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PRX gene
Known as:
KIAA1620
, PERIAXIN
, PRX
National Institutes of Health
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Related topics
1 relation
periaxin
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Contribution of Schwann Cells to Remyelination in a Naturally Occurring Canine Model of CNS Neuroinflammation
K. Kegler
,
I. Spitzbarth
,
I. Imbschweiler
,
K. Wewetzer
,
W. Baumgärtner
,
F. Seehusen
PLoS ONE
2015
Corpus ID: 16712245
Gliogenesis under pathophysiological conditions is of particular clinical relevance since it may provide evidence for…
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2015
2015
Associated occurrence of p75 neurotrophin receptor expressing aldynoglia and microglia/macrophages in long term organotypic murine brain slice cultures
I. Spitzbarth
,
Armend Cana
,
K. Hahn
,
F. Hansmann
,
W. Baumgärtner
Brain Research
2015
Corpus ID: 23723375
2014
2014
Differential gene expression in proximal and distal nerve segments of rats with sciatic nerve injury during Wallerian degeneration
Nan Jiang
,
Huaiqin Li
,
+4 authors
D. Yao
Neural Regeneration Research
2014
Corpus ID: 44538017
Wallerian degeneration is a subject of major interest in neuroscience. A large number of genes are differentially regulated…
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2014
2014
Periaxin and AHNAK Nucleoprotein 2 Form Intertwined Homodimers through Domain Swapping*
Huijong Han
,
P. Kursula
Journal of Biological Chemistry
2014
Corpus ID: 22536302
Background: Periaxin and AHNAK nucleoprotein 2 contain a poorly conserved PDZ domain. Results: The crystal structures for the PDZ…
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2013
2013
New mutation in periaxin gene causing Charcot Marie Tooth disease in a Puerto Rican young male.
E. Noriega
,
E. Ramos
Journal of Clinical Neuromuscular Disease
2013
Corpus ID: 11514285
Charcot-Marie-Tooth (CMT) disease is an inherited peripheral neuropathy caused by mutations in more than 30 different genes. One…
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2012
2012
Self‐regulated alternative splicing at the AHNAK locus
A. Morrée
,
M. Droog
,
+5 authors
S. Maarel
The FASEB Journal
2012
Corpus ID: 26042541
AHNAK is a 700‐kDa protein involved in cytoarchitecture and calcium signaling. It is secondarily reduced in muscle of…
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Highly Cited
2008
Highly Cited
2008
Two novel mutations in the GDAP1 and PRX genes in early onset Charcot-Marie-Tooth syndrome.
M. Auer-Grumbach
,
Carina Fischer
,
+12 authors
A. Janecke
Neuropediatrics
2008
Corpus ID: 205026941
Autosomal recessive Charcot-Marie-Tooth syndrome (AR-CMT) is often characterised by an infantile disease onset and a severe…
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2006
2006
Periaxin mutation in Japanese patients with Charcot-Marie-Tooth disease
T. Otagiri
,
K. Sugai
,
+4 authors
K. Hayasaka
Journal of Human Genetics
2006
Corpus ID: 22182566
AbstractPeriaxin (PRX) plays an important role in the myelination of the peripheral nerve and consequently in the pathogenesis of…
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Review
2005
Review
2005
Autosomal-Recessive Charcot-Marie-Tooth Diseases
J. Vallat
,
M. Tazir
,
C. Magdelaine
,
F. Sturtz
,
D. Grid
Journal of Neuropathology and Experimental…
2005
Corpus ID: 9481746
In certain countries around the Mediterranean basin such as Algeria, which have a high prevalence of consanguineous marriages…
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2004
2004
Autosomal recessive forms of Charcot-Marie-Tooth disease
J. Vallat
,
D. Grid
,
C. Magdelaine
,
F. Sturtz
,
M. Tazir
Current Neurology and Neuroscience Reports
2004
Corpus ID: 19822675
In some countries with a high prevalence of consanguineous marriages, autosomal recessive inheritance is likely to account for…
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