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  • 1
    Publication Date: 1992-12-11
    Description: There has long been debate about the relative importance of abrasion versus selective deposition of the coarsest clasts in causing downstream fining of sediment in river systems. Although high fining rates observed in many natural rivers seem to require strong selective deposition, the ability of selective deposition to produce downstream size sorting has never been measured under controlled conditions. In an experiment using a long flume and a poorly sorted, bimodal gravel feed, downstream fining was produced by a factor of 1.3 in median size and 1.8 in 90th percentile size, over a distance of 21 meters. The experimental conditions rule out abrasion effects. Selective deposition appears to be a natural consequence of the transport and deposition of sufficiently poorly sorted or bimodal gravels and appears to be capable of accounting for fining rates observed in natural gravel rivers.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Paola, C -- Parker, G -- Seal, R -- Sinha, S K -- Southard, J B -- Wilcock, P R -- New York, N.Y. -- Science. 1992 Dec 11;258(5089):1757-60.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17831656" target="_blank"〉PubMed〈/a〉
    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: 1993-08-20
    Description: Surface tension measurements reveal surface freezing in liquid n-alkanes. A solid monolayer of molecules is found to exist up to 30 degrees C above the bulk freezing point. This surface phase exists only for carbon numbers 14 n 〈/= 50. The measured carbon number and temperature dependence of the surface tension is interpreted within a simple thermodynamical model based on known bulk latent heat data and surface energy considerations. The vanishing of the surface phase for n 〈/= 14 is a possible transition from surface freezing to surface melting behavior.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wu, X Z -- Ocko, B M -- Sirota, E B -- Sinha, S K -- Deutsch, M -- Cao, B H -- Kim, M W -- New York, N.Y. -- Science. 1993 Aug 20;261(5124):1018-21.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17739620" target="_blank"〉PubMed〈/a〉
    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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  • 3
    Publication Date: 1978-04-14
    Description: Aggregation of human blood platelets induced by adenosine diphosphate or 1-epinephrine was inhibited when the platelets were suspended in plasma which had been previously exposed to an insolubilized omega-aminohexylagarose derivative of prostaglandin E1. This decrease of platelet aggregation was not accompanied by a change in the concentration of adenosine 3',5'-monophosphate (cyclic AMP) in platelets. The results demonstrate the existence of an alternative pathway independent of cyclic AMP for the inhibition of platelet aggregation by plasma.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sinha, A K -- Colman, R W -- New York, N.Y. -- Science. 1978 Apr 14;200(4338):202-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/204997" target="_blank"〉PubMed〈/a〉
    Keywords: Adenosine Diphosphate/antagonists & inhibitors ; Cyclic AMP/*blood ; Epinephrine/antagonists & inhibitors ; Humans ; Plasma/physiology ; Platelet Aggregation/*drug effects ; Prostaglandins E, Synthetic/*pharmacology ; Sepharose/analogs & derivatives ; Solubility
    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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  • 4
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1980-07-25
    Description: The study involved quantitative measurement of arterial and venous oxygen saturation, oxygen extraction, blood flow, and oxygen consumption in specific areas of the brain. No regional differences in oxygen consumption were found in anesthetized cat brain, and the amount of oxygen available to all regions studied was more than 2.5 times the consumption throughout the brain.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Buckweitz, E -- Sinha, A K -- Weiss, H R -- New York, N.Y. -- Science. 1980 Jul 25;209(4455):499-501.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7394515" target="_blank"〉PubMed〈/a〉
    Keywords: Anesthesia, General ; Animals ; Brain/blood supply/drug effects/*metabolism ; Cats ; Chloralose/*pharmacology ; Female ; Male ; Oxygen/*blood ; Oxygen Consumption/*drug effects ; Regional Blood Flow ; Tissue Distribution
    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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  • 5
    Publication Date: 1986-01-24
    Description: When platelets were incubated with prostacyclin, prostaglandin E1, or prostaglandin D2 at concentrations insufficient to increase the level of adenosine 3',5'-monophosphate (cyclic AMP), coagulation factor X was activated by a platelet cysteine protease. Prostacyclin or prostaglandin E1 at higher concentrations increased the cyclic AMP level and inhibited the activation of factor X by platelets. Inhibition of platelet adenylate cyclase by 2',5'-dideoxyadenosine allowed the activation of the protease at higher concentrations of the autocoids. Prostaglandins A1, A2, B1, B2, E2, F2 alpha, 6-keto-prostaglandin F1 alpha, and thromboxane B2, which do not affect platelet cyclic AMP level, did not stimulate the protease.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dutta-Roy, A K -- Ray, T K -- Sinha, A K -- New York, N.Y. -- Science. 1986 Jan 24;231(4736):385-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3001935" target="_blank"〉PubMed〈/a〉
    Keywords: Adenylyl Cyclases/metabolism ; Alprostadil/pharmacology ; Animals ; Blood Platelets/*drug effects/metabolism/physiology ; Cattle ; Cyclic AMP/metabolism ; Deoxyadenosines/analogs & derivatives/pharmacology ; *Dideoxyadenosine/*analogs & derivatives ; Epoprostenol/*pharmacology ; Factor X/*physiology ; Humans ; Peptide Hydrolases/metabolism ; Prostaglandin D2 ; Prostaglandins/pharmacology ; Prostaglandins D/pharmacology
    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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  • 6
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    American Association for the Advancement of Science (AAAS)
    In: Science
    Publication Date: 2017-01-20
    Description: Adenosine 5′-triphosphate (ATP)–dependent chromatin remodeling enzymes play essential biological roles by mobilizing nucleosomal DNA. Yet, how DNA is mobilized despite the steric constraints placed by the histone octamer remains unknown. Using methyl transverse relaxation–optimized nuclear magnetic resonance spectroscopy on a 450-kilodalton complex, we show that the chromatin remodeler, SNF2h, distorts the histone octamer. Binding of SNF2h in an activated ATP state changes the dynamics of buried histone residues. Preventing octamer distortion by site-specific disulfide linkages inhibits nucleosome sliding by SNF2h while promoting octamer eviction by the SWI-SNF complex, RSC. Our findings indicate that the histone core of a nucleosome is more plastic than previously imagined and that octamer deformation plays different roles based on the type of chromatin remodeler. Octamer plasticity may contribute to chromatin regulation beyond ATP-dependent remodeling. Authors: Kalyan K. Sinha, John D. Gross, Geeta J. Narlikar
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Geosciences , Computer Science , Medicine , Natural Sciences in General , Physics
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