Efficient amplification using 'megaprimer' by asymmetric polymerase chain reaction.
about
A Cajal body-specific pseudouridylation guide RNA is composed of two box H/ACA snoRNA-like domains.Coupling of cell division to cell growth by translational control of the G1 cyclin CLN3 in yeastA persulfurated cysteine promotes active site reactivity in Azotobacter vinelandii RhodaneseTetramerization and ATP binding by a protein comprising the A, B, and C domains of rat synapsin IThe 'pair of sugar tongs' site on the non-catalytic domain C of barley alpha-amylase participates in substrate binding and activityStructural insights into the catalytic reaction that is involved in the reorientation of Trp238 at the substrate-binding site in GH13 dextran glucosidaseStructural model of a malonyl-CoA-binding site of carnitine octanoyltransferase and carnitine palmitoyltransferase I: mutational analysis of a malonyl-CoA affinity domainInhibition by etomoxir of rat liver carnitine octanoyltransferase is produced through the co-ordinate interaction with two histidine residuesAnalysis of promoters recognized by PvdS, an extracytoplasmic-function sigma factor protein from Pseudomonas aeruginosa.Determination of disulfide bond assignment of human vitamin K-dependent gamma-glutamyl carboxylase by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.A novel DNA-binding motif, hallmark of a new family of plant transcription factors.Chemical modification of cysteine residues is a misleading indicator of their status as active site residues in the vitamin K-dependent gamma-glutamyl carboxylation reaction.Mechanism of platelet factor 4 (PF4) deficiency with RUNX1 haplodeficiency: RUNX1 is a transcriptional regulator of PF4.Differences in the Enterococcus faecalis lsa locus that influence susceptibility to quinupristin-dalfopristin and clindamycinNovel regulatory factors interacting with the promoter of the gene encoding the mRNA cap binding protein (eIF4E) and their function in growth regulation.Use of a transient assay for studying the genetic determinants of Fv1 restriction.Polypeptide p41 of a Norwalk-like virus is a nucleic acid-independent nucleoside triphosphataseElements essential for accumulation and function of small nucleolar RNAs directing site-specific pseudouridylation of ribosomal RNAs.Localization of an exonic splicing enhancer responsible for mammalian natural trans-splicing.A protein linkage map of the P2 nonstructural proteins of poliovirus.The competence transcription factor of Bacillus subtilis recognizes short A/T-rich sequences arranged in a unique, flexible pattern along the DNA helix.Novel dextranase catalyzing cycloisomaltooligosaccharide formation and identification of catalytic amino acids and their functions using chemical rescue approach.Robust one-tube Ω-PCR strategy accelerates precise sequence modification of plasmids for functional genomics.Decreased metallation and activity in subsets of mutant superoxide dismutases associated with familial amyotrophic lateral sclerosis.Modulation of activity and substrate binding modes by mutation of single and double subsites +1/+2 and -5/-6 of barley alpha-amylase 1.Conserved cysteines in the sialyltransferase sialylmotifs form an essential disulfide bond.Role of pro-297 in the catalytic mechanism of sheep liver serine hydroxymethyltransferase.His230 of serine hydroxymethyltransferase facilitates the proton abstraction step in catalysis.Oligosaccharide binding to barley alpha-amylase 1.Characterization of the nucleoside triphosphatase activity of poliovirus protein 2C reveals a mechanism by which guanidine inhibits poliovirus replication.Mutation of the sialyltransferase S-sialylmotif alters the kinetics of the donor and acceptor substrates.A novel transcription factor involved in plant defense endowed with protein phosphatase activity.Barley alpha-amylase Met53 situated at the high-affinity subsite -2 belongs to a substrate binding motif in the beta-->alpha loop 2 of the catalytic (beta/alpha)8-barrel and is critical for activity and substrate specificity.The wing in yeast heat shock transcription factor (HSF) DNA-binding domain is required for full activityExpression of the isoamylase gene of Flavobacterium odoratum KU in Escherichia coli and identification of essential residues of the enzyme by site-directed mutagenesis.Rapid and efficient site-directed mutagenesis by single-tube 'megaprimer' PCR method.A common sequence motif determines the Cajal body-specific localization of box H/ACA scaRNAs.Human intron-encoded AluACA RNAs and telomerase RNA share a common element promoting RNA accumulation.Isolation and characterization of the human A-myb promoter: regulation by NF-Y and Sp1.Expression of a transactivation-deficient form of thyroid transcription factor I decreases the activity of co-transfected thyroglobulin and thyroperoxidase promoters.
P2860
Q24540398-1D6EB7D6-6216-42B4-9E9F-5F3C90C93582Q24606696-10406565-6551-4184-A571-DAEC97254984Q27635298-A5BC0C85-7F7F-450A-9C01-F57B9A369E80Q27642834-229E4EB0-101D-41F7-ACED-2E02F1E462AEQ27647824-26CD09DF-B44E-44DD-994D-887206A50321Q27697572-D831CD25-C642-43F1-972B-852FB4F431E2Q28564300-0FD6D7A2-DD5E-4985-BC40-3E19CAF4402CQ28581761-09CFD480-3A2F-4F60-B5ED-F846899111E9Q29346794-0D5706B5-B1FB-49DB-A2AF-E490BBFDA03FQ30980882-228701BA-4697-4049-BDD2-466FE98C3411Q30982748-823E4E76-8F2A-48F6-A7BB-6D029C27CAFBQ33208040-F3506C3D-0F71-4682-BC4B-6D11AFDBC6EEQ33393133-908FB030-D8DA-4043-AA18-76BEB80E4FCFQ33555837-C427826E-63B5-475F-A484-6AFD304F9FFFQ33779671-F7BB3EB7-8B45-47AD-83FD-634B5F11A1F1Q33809632-6E5E4BD3-2378-4979-9356-5D70E72A098AQ33837197-0822972B-AD2D-4A6A-9842-CEB74048AB63Q33890338-62F0274F-258E-4BB8-BE06-34E198127709Q33940650-6D746CBE-C44A-4F84-A095-7162764824B7Q34069651-BE05214E-3C57-4B68-BE62-110842E4D380Q35200591-2F17AD21-7243-48DE-ADB1-0AA9210D1289Q36016786-EE696DE2-086E-4BFC-B486-82FD9B60CDF5Q36728275-59593DC2-36E6-4BEE-B821-6A8405D0068FQ38291855-CE8B58B3-11C5-43DF-BC06-9A79073B37B2Q38294120-4D2C85F7-14D3-4A71-9B1C-49DA6DC13B66Q38302620-99D098D8-89A7-4282-9B84-D1012BC21A42Q38308700-0FD77D27-7BEE-4D24-8E84-906D72D5DC94Q38315055-DCBFAC53-1042-4C0E-B9A8-2B4D4B91001FQ38323448-4354587A-62D2-49D2-94C6-0D9302B90D90Q38327453-3B801567-069E-43E7-B6D7-551A0FDF97F6Q38337475-5F5D028B-3FC3-4824-9C6A-8B549C5D42D4Q38353006-7C4B7847-73FA-442D-B805-7A17952285ADQ38361227-7FFF31D4-F009-4D83-9E2D-A0CEA60400B2Q38679138-D4FE6995-05BD-4B3E-A6BB-6AF907490E62Q39527896-189ED515-B951-4809-BDAC-E5458F9EDD93Q39720908-FF90B2A1-2ED5-45C4-8EC4-4FDBD6FE9D11Q39831945-31F8C734-AC64-4DA4-BAB7-FF84FA393218Q40568869-1217B1A6-B300-4F30-80AE-943EB341FFD9Q40860016-8CAA07FF-D1DB-406A-8F9C-C6EC13D8EB6DQ41145673-DA711DBC-C706-4E48-BE48-8EA6E16DAC8C
P2860
Efficient amplification using 'megaprimer' by asymmetric polymerase chain reaction.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Efficient amplification using 'megaprimer' by asymmetric polymerase chain reaction.
@en
type
label
Efficient amplification using 'megaprimer' by asymmetric polymerase chain reaction.
@en
prefLabel
Efficient amplification using 'megaprimer' by asymmetric polymerase chain reaction.
@en
P2860
P356
P1476
Efficient amplification using 'megaprimer' by asymmetric polymerase chain reaction.
@en
P2093
P2860
P304
P356
10.1093/NAR/23.21.4530
P577
1995-11-01T00:00:00Z