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ATP7A gene

Known as: ATPase copper transporting alpha, ATPase, Cu++ Transporting, Alpha Polypeptide (Menkes Syndrome) Gene, copper-transporting ATPase 1 
This gene is involved in copper transport.
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
멘케스병은 ATP7A 유전자의 돌연변이에 의한 드문 신경변성 구리대사질환이다. 임상증상으로는 경련, 성장지연, 근력저하, 피부 과신전, 모발변형 및 비뇨기계 이상 등을 나타낸다. 하지만 이런 임상증상은 생후 2-3… 
2015
2015
Cuproproteins such as PHM and DBM mature in late endosmal vesicles of the mammalian secretory pathway where changes in vesicle pH… 
2010
2010
From the Strategic Research Centre for Molecular and Medical Research and Centre for Cellular and Molecular Biology, School of… 
2010
2010
A natural missing link between activated and downhill protein folding scenarios Feng Liu, Caroline Maynard, Gregory Scott, Artem… 
2008
2008
The protein affected in Menkes disease, ATP7A, is a copper (Cu)-transporting P-type ATPase that plays an important role in Cu… 
2004
2004
本发明涉及ATP7A-相互作用分子在制备用于治疗神经变性疾病的药物组合物中的应用。 其中ATP7A-相互作用分子优选地是ATP7A…