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DUOXA2 gene

Known as: DUAL OXIDASE MATURATION FACTOR 2, DUOXA2 
National Institutes of Health

Papers overview

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Review
2019
Review
2019
Genetics of Thyroid Disorders
Abstract Background: Thyroid diseases are the most common endocrine pathologies second to diabetes. They have been shown to have… 
2019
2019
Functional Characterization of DUOX Enzymes in Reconstituted Cell Models.
Biosynthesis of active human dual oxidases (DUOX1 and DUOX2) requires maturation factors, a.k.a. DUOX activator proteins (DUOXA1… 
2018
2018
Mutational Spectrum Analysis of Seven Genes Associated with Thyroid Dyshormonogenesis
Objective Thyroid dyshormonogenesis (DH) is a genetically heterogeneous inherited disorder caused by thyroid hormone synthesis… 
2018
2018
Fetal Goitrous Hypothyroidism and Polyhydramnios in a Patient with Compound Heterozygous DUOXA2 Mutations
Background: Fetal goiter is only rarely observed in pregnant women without autoimmune thyroid disorders, and there is no… 
2017
2017
Compound Heterozygous Mutations in the DUOX2/DUOXA2 Genes Cause Congenital Hypothyroidism
The mutations in the dual oxidase 2 (DUOX2) and dual oxidase maturation factor 2 (DUOXA2) genes can cause congenital… 
2016
2016
A Novel c.554+5C>T Mutation in the DUOXA2 Gene Combined with p.R885Q Mutation in the DUOX2 Gene Causing Congenital Hypothyroidism
The coexistence of mutations in the dual oxidase maturation factor 2 (DUOXA2) and dual oxidase 2 (DUOX2) genes is rarely… 
2016
2016
Heterozygous Mutations of the DUOXA2 and DUOX2 Genes in Dizygotic Twins with Congenital Hypothyroidism.
BACKGROUND The mutations in the dual oxidase maturation factor 2 (DUOXA2) and dual oxidase 2 (DUOX2) genes have been identified… 
2016
2016
Frequent occurrence of DUOX2 and DUOXA2 mutations in cases with borderline bloodspot screening TSH who develop 'True' congenital hypothyroidism
2016
2016
Compound heterozygous mutations (p.T561M and c.2422delT) in the TPO gene associated with congenital hypothyroidism
Abstract Background: The objective of the study was to determine the genetic basis of goitrous congenital hypothyroidism (GCH) in… 
2014
2014
Screening aberrant methylation profile in esophageal squamous cell carcinoma for Kazakhs in Xinjiang area of China
To screen the aberrant methylation genes in esophageal squamous cell carcinoma (ESCC) for Kazakh nationality in Xinjiang, and the… 
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