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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Developmental Dynamics 198 (1993), S. 86-96 
    ISSN: 1058-8388
    Keywords: Rat embryos ; Somites ; Limb bud ; Myogenic cells ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: DiI, a fluorescent lipophilic dye, was micro-injected into the brachial somites of 10.5 day rat embryos to determine whether these somites can contribute cells to the development of the fore-limb bud. The injected embryos were cultured and harvested at the 20-25-somite stage. The dye did not interfere with somitogenesis because, at the injection site, the DiI-labelled somites were able to differentiate into dermomyotome and sclerotome. We have analyzed cryo-sections of 20-21-somite stage embryos and were unable detect the presence of DiI-labelled cells in the fore-limb buds. However, at the 22-somite stage, a few DiI-positive cells were found in the proximal region of the limb bud. These labelled cells had migrated into the limb from the lateral border of the dermomyotome. From the 23-somite stage onwards, there were even more DiI-positive cells inside the limb. We have performed an additional set of experiments to confirm that the somitic cells do have the ability to invade and colonize the limb bud. This was achieved by first labelling newly formed somites isolated from the caudal region of 10.5 day embryos with DiI and then grafting them into corresponding regions in 8-11-somite stage hosts. The donor somites were not orientated when they were implanted into the host. However, this did not disrupt their ability to undergo normal somitogenesis. We have detected the presence of DiI-positive cells in the limb buds of approximately 71% of the 19-30-somite stage embryos that have been examined. This is similar to what we obtained for the injected embryos. Nevertheless, there is one slight difference and that is the stage the somitic cells begin their invasion of the limb. For the injected embryos, migration began at the 22-somite stage but in the transplanted embryos, it commenced as early as the 18-somite stage. We have also investigated the myogenic potential of the fore-limb bud at various stages of development to ascertain whether there is a correlation between the stage the somitic cells first appear in the limb bud and the stage the bud acquires the capacity to form skeletal muscles. This was realized by culturing fore-limb buds excised from 18-30-somite stage embryos conventionally and in the kidney capsules of adult rats. In both methods, bone and cartilage were present in all of the cultures whereas skeletal muscles were only present in cultured explants older than the 21-22-somite stage. The appearances of skeletal muscles in the cultures correlated exactly with the stage somitic cells began their invasion of limb (as seen in the DiI injected embryos). Based upon the indirect evidence that has been obtained, we tentatively propose that the brachial musculature of the rat embryo is derived from the somites while bone and cartilage are formed by the somatopleure of the limb. © 1993 Wiley-Liss, Inc.
    Additional Material: 4 Ill.
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  • 2
    ISSN: 1058-8388
    Keywords: Cell death ; Interdigital chondrogenesis ; Type II procollagen mRNA ; Retinoic acid ; Hind limb bud ; Mouse embryo ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: We have cultured tissues isolated from the interdigital zones (IDZ) of the mouse footplate in the presence of the digits, ectoderm, and all-trans retionic acid. The objective was to understand how these various factors influence the developmental fate of the interdigital tissues. Neutral red staining showed that these tissues normally differentiate by dying between day 12.5-14.5. However, if they were isolated from the footplate between day 12.5-13.5 (when cell death is not overtly obvious in the IDZ) and maintained in organ culture, these tissues would develop into cartilage and soft connective tissues. In culture, chondrogenesis is initiated very rapidly in the interdigital explants as revealed by in situ hybridization with riboprobes specific for type IIA and IIB procollagen mRNAs. The ability of interdigital tissues to form cartilage is not attributed to factors present in the serum of the culture medium as this phenomenon is also observed in serumless cultures. We have found that if all-trans retinoic acid, at concentrations of 10-50 ng/ml culture medium, were added to the explants it could inhibit chondrogenesis and promote cell death. Moreover, in some of the cultures, a single digit was left attached to the interdigital tissue. This also dramatically reduced the incidence of chondrogenesis. We have tried to determine whether the digits and ectoderm can produce a diffusible factor that can prevent cartilage from developing by culturing day 12.5 interdigital tissues in ectoderm and digit conditioned media. The ectoderm conditioned medium had no effects on interdigital growth or chondrogenesis. In contrast, the size of interdigital explants cultured in the presence of digit conditioned medium was shown to be significantly smaller than the control. These explants also produced a smaller quantity of cartilage as revealed by Alcian blue binding assay. In sum, our results showed that the fate of the interdigital tissues are not fully determined until after day 13.5. These tissues have the potentials to form cartilage and soft connective tissues. We tentatively propose that these interdigital tissues do not normally realize their histogenetic potentials because of the antichondrogenic influence of the digits and retinoic acid. © 1994 Wiley-Liss, Inc.
    Additional Material: 10 Ill.
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  • 3
    ISSN: 0009-2940
    Keywords: Rhenium complexes ; Silylene complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions of (η5-C5H5)Re(NO)(PPh3)(SiMe2H) (1) and CHCl3, CBr4, and CHI3 give halosilyl complexes (η5-C5H5)Re(NO)-(PPh3)(SiMe2X) [X = Cl (2), Br (3), I (4); 66-84%]. Addition of Me3SiOTf to 2 gives triflate (η5-C5H5)Re(NO)(PPh3)(SiMe2OTf) (5; 97%), which in turn reacts with (Me2N)3S⊕ [SiMe3F2]⊖ to give (η5-C5H5)Re(NO)(PPh3)(SiMe2F) (6; 77%). Reaction of 5 and pyridine gives the base-stabilized silylene complex [(η5-C5H5)Re(NO)(PPh3){SiMe2(NC5H5)}]⊕ TfO⊖ (7; 84%). CH2Cl2 solutions of (η5-C5H5)Re(NO)(PPh3)(CH3) (8) or 2 and Lewis acids are studied by IR and NMR. As assayed by IR, 8/ECl3 solutions (E = B, Al) show ReNO-ECl3 (major) and Re-ECl3 (minor) adducts. Solutions of 2/BCl3 show analogous adducts (-78°C), and in the presence of excess BCl3 (η5-C5H5)Re-(NO-BCl3)(PPh3)(SiMe2Cl) (11) crystallizes. Solutions of 2/AlCl3 show uncomplexed 2 and Re-AlCl3 (major) and ReNO-AlCl3 (minor) adducts. In contrast to 2-7 and 2/BCl3, 1H- and 13C-NMR spectra of 2/AlCl3 suggest an equilibrium with the base-free silylene complex [(η5-C5H5)Re(NO)(PPh3)-( = SiMe2)]⊕ X⊖.
    Additional Material: 2 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 25 (1987), S. 176-178 
    ISSN: 0749-1581
    Keywords: INADEQUATE ; 2D NMR ; Carbon-carbon scalar coupling ; Polarization transfer ; Quaternary carbons ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The two-dimensional INEPT-INADEQUATE experiment gives correlation peaks for unprotonated carbons which show only half of the total available signal, because the enhanced 13C signal generated by polarization transfer is shared equally between protonated and unprotonated coupling partners by the double quantum filtration step. If precautions are taken to attenuate unwanted signals from protonated carbons, then the double quantum filtration step may be dispensed with, leaving a hydrogen-carbon-carbon relay sequence. This gives unidirectional coherence transfer, ensuring that the maximum possible signal is concentrated in a single cross-peak identifying the correlation between protonated and unprotonated carbons. By extending the basic HCC relay sequence to include an evolution period an enhanced 13C-13C COSY 2D spectrum may be produced, with the further advantage over the 2D INADEQUATE experiment that the range of 13C-13C coupling constants detectable is limited only by the available resolution.
    Additional Material: 3 Ill.
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  • 5
    Publication Date: 2014-01-26
    Description: Purpose To obtain robust estimates of 31 P metabolite content in mouse skeletal muscles using our recently developed MR absolute quantification method and a custom-built 1 H/ 31 P dual tuned radiofrequency (RF) coil optimized for mouse leg. Materials and Methods We designed and fabricated a probe consisting of two dual tuned 1 H/ 31 P solenoid coils: one leg was inserted to each solenoid. The mouse leg volume coil was incorporated with injector coils for MR absolute quantification. The absolute quantification method uses a synthetic reference signal injection approach and solves several challenges in MR absolute quantification including changes of coil loading and receiver gains. Results The 1 H/ 31 P dual tuned probe was composed of two separate solenoid coils, one for each leg, to increase coil filling factors and signal-to-noise ratio. Each solenoid was equipped with a second coil to allow injection of reference signals. 31 P metabolite concentrations determined for normal mice were well within the expected range reported in the literature. Conclusion We developed an RF probe and an absolute quantification approach adapted for mouse skeletal muscle. J. Magn. Reson. Imaging 2013; . © 2013 Wiley Periodicals, Inc .
    Print ISSN: 1053-1807
    Electronic ISSN: 1522-2586
    Topics: Medicine
    Published by Wiley-Blackwell
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  • 6
    Publication Date: 2014-07-10
    Description: ABSTRACT Although triphenyltin (TPT) compounds are ubiquitous pollutants in urbanised coastal environments in Asian regions, their toxicities to marine organisms are still poorly known. This study was designed to investigate the toxicity of triphenyltin chloride (TPTCl) on the rotifer Brachionus koreanus across different levels of biological organisation. Firstly, we concurrently performed a 24 h static-acute toxicity test and a 6-day semi-static multigenerational life-cycle test using the rotifer. Our results demonstrated that the 24-h median lethal concentration of TPTCl for the rotifer was 29.6 μg/L and the 6-day median effect concentration, based on the population growth inhibition, was 3.31 μg/L. Secondly, we examined the expression of 12 heat shock protein ( hsp ) genes, four glutathione S-transferase ( GST ) genes, one retinoid X receptor ( RXR ) gene and 13 cytochrome P450 ( CYP ) genes in the rotifers after exposure to 20 µg/L TPTCl for 24 h. Among these studied genes, hsp90α2 , GST-O and CYP3045C1 were the most significantly up-regulated genes with a relative expression level up to 32.9, 4.4 and 62.6 folds, respectively. The expression of these three genes in the rotifers showed an increasing trend in the first few hours of TPTCl exposure, peaked at 3 h ( hsp90α2 and GST-O ) and 12 h ( CYP3045C1 ) respectively, and then gradually returned to a lower level at 24 h. Such up-regulations of hsp and GST genes probably offer cellular protection against the TPT-mediated oxidative stress while the accelerated induction of CYP genes possibly facilitates the detoxification of this toxicant in the rotifer. © 2014 Wiley Periodicals, Inc. Environ Toxicol, 2014.
    Print ISSN: 1520-4081
    Electronic ISSN: 1522-7278
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Published by Wiley-Blackwell
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  • 7
    Publication Date: 2014-10-11
    Description: Skull bone metastasis (SBM) presents as solitary bone mass, which may spread either outward to the scalp or inward to the dura and the subdural tissues. SBM may occur in 4% -22% of all cancer patients and is thought to be haematogenous in origin at late disease stage 1,2 . However, SBM as initial clinical presentation is rare. Although breast is the most common source for SBM, diagnosis can be difficult due to the lack of specific symptoms, particularly in patients without cancer history. This article is protected by copyright. All rights reserved.
    Print ISSN: 0309-0167
    Electronic ISSN: 1365-2559
    Topics: Medicine
    Published by Wiley-Blackwell
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