(Q42278150)

English

Selection of normalization factors for quantitative real time RT-PCR studies in Japanese flounder (Paralichthys olivaceus) and turbot (Scophthalmus maximus) under conditions of viral infection

scientific article published on 4 January 2013

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Europe PubMed Central

PubMed publication ID

19 October 2017

Selection of normalization factors for quantitative real time RT-PCR studies in Japanese flounder (Paralichthys olivaceus) and turbot (Scophthalmus maximus) under conditions of viral infection (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

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author name string

Jian Zhang

1

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

Yong-hua Hu

2

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Europe PubMed Central

PubMed publication ID

19 October 2017

Bo-guang Sun

3

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

Zhi-zhong Xiao

4

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Europe PubMed Central

PubMed publication ID

19 October 2017

Li Sun

5

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Europe PubMed Central

PubMed publication ID

19 October 2017

publication date

4 January 2013

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Europe PubMed Central

PubMed publication ID

19 October 2017

Veterinary Immunology and Immunopathology

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Europe PubMed Central

PubMed publication ID

19 October 2017

152

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Europe PubMed Central

PubMed publication ID

19 October 2017

3-4

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Europe PubMed Central

PubMed publication ID

19 October 2017

303-316

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

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1 reference

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Validation of housekeeping genes for normalizing RNA expression in real-time PCR.

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Phylogenetic analysis of the major capsid protein gene of iridovirus isolates from cultured flounders Paralichthys olivaceus in Korea

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Pathogenicity of Edwardsiella tarda to olive flounder, Paralichthys olivaceus (Temminck & Schlegel).

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7 January 2021

Real-time RT-PCR normalisation; strategies and considerations.

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7 January 2021

The real-time polymerase chain reaction

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Transcription of reference genes used for quantitative RT-PCR in Atlantic salmon is affected by viral infection

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beta-Actin is a useful internal control for tissue-specific gene expression studies using quantitative real-time PCR in the half-smooth tongue sole Cynoglossus semilaevis challenged with LPS or Vibrio anguillarum

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Cell cycle regulation of the glyceraldehyde-3-phosphate dehydrogenase/uracil DNA glycosylase gene in normal human cells

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Phenotypic characteristics of Streptococcus iniae and Streptococcus parauberis isolated from olive flounder (Paralichthys olivaceus).

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Evaluation of potential reference genes for real time RT-PCR studies in Atlantic halibut (Hippoglossus Hippoglossus L.); during development, in tissues of healthy and NNV-injected fish, and in anterior kidney leucocytes

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Guideline to reference gene selection for quantitative real-time PCR

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Effect of experimental treatment on housekeeping gene expression: validation by real-time, quantitative RT-PCR.

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Complete genome sequence of a Megalocytivirus (family Iridoviridae) associated with turbot mortality in China

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Stability of reference genes for real-time PCR analyses in channel catfish (Ictalurus punctatus) tissues under varying physiological conditions

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7 January 2021

Housekeeping genes as internal standards: use and limits

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Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes

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Determination of internal controls for quantitative real time RT-PCR analysis of the effect of Edwardsiella tarda infection on gene expression in turbot (Scophthalmus maximus).

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Effect of temperature on immune response of Japanese flounder (Paralichthys olivaceus) to inactivated lymphocystis disease virus (LCDV).

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Complete genome sequence of lymphocystis disease virus isolated from China

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Evaluation of housekeeping genes as references for quantitative real time RT-PCR analysis of gene expression in Japanese flounder (Paralichthys olivaceus).

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Expression profiling and validation of potential reference genes during Paralichthys olivaceus embryogenesis.

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Identifiers

10.1016/J.VETIMM.2012.12.018

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

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