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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… 
2019
2019
Identification of Restless Legs Syndrome Genes by Mutational Load Analysis
Restless legs syndrome is a frequent neurological disorder with substantial burden on individual well‐being and public health… 
2017
2017
A prognostic mutation panel for predicting cancer recurrence in stages II and III colorectal cancer
Approximately 20‐40% of stage II/III colorectal cancer (CRC) patients develop relapse. Clinicopathological factors alone are… 
2016
2016
Targeted next generation sequencing: the diagnostic value in early-onset epileptic encephalopathy
We investigated the genetic background of early-onset epileptic encephalopathy (EE) using targeted next generation sequencing… 
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… 
Highly Cited
2013
Highly Cited
2013
Transcriptome Profile at Different Physiological Stages Reveals Potential Mode for Curly Fleece in Chinese Tan Sheep
Tan sheep (Ovis aries), a Chinese indigenous breed, has special curly fleece after birth, especially at one month old. However… 
2011
2011
Functional variants of the genes involved in neurodevelopment and susceptibility to schizophrenia in an Armenian population.
Highly Cited
2009
Highly Cited
2009
Analysis of severely affected patients with dihydropyrimidine dehydrogenase deficiency reveals large intragenic rearrangements of DPYD and a de novo interstitial deletion del(1)(p13.3p21.3)
Dihydropyrimidine dehydrogenase (DPD) deficiency is an infrequently described autosomal recessive disorder of the pyrimidine… 
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… 
2005
2005
Human netrin-G1 isoforms show evidence of differential expression.
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