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  • 1
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 510 (1987), 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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  • 3
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. A prominent population of olfactory receptor cells from the lobsterHomarus americanus is narrowly tuned to trans-4-hydroxyl-L-proline (Hyp, Fig. 1) suggesting that Hyp may be an important chemical signal for this animal (Johnson and Atema 1983). However, Hyp is usually bound in connective tissue proteins of lobster prey and thus may be unavailable in sufficient quantities as a free amino acid to stimulate chemoreceptors. To determine other possible adequate stimuli for Hyp sensitive cells we further examined their tuning using a variety of substances including other amino acids also found in collagens, Hyp isomers (Fig. 1), synaptic receptor agonists, ecdysones, purified natural collagens and their gelatins (Fig. 2), and different molecular weight fractions of a commercial gelatin solution (Table 1). 2. Of a first group of Hyp sensitive cells (N=29) tested with the compounds in Table 1 A, 21 responded best to Hyp. Only a commercial gelatin solution (SG1) and its one-tenth dilution consistently elicited responses from these cells (Fig. 3). The remaining 8 cells responded best to the SG1 solutions (5 cells) or to one of the other test substances (Table 2). 3. Of a second group of Hyp sensitive cells (N=27) tested with the collagen and gelatin solutions (Table 1b), 19 responded best to Hyp. Again, the Hyp best cells rarely responded to any test substance other than Hyp and a commercial gelatin solution, SG2, and its greater than 12 kD fraction, SG2-12 (Fig. 4). SG2 and SG2-12 were equally effective for the Hyp best cells. The remaining 8 cells responded best to either SG2 (2 cells), SG2-12 (2 cells) or one of the purified gelatin or collagen solutions (Table 3). 4. A third group of Hyp sensitive cells (N=21) was tested with SG2, SG2-12, and a greater than 1 kD fraction of SG2 (SG2-1; Table 1c). Based on the mean response, the most effective stimulus for these cells was SG2-12, followed by SG2-1, SG2 and Hyp. The high mean response for the SG2 solutions was mainly due to a few cells giving large responses to these stimuli (Fig. 6). Ten of these 21 cells responded best to Hyp; all but 2 responded to one or more of the SG2 solutions; the other 11 cells responded best to either SG2, SG2-12 or SG2-1, which were all best stimuli for different cells (Fig. 5). 5. Overall, the 77 Hyp sensitive cells tested here can be divided into two main types; 65% Hyp best cells and 31% gelatin best cells. The Hyp best cells seem to be a distinct population of receptors: they have no spontaneous activity and give low responses (15 spikes in 5 s) even to their ‘best’ stimulus, Hyp. In contrast, the gelatin best cells are not infrequently spontaneously active and can give high responses to their best stimulus (up to 150 spikes in 5 s). In addition, when tested specifically in the third group, the Hyp cells appear to have a tuning spectrum distinct from the gelatin best cells (Fig. 7). 6. Stimulation of Hyp cells by gelatin solutions may be due to Hyp-containing peptides derived from the gelatin. Enzymatic tissue breakdown from the lobster's prey could produce chemical mixtures that stimulate prominent receptor populations which respond to both high (gelatin best cells) and low (Hyp best cells) molecular weight substances. This could create a central representation of food based on parallel receptor lines of somewhat overlapping sensitivity. Together, Hyp best and gelatin best receptor cell populations may give important information on the presence and state of decay of the lobster's food.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-7276
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The invasive and metastatic characteristics of cloned cells derived from the K-1735 murine melanoma were investigated. Cell lines which are highly metastatic in mice were found to be invasivein vitro, and to show an enhanced attachment to, spreading on and migration toward laminin. As attachment, spreading and directional migration are thought to be receptor-mediated events, the binding of laminin to these cells was studied. Biotinylated laminin was used to evaluate receptor binding by fluorescence activated cell sorting (FACS) and this method was compared with that in which the binding of radioactive laminin is measured. Both studies revealed that metastatic K-1735 cells (a) have more receptors for laminin compared with non-metastatic cells and (b) exhibit a second population of low-affinity binding sites not present on the non-metastatic cells. The differences in receptor number and type may account for the greater interaction of metastatic cells with laminin and their invasive phenotype.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 65 (1978), S. 115-126 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Nucleoli were purified from the slime mold Physarum polycephalum and assayed for enrichment in ribosomal DNA by analytical ultracentrifugation. Greater than 90% of the DNA from nucleoli comprises a satellite band characteristic of Physarum ribosomal DNA (rDNA) in a CsCl equilibrium sedimentation gradient. Over 75% of the nucleolar DNA molecules are 37×106 Daltons, a further characteristic of Physarum rDNA. Nucleoli incubated with micrococcal nuclease yield a distribution of discrete DNA fragments indicative of nucleosome subunits; these digestion products are indistinguishable in size from those of total nuclear chromatin. The nucleosome DNA repeat length varied with increasing digestion from 175 down to 150 base pairs. A palindrome structure for the ribosomal nucleoprotein molecules is demonstrated by electron microscopy of actively transcribing ribosomal RNA genes, which required modification of usual methods for dispersing chromatin. In the center of each palindrome is a 6.0–6.5 μm non-transcribed “spacer” region which exhibits a beaded nucleosome structure. Transcription initiates at points on either side of the central spacer, as evidenced by 4.0–4.2 μm matrices of growing rRNA fibrils extending to each end of the palindrome. The polarity of transcription matrices, together with information about the sites of rRNA coding sequences, imply that 19S rRNA is transcribed prior to 26S rRNA.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1573-4935
    Keywords: collagen receptor ; RGD-peptides ; integrins ; embryonic cell surface
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Several cell surface proteins (Mr=120,000, 90,000, 63,000 and 47,000) apparently integral to embryonic fibroblast plasma membranes were extracted with detergent and isolated by collagen affinity chromatography. Certain of these proteins (Mr=120,000, 90,000 and 47,000) were specifically eluted from collagen affinity columns by synthetic peptides containing the amino acid sequence arginyl-glycyl-aspartic acid (RGD). These data show that a number of collagen binding proteins exist on the embryonic fibroblast cell surface. Some of the proteins may be collagen receptors binding to RGD sequences in the collagen molecule while at least one of the proteins (Mr=63,000) recognizes features other than RGD.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Developmental Dynamics 198 (1993), S. 312-322 
    ISSN: 1058-8388
    Keywords: Development ; Tissue interactions ; Morphogenesis ; Cranial sutures ; Dura mater ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Cranial sutures play a critical role in calvarial morphogenesis, serving as growth centers during skull development. Both biomechanical tensile forces originating in the cranial base and biochemical factors present in dura mater have been postulated as determinants of suture morphogenesis and patency. A rat transplant model free of the putative biomechanical influence of the dura and cranial base was used to investigate the role of the dura mater in both the initial morphogenesis and maintenance of sutures during skull growth. Day 19 fetal presumptive (F19) and day 1 neonatal differentiated (N1) coronal sutures, including associated frontal and parietal bones, were transplanted with or without underlying dura mater to the center of adult parietal bones. After 1, 2, and 3 weeks, transplanted tissues were examined histologically and histomorphometrically to determine whether sutures formed and whether they were obliterated by ossification in the absence of dura mater. Both F19 and N1 sutures remained patent for 2 weeks either in the presence or the absence of transplant dura mater. However, at 3 weeks, in the absence of transplant dura mater, sutures were obliterated by bone, while in the presence of dura mater sutures resisted ossification, demonstrating an essential requirement for interactions with the transplant dura mater in maintaining functional sutures. Both F19 and N1 transplants showed comparable bone growth (cross-sectional surface area), regardless of the presence of transplant dura mater. These experiments suggest that tissue interactions of a biochemical nature, rather than biomechanical forces generated through the cranial base, are required to maintain the suture as a non-ossified growth center. Furthermore, while the presence of dura mater was essential for maintenance of suture patency, fetal dura mater was not required for initial suture formation. © 1993 Wiley-Liss, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Hoboken, NJ [u.a.] : Wiley-Blackwell
    Journal of Orthopaedic Research 2 (1984), S. 134-142 
    ISSN: 0736-0266
    Keywords: Cartilage ; Collagen ; Biosynthesis ; Growth ; Growth plate ; Life and Medical Sciences
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The distribution, structure, and biosynthesis of various collagen types have been studied in growth and structural cartilage from young rabbits. The major collagen of cartilage is α1(II); however, all cartilage matrix also contains 1α, 2α, 3α (Type Cm), as well as a high molecular weight disulfidelinked collagen (Type M). Cartilage fragments in organ culture demonstrate synthesis of precursors of collagen α chains and processing to their final forms. Although Type Cm collagen is present in the same proportion in the matrix of growth and structural cartilage, in vitro radiolabeling of rabbit cartilage showed that only growth cartilage is capable of actively synthesizing Type Cm, except in the newborn period when synthesis of Type Cm does occur in structural cartilage. A low molecular weight collagen (designated G collagen) is synthesized in vitro by growth cartilage but not by structural or articular cartilage. Preferential distribution of these minor collagens in growth cartilage suggests a role in development during normal cartilage growth.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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