SLC26A4 gene

Known as: SLC26A4, PENDRIN, PDS 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1981-2017
0204019812017

Papers overview

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Highly Cited
2009
Highly Cited
2009
I present dispersal distances for 44 species with data on propagule duration (PD) for 40 of these. Data were combined with those… (More)
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Highly Cited
2006
Highly Cited
2006
Sensorineural hearing loss is the most frequent sensory deficit of childhood and is of genetic origin in up to 75% of cases. It… (More)
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Highly Cited
2003
Highly Cited
2003
Recessive mutations of SLC26A4 (PDS) are a common cause of Pendred syndrome and non-syndromic deafness in western populations… (More)
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Highly Cited
2001
Highly Cited
2001
Pendrin is an anion transporter encoded by the PDS/Pds gene. In humans, mutations in PDS cause the genetic disorder Pendred… (More)
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Highly Cited
2001
Highly Cited
2001
Following the positional cloning of PDS, the gene mutated in the deafness/goitre disorder Pendred syndrome (PS), numerous studies… (More)
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Highly Cited
2000
Highly Cited
2000
Pendred syndrome is an autosomal recessive disorder characterized by congenital deafness and thyroid goiter. The thyroid disease… (More)
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Highly Cited
1999
Highly Cited
1999
Pendred syndrome is the most common form of syndromic deafness and characterized by congenital sensorineural hearing loss and… (More)
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Highly Cited
1999
Highly Cited
1999
Pendred's syndrome is an autosomal-recessive disorder characterized by deafness and goiter. After our recent identification of… (More)
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Highly Cited
1998
Highly Cited
1998
The phytoene desaturase (PDS) gene of Nicotiana benthamiana was silenced in plants infected with potato virus X (PVX) vectors… (More)
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Highly Cited
1997
Highly Cited
1997
Pendred syndrome is a recessively inherited disorder with the hallmark features of congenital deafness and thyroid goitre. By… (More)
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