BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

167 related articles for article (PubMed ID: 7704020)

  • 1. Targeted mutation in the col5a2 gene reveals a regulatory role for type V collagen during matrix assembly.
    Andrikopoulos K; Liu X; Keene DR; Jaenisch R; Ramirez F
    Nat Genet; 1995 Jan; 9(1):31-6. PubMed ID: 7704020
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Developmental pattern of expression of the mouse alpha 1 (XI) collagen gene (Col11a1).
    Yoshioka H; Iyama K; Inoguchi K; Khaleduzzaman M; Ninomiya Y; Ramirez F
    Dev Dyn; 1995 Sep; 204(1):41-7. PubMed ID: 8563024
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Skin is a window on heritable disorders of connective tissue.
    Holbrook KA; Byers PH
    Am J Med Genet; 1989 Sep; 34(1):105-21. PubMed ID: 2683775
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Induction of skin fibrosis and autoantibodies by infusion of immunocompetent cells from tight skin mice into C57BL/6 Pa/Pa mice.
    Phelps RG; Daian C; Shibata S; Fleischmajer R; Bona CA
    J Autoimmun; 1993 Dec; 6(6):701-18. PubMed ID: 8155252
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Transforming growth factor-beta 1 and collagen gene expression during postnatal skin development and fibrosis in the tight-skin mouse.
    Pablos JL; Everett ET; Harley R; LeRoy EC; Norris JS
    Lab Invest; 1995 Jun; 72(6):670-8. PubMed ID: 7783425
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Disproportionate micromelia (Dmm) in mice caused by a mutation in the C-propeptide coding region of Col2a1.
    Pace JM; Li Y; Seegmiller RE; Teuscher C; Taylor BA; Olsen BR
    Dev Dyn; 1997 Jan; 208(1):25-33. PubMed ID: 8989518
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Type XII collagen contributes to diversities in human corneal and limbal extracellular matrices.
    Wessel H; Anderson S; Fite D; Halvas E; Hempel J; SundarRaj N
    Invest Ophthalmol Vis Sci; 1997 Oct; 38(11):2408-22. PubMed ID: 9344363
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Quantitative analysis of gene expression in a rabbit model of intervertebral disc degeneration by real-time polymerase chain reaction.
    Sobajima S; Shimer AL; Chadderdon RC; Kompel JF; Kim JS; Gilbertson LG; Kang JD
    Spine J; 2005; 5(1):14-23. PubMed ID: 15653081
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Collagen loss and impaired wound healing is associated with c-Myb deficiency.
    Kopecki Z; Luchetti MM; Adams DH; Strudwick X; Mantamadiotis T; Stoppacciaro A; Gabrielli A; Ramsay RG; Cowin AJ
    J Pathol; 2007 Feb; 211(3):351-61. PubMed ID: 17152050
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Stickler syndrome: further mutations in COL11A1 and evidence for additional locus heterogeneity.
    Martin S; Richards AJ; Yates JR; Scott JD; Pope M; Snead MP
    Eur J Hum Genet; 1999; 7(7):807-14. PubMed ID: 10573014
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Type I collagen-deficient Mov-13 mice do not retain SPARC in the extracellular matrix: implications for fibroblast function.
    Iruela-Arispe ML; Vernon RB; Wu H; Jaenisch R; Sage EH
    Dev Dyn; 1996 Oct; 207(2):171-83. PubMed ID: 8906420
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Targeted disruption of Col11a2 produces a mild cartilage phenotype in transgenic mice: comparison with the human disorder otospondylomegaepiphyseal dysplasia (OSMED).
    Li SW; Takanosu M; Arita M; Bao Y; Ren ZX; Maier A; Prockop DJ; Mayne R
    Dev Dyn; 2001 Oct; 222(2):141-52. PubMed ID: 11668593
    [TBL] [Abstract][Full Text] [Related]  

  • 13. ColVa1 and ColXIa1 are required for myocardial morphogenesis and heart valve development.
    Lincoln J; Florer JB; Deutsch GH; Wenstrup RJ; Yutzey KE
    Dev Dyn; 2006 Dec; 235(12):3295-305. PubMed ID: 17029294
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A mouse model for Stickler's syndrome: ocular phenotype of mice carrying a targeted heterozygous inactivation of type II (pro)collagen gene (Col2a1).
    Kaarniranta K; Ihanamäki T; Sahlman J; Pulkkinen H; Uusitalo H; Arita M; Tammi R; Lammi MJ; Helminen HJ
    Exp Eye Res; 2006 Aug; 83(2):297-303. PubMed ID: 16546167
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular cloning of a cDNA encoding the porcine type XVII collagen noncollagenous 16 A domain and localization of the domain to the upper part of porcine skin basement membrane zone.
    Xu L; Olivry T; Chan LS
    Vet Dermatol; 2004 Jun; 15(3):146-51. PubMed ID: 15214950
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Tenascin-X deficiency mimics Ehlers-Danlos syndrome in mice through alteration of collagen deposition.
    Mao JR; Taylor G; Dean WB; Wagner DR; Afzal V; Lotz JC; Rubin EM; Bristow J
    Nat Genet; 2002 Apr; 30(4):421-5. PubMed ID: 11925569
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mice lacking matrilin-1 (cartilage matrix protein) have alterations in type II collagen fibrillogenesis and fibril organization.
    Huang X; Birk DE; Goetinck PF
    Dev Dyn; 1999 Dec; 216(4-5):434-41. PubMed ID: 10633862
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Abnormality of type IX collagen in a patient with diastrophic dysplasia.
    Diab M; Wu JJ; Shapiro F; Eyre D
    Am J Med Genet; 1994 Feb; 49(4):402-9. PubMed ID: 8160734
    [TBL] [Abstract][Full Text] [Related]  

  • 19. BUB/BnJ (H-2q) is a TCR deletion mutant mouse strain (TCR V beta a, KJ16-) that is susceptible to type II collagen-induced arthritis.
    Ortman RA; Holderbaum D; Qu XM; Banerjee S; Haqqi TM
    J Immunol; 1994 Apr; 152(8):4175-82. PubMed ID: 8144978
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Insulin-like growth factor binding protein 5 induces skin fibrosis: A novel murine model for dermal fibrosis.
    Yasuoka H; Jukic DM; Zhou Z; Choi AM; Feghali-Bostwick CA
    Arthritis Rheum; 2006 Sep; 54(9):3001-10. PubMed ID: 16947625
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.