Amplification of bacterial genomic DNA by the polymerase chain reaction and direct sequencing after asymmetric amplification: application to the study of periplasmic permeases

Amplification of bacterial genomic DNA by the polymerase chain reaction and direct sequencing after asymmetric amplification: application to the study of periplasmic permeases

Item
http://www.wikidata.org/entity/Q36175163
Tandem chromosomal duplications: role of REP sequences in the recombination event at the join-point.Differential suppression of priA2::kan phenotypes in Escherichia coli K-12 by mutations in priA, lexA, and dnaCTranscriptional regulation of the cryIVD gene operon from Bacillus thuringiensis subsp. israelensisMonitoring the enrichment and isolation of sulfate-reducing bacteria by using oligonucleotide hybridization probes designed from environmentally derived 16S rRNA sequences.RocR, a novel regulatory protein controlling arginine utilization in Bacillus subtilis, belongs to the NtrC/NifA family of transcriptional activators.Salmonella typhimurium histidine periplasmic permease mutations that allow transport in the absence of histidine-binding proteins.DegS-DegU and ComP-ComA modulator-effector pairs control expression of the Bacillus subtilis pleiotropic regulatory gene degQ.Mutational analysis of the Bacillus subtilis DegU regulator and its phosphorylation by the DegS protein kinase.Sequence invariance of the antigen-coding central region of the phase 1 flagellar filament gene (fliC) among strains of Salmonella typhimurium.The product of the nitrogen fixation regulatory gene nfrX of Azotobacter vinelandii is functionally and structurally homologous to the uridylyltransferase encoded by glnD in enteric bacteriaCTX genetic element encodes a site-specific recombination system and an intestinal colonization factor.Use of polymerase chain reaction for detection of Chlamydia trachomatis.An aspartate deletion mutation defines a binding site of the multifunctional FhuA outer membrane receptor of Escherichia coli K-12.Identification of the pheS5 mutation, which causes thermosensitivity of Escherichia coli mutant NP37.
P2860

Amplification of bacterial genomic DNA by the polymerase chain reaction and direct sequencing after asymmetric amplification: application to the study of periplasmic permeases

Item
http://www.wikidata.org/entity/Q36175163
description
1989 nî lūn-bûn
@nan
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
1989年论文
@zh
1989年论文
@zh-cn
name
Amplification of bacterial gen ...... study of periplasmic permeases
@ast
Amplification of bacterial gen ...... study of periplasmic permeases
@en
type
label
Amplification of bacterial gen ...... study of periplasmic permeases
@ast
Amplification of bacterial gen ...... study of periplasmic permeases
@en
prefLabel
Amplification of bacterial gen ...... study of periplasmic permeases
@ast
Amplification of bacterial gen ...... study of periplasmic permeases
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
P577
P698
P932
P356
P1433
P1476
Amplification of bacterial gen ...... study of periplasmic permeases
@en
P2093
P2860
P304
P31
P356
10.1128/JB.171.3.1602-1608.1989
P407
P433
P478
P577
P698
P932