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International Journal of Molecular Sciences|June 19, 2024
An Overview of Epigenetic Changes in the Parkinson's Disease BrainAnthony Klokkaris, Anna Migdalska-Richards
Journal of Neurochemistry|February 11, 2016
The relationship between glucocerebrosidase mutations and Parkinson diseaseAnna Migdalska-Richards, Anthony H V Schapira
Medycyna Wieku Rozwojowego|October 10, 2006
[Attention deficit hyperactivity disorder (ADHD)--molecular and genetic aspects]Anna Migdalska, Magdalena Nawara, Jerzy Bal, et al.
Annals of Neurology|November 19, 2016
Ambroxol effects in glucocerebrosidase and α-synuclein transgenic miceAnna Migdalska-Richards, Liam Daly, Erwan Bezard, et al.
Synapse (New York, N.Y.)|March 16, 2017
Oral ambroxol increases brain glucocerebrosidase activity in a nonhuman primateAnna Migdalska-Richards, Wai Kin D Ko, Qin Li, et al.
International Journal of Molecular Sciences|February 11, 2023
DNA Methylation of α-Synuclein Intron 1 Is Significantly Decreased in the Frontal Cortex of Parkinson's Individuals with GBA1 MutationsAdam R Smith, David M Richards, Katie Lunnon, et al.
Human Molecular Genetics|July 6, 2016
Autophagic lysosome reformation dysfunction in glucocerebrosidase deficient cells: relevance to Parkinson diseaseJoana Magalhaes, Matthew E Gegg, Anna Migdalska-Richards, et al.
Plos One|August 25, 2020
L444P Gba1 mutation increases formation and spread of α-synuclein deposits in mice injected with mouse α-synuclein pre-formed fibrilsAnna Migdalska-Richards, Michal Wegrzynowicz, Ian F Harrison, et al.
Brain : a Journal of Neurology|October 4, 2017
The L444P Gba1 mutation enhances alpha-synuclein induced loss of nigral dopaminergic neurons in miceAnna Migdalska-Richards, Michal Wegrzynowicz, Raffaella Rusconi, et al.
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