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1989-52-2

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关键词:'1989-52-2'
显示 1-11 共 11 条结果 关于 "1989-52-2" 范围 论文
J M Ritzler et al.
Genomics, 12(3), 567-572 (1992-03-01)
The chromosomal loci of the human parvalbumin and oncomodulin single-copy genes that encode structurally and evolutionarily closely related Ca(2+)-binding proteins were determined by somatic cell hybrid analysis. Southern blot analysis of genomic DNA from 25 human-hamster somatic cell hybrids showed
D J Hayzer et al.
The Biochemical journal, 270(1), 261-263 (1990-08-15)
The sequences of two near full-length cDNAs encoding rat liver glucokinase are reported. One of the cDNAs is essentially identical to the cDNA cloned by Andreone, Printz, Pilkis, Magnuson & Granner. [(1989) J. Biol. Chem. 264, 363-369]. The other cDNA
S Bjoern et al.
The Journal of biological chemistry, 266(17), 11051-11057 (1991-06-15)
Factor VII is a multidomain, vitamin K-dependent plasma glycoprotein that participates in the extrinsic pathway of blood coagulation. Earlier studies demonstrated a novel disaccharide (Xyl-Glc) or trisaccharide (Xyl2-Glc) O-glycosidically linked to serine 52 in human plasma factor VII (Nishimura, H.
Petros Christopoulos et al.
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 18(9), 1430-1437 (2012-03-21)
Total body irradiation has been the mainstay of conditioning since the inception of allogeneic hematopoietic cell transplantation, but toxicity often precludes its use. For less-fit patients with acute lymphoblastic leukemia and other hematologic malignancies frequently affecting the central nervous system
X Liang et al.
The Journal of biological chemistry, 274(20), 13830-13835 (1999-05-13)
The mitochondrial metabolism of unsaturated fatty acids with conjugated double bonds at odd-numbered positions, e.g. 9-cis, 11-trans-octadecadienoic acid, was investigated. These fatty acids are substrates of beta-oxidation in isolated rat liver mitochondria and hence are expected to yield 5,7-dienoyl-CoA intermediates.
S Hada et al.
Journal of biochemistry, 113(1), 13-18 (1993-01-01)
Initial velocity data for the hydrolysis of micellar 1,2-diheptanoyl-sn-glycero-3-phosphorylcholine (diC7PC) catalyzed by bovine pancreatic PLA2 (Group I) were analyzed using the Michaelis-Menten equation. The Km value for the micellar substrate was found to be independent of Ca2+ concentration, as was
J Ozols
Archives of biochemistry and biophysics, 290(1), 103-115 (1991-10-01)
Hepatic flavin-containing monooxygenases catalyze NADPH-dependent oxygenation of a wide variety of drugs that possess a nucleophilic heteroatom. Two forms of these enzymes (form 1 and 2) have been isolated from rabbit liver microsomes and partially characterized (Ozols, J., 1989, Biochem.
D R Tulsiani et al.
The Biochemical journal, 290 ( Pt 2), 427-436 (1993-03-01)
We have previously reported the occurrence and partial characterization of a novel alpha-D-mannosidase activity on rat sperm plasma membranes [Tulsiani, Skudlarek and Orgebin-Crist (1989) J. Cell Biol. 109, 1257-1267]. Here, we report the presence of a similar alpha-D-mannosidase activity in
H T Jia et al.
Cellular and molecular neurobiology, 12(3), 241-258 (1992-06-01)
1. The skeletal muscle acetylcholine receptor comprises several subunits whose coordinated expression during myogenesis is probably controlled by cis elements in the individual subunit genes. We have previously analyzed promoter regions of the alpha and delta genes (Wang et al.
F Jänicke et al.
Cancer research, 54(10), 2527-2530 (1994-05-15)
The serine protease urokinase-type plasminogen activator (uPA) plays a key role in tumor-associated proteolysis in malignant solid tumors. Proteolytic activity of uPA is controlled by its naturally occurring plasminogen activator inhibitor type 1. As an initial observation, a correlation of
Bruno Van Deuren et al.
Journal of pharmacological and toxicological methods, 60(1), 11-23 (2009-05-09)
The purpose of conducting cardiovascular safety pharmacology studies is to investigate the pharmacological profiles of new molecular entities (NMEs) and provide data that can be used for optimization of a possible new drug, and help make a selection of NMEs
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