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SLC9A9 gene

Known as: NHE9, FLJ35613, solute carrier family 9 member A9 
This gene is involved in intracellular organelle ion homeostasis.
National Institutes of Health

Related topics

Related topics

8 relations
Acid-Base EquilibriumHomo sapiensIonophore activityLigand Binding

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Abstract P6-04-03: In-depth genomic analysis of acquired resistance to multiple sequential lines of endocrine therapy in breast cancer
Background: 80% of all breast cancers (BCs) are ER+. Not all respond to endocrine therapy (ET) and many eventually develop… 
2018
2018
Structural insights and characterization of human Npas4 protein
Npas4 is an activity dependent transcription factor which is responsible for gearing the expression of target genes involved in… 
2017
2017
Dataset pertaining to the publication “Polymorphisms in B3GAT1, SLC9A9 and MGAT5 are associated with variation within the human plasma N-glycome of 3533 European adults.”
2017
2017
Abstract 21108: Early Evidence That the Female Genome Does Matter for Acute Coronary Syndrome Risk
Introduction: Women of all ethnicities have the highest rates of Acute Coronary Syndrome (ACS) misdiagnosis, delayed treatment… 
2016
2016
Genome-Wide Study of Response to Platinum, Taxane, and Combination Therapy in Ovarian Cancer: In vitro Phenotypes, Inherited Variation, and Disease Recurrence
Background: The standard treatment for epithelial ovarian cancer (EOC) patients with advanced disease is carboplatin-paclitaxel… 
2014
2014
Genetic variants in SLC9A9 gene coding for sodium/hydrogen exchanger 9 are not associated with diabetic kidney disease
Wstep. W kilku niezaleznych badaniach stwierdzono sprzezenie pomiedzy fragmentem chromosomu 3q22 a cukrzycową chorobą nerek… 
2014
2014
Brak związku wariantów genetycznych w genie SLC9A9 kodującym antyporter sodowo-protonowy 9 z cukrzycową chorobą nerek
Background. Several independent studies found a linkage between diabetic kidney disease and chromosome 3q22. Following studies… 
2011
2011
Abstracts & Insights on Biomarkers From the 2011 European Meeting in Multiple Sclerosis CME
s & Insights on Biomarkers From the 2011 European Meeting in Multiple Sclerosis CME/CE INTRoDuCTIoN The diagnosis of multiple… 
2010
2010
Association of attention-deficit/hyperactivity disorder symptoms with the solute carrier family (sodium/hydrogen exchanger) isoform 9 (SLC9A9)
Introduction: Attention-deficit/hyperactivity disorder (ADHD) is a multifactorial, highly heritable developmental disorder which… 
2008
2008
Replication of a genome‐wide case–control study of esophageal squamous cell carcinoma
In a previous pilot case–control study of individuals diagnosed with esophageal squamous cell carcinoma (ESCC) and matched… 
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