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