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ANOS1 gene

Known as: ANOS1, anosmin-1, WAP four-disulfide core domain 19 
This gene may play a role in both cell adhesion and protease inhibition.
National Institutes of Health

Related topics

Related topics

11 relations
Cell AdhesionCell MovementFGFR1 geneKAL1 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Serum levels of ANOS1 serve as a diagnostic biomarker of gastric cancer: a prospective multicenter observational study
Background Development of high-performance serum biomarkers will likely improve treatment outcomes of patients with gastric… 
2018
2018
Targeted Gene Panel Sequencing for Molecular Diagnosis of Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism.
BACKGROUND Isolated gonadotropin-releasing hormone (GnRH) deficiency (IGD) is classified either as Kallmann syndrome (KS) with… 
2017
2017
Expanding the genetic spectrum of ANOS1 mutations in patients with congenital hypogonadotropic hypogonadism
STUDY QUESTION What is the prevalence and functional consequence of ANOS1 (KAL1) mutations in a group of men with congenital… 
Highly Cited
2016
Highly Cited
2016
Function and diagnostic value of Anosmin‐1 in gastric cancer progression
Gastric cancer (GC) is a major global health problem that urgently requires novel molecular biomarkers for patient stratification… 
2013
2013
Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome.
2009
2009
Anosmin-1 involved in neuronal cell migration is hypoxia inducible and cancer regulated
Functional expression of KAL1 gene is critical in the migration of GnRH neurons from the olfactory placode to the hypothalamus in… 
Review
2006
Review
2006
Mechanisms of Disease: insights into X-linked and autosomal-dominant Kallmann syndrome
Kallmann syndrome (KS) is a disorder characterized by hypogonadotropic hypogonadism and anosmia. Although KS is genetically… 
Highly Cited
2006
Highly Cited
2006
Novel fibroblast growth factor receptor 1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmia.
CONTEXT Kallmann syndrome is a clinically and genetically heterogeneous disorder. To date, loss-of-function mutations in the… 
Review
1993
Review
1993
The Kallmann's syndrome variant (KSV) model of the schizophrenias
Highly Cited
1992
Highly Cited
1992
Brief report: intragenic deletion of the KALIG-1 gene in Kallmann's syndrome.
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