Animal models of Parkinson's disease: a source of novel treatments and clues to the cause of the disease
S Duty, P Jenner - British journal of pharmacology, 2011 - Wiley Online Library
Animal models of Parkinson's disease (PD) have proved highly effective in the discovery of
novel treatments for motor symptoms of PD and in the search for clues to the underlying …
novel treatments for motor symptoms of PD and in the search for clues to the underlying …
[HTML][HTML] Cat-Map: putting cataract on the map
A Shiels, TM Bennett, JF Hejtmancik - Molecular vision, 2010 - ncbi.nlm.nih.gov
Lens opacities, or cataract (s), may be inherited as a classic Mendelian disorder usually with
early-onset or, more commonly, acquired with age as a multi-factorial or complex trait. Many …
early-onset or, more commonly, acquired with age as a multi-factorial or complex trait. Many …
Transcription factor Nurr1 maintains fiber integrity and nuclear-encoded mitochondrial gene expression in dopamine neurons
B Kadkhodaei, A Alvarsson, N Schintu… - Proceedings of the …, 2013 - National Acad Sciences
Developmental transcription factors important in early neuron specification and
differentiation often remain expressed in the adult brain. However, how these transcription …
differentiation often remain expressed in the adult brain. However, how these transcription …
Mitochondrial function and dynamics in neural stem cells and neurogenesis: Implications for neurodegenerative diseases
P Coelho, L Fão, S Mota, AC Rego - Ageing research reviews, 2022 - Elsevier
Mitochondria have been largely described as the powerhouse of the cell and recent findings
demonstrate that this organelle is fundamental for neurogenesis. The mechanisms …
demonstrate that this organelle is fundamental for neurogenesis. The mechanisms …
Animal models of the non-motor features of Parkinson's disease
K McDowell, MF Chesselet - Neurobiology of disease, 2012 - Elsevier
The non-motor symptoms (NMS) of Parkinson's disease (PD) occur in roughly 90% of
patients, have a profound negative impact on their quality of life, and often go undiagnosed …
patients, have a profound negative impact on their quality of life, and often go undiagnosed …
Genetics of anterior segment dysgenesis disorders
LM Reis, EV Semina - Current opinion in ophthalmology, 2011 - journals.lww.com
Although a number of genetic causes have been identified, many ASD conditions are still
awaiting genetic elucidation. The majority of characterized ASD genes encode transcription …
awaiting genetic elucidation. The majority of characterized ASD genes encode transcription …
Association of Nrf2-encoding NFE2L2 haplotypes with Parkinson's disease
M von Otter, S Landgren, S Nilsson, D Celojevic… - BMC medical …, 2010 - Springer
Background Oxidative stress is heavily implicated in the pathogenic process of Parkinson's
disease. Varying capacity to detoxify radical oxygen species through induction of phase II …
disease. Varying capacity to detoxify radical oxygen species through induction of phase II …
MicroRNAs in neurodegeneration
N Bushati, SM Cohen - Current opinion in neurobiology, 2008 - Elsevier
microRNAs (miRNAs) act as post-transcriptional regulators of gene expression in diverse
cellular and developmental processes. Many miRNAs are expressed specifically in the …
cellular and developmental processes. Many miRNAs are expressed specifically in the …
Genetic associations of Nrf2-encoding NFE2L2 variants with Parkinson's disease – a multicenter study
M von Otter, P Bergström, A Quattrone… - BMC medical …, 2014 - Springer
Abstract Background The transcription factor Nrf2, encoded by the NFE2L2 gene, is an
important regulator of the cellular protection against oxidative stress. Parkinson's disease is …
important regulator of the cellular protection against oxidative stress. Parkinson's disease is …
Dopaminergic control of autophagic-lysosomal function implicates Lmx1b in Parkinson's disease
A Laguna, N Schintu, A Nobre, A Alvarsson… - Nature …, 2015 - nature.com
The role of developmental transcription factors in maintenance of neuronal properties and in
disease remains poorly understood. Lmx1a and Lmx1b are key transcription factors required …
disease remains poorly understood. Lmx1a and Lmx1b are key transcription factors required …