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Parkinson Disease 13

Known as: PARK13 
 
National Institutes of Health

Papers overview

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2018
2018
Deletion at 22q11.2 responsible for Di George syndrome (DGs) is a risk factor for early-onset Parkinson's disease (EOPD). To date… Expand
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2017
2017
Background. HTRA2 has already been nominated as PARK13 which may cause Parkinson's disease, though there are still discrepancies… Expand
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Review
2017
Review
2017
High-temperature-requirement A2 (HtrA2)/Omi/PARK13 is a serine protease with extensive homology to the Escherichia coli HtrAs… Expand
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2016
2016
Although mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are the most common cause of genetic Parkinson's disease… Expand
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2014
2014
Background: Mutations in PARK13 have been implicated in Parkinson disease. Results: AtPARK13 confers thermotolerance in… Expand
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Highly Cited
2011
Highly Cited
2011
High-profile studies have provided conflicting results regarding the involvement of the Omi/HtrA2 gene in Parkinson's disease (PD… Expand
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Highly Cited
2007
Highly Cited
2007
In mice, targeted deletion of the serine protease HtrA2 (also known as Omi) causes mitochondrial dysfunction leading to a… Expand
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2007
2007
Intensive Forschung innerhalb des letzten Jahrzehnts hat die Rolle genetischer Veranderungen bei der Entstehung des… Expand
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