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 *

124 related articles for article (PubMed ID: 9205941)

  • 1. Murine models of human genetic skeletal disorders.
    Li Y; Olsen BR
    Matrix Biol; 1997 May; 16(2):49-52. PubMed ID: 9205941
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Chondrodysplasia of gene knockout mice for aggrecan and link protein.
    Watanabe H; Yamada Y
    Glycoconj J; 2002; 19(4-5):269-73. PubMed ID: 12975605
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in collagen genes resulting in metaphyseal and epiphyseal dysplasias.
    Olsen BR
    Bone; 1995 Aug; 17(2 Suppl):45S-49S. PubMed ID: 8579897
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The comparative biology of chondrodysplasias in mice.
    Brown KS
    Pathol Immunopathol Res; 1988; 7(1-2):55-61. PubMed ID: 3222208
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Histochemical, immunofluorescence, and ultrastructural differences in fetal cartilage among three genetically distinct chondrodystrophic mice.
    Seegmiller RE; Brown K; Chandrasekhar S
    Teratology; 1988 Dec; 38(6):579-92. PubMed ID: 3070812
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Transgenic mouse models in studies of skeletal disorders.
    Jacenko O; Olsen BR
    J Rheumatol Suppl; 1995 Feb; 43():39-41. PubMed ID: 7752133
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Disproportionate micromelia (Dmm): an incomplete dominant mouse dwarfism with abnormal cartilage matrix.
    Brown KS; Cranley RE; Greene R; Kleinman HK; Pennypacker JP
    J Embryol Exp Morphol; 1981 Apr; 62():165-82. PubMed ID: 7276808
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Understanding chondrodysplasia (cho): A comprehensive review of cho as an animal model of birth defects, disorders, and molecular mechanisms.
    Seegmiller RE; Foster C; Burnham JL
    Birth Defects Res; 2019 Mar; 111(5):237-247. PubMed ID: 30719872
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Fine structure of extracellular matrix and basal laminae in two types of abnormal collagen production: L-proline analog-treated otocyst cultures and disproportionate micromelia (Dmm/Dmm) mutants.
    Berggren D; Frenz D; Galinovic-Schwartz V; Van de Water TR
    Hear Res; 1997 May; 107(1-2):125-35. PubMed ID: 9165353
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Heritable diseases of the skeleton. Part II: Molecular insights into skeletal development-matrix components and their homeostasis.
    Mundlos S; Olsen BR
    FASEB J; 1997 Mar; 11(4):227-33. PubMed ID: 9068611
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A fibrillar collagen gene, Col11a1, is essential for skeletal morphogenesis.
    Li Y; Lacerda DA; Warman ML; Beier DR; Yoshioka H; Ninomiya Y; Oxford JT; Morris NP; Andrikopoulos K; Ramirez F
    Cell; 1995 Feb; 80(3):423-30. PubMed ID: 7859283
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The heterozygous disproportionate micromelia (dmm) mouse: morphological changes in fetal cartilage precede postnatal dwarfism and compared with lethal homozygotes can explain the mild phenotype.
    Seegmiller RE; Bomsta BD; Bridgewater LC; Niederhauser CM; Montaño C; Sudweeks S; Eyre DR; Fernandes RJ
    J Histochem Cytochem; 2008 Nov; 56(11):1003-11. PubMed ID: 18678883
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular genetics of chondrodysplasias, including clues to development, structure, and function.
    Byers PH
    Curr Opin Rheumatol; 1994 May; 6(3):345-50. PubMed ID: 8060773
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Disrupted expression of matrix genes in the growth plate of the mouse cartilage matrix deficiency (cmd) mutant.
    Wai AW; Ng LJ; Watanabe H; Yamada Y; Tam PP; Cheah KS
    Dev Genet; 1998; 22(4):349-58. PubMed ID: 9664687
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus.
    Vikkula M; Mariman EC; Lui VC; Zhidkova NI; Tiller GE; Goldring MB; van Beersum SE; de Waal Malefijt MC; van den Hoogen FH; Ropers HH
    Cell; 1995 Feb; 80(3):431-7. PubMed ID: 7859284
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Brachymorphic (bmm/bmm) cartilage matrix deficiency (cmd/cmd) and disproportionate micromelia (Dmm/Dmm); three inborn errors of cartilage biosynthesis in mice.
    Brown KS; Harne L
    Prog Clin Biol Res; 1982; 94():245-9. PubMed ID: 7122617
    [No Abstract]   [Full Text] [Related]  

  • 18. Impact of mutations of cartilage matrix genes on matrix structure, gene activity and chondrogenesis.
    So CL; Kaluarachchi K; Tam PP; Cheah KS
    Osteoarthritis Cartilage; 2001; 9 Suppl A():S160-73. PubMed ID: 11680681
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Osteoarthritis-like changes and decreased mechanical function of articular cartilage in the joints of mice with the chondrodysplasia gene (cho).
    Xu L; Flahiff CM; Waldman BA; Wu D; Olsen BR; Setton LA; Li Y
    Arthritis Rheum; 2003 Sep; 48(9):2509-18. PubMed ID: 13130470
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Spondylometaphyseal dysplasia in mice carrying a dominant negative mutation in a matrix protein specific for cartilage-to-bone transition.
    Jacenko O; LuValle PA; Olsen BR
    Nature; 1993 Sep; 365(6441):56-61. PubMed ID: 8361538
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.