Quantitative real-time reverse transcription polymerase chain reaction: normalization to rRNA or single housekeeping genes is inappropriate for human tissue biopsies.
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MicroRNA expression profiling to identify and validate reference genes for relative quantification in colorectal cancerInsights into the role of differential gene expression on the ecological adaptation of the snail Littorina saxatilis'Desperate house genes': the dramatic example of hypoxiaThe 'permeome' of the malaria parasite: an overview of the membrane transport proteins of Plasmodium falciparum.Real-time PCR in clinical microbiology: applications for routine laboratory testing.De-regulation of common housekeeping genes in hepatocellular carcinomaIdentification of reference genes across physiological states for qRT-PCR through microarray meta-analysisIdentification of miR-23a as a novel microRNA normalizer for relative quantification in human uterine cervical tissuescDNA microarrays as a tool for identification of biomineralization proteins in the coccolithophorid Emiliania huxleyi (Haptophyta)Validation of reference genes aiming accurate normalization of qRT-PCR data in Dendrocalamus latiflorus MunroAn analysis of critical factors for quantitative immunoblotting.Cardiovascular and Cerebrovascular Disease Associated microRNAs Are Dysregulated in Placental Tissues Affected with Gestational Hypertension, Preeclampsia and Intrauterine Growth Restriction.Improved data normalization methods for reverse phase protein microarray analysis of complex biological samples.Quantitative TaqMan real-time PCR assays for gene expression normalisation in feline tissues.Selecting housekeeping genes as references for the normalization of quantitative PCR data in breast cancer.The choice of reference gene affects statistical efficiency in quantitative PCR data analysis.Reference genes for quantitative RT-PCR data in gastric tissues and cell linesQuantifying mRNA and microRNA with qPCR in cervical carcinogenesis: a validation of reference genes to ensure accurate dataEndogenous control genes in complex vascular tissue samples.Validation of endogenous reference genes in Buglossoides arvensis for normalizing RT-qPCR-based gene expression data.Data integration: challenges for drug discovery.LEMming: A Linear Error Model to Normalize Parallel Quantitative Real-Time PCR (qPCR) Data as an Alternative to Reference Gene Based Methods.Identification of genes for normalization of real-time RT-PCR data in breast carcinomas.Cooccurrence of ScDSP gene expression, cell death, and DNA fragmentation in a marine diatom, Skeletonema costatumQuantitative evaluation and selection of reference genes in mouse oocytes and embryos cultured in vivo and in vitro.Evaluation of reference genes for real-time RT-PCR expression studies in the plant pathogen Pectobacterium atrosepticumIdentifying the most suitable endogenous control for determining gene expression in hearts from organ donorsCDKN1C/p57kip2 is a candidate tumor suppressor gene in human breast cancer.Gene expression analysis in the human hypothalamus in depression by laser microdissection and real-time PCR: the presence of multiple receptor imbalances.Validation of internal control for gene expression study in soybean by quantitative real-time PCR.Defining diversity, specialization, and gene specificity in transcriptomes through information theory.Selection of housekeeping genes for gene expression studies in the adult rat submandibular gland under normal, inflamed, atrophic and regenerative states.Selection and validation of reference genes for quantitative RT-PCR expression studies of the non-model crop Musa.Expression profiles of the pluripotency marker gene POU5F1 and validation of reference genes in rabbit oocytes and preimplantation stage embryos.Identification of suitable endogenous control genes for microRNA gene expression analysis in human breast cancer.Selection of internal reference genes for SYBR green qRT-PCR studies of rhesus monkey (Macaca mulatta) tissues.Characterization of housekeeping genes in zebrafish: male-female differences and effects of tissue type, developmental stage and chemical treatment.Validation of putative reference genes for gene expression studies in human hepatocellular carcinoma using real-time quantitative RT-PCR.Genomic selection of reference genes for real-time PCR in human myocardium.Identification of suitable internal control genes for expression studies in Coffea arabica under different experimental conditions.
P2860
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P2860
Quantitative real-time reverse transcription polymerase chain reaction: normalization to rRNA or single housekeeping genes is inappropriate for human tissue biopsies.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh-hant
name
Quantitative real-time reverse ...... ate for human tissue biopsies.
@en
Quantitative real-time reverse ...... ate for human tissue biopsies.
@nl
type
label
Quantitative real-time reverse ...... ate for human tissue biopsies.
@en
Quantitative real-time reverse ...... ate for human tissue biopsies.
@nl
prefLabel
Quantitative real-time reverse ...... ate for human tissue biopsies.
@en
Quantitative real-time reverse ...... ate for human tissue biopsies.
@nl
P2093
P1476
Quantitative real-time reverse ...... iate for human tissue biopsies
@en
P2093
Carmela Tricarico
Claudio Orlando
Milena Paglierani
Pamela Pinzani
Simonetta Bianchi
Vito Distante
P304
P356
10.1016/S0003-2697(02)00311-1
P407
P577
2002-10-01T00:00:00Z