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  • Articles: DFG German National Licenses  (3)
  • 2000-2004  (1)
  • 1970-1974  (2)
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  • Articles: DFG German National Licenses  (3)
Material
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 228 (1974), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 12 (1971), S. 283-294 
    ISSN: 1432-1106
    Keywords: Spinal border cells ; Ventral spinocerebellar tract
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. Extra- and intracellular recording has been made in cats from the spinal border cells (SBCs) of Cooper and Sherrington (1940). The SBCs were identified by their location in the lateral part of the ventral horn in the lumbar segments 3–6 and by their antidromic invasion from the contralateral thoracic spinal cord. 2. The conduction velocity of SBC axons ranged from 40–140 m/sec with a mean of 85 m/sec. 3. Lesion experiments showed that the SBC axons ascend in the ventrolateral region of the spinal cord. 4. Of 90 SBCs tested, 85 were invaded antidromically by stimulation of the cerebellar cortex. 5. It is concluded that SBCs give rise to ventral spinocerebellar axons and suggested that they are the major source of this tract.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-0568
    Keywords: Key words Fibrillin-1 ; Microfibrils ; Embryonic development ; Extracellular matrix ; Marfan
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  Fibrillin microfibrils are widely distributed components of extracellular matrices that function in the formation of elastin, serve structural roles and provide substrates for cell adhesion. To determine when and how fibrillin-1 (fib-1) may function in early development we have examined the temporal and spatial distribution of fib-1 in chicken embryos. Using homologous PCR we amplified and cloned a 407 nt fragment of chicken cDNA that appears to code for an orthologue of FBN-1. Bacterially expressed protein was used to prepare two monoclonal antibodies, both of which recognize a 350 kD band in immunoblots or immunoprecipitates in supernatants of chicken embryonic aorta cells or human MG-63 cells. Both antibodies recognize fibrillar material associated with the surfaces of cultured cells. The antibodies appear to be specific for fib-1 as there was only weak cross reactivity to a bacterially expressed fragment from the corresponding region of fib-2 and the pattern of immunofluorescence in embryonic tissue is distinctly different from that of JB-3, a fib-2 specific antibody (Rongish et al. 1998). In embryos, fib-1 is first detected at stage 6 in the epiblast during gastrulation. In subsequent stages fib-1 fibers appear in all tissues and are present throughout the first 6 days of development. Immunoreactive fibers are present in basal laminae and mesenchyme filled spaces, but they also form random arrays with an apical-basal polarity within epithelia. Using primers specific for FBN-1 and FBN-2 in RT-PCR reactions we confirm the presence of fib-1 and fib-2 mRNA in early embryonic stages. This temporal and spatial distribution indicates fib-1 has functions in early development that are distinct from fib-2.
    Type of Medium: Electronic Resource
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