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  • 1995-1999  (2)
  • 1955-1959  (1)
  • 1925-1929  (1)
  • Cell & Developmental Biology  (4)
  • Life and Medical Sciences  (4)
  • 1
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 48 (1929), S. 105-121 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Two types of cytoplasmic inclusions, differing in reactions to vital dyes and to osmic fixation and impregnation have been demonstrated in Peranema trichophorum. The mitochondria are rod-like and lie in more or less spiral rows, forming a single layer beneath the periplast. They are stained supravitally with Janus green, but not with neutral red. They may be demonstrated by staining in iron hematoxylin after Mann-Kopsch fixation. They are also blackened in prolonged osmic impregnation, but are bleached readily with hydrogen peroxide.The small spherical osmiophilic inclusions are scattered in distribution, although sometimes more numerous in the anterior third of the organism. These bodies are stainable supravitally with neutral red, neutral violet, and brilliant cresyl blue. They are densely blackened in osmic impregnation, and are not bleached in the usual treatment with hydrogen peroxide. They are not however, demonstrated by Mann-Kopsch fixation and iron hematoxylin. After being stained supravitally with neutral red, these inclusions may be blackened under direct observation by exposure to osmic vapor in hanging-drop preparations.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Developmental Dynamics 203 (1995), S. 477-490 
    ISSN: 1058-8388
    Keywords: Thrombospondin ; Development ; Extracellular matrix ; In situ hybridization ; Chondrogenesis ; Osteogenesis ; Cornea ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The thrombospondins are a family of related glycoproteins found in the embryonic extracellular matrix. To date, five members of this family have been identified. Thrombospondin-1 and thrombospondin-2 have similar primary structure, but are expressed in different tissues at different times during development. Thrombospondins-3, -4, and cartilage oligomeric protein belong to a second thrombospondin subgroup in which the carboxyl-half of each molecule is most similar to thrombospondin-1 and -2. Here, we report the cloning and sequencing of a novel probe to avian thrombospondin-4. We have used this probe to determine the origins of thrombospondin-4 in the chick embryo by in situ hybridization. Thrombospondin-4 transcripts first appear in the mesenchyme surrounding bone anlage coinciding with the initial stages of osteogenesis. The expression in osteogenic tissues is transient: thrombospondin-4 mRNAs are not seen in the osteoblasts of bone collars in developing long bones. This pattern is distinct from avian thrombospondin-2, which is expressed in perichondrium and embryonic fibrous connective tissues. Our observations indicate that connective tissues are the principal site of thrombospondin-4 expression in the chick. The diverse origins of different thrombospondin gene family members imply distinctive roles for these proteins related to the growth and differentiation of cartilage, tendons, and bone. ©1995 Wiley-Liss, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: A new pH indicator, seminaphthofluorescein (SNAFL)-calcein acetoxymethyl ester, was used for intracellular pH (pHi) measurement in living MDCK cells with a laser scanning confocal microscope (LSCM) equipped with an Argon/Krypton laser and dual-excitation and dual-emission (FITC/Texas Red) filter set. SNAFL-calcein excitation maxima are ∼492/540 nm (acid/base) and emission maxima are ∼535/625 nm (acid/base) with a pKa value at ∼7.0. The absorption/emission spectra of SNAFL-calcein indicate that the ratio of emission intensities of its basic/acidic forms is pH dependent. With an Argon/Krypton LSCM, we were able to monitor the acidic and basic forms of this dye simultaneously using dualexcitation (488/568 nm) and dual-emission (525-614 nm/∼615 nm) wavelengths (λs). The simultaneous dual-excitation/emission LSCM system allows for efficient recording of pHi dynamics (time resolution ≍ 1 sec) in living cells. We have analyzed emission stability of the dye at different temperatures (22°C and 37°C) and constant pH, and at the same temperature (22D°C) but various pHs (6.6, 7.0, and 7.4). Bleaching rate is slightly higher at 37°C than that at 22°C. The basic form of the dye (λEm ≍ 625 nm) has a slightly higher bleaching rate than the acidic form (λEm ≍ 535 nm) in standard culture medium (pH 7.3) at either 22°C or 37°C. The pHi in MDCK cells calculated from ratio images (535 nm/625 nm) was 7.19 ± 0.03 (mean ± SEM, n = 20). Calibration experiments show that the useful pH range of SNAFL-calcein appears to be between 6.2 and 7.8, as the dye is difficult to calibrate outside this pH range. © 1995 Wiley-Liss, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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