نتایج جستجو برای: nco concentration

تعداد نتایج: 381550  

Journal: :Journal of bacteriology 2007
George S Espie Farid Jalali Tommy Tong Natalie J Zacal Anthony K-C So

The cyanobacteria Synechococcus elongatus strain PCC7942 and Synechococcus sp. strain UTEX625 decomposed exogenously supplied cyanate (NCO-) to CO2 and NH3 through the action of a cytosolic cyanase which required HCO3- as a second substrate. The ability to metabolize NCO- relied on three essential elements: proteins encoded by the cynABDS operon, the biophysical activity of the CO2-concentratin...

Journal: :The Journal of clinical investigation 1973
P F Milner S Charache

By using three isotopes of diisopropyl-phosphofluoridate ([(3)H]-, [(14)C]-, and [(32)P]DFP) simultaneously, the life span of red cells from 20 patients with sickle cell anemia (Hb SS) has been studied after varying degrees of carbamylation in vitro with cyanate (NCO) and carbamyl phosphate (CP). The results are expressed in terms of the red cell mean life span (MLS). The MLS of red cells in th...

Journal: :Monthly Notices of the Royal Astronomical Society 1978

2009
N. G. INMAN-BAMBER

There are several areas in the South African sugar industry where the ubiquitous variety, NCo 376, is beingsuperseded by newer varieties. Growers have a choice of varieties which have outyielded NCo 376 in trials under a wide range of conditions. There are others which have yielded more than NCo 376 in certain conditions. It is opportune to report the results of trials that have been conducted ...

Journal: :AIP Advances 2023

Inverse spinel oxide NiCo2O4 (NCO) is known to exhibit ferrimagnetic characteristics and electrical conductivity. First-principles calculations predict NCO be a half-metal with negative polarization of −100%. In this study, we fabricated epitaxial NCO/MgO/Fe magnetic tunnel junctions by reactive molecular beam epitaxy observed an inverse magnetoresistance (TMR) effect −19.1% at 14 K, indicating...

2013
Katrina Mitchel Kevin Lehner Sue Jinks-Robertson

The contributions of the Sgs1, Mph1, and Srs2 DNA helicases during mitotic double-strand break (DSB) repair in yeast were investigated using a gap-repair assay. A diverged chromosomal substrate was used as a repair template for the gapped plasmid, allowing mismatch-containing heteroduplex DNA (hDNA) formed during recombination to be monitored. Overall DSB repair efficiencies and the proportions...

Journal: :Molecular pharmacology 2003
Kerri A Schoedel Edward M Sellers Roberta Palmour Rachel F Tyndale

Nicotine metabolism is decreased in smokers compared with nonsmokers, but the mechanism(s) responsible for the slower metabolism are unknown. Nicotine is inactivated to cotinine by CYP2A6 in human liver [nicotine C-oxidation (NCO)]. CYP2B6 also metabolizes nicotine to cotinine but with lower affinity than CYP2A6. To evaluate the effects of long-term nicotine treatment on hepatic levels of CYP2A...

Journal: :Chemical communications 2007
Daniele Belletti Pierre Braunstein Abdelatif Messaoudi Roberto Pattacini Giovanni Predieri Antonio Tiripicchio

In the clusters [Ru3(micro(3)-NPPh(3))(micro(3)-OSiMe(3))(micro-X)(micro(C,O)-OC[double bond]NPPh(3))(micro-CO)(CO)6] (X = NCO, 2; X = Cl, 3), which were prepared by a pyrolytic reaction of Ph(3)PNSiMe(3) with Ru(3)(CO)12, the ligands result from a cluster-mediated pseudo-Hofmann rearrangement involving the micro-NCO, micro(C,O)-Ph(3)P[double bond]N-CO and micro(3)-NPPh(3) fragments.

Journal: :Genetics 2008
Caroline Welz-Voegele Sue Jinks-Robertson

Homologous recombination between dispersed repeated sequences is important in shaping eukaryotic genome structure, and such ectopic interactions are affected by repeat size and sequence identity. A transformation-based, gap-repair assay was used to examine the effect of 2% sequence divergence on the efficiency of mitotic double-strand break repair templated by chromosomal sequences in yeast. Be...

Journal: :Arteriosclerosis and thrombosis : a journal of vascular biology 1994
Y I Ahn M I Kamboh C E Aston R E Ferrell R F Hamman

A large number of rare mutations in the low-density lipoprotein (LDL) receptor gene cause the autosomal dominant disorder familial hypercholesterolemia. In addition, a number of common DNA polymorphisms have been identified in the LDL receptor gene, but their significance in affecting plasma cholesterol levels in the general population has not been studied widely. We investigated the role of tw...

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