Skip to search formSkip to main contentSkip to account menu

AKAP10 gene

Known as: A-kinase anchoring protein 10, dual-specificity A-kinase anchoring protein 2, mitochondrial A kinase PPKA anchor protein 10 
This gene plays a role in the regulation of protein kinase A activity.
National Institutes of Health

Related topics

Related topics

5 relations
A-Kinase Anchor Protein 10, MitochondrialBlood coagulationSignal Transductionprotein protein interaction

Narrower (1)

AKAP10 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Centenarian Exomes as a Tool for Evaluating the Clinical Relevance of Germline Tumor Suppressor Mutations
Objectives: The aim of the present study was to evaluate the clinical relevance of mutations in tumor suppressor genes using… 
2018
2018
Predisposition of functional genetic variants of A-kinase anchoring protein 10 toward acquired repolarization disorders in high-risk vascular surgery patients
Purpose We aimed at assessing the predisposition of A-kinase anchoring protein 10 (AKAP10) polymorphism toward acquired… 
2013
2013
Association of 1936A > G in AKAP10 (A-kinase anchoring protein 10) and blood pressure in Polish full-term newborns
Abstract Objective. The 1936G AKAP10 allele is associated with increased adult basal heart rate (HR) and decreased variability… 
2013
2013
Polymorphism 1936A>G in the AKAP10 gene (encoding A-kinase-anchoring protein 10) is associated with higher cholesterol cord blood concentration in Polish full-term newborns
Abstract Aims: A-Kinase anchoring proteins (AKAPs) coordinate the specificity of protein kinase A signaling by localizing the… 
2012
2012
1936A→G (I646 V) Polymorphism in the AKAP10 Gene Encoding A-Kinase-Anchoring Protein 10 in Very Long-Lived Poles is Similar to that in Newborns
Background/Study Context: The common 1936A→G transition (rs203462) in the AKAP10 gene encoding the A-kinase-anchoring protein 10… 
2009
2009
Editor's Summary and Q&A: Cone-beam computed tomography evaluation of orthodontic miniplate anchoring screws in the posterior maxilla
2009
2009
[Genotyping of AKAP10 gene 2073A/G single nucleotide polymorphism by TaqMan probe real-time PCR].
OBJECTIVE To detect AKAP10 gene 2073A/G single nucleotide polymorphism (SNP) genotyping by TaqMan probe real-time PCR. METHODS… 
2009
2009
Association of a1936g (rs203462) polymorphism of a-kinase anchoring protein 10 with qt interval prolongation during kidney transplantation
2002
2002
Different phenotypes in recessive dystrophic epidermolysis bullosa patients sharing the same mutation in compound heterozygosity with two novel mutations in the type VII collagen gene
Background Dystrophic epidermolysis bullosa (DEB) is a bullous skin disease caused by mutations in the type VII collagen gene… 
1999
1999
Three homozygous PTC mutations in the collagen type VII gene of patients affected by recessive dystrophic epidermolysis bullosa: Analysis of transcript levels in dermal fibroblasts
The Hallopeau‐Siemens variant of recessive dystrophic epidermolysis bullosa (HS‐RDEB) is a severe inherited skin disease… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)