HYDIN gene

Known as: KIAA1864, DKFZp434D0513, protein phosphatase 1, regulatory subunit 31 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2003-2018
02420032018

Papers overview

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2017
2017
Gene innovation by duplication is a fundamental evolutionary process but is difficult to study in humans due to the large size… (More)
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2014
2014
Mouse genetics is a powerful approach for discovering genes and other genome features influencing human pain sensitivity. Genetic… (More)
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2013
2013
A mutation in the hydin gene has been recently described as one possible mechanism leading to lethal congenital hydrocephalus in… (More)
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Highly Cited
2012
Highly Cited
2012
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder characterized by defective cilia and flagella… (More)
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Highly Cited
2008
Highly Cited
2008
Chlamydomonas reinhardtii hydin is a central pair protein required for flagellar motility, and mice with Hydin defects develop… (More)
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Highly Cited
2008
Highly Cited
2008
Chromosome region 1q21.1 contains extensive and complex low-copy repeats, and copy number variants (CNVs) in this region have… (More)
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2007
2007
Mutations in Hydin cause hydrocephalus in mice, and HYDIN is a strong candidate for causing hydrocephalus in humans. The gene is… (More)
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2006
2006
The HYDIN gene located in human chromosome band 16q22.2 is a large gene encompassing 423 kb of genomic DNA that has been… (More)
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2006
2006
Impairment of cilia and flagella function underlies a growing number of human genetic diseases. Mutations in hydin in hy3 mice… (More)
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Highly Cited
2003
Highly Cited
2003
The autosomal-recessive mutation hydrocephalus3 (hy3) results in lethal communicating hydrocephalus with perinatal onset. We… (More)
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