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“Parkinson LRRK2” Clear search

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LRRK2 Mutation Alters Dopamine D2 Receptor Localization in Induced Pluripotent Stem Cells-Derived Astrocytes From Parkinson's Disease Patients: Implications for Neuronal Damage.

Mutti V, Bono F, Tomasoni Z, Fadel D, Gnutti C, Sbrini G, Gaudenzi C, Salvi V, Bosisio D, Russo I, Bolognin S, Schwamborn JC, Missale C, Fiorentini C.

J Neurochem · 2026-07-01

DOI: 10.1111/jnc.70510PMID: 42381446

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
Open access

NERINE reveals rare variant associations in gene networks across phenotypes and implicates an SNCA-PRL-LRRK2 subnetwork in Parkinson's disease.

Nazeen S, Wang X, Morrow AR, Strom R, Ethier E, Ritter D, Henderson ABH, Afroz J, Cassa CS, Stitziel NO, Gupta RM, Luk KC, Studer L, Khurana V, Sunyaev SR.

Cell Genom · 2026-06-22

DOI: 10.1016/j.xgen.2026.101284PMID: 42330948

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
Open access

Single-cell RNA profiling of oligodendroglial lineage cells derived from iPSCs carrying Parkinson's disease-relevant LRRK2-G2019S mutation.

Karmali N, Kessler W, Dehestani M, Sun W, Drwesh L, Volos P, Tsitkov S, Dhingra A, Thomas C, Rodriguez-Nieto S, Tietz J, Schafflick D, Fernandes N, Fitzgerald J, Fraenkel E, Gasser T, Rafiq NM, Kuhlmann T, Bansal V.

iScience · 2026-06-19

DOI: 10.1016/j.isci.2026.116368PMID: 42383004

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

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