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 *

143 related articles for article (PubMed ID: 3269104)

  • 1. The Gordon Wilson lecture. Mutations in type I procollagen genes. An explanation for brittle bones and a paradigm for other diseases of connective tissue.
    Prockop DJ
    Trans Am Clin Climatol Assoc; 1989; 100():70-80. PubMed ID: 3269104
    [No Abstract]   [Full Text] [Related]  

  • 2. Osteogenesis imperfecta. A model for genetic causes of osteoporosis and perhaps several other common diseases of connective tissue.
    Prockop DJ
    Arthritis Rheum; 1988 Jan; 31(1):1-8. PubMed ID: 3345218
    [No Abstract]   [Full Text] [Related]  

  • 3. Type I procollagen: the gene-protein system that harbors most of the mutations causing osteogenesis imperfecta and probably more common heritable disorders of connective tissue.
    Prockop DJ; Constantinou CD; Dombrowski KE; Hojima Y; Kadler KE; Kuivaniemi H; Tromp G; Vogel BE
    Am J Med Genet; 1989 Sep; 34(1):60-7. PubMed ID: 2683782
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Heritable defects in connective tissue.
    Pyeritz RE
    Hosp Pract (Off Ed); 1987 Feb; 22(2):153-9, 162-8. PubMed ID: 3100562
    [No Abstract]   [Full Text] [Related]  

  • 5. [Biochemical defects in hereditary diseases of the connective tissue (review)].
    Del'vig AA
    Vopr Med Khim; 1986; 32(2):2-14. PubMed ID: 3518233
    [No Abstract]   [Full Text] [Related]  

  • 6. Genetic disorders of connective tissues.
    Mundlos S; Spranger J
    Curr Opin Rheumatol; 1991 Oct; 3(5):832-7. PubMed ID: 1751316
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Collagen genes and brittle bones.
    Shapiro JR; Rowe DW
    Ann Intern Med; 1983 Nov; 99(5):700-4. PubMed ID: 6638727
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Bone fragility in transgenic mice expressing a mutated gene for type I procollagen (COL1A1) parallels the age-dependent phenotype of human osteogenesis imperfecta.
    Pereira RF; Hume EL; Halford KW; Prockop DJ
    J Bone Miner Res; 1995 Dec; 10(12):1837-43. PubMed ID: 8619363
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Learning how mutations in type I collagen genes cause connective tissue disease.
    Kadler KE
    Int J Exp Pathol; 1993 Aug; 74(4):319-23. PubMed ID: 8398803
    [No Abstract]   [Full Text] [Related]  

  • 10. Osteogenesis imperfecta--a model for the analysis of inborn errors of connective tissue.
    Ramirez F
    Basic Life Sci; 1988; 48():45-51. PubMed ID: 3071359
    [No Abstract]   [Full Text] [Related]  

  • 11. Mutations in collagen genes. Consequences for rare and common diseases.
    Prockop DJ
    J Clin Invest; 1985 Mar; 75(3):783-7. PubMed ID: 3884665
    [No Abstract]   [Full Text] [Related]  

  • 12. [Osteoporosis in congenital disorders].
    Tsuda M; Sakiyama T
    Nihon Rinsho; 1994 Sep; 52(9):2426-9. PubMed ID: 7967092
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutations in type 1 procollagen that cause osteogenesis imperfecta: effects of the mutations on the assembly of collagen into fibrils, the basis of phenotypic variations, and potential antisense therapies.
    Prockop DJ; Colige A; Helminen H; Khillan JS; Pereira R; Vandenberg P
    J Bone Miner Res; 1993 Dec; 8 Suppl 2():S489-92. PubMed ID: 8122517
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic defects of collagen.
    Prockop DJ
    Hosp Pract (Off Ed); 1986 Feb; 21(2):125-9, 133-5, 138-40. PubMed ID: 3081529
    [No Abstract]   [Full Text] [Related]  

  • 15. Mutation analysis of coding sequences for type I procollagen in individuals with low bone density.
    Spotila LD; Colige A; Sereda L; Constantinou-Deltas CD; Whyte MP; Riggs BL; Shaker JL; Spector TD; Hume E; Olsen N
    J Bone Miner Res; 1994 Jun; 9(6):923-32. PubMed ID: 8079666
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations in type I procollagen genes that cause osteogenesis imperfecta.
    Prockop DJ; Baldwin CT; Constantinou CD
    Adv Hum Genet; 1990; 19():105-32. PubMed ID: 2193488
    [No Abstract]   [Full Text] [Related]  

  • 17. A lethal variant of osteogenesis imperfecta has a single base mutation that substitutes cysteine for glycine 904 of the alpha 1(I) chain of type I procollagen. The asymptomatic mother has an unidentified mutation producing an overmodified and unstable type I procollagen.
    Constantinou CD; Nielsen KB; Prockop DJ
    J Clin Invest; 1989 Feb; 83(2):574-84. PubMed ID: 2913053
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutations in collagen genes: causes of rare and some common diseases in humans.
    Kuivaniemi H; Tromp G; Prockop DJ
    FASEB J; 1991 Apr; 5(7):2052-60. PubMed ID: 2010058
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Syndromes with congenital brittle bones.
    Plotkin H
    BMC Pediatr; 2004 Aug; 4():16. PubMed ID: 15339338
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An osteopenic nonfracture syndrome with features of mild osteogenesis imperfecta associated with the substitution of a cysteine for glycine at triple helix position 43 in the pro alpha 1(I) chain of type I collagen.
    Shapiro JR; Stover ML; Burn VE; McKinstry MB; Burshell AL; Chipman SD; Rowe DW
    J Clin Invest; 1992 Feb; 89(2):567-73. PubMed ID: 1737847
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.