 15681832
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dual transgene amelioration of Lama2-null muscular dystrophy.
    McKee KK; Yurchenco PD
    Matrix Biol; 2023 Apr; 118():1-15. PubMed ID: 36878377
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Merosin and congenital muscular dystrophy.
    Miyagoe-Suzuki Y; Nakagawa M; Takeda S
    Microsc Res Tech; 2000 Feb 1-15; 48(3-4):181-91. PubMed ID: 10679965
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Effects of metformin on congenital muscular dystrophy type 1A disease progression in mice: a gender impact study.
    Fontes-Oliveira CC; M Soares Oliveira B; Körner Z; M Harandi V; Durbeej M
    Sci Rep; 2018 Nov; 8(1):16302. PubMed ID: 30389963
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Highly efficient in vivo delivery of PMO into regenerating myotubes and rescue in laminin-α2 chain-null congenital muscular dystrophy mice.
    Aoki Y; Nagata T; Yokota T; Nakamura A; Wood MJ; Partridge T; Takeda S
    Hum Mol Genet; 2013 Dec; 22(24):4914-28. PubMed ID: 23882132
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Overexpression of mini-agrin in skeletal muscle increases muscle integrity and regenerative capacity in laminin-alpha2-deficient mice.
    Bentzinger CF; Barzaghi P; Lin S; Ruegg MA
    FASEB J; 2005 Jun; 19(8):934-42. PubMed ID: 15923403
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A splice site mutation in laminin-α2 results in a severe muscular dystrophy and growth abnormalities in zebrafish.
    Gupta VA; Kawahara G; Myers JA; Chen AT; Hall TE; Manzini MC; Currie PD; Zhou Y; Zon LI; Kunkel LM; Beggs AH
    PLoS One; 2012; 7(8):e43794. PubMed ID: 22952766
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Laminin-111 protein therapy reduces muscle pathology and improves viability of a mouse model of merosin-deficient congenital muscular dystrophy.
    Rooney JE; Knapp JR; Hodges BL; Wuebbles RD; Burkin DJ
    Am J Pathol; 2012 Apr; 180(4):1593-602. PubMed ID: 22322301
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Expression of laminin alpha1, alpha2, alpha4, and alpha5 chains, fibronectin, and tenascin-C in skeletal muscle of dystrophic 129ReJ dy/dy mice.
    Ringelmann B; Röder C; Hallmann R; Maley M; Davies M; Grounds M; Sorokin L
    Exp Cell Res; 1999 Jan; 246(1):165-82. PubMed ID: 9882526
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A Family of Laminin α2 Chain-Deficient Mouse Mutants: Advancing the Research on LAMA2-CMD.
    Gawlik KI; Durbeej M
    Front Mol Neurosci; 2020; 13():59. PubMed ID: 32457577
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.