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NTNG1 gene

Known as: Lmnt1, KIAA0976, NETRIN G1 
This gene is involved in axon formation.
National Institutes of Health

Related topics

Related topics

4 relations
NTNG1 protein, humanNeurogenesisRegulation of Cell Shapeprotein protein interaction

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Gene expression-based analysis identified NTNG1 and HGF as biomarkers for diabetic kidney disease
Abstract Diabetic kidney disease (DKD) is a leading cause of end-stage renal disease. Because the molecular mechanisms of DKD are… 
2020
2020
SARS-CoV-2 orf1b Gene Sequence in the NTNG1 Gene on Human Chromosome 1.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a positive-sense single-stranded RNA virus. It is contagious in… 
2020
2020
Human Gene Sequences in SARS-CoV-2 and Other Viruses.
In a previous study, we identified a 117 base severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) sequence in the human… 
2018
2018
Netrin G1: its downregulation in the nucleus accumbens of cocaine‐conditioned mice and genetic association in human cocaine dependence
Netrin G1 is a presynaptic ligand involved in axonal projection. Although molecular mechanisms underlying cocaine addiction are… 
2014
2014
Replication of NTNG1 association in schizophrenia
This is a case–control study of the association of NTNG1 subtypes with schizophrenia among a group of individuals from a… 
2013
2013
The netrin G1 gene rs628117 polymorphism is associated with ischemic stroke
Review
2013
Review
2013
Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review.
2010
2010
Comparison of the neural crest stem cell characteristics derived from dorsal root ganglia, whisker pad and bone marrow in neonate rodents
2010
2010
Temporally-regulated generation of distinct descendants by sonic hedgehog-expressing progenitors in the forebrain
2007
2007
Interstitial deletion of the short arm of chromosome 1 (1p13.1p21.1) in a girl with mental retardation, short stature and colobomata
Interstitial deletions on the short arm of chromosome 1 are rare. We describe a girl with severe mental retardation, short… 
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