Modified linker-PCR primers facilitate complete sequencing of DGGE DNA fragments.
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Complex coupled metabolic and prokaryotic community responses to increasing temperatures in anaerobic marine sediments: critical temperatures and substrate changes.Culture-independent analysis of bacterial fuel contamination provides insight into the level of concordance with the standard industry practice of aerobic cultivationDynamic microbial community associated with iron-arsenic co-precipitation products from a groundwater storage system in Bangladesh.Culturable prokaryotic diversity of deep, gas hydrate sediments: first use of a continuous high-pressure, anaerobic, enrichment and isolation system for subseafloor sediments (DeepIsoBUG)Role of postnatal acquisition of the intestinal microbiome in the early development of immune function.Microbial diversity in Frenulata (Siboglinidae, Polychaeta) species from mud volcanoes in the Gulf of Cadiz (NE Atlantic).Microbial diversity of active layer and permafrost in an acidic wetland from the Canadian High Arctic.Toll-like receptor 4 is protective against neonatal murine ischemia-reperfusion intestinal injury.Stability of a biogas-producing bacterial, archaeal and fungal community degrading food residues.Live feed is not a major determinant of the microbiota associated with cod larvae (Gadus morhua).NaOH-debittering induces changes in bacterial ecology during table olives fermentation.Cellulosic ethanol production by natural bacterial consortia is enhanced by Pseudoxanthomonas taiwanensis.Comparative survey of bacterial and archaeal communities in high arsenic shallow aquifers using 454 pyrosequencing and traditional methods.Unique sequence characteristics account for good DGGE separation of almost full-length 18S rDNAs.Survival of Desulfotomaculum spores from estuarine sediments after serial autoclaving and high-temperature exposureEffects of storage temperature on bacterial growth rates and community structure in fresh retail sushi.
P2860
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P2860
Modified linker-PCR primers facilitate complete sequencing of DGGE DNA fragments.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
Modified linker-PCR primers facilitate complete sequencing of DGGE DNA fragments.
@en
Modified linker-PCR primers facilitate complete sequencing of DGGE DNA fragments.
@nl
type
label
Modified linker-PCR primers facilitate complete sequencing of DGGE DNA fragments.
@en
Modified linker-PCR primers facilitate complete sequencing of DGGE DNA fragments.
@nl
prefLabel
Modified linker-PCR primers facilitate complete sequencing of DGGE DNA fragments.
@en
Modified linker-PCR primers facilitate complete sequencing of DGGE DNA fragments.
@nl
P2093
P1476
Modified linker-PCR primers facilitate complete sequencing of DGGE DNA fragments.
@en
P2093
John C Fry
Louise A O'Sullivan
R John Parkes
P304
P356
10.1016/J.MIMET.2008.08.006
P577
2008-08-26T00:00:00Z