KCNAB2 gene

Known as: HKvbeta2.1, AKR6A5, KCNA2B 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1998-2017
01219982017

Papers overview

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2017
2017
Redox-sensitive potassium channels consisting of the voltage-gated K+ (KV) channel pore subunit KV1.5 regulate resting membrane… (More)
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2016
2016
BACKGROUND The Brugada syndrome is an inherited cardiac arrhythmia associated with high risk of sudden death. Although 20% of… (More)
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2015
2015
OBJECTIVE Monosomy 1p36 syndrome is the most commonly observed subtelomeric deletion syndrome. Patients with this syndrome… (More)
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2014
2014
Pituitary adenomas (PAs) are neoplasms that may cause a variety of neurological and endocrine effects. Although known causal… (More)
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2013
2013
AIMS Genetic factors may be important in the development of atrial fibrillation (AF) in the young. KCNA5 encodes the potassium… (More)
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2011
2011
Ablation of the distal end of the short arm of chromosome 1 [1p36 deletion syndrome (1p36DS)] is one of the most commonly… (More)
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2009
2009
Aldo-keto reductases (AKRs) are a major superfamily of monomeric NADPH-dependent carbonyl oxidoreductases. They are characterized… (More)
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2008
2008
Chronic metabolic acidosis (CMA) affects ion transport, permeability, and metabolism of the intestinal absorptive cells. Most… (More)
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2001
2001
PURPOSE Clinical features associated with chromosome 1p36 deletion include characteristic craniofacial abnormalities, mental… (More)
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2000
2000
We tested the hypothesis that Bis1, a gene involved in seizure regulation in mice which has been localized to the distal part of… (More)
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