CCDC40 gene

Known as: CCDC40, coiled-coil domain containing 40, FLJ20753 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2010-2018
01220102018

Papers overview

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Review
2018
Review
2018
Objective: To analyze the clinical manifestations, cilia ultrastructure and gene variations of primary ciliary dyskinesia (PCD… (More)
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2015
2015
RATIONALE The relationship between clinical phenotype of childhood primary ciliary dyskinesia (PCD) and ultrastructural defects… (More)
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2015
2015
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous, autosomal recessive disorder that results from functional and… (More)
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2015
2015
CCDC39 and CCDC40 were first identified as causative mutations in primary ciliary dyskinesia patients; cilia from patients show… (More)
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2014
2014
Primary ciliary dyskinesia (PCD) is a rare genetic disorder leading to recurrent respiratory tract infections. High-speed video… (More)
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2014
2014
Existence of cellular structures with specific size raises a fundamental question in biology: How do cells measure length? One… (More)
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2013
2013
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder caused by cilia and sperm dysmotility. About 12% of… (More)
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2013
2013
Pompe disease is an uncommon autosomal recessive glycogen storage disorder caused by deficiency of acid α-glucosidase. Classic… (More)
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2012
2012
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous inherited disorder characterised by recurrent respiratory tract… (More)
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2010
2010
To understand transcriptional regulation, it is necessary to understand the factors that determine where a particular… (More)
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