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  • 1
    Publication Date: 1981-06-19
    Description: Intense rapid eye movements (REM) during sleep were investigated as a possible indication of delay in the neurodevelopment of infants. The rate of occurrence of REM storms was determined by monitoring the sleep of 15 normal, first-born infants during weeks 2 through 5 and at 3, 6, 12 months. The amount of REM within each 10-second interval of active sleep was rated on a four-point scale based on frequency and intensity of eye movements. When the babies were 12 months old, the Bayley Scales of Mental Development were administered. A significant negative correlation was found between the frequency of REM storms of 14 subjects was also studied. The negative correlation was confirmed. The findings support the suggestion that by 6 months of age REM storms express dysfunction or delay in the development of central inhibitory feedback controls for sleep organization and phasic sleep-related activities.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Becker, P T -- Thoman, E B -- HD-12948/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 1981 Jun 19;212(4501):1415-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7233232" target="_blank"〉PubMed〈/a〉
    Keywords: Age Factors ; *Child Development ; Humans ; *Infant ; *Infant, Newborn ; Neurons/physiology ; *Sleep, REM
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2015-08-18
    Description: Chromatin immunoprecipitation (ChIP) is widely used to identify chromosomal binding sites. Chromatin proteins are cross-linked to their target sequences in living cells. The purified chromatin is sheared and the relevant protein is enriched by immunoprecipitation with specific antibodies. The co-purifying genomic DNA is then determined by massive parallel sequencing (ChIP-seq). We applied ChIP-seq to map the chromosomal binding sites for two ISWI-containing nucleosome remodeling factors, ACF and RSF, in Drosophila embryos. Employing several polyclonal and monoclonal antibodies directed against their signature subunits, ACF1 and RSF-1, robust profiles were obtained indicating that both remodelers co-occupied a large set of active promoters. Further validation included controls using chromatin of mutant embryos that do not express ACF1 or RSF-1. Surprisingly, the ChIP-seq profiles were unchanged, suggesting that they were not due to specific immunoprecipitation. Conservative analysis lists about 3000 chromosomal loci, mostly active promoters that are prone to non-specific enrichment in ChIP and appear as ‘Phantom Peaks’. These peaks are not obtained with pre-immune serum and are not prominent in input chromatin. Mining the modENCODE ChIP-seq profiles identifies potential Phantom Peaks in many profiles of epigenetic regulators. These profiles and other ChIP-seq data featuring prominent Phantom Peaks must be validated with chromatin from cells in which the protein of interest has been depleted.
    Print ISSN: 0305-1048
    Electronic ISSN: 1362-4962
    Topics: Biology
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