(Q28207838)

Europe PubMed Central

PubMed publication ID

1302009

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1302009

10 September 2022

author name string

D B Parkinson

series ordinal

1

0 references

R V Thakker

series ordinal

2

0 references

Parkinson DB

series ordinal

1

1 reference

Europe PubMed Central

PubMed publication ID

1302009

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1302009

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

10 September 2022

language of work or name

English

0 references

publication date

May 1992

0 references

published in

Nature Genetics

0 references

volume

1

0 references

issue

2

0 references

page(s)

149-52

0 references

cites work

1 reference

https://api.crossref.org/works/10.1038/NG0592-149

The scanning model for translation: an update

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0592-149

A mechanism of protein localization: the signal hypothesis and bacteria

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0592-149

Familial Isolated Hypoparathyroidism

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-149

Effect of 5' splice site mutations on splicing of the preceding intron

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-149

Familial Idiopathic Hypoparathyroidism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-149

7 January 2021

Idiopathic hypoparathyroidism presenting with seizures during infancy: X-linked recessive inheritance in a large Missouri kindred

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-149

7 January 2021

Complete amino acid sequence of human parathyroid hormone

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-149

7 January 2021

Human parathyroid hormone gene (PTH) is on short arm of chromosome 11

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-149

7 January 2021

Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-149

7 January 2021

Mutation of the signal peptide-encoding region of the preproparathyroid hormone gene in familial isolated hypoparathyroidism

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-149

7 January 2021

Illegitimate transcription: transcription of any gene in any cell type

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-149

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/10.1038%2FNG0592-149

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-149

7 January 2021

Restriction fragment length polymorphisms at the human parathyroid hormone gene locus

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-149

7 January 2021

Nucleotide sequence of the human parathyroid hormone gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-149

7 January 2021

Ovalbumin gene: evidence for a leader sequence in mRNA and DNA sequences at the exon-intron boundaries

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-149

7 January 2021

Specific transcription and RNA splicing defects in five cloned β-thalassaemia genes

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-149

7 January 2021

Ehlers-Danlos syndrome type VII: a single base change that causes exon skipping in the type I collagen ?2(I) chain

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-149

7 January 2021

Control of Alternative Splicing by the Differential Binding of U1 Small Nuclear Ribonucleoprotein Particle

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-149

7 January 2021

Renal responsiveness to synthetic human parathyroid hormone 1-38 in healthy subjects

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-149

7 January 2021

Improvement of PCR amplified DNA sequencing with the aid of detergents

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-149

7 January 2021

Identifiers

DOI

10.1038/NG0592-149

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

1302009

1 reference

Consolidated OpenCitations Corpus – April 2017