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NREP gene

Known as: P311, CHROMOSOME 5 OPEN READING FRAME 13, SEZ17 
National Institutes of Health

Related topics

Related topics

4 relations
FAM114A2 geneFAM13B geneFAXDC2 geneRELL2 gene

Papers overview

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Highly Cited
2018
Highly Cited
2018
Signatures within the esophageal microbiome are associated with host genetics, age, and disease
The esophageal microbiome has been proposed to be involved in a range of diseases including the esophageal adenocarcinoma cascade… 
Highly Cited
2018
Highly Cited
2018
MicroRNA degradation by a conserved target RNA regulates animal behavior
microRNAs (miRNAs) repress target transcripts through partial complementarity. By contrast, highly complementary miRNA-binding… 
2016
2016
P311 induces the transdifferentiation of epidermal stem cells to myofibroblast-like cells by stimulating transforming growth factor β1 expression
Epithelial to mesenchymal transition, especially to myofibroblasts, plays an important role in wound healing, fibrosis, and… 
Highly Cited
2013
Highly Cited
2013
MeCP2 modulates gene expression pathways in astrocytes
BackgroundMutations in MECP2 encoding methyl-CpG-binding protein 2 (MeCP2) cause the X-linked neurodevelopmental disorder Rett… 
Highly Cited
2010
Highly Cited
2010
Investigating the Role of P311 in the Hypertrophic Scar
The mechanisms of hypertrophic scar formation are not fully understood. We previously screened the differentially expressed genes… 
Highly Cited
2007
Highly Cited
2007
Artificial Neural Network Classification Using a Minimal Training Set : Comparison to Conventional Supervised Classification
Recent research has shown an artificial neural network (ANN) to be capable of pattern recognition and the classification of image… 
Highly Cited
2002
Highly Cited
2002
P311 induces a TGF-beta1-independent, nonfibrogenic myofibroblast phenotype.
P311, also called PTZ17, was identified by suppressive subtraction hybridization as potentially involved in smooth muscle (SM… 
1989
1989
Central venous O2 saturation and rate of arterial desaturation during obstructive apnea.
We examined the rate of fall of arterial O2 saturation (dSao2/dt) after apnea onset in four spontaneously breathing adult male… 
Highly Cited
1988
Highly Cited
1988
Construction of a NotI linking library and isolation of new markers close to the Huntington's disease gene.
Linking clones contain sequences flanking recognition sites for enzymes cutting rarely in mammalian DNA. They can be used to… 
1988
1988
Mapping of D4S98/S114/S113 confines the Huntington's defect to a reduced physical region at the telomere of chromosome 4.
The dominant gene defect in Huntington's disease (HD) is linked to the DNA marker D4S10, near the telomere of the chromosome 4… 
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