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  • bone morphogenetic protein  (2)
  • Key words Murine cataract  (1)
  • 1
    ISSN: 1617-4623
    Keywords: Key words Murine cataract ; Linkage studies ; Candidate genes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Cat3 vl and Cat3 vao are two allelic, dominant cataract mutations that arose independently in the F1 generation after γ-irradiation of male mice. The cataracts are already present at birth. Examination of the eyes with a slit lamp revealed completely vacuolated lenses in Cat3 vl mutants and anteriorly located opacity in Cat3 vao mutants. The appearance of the opacities does not differ between the individuals or between heterozygotes and homozygotes. Penetrance of the mutations is complete. Viability and fertility of the mutants are normal except in the case of the Cat3 vl homozygotes. Cat3 vao was assigned to the distal part of mouse chromosome 10, 3.2±0.9 cM away from the visible marker Steel (Sl gbH ). Using polymorphic markers the following locus order was found: D10Mit230–(0.2±0.1 cM)–Cat3 vao –(2.5±0.6 cM)–D10Mit70. No recombinants were found between Cat3 vao and the markers D10Mit41 and D10Mit95 among 921 offspring. The results exclude allelism of Cat3 vao with Cat Lop or To2, which also map to chromosome 10. Candidate genes were tested by examination of their expression in the eye of newborn mice and by analysis of cDNA sequences. So far, negative results have been obtained for the genes encoding the proteoglycans lumican and decorin, the nuclear orphan receptor Tr2-11 and the transcription factor Elk3. Based on syntenic homology of the Cat3 region to the human chromosome 12q, the Cat3 mutants are discussed as mouse models for cornea plana congenita in man. The recovery of the Cat3 mutations demonstrates the importance of the corresponding locus for proper eye development.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 43 (1998), S. 356-364 
    ISSN: 0021-9304
    Keywords: bone morphogenetic protein ; bone regeneration ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The study reported describes a combination of recombinant human bone morphogenetic protein-2 (rhBMP-2) and collagen (C) to regenerate bone. Unilateral critical-sized defects (CSDs) were prepared in radii of 32 skeletally mature New Zealand white rabbits. Rabbits were divided evenly among four treatments: autograft, absorbable C (Helistat®), 35 μg of rhBMP-2 combined with absorbable C (rhBMP-2/C), and untreated CSDs. The two euthanasia periods were 4 and 8 weeks. Radiographs were taken the day of surgery, every 2 weeks, and at term and the percent of radiopacity was measured. Data analysis revealed a time-dependent increase in the percent radiopacity with rhBMP-2/C. Histological examination revealed the rhBMP-2/C treatment regenerated osseous contour by 8 weeks. According to quantitative histomorphometry, the CSD and C groups had significantly less new bone than either autograft or rhBMP-2/C (p ≤ 0.05). The results suggest that rhBMP-2/C could be an effective therapy to restore segmental bone defects. © 1998 John Wiley & Sons, Inc. J Biomed Mater Res (Appl Biomater) 43: 356-364, 1998
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0021-9304
    Keywords: bone morphogenetic protein ; bone regeneration ; critical size defect ; rabbit ; biomechanics ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The study objective was to determine the mechanical integrity and radiopacity of regenerated bone within critical-sized defects (CSDs) in radii of rabbits using recombinant human bone morphogenetic protein 2 (rhBMP-2) with a porous, biodegradable poly(D,L-lactic acid) (PDLLA) carrier (designated PLA). Twenty millimeter, unilateral radial ostectomies were created in 96 skeletally mature New Zealand white rabbits. The rabbits were randomly assigned to six treatment groups with two euthanasia periods. Treatment groups included unfilled defect (n = 8), segmental autograft (n = 8), PLA + 0 μg rhBMP-2 (n = 8), PLA + 17 μg rhBMP-2 (n = 8), PLA + 35 μg rhBMP-2 (n = 8), and PLA + 70 μg rhBMP-2 (n = 8). The radiopacity was significantly greater for the 35- and 70-μg rhBMP-2 groups at 4 weeks compared to unfilled controls, PLA only, and 17-μg rhBMP-2 groups and equivalent to the autograft. At 8 weeks all groups receiving rhBMP-2 were equivalent to the autograft and significantly greater than unfilled defects and PLA alone. Similarly, the biomechanical analysis indicated significantly greater torque at failure for the 35-μg rhBMP-2 group compared to all other groups at 4 weeks. By 8 weeks all groups receiving rhBMP-2 and autograft had significantly greater torque than unfilled controls and PLA alone. These radiomorphometric and biomechanical results indicate PLA may be a suitable carrier for rhBMP-2 used for skeletal regeneration. © 1998 John Wiley & Sons, Inc. J Biomed Mater Res (Appl Biomater) 43: 365-373, 1998
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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