(Q52192082)

English

Quantification of alternatively spliced RUSH mRNA isoforms by QRT-PCR and IP-RP-HPLC analysis: a new approach to measuring regulated splicing efficiency.

scientific article published in October 1997

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scholarly article

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/9370258

Quantification of alternatively spliced RUSH mRNA isoforms by QRT-PCR and IP-RP-HPLC analysis: a new approach to measuring regulated splicing efficiency. (English)

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/9370258

author name string

Robinson CA

1

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/9370258

Hayward-Lester A

2

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/9370258

Hewetson A

3

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/9370258

Oefner PJ

4

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/9370258

Doris PA

5

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/9370258

Chilton BS

6

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/9370258

language of work or name

0 references

publication date

1 October 1997

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/9370258

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/9370258

198

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/9370258

1-2

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/9370258

1-4

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/9370258

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

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More is better: Activators and repressors from the same gene

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Cloning, characterization, and steroid-dependent posttranscriptional processing of RUSH-1 alpha and beta, two uteroglobin promoter-binding proteins.

1 reference

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Rapid quantification of gene expression by competitive RT-PCR and ion-pair reversed-phase HPLC.

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Accurate and absolute quantitative measurement of gene expression by single-tube RT-PCR and HPLC

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The yeast SNF2/SWI2 protein has DNA-stimulated ATPase activity required for transcriptional activation

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Alternative mRNA splicing

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Quantitative PCR: theoretical considerations with practical implications.

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Splicing of pre-mRNA: mechanism, regulation and role in development

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Split genes and RNA splicing

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Cloning of an SNF2/SWI2-related protein that binds specifically to the SPH motifs of the SV40 enhancer and to the HIV-1 promoter

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Alternative splicing in the control of gene expression

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Identifiers

10.1016/S0378-1119(97)00305-3

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/9370258

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/9370258

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