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ACTA1 gene

Known as: nemaline myopathy type 3, actin, alpha 1, skeletal muscle, ACTA1 
National Institutes of Health

Related topics

Related topics

3 relations
ActinsCongenital Fiber Type DisproportionNemaline myopathy 3

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2019
Highly Cited
2019
Identification of SERPINE1, PLAU and ACTA1 as biomarkers of head and neck squamous cell carcinoma based on integrated bioinformatics analysis
BackgroundHead and neck squamous cell carcinoma (HNSCC) is the six leading cancer by incidence worldwide. The 5-year survival… 
Review
2017
Review
2017
Clinical and Histologic Findings in ACTA1-Related Nemaline Myopathy: Case Series and Review of the Literature.
2017
2017
HUBUNGAN TINGKAT KECEMASAN DENGAN KEJADIAN ASMA PADA PASIEN ASMA BRONKIAL DI WILAYAH KERJA PUSKESMAS KUIN RAYA BANJARMASIN
Latar Belakang : Asma merupakan masalah kesehatan dunia yang tidak hanya terjangkit di negara maju tetapi juga di negara… 
2015
2015
Association of a Novel ACTA1 Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended Family.
IMPORTANCE New genomic strategies can now be applied to identify a diagnosis in patients and families with previously undiagnosed… 
2014
2014
Congenital fiber type disproportion myopathy caused by LMNA mutations
2013
2013
A de novo dominant mutation in ACTA1 causing congenital nemaline myopathy associated with a milder phenotype: Expanding the spectrum of dominant ACTA1 mutations
2011
2011
GH overexpression causes muscle hypertrophy independent from local IGF-I in a zebrafish transgenic model
The aim of the present study was to analyse the morphology of white skeletal muscle in males and females from the GH-transgenic… 
2010
2010
TÜİK Verilerine Göre Türkiye’de İntihar Olgularının Değerlendirilmesi
Intiharlar tum dunyada sosyo-ekonomik fark gozetmeksizin onemli bir halk ve ruh sagligi sorunu olarak degerlendirilmektedir… 
Highly Cited
2007
Highly Cited
2007
The pathogenesis of ACTA1‐related congenital fiber type disproportion
Mutations in ACTA1 have been associated with a variety of changes in muscle histology that likely result from fundamental… 
1995
1995
Molecular analysis of asmA, a locus identified as the suppressor of OmpF assembly mutants of Escherichia coli K‐12
We present the molecular characterization of the asmA gene, whose product is involved in the assembly of outer membrane proteins… 
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