(Q24294990)

English

Defining alpha-skeletal and alpha-cardiac actin expression in human heart and skeletal muscle explains the absence of cardiac involvement in ACTA1 nemaline myopathy

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16288873%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Defining alpha-skeletal and alpha-cardiac actin expression in human heart and skeletal muscle explains the absence of cardiac involvement in ACTA1 nemaline myopathy (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16288873%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Actin alpha cardiac muscle 1

1 reference

GOA release 2020-03-11

nemaline myopathy

1 reference

based on heuristic

inferred from title

4

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16288873%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Sandra T Cooper

5

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16288873%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

author name string

Biljana Ilkovski

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16288873%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Sophie Clement

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16288873%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Caroline Sewry

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16288873%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

language of work or name

0 references

publication date

8 November 2005

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16288873%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Neuromuscular Disorders

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16288873%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

15

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16288873%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

12

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16288873%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

829-835

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16288873%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Nemaline myopathy: a clinical study of 143 cases

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

Actin mutations are one cause of congenital fibre type disproportion

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

α-Actin isoform distribution in normal and failing human heart: a morphological, morphometric, and biochemical study

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

A comprehensive analysis of the developmental and tissue-specific expression of the isoactin multigene family in the rat

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

Actin and myosin genes are transcriptionally regulated during mouse skeletal muscle development

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

A fetal skeletal muscle actin mRNA in the mouse and its identity with cardiac actin mRNA.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

Muscle disease caused by mutations in the skeletal muscle alpha-actin gene (ACTA1).

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

Specific immunohistochemical detection of cardiac/fetal alpha-actin in human cardiomyocytes and regenerating skeletal muscle cells.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

Mammalian cytoplasmic actins are the products of at least two genes and differ in primary structure in at least 25 identified positions from skeletal muscle actins

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

Nemaline myopathy caused by mutations in the muscle alpha-skeletal-actin gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26).

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

Evidence for a dominant-negative effect in ACTA1 nemaline myopathy caused by abnormal folding, aggregation and altered polymerization of mutant actin isoforms

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression of the genes coding for the skeletal muscle and cardiac actions in the heart.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

alpha-Cardiac actin is the major sarcomeric isoform expressed in embryonic avian skeletal muscle.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

Mice lacking skeletal muscle actin show reduced muscle strength and growth deficits and die during the neonatal period

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

alpha-skeletal and alpha-cardiac actin genes are coexpressed in adult human skeletal muscle and heart

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

Cardiac actin is the major actin gene product in skeletal muscle cell differentiation in vitro

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

The development expression of the rat alpha-vascular and gamma-enteric smooth muscle isoactins: isolation and characterization of a rat gamma-enteric actin cDNA.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

Missense mutations of ACTA1 cause dominant congenital myopathy with cores

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

Nemaline myopathy: current concepts. The ENMC International Consortium and Nemaline Myopathy

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26)

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

A subpopulation of cardiomyocytes expressing alpha-skeletal actin is identified by a specific polyclonal antibody

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

Skeletal actin mRNA increases in the human heart during ontogenic development and is the major isoform of control and failing adult hearts

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical course correlates poorly with muscle pathology in nemaline myopathy.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

Single section Western blot: Improving the molecular diagnosis of the muscular dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FJ.NMD.2005.08.004

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q24294990&oldid=1985693103"