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  • Articles: DFG German National Licenses  (4)
  • 1970-1974  (4)
Source
  • Articles: DFG German National Licenses  (4)
Material
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 169 (1971), S. 585-591 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: A three-dimensional reconstruction of the rod profiles seen in inner and outer rat incisor enamel was made from serial 1 μ cross sections of a decalcified upper incisor. The enamel rod was found to be an elongated structure which travelled incisally relative to its origin and ran continuously from the dentino-enamel junction to the enamel surface. The rod was divisible into an inner and outer enamel portion. The inner enamel portion began at the dentinoenamel junction and travelled incisally for about 20 μ with either a mesial or lateral tilt towards the outer enamel. The outer enamel portion of the rod was straight and ran incisally for about 60 μ as it gradually approached the enamel surface.Inner enamel portions of rods were arranged in rows parallel to the cross sectional plane of the incisor. All the rods in each row were tilted either mesially or laterally such that individual rods of adjacent rows crossed each other at 90°. Outer enamel portions of rods were not arranged in rows but all passed incisally parallel to one another.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 169 (1971), S. 559-583 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The structure of the organic matrix close to the mature enamel in 100 gm rat incisors was studied by light and electron microscopy using EDTA decalcified teeth.Under the light microscope, in 0.5 μ Epon sections, the enamel layer of cross sectioned upper incisors was about 60 μ thick. The inner enamel was about 40 μ thick and consisted of an initial enamel layer (4 μ) adjacent to the dentin in which no rod profiles were seen, and an inner layer proper which contained six to eight rows of oval-shaped rod profiles set in a homogeneous background. The profiles in any given row were inclined mesially or laterally and alternated in adjacent rows. The outer enamel was about 20 μ thick and consisted of an outer enamel proper and a 2-4 μ thick final enamel layer which smoothed out the enamel surface. The outer enamel proper contained smaller elliptical rod profiles in a more abundant background. These profiles were not arranged in rows and were oriented at right angles to the enamel surface. The final enamel layer contained no rod profiles and was lined on its outer surface by a PA-Schiff positive layer resembling a basement membrane.Under the electron microscope the matrix of rod profiles and interrod material could be distinguished. This consisted of aggregated tubular (and filamentous) subunits, 250 Å in diameter, with empty space between them. Within the rod profiles the subunits ran parallel to the rod's long axis, whereas in the interrod material the subunits were again parallel but but running at right angles to the subunits of the rods. In addition to forming the material between the rods, the interrod material also formed the initial and final enamel layers.
    Additional Material: 24 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 179 (1974), S. 423-445 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Longitudinal sections through the incisors of the rat show a continuous layer of ameloblasts on the labial surface of the tooth. This layer contains the entire sequence of developmental stages in enamel production. Using 1 μm Epon sections from the upper and lower incisors of 100 gm male rats, the ameloblast layer was divided into three main zones which were themselves subdivided into regions: (1) Presecretory zone which includes (a) region of ameloblasts facing pulp, itself comprising a posterior portion (upper 172 ± 35 μm; lower 187 ± 37 μm) and an anterior portion (upper 458 ± 28 μm; lower 503 ± 36 μm); (b) region of ameloblasts facing dentin (upper 1210 ± 81 μm; lower 1381 ± 90 μm). (2) Secretory zone, (a) region of inner enamel secretion (upper 2573 ± 141 μm; lower 4274 ± 160 μm); (b) region of outer enamel secretion (upper 1211 ± 60 μm; lower 868 ± 72 μm). (3) Maturation zone (upper 7335 μm; lower 10615 μm), (a) region of postsecretory transition; (b) region of maturation proper, consisting of portions of ameloblasts with striated border and portions of ameloblasts with unmodified apices; (c) region of pigmentation; (d) region of reduced ameloblasts.These regions are readily identified using clear cut morphological criteria. Length measurements made on a group of 40 rats established the reproducibility of this classification. Therefore, this classification will be used as a basis for future studies of cell population kinetics.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The South American rattlesnake venom gland is made up of secretory tubules lined by a simple columnar epithelium containing horizontal cells, mitochondria-rich cells, and the principal cell type, the columnar secretory cells. This cell has a round basal nucleus and abundant rough endoplasmic reticulum, the cisternae of which are variably distended with flocculent material containing many dense intracisternal granules. The supranuclear Golgi apparatus is spherical, with stacks of flattened saccules at the periphery and large vacuoles containing masses of dense material, and other dense granules in the center. Similar but smaller granules are present at the apex where they fuse with the microvillus-covered apical membrane and release their content into the lumen. Protein synthesis was studied in snakes injected with 3H-tyrosine and sacrificed at several times after injection. Radioautographs showed reactions at one half and one hour over the ribosomes and membranes of the rough endoplasmic reticulum. At two hours the immature face of the Golgi apparatus was labeled. At four hours Golgi saccules and vacuoles with dense masses (secretory granules) were labeled, and at eight hours the dense masses within the secretory granules were heavily labeled both in the Golgi region and in the apex near the lumen. Labeled material was found in the lumen at two days. Intracisternal granules were first labeled at eight hours, and by two days reactions remained only over the flocculent content and intracisternal granules of the rough endoplasmic reticulum. Thus, venom protein was synthesized on the rough endoplasmic reticulum, migrated through the Golgi apparatus and accumulated in the dense masses of the secretory granules, which moved to the apex and were extruded. The labeling of intracisternal granules at eight hours and two days after injection indicated a storage nature for these granules.
    Type of Medium: Electronic Resource
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