(Q35221865)

7 August 2017

1 reference

title

Illegitimate transcription: its use in the study of inherited disease (English)

1 reference

7 August 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1301944

10 September 2022

author name string

Kaplan JC

series ordinal

1

1 reference

7 August 2017

Kahn A

series ordinal

2

1 reference

7 August 2017

Chelly J

series ordinal

3

1 reference

7 August 2017

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1301944

10 September 2022

publication date

1 January 1992

1 reference

7 August 2017

1 reference

7 August 2017

1

1 reference

7 August 2017

357-360

1 reference

7 August 2017

5

1 reference

Detection of a novel point mutation causing haemophilia A by PCR/direct sequencing of ectopically-transcribed factor VIII mRNA.

7 August 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010502

7 January 2021

Lymphocyte mRNA as a resource for detection of mutations and polymorphisms in the CF gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010502

7 January 2021

Transcription of the dystrophin gene in human muscle and non-muscle tissue

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010502

7 January 2021

Illegitimate transcription: transcription of any gene in any cell type

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010502

7 January 2021

Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010502

7 January 2021

Illegitimate (or ectopic) transcription proceeds through the usual promoters

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010502

7 January 2021

Illegitimate transcription. Application to the analysis of truncated transcripts of the dystrophin gene in nonmuscle cultured cells from Duchenne and Becker patients

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010502

7 January 2021

CFTR illegitimate transcription in lymphoid cells: quantification and applications to the investigation of pathological transcripts

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010502

7 January 2021

Skipping of exon 5 as a consequence of the 711 + 1 G-->T mutation in the CFTR gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010502

7 January 2021

Mouse globin gene expression in erythroid and non-erythroid tissues

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010502

7 January 2021

Anti-Müllerian hormone Bruxelles: a nonsense mutation associated with the persistent Müllerian duct syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010502

7 January 2021

Are tissues a patch quilt of ectopic gene expression?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010502

7 January 2021

Detection of three novel mutations in two haemophilia A patients by rapid screening of whole essential region of factor VIII gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010502

7 January 2021

A donor splice site mutation in the parathyroid hormone gene is associated with autosomal recessive hypoparathyroidism

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010502

7 January 2021

Illegitimate transcription of phenylalanine hydroxylase for detection of mutations in patients with phenylketonuria

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010502

7 January 2021

Direct diagnosis of carriers of Duchenne and Becker muscular dystrophy by amplification of lymphocyte RNA

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010502

7 January 2021

Point mutations in the dystrophin gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010502

7 January 2021

Preclinical diagnosis of familial hypertrophic cardiomyopathy by genetic analysis of blood lymphocytes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010502

7 January 2021

Access to a messenger RNA sequence or its protein product is not limited by tissue or species specificity

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010502

7 January 2021

Detection of human spermatid-specific transcripts in peripheral blood lymphocytes of males and females

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010502

7 January 2021

Identifiers

DOI

10.1002/HUMU.1380010502

1 reference

7 August 2017

1 reference