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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.
2016
2016
Intermolecular disulfide bond in the dimerization of S-periaxin mediated by Cys88 and Cys139.
Yan Yang
,
Y. Ren
,
Yawei Shi
Acta Biochimica et Biophysica Sinica
2016
Corpus ID: 42346499
Periaxin is expressed in mammalian Schwann cells and lens fiber cells, and has been identified in a screen for cytoskeleton…
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2016
2016
[Establishment of L-periaxin gene knock-out RSC96 cell line].
M. Liang
,
Tingting Peng
,
Yawei Shi
Sheng wu gong cheng xue bao = Chinese journal of…
2016
Corpus ID: 46808321
Periaxin, a protein of noncompact myelin, is specifically expressed in the peripheral nervous system (PNS). There are two protein…
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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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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
Late-onset Charcot-Marie-Tooth disease 4F caused by periaxin gene mutation
徳永 章子
2012
Corpus ID: 87137226
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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2008
2008
A 71‐nucleotide deletion in the periaxin gene in a Romani patient with early‐onset slowly progressive demyelinating CMT
L. Báranková
,
D. Šišková
,
+5 authors
Pavel Seeman
European Journal of Neurology
2008
Corpus ID: 24642229
Background: Mutations in the periaxin (PRX) gene cause autosomal recessive demyelinating neuropathy Charcot–Marie–Tooth (CMT…
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Review
2005
Review
2005
[Autosomal recessive forms of Charcot-Marie-Tooth disease].
J. Vallat
,
D. Grid
,
C. Magdelaine
,
F. Sturtz
,
N. Lévy
,
M. Tazir
Bulletin de l'Académie Nationale de Médecine
2005
Corpus ID: 31694322
In some countries with a high prevalence of consanguineous mariage, autosomal recessive inheritance probably accounts for the…
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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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