PRX gene

Known as: KIAA1620, PERIAXIN, PRX 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1994-2018
024619942018

Papers overview

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2012
2012
We identified the main features of Charcot–Marie–Tooth (CMT) disease, type 4F, caused by a periaxin gene (PRX) mutation in… (More)
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2007
2007
Myelination in the PNS is accompanied by a large induction of the myelin protein zero (Mpz) gene to produce the most abundant… (More)
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2006
2006
Mutations in the DNA-binding domain of EGR2 are associated with severe autosomal dominant forms of peripheral neuropathy. In this… (More)
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Highly Cited
2004
Highly Cited
2004
The transcription factor Krox-20 controls Schwann cell myelination. Schwann cells in Krox-20 null mice fail to myelinate, and… (More)
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Highly Cited
2003
Highly Cited
2003
The anucleate prismoid fiber cells of the eye lens are densely packed to form a tissue in which the plasma membranes and their… (More)
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2003
2003
We investigated the role of Krox-20 (Egr2), a transcription factor that regulates myelination, in controlling the myelin… (More)
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Highly Cited
2001
Highly Cited
2001
Charcot-Marie-Tooth (CMT) disease is a heterogeneous group of inherited peripheral motor and sensory neuropathies characterized… (More)
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1998
1998
Periaxin was first described as a 147-kDa protein that was suggested to have a potential role in the initiation of myelin… (More)
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1995
1995
Periaxin is a newly described protein that is expressed exclusively by myelinating Schwann cells. In developing nerves, periaxin… (More)
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Highly Cited
1994
Highly Cited
1994
We report the cloning and subcellular localization of a novel Schwann cell-specific protein of 147 kd that we have named periaxin… (More)
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