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The multifaceted role of LRRK2 in Parkinson's disease: From human iPSC to organoids

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dc.creator Sabogal-Guaqueta, Angelica Maria
dc.creator Galuh, Sekar
dc.creator Alexander, Anastasia
dc.creator Dolga, Amalia M.
dc.creator Oun, Asmaa
dc.creator Kortholt, Arjan
dc.date 2022-10-01T00:00:00Z
dc.date.accessioned 2023-01-09T12:01:38Z
dc.date.available 2023-01-09T12:01:38Z
dc.identifier 3921b01f-e3f9-4664-ab8e-cb7767e8a5d3
dc.identifier 10.1016/j.nbd.2022.105837
dc.identifier https://avesis.sdu.edu.tr/publication/details/3921b01f-e3f9-4664-ab8e-cb7767e8a5d3/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/97750
dc.description Parkinson's disease (PD) is the second most common neurodegenerative disease affecting elderly people. Pathogenic mutations in Leucine-Rich Repeat Kinase 2 (LRRK2) are the most common cause of autosomal dominant PD. LRRK2 activity is enhanced in both familial and idiopathic PD, thereby studies on LRRK2-related PD research are essential for understanding PD pathology. Finding an appropriate model to mimic PD pathology is crucial for revealing the molecular mechanisms underlying disease progression, and aiding drug discovery. In the last few years, the use of human-induced pluripotent stem cells (hiPSCs) grew exponentially, especially in studying neurodegenerative diseases like PD, where working with brain neurons and glial cells was mainly possible using postmortem samples. In this review, we will discuss the use of hiPSCs as a model for PD pathology and research on the LRRK2 function in both neuronal and immune cells, together with reviewing the recent advances in 3D organoid models and microfluidics.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title The multifaceted role of LRRK2 in Parkinson's disease: From human iPSC to organoids
dc.type info:eu-repo/semantics/article


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