about
The elimination of primer-dimer accumulation in PCRA new reverse transcription-polymerase chain reaction method for accurate quantificationGeographical distance and barriers explain population genetic patterns in an endangered island perennialGENOMEMASKER package for designing unique genomic PCR primersGenome-wide functional analysis of the cotton transcriptome by creating an integrated EST database.De novo sequencing and a comprehensive analysis of purple sweet potato (Impomoea batatas L.) transcriptome.Multiplex allele-specific target amplification based on PCR suppression.Towards a more holistic research approach to plant conservation: the case of rare plants on oceanic islandsModelling evolution on design-by-contract predicts an origin of life through an abiotic double-stranded RNA world.2.7 million samples genotyped for HLA by next generation sequencing: lessons learnedGenoFrag: software to design primers optimized for whole genome scanning by long-range PCR amplificationLigand-dependent exponential amplification of self-replicating RNA enzymes.Molecular (PCR-DGGE) versus morphological approach: analysis of taxonomic composition of potentially toxic cyanobacteria in freshwater lakes.Anchored multiplex amplification on a microelectronic chip array.Computer aided gene mining for gingerol biosynthesisRapid and sensitive diagnoses of dry root rot pathogen of chickpea (Rhizoctonia bataticola (Taub.) Butler) using loop-mediated isothermal amplification assay.Regionalized GC content of template DNA as a predictor of PCR successHigh-resolution differentiation of Cyanobacteria by using rRNA-internal transcribed spacer denaturing gradient gel electrophoresis.A PCR-Based Assay Targeting the Major Capsid Protein Gene of a Dinorna-Like ssRNA Virus That Infects Coral Photosymbionts.Highly sensitive and specific Alu-based quantification of human cells among rodent cells.Development and characterization of SCAR markers linked to the citrus tristeza virus resistance gene from Poncirus trifoliata.Variability and cost implications of three generations of the Roche LightCycler® 480.2'-MeO-RNA containing oligodeoxyribonucleotide primers can prevent template-independent base extension on microarrays.Tick-borne zoonoses in the Order Rickettsiales and Legionellales in Iran: A systematic reviewGeography, geology and ecology influence population genetic diversity and structure in the endangered endemic Azorean Ammi (Apiaceae)Microsatellite markers unravel the population genetic structure of the Azorean Leontodon: implications in conservationPopulation genetic structure and conservation of the Azorean tree Prunus azorica (Rosaceae)
P2860
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P2860
description
1995 nî lūn-bûn
@nan
1995 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年学术文章
@wuu
1995年学术文章
@zh-cn
1995年学术文章
@zh-hans
1995年学术文章
@zh-my
1995年学术文章
@zh-sg
1995年學術文章
@yue
name
Selection of primers for polymerase chain reaction.
@ast
Selection of primers for polymerase chain reaction.
@en
Selection of primers for polymerase chain reaction.
@nl
type
label
Selection of primers for polymerase chain reaction.
@ast
Selection of primers for polymerase chain reaction.
@en
Selection of primers for polymerase chain reaction.
@nl
prefLabel
Selection of primers for polymerase chain reaction.
@ast
Selection of primers for polymerase chain reaction.
@en
Selection of primers for polymerase chain reaction.
@nl
P356
P1476
Selection of primers for polymerase chain reaction.
@en
P2093
P2888
P304
P356
10.1007/BF02789108
P577
1995-04-01T00:00:00Z