Andrew B. West mostly deals with Molecular biology, LRRK2, Genetics, Parkin and Parkinson's disease. In his study, Point mutation, Gene expression and Ubiquitin ligase is inextricably linked to Neurodegeneration, which falls within the broad field of Molecular biology. The study incorporates disciplines such as Microglia, Leucine-rich repeat, Kinase activity and ASK1 in addition to LRRK2.
His Kinase activity research is multidisciplinary, relying on both Cyclin-dependent kinase 4, MAP3K7, Cyclin-dependent kinase 9 and Cyclin-dependent kinase 2. His Parkin research includes elements of Ubiquitin, Pathogenesis, Mutation, Age of onset and Degenerative disease. His studies in Parkinson's disease integrate themes in fields like Neuroscience, Mitochondrion and Proteasome.
His scientific interests lie mostly in LRRK2, Disease, Kinase, Parkinson's disease and Neurodegeneration. His LRRK2 study incorporates themes from Molecular biology, Cell biology, Neuroprotection and Kinase activity. His Disease research is multidisciplinary, incorporating perspectives in Biomarker, Genetics, Gene and Bioinformatics.
His Kinase research is multidisciplinary, incorporating elements of Cancer research, GTPase, Pharmacology and Phosphorylation. A large part of his Parkinson's disease studies is devoted to Parkin. His biological study spans a wide range of topics, including Substantia nigra, Neuroinflammation, Neuroscience and Innate immune system.
Andrew B. West mainly investigates LRRK2, Cell biology, Disease, Neurodegeneration and Kinase. His LRRK2 research includes elements of Missense mutation, Movement disorders, Montreal Cognitive Assessment and Kinase activity. His Cell biology study also includes fields such as
He is involved in the study of Disease that focuses on Parkinson's disease in particular. Andrew B. West interconnects Dementia with Lewy bodies, Dementia and Dopaminergic in the investigation of issues within Neurodegeneration. His Kinase research is multidisciplinary, incorporating elements of Pharmacology and Phosphorylation.
The scientist’s investigation covers issues in LRRK2, Neurodegeneration, Disease, Cell biology and Exosome. His study on LRRK2 is mostly dedicated to connecting different topics, such as Kinase. The various areas that he examines in his Kinase study include GTPase, Mutation, Substantia nigra, Dopaminergic and Neuroprotection.
The concepts of his Disease study are interwoven with issues in Biomarker, Neuroscience and Bioinformatics. Endosome is the focus of his Cell biology research. His studies in Parkinson's disease integrate themes in fields like Neuroinflammation, Mitochondrion and Kinase activity.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
MOLECULAR PATHOPHYSIOLOGY OF PARKINSON'S DISEASE
Darren J. Moore;Andrew B. West;Valina L. Dawson;Ted M. Dawson.
Neuroscience (2005)
Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activity
Andrew B. West;Darren J. Moore;Saskia Biskup;Artem Bugayenko.
Proceedings of the National Academy of Sciences of the United States of America (2005)
A genome-wide linkage and association scan reveals novel loci for autism
Lauren A. Weiss;Lauren A. Weiss;Dan E. Arking;Mark J. Daly;Mark J. Daly;Aravinda Chakravarti.
Nature (2009)
Parkinson's disease-associated mutations in LRRK2 link enhanced GTP-binding and kinase activities to neuronal toxicity
Andrew B. West;Darren J. Moore;Catherine Choi;Shaida A. Andrabi.
Human Molecular Genetics (2007)
Localization of LRRK2 to membranous and vesicular structures in mammalian brain.
Saskia Biskup;Darren J. Moore;Fulvio Celsi;Shinji Higashi;Shinji Higashi.
Annals of Neurology (2006)
Leucine-rich repeat kinase 2 (LRRK2) interacts with parkin, and mutant LRRK2 induces neuronal degeneration
Wanli W. Smith;Zhong Pei;Haibing Jiang;Darren J. Moore.
Proceedings of the National Academy of Sciences of the United States of America (2005)
Transcriptome analysis reveals dysregulation of innate immune response genes and neuronal activity-dependent genes in autism.
Simone Gupta;Shannon E. Ellis;Foram N. Ashar;Anna Moes.
Nature Communications (2014)
α-synuclein gene haplotypes are associated with Parkinson’s disease
Matt Farrer;Demetrius M. Maraganore;Paul Lockhart;Andrew Singleton.
Human Molecular Genetics (2001)
LRRK2 inhibition attenuates microglial inflammatory responses.
Mark S. Moehle;Philip J. Webber;Tonia Tse;Nour Sukar.
The Journal of Neuroscience (2012)
Inhibitors of leucine-rich repeat kinase-2 protect against models of Parkinson's disease
Byoung Dae Lee;Joo Ho Shin;Jackalina Vankampen;Leonard Petrucelli.
Nature Medicine (2010)
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