[HTML][HTML] Biomarkers in neurodegenerative diseases: proteomics spotlight on ALS and Parkinson's disease
R Raghunathan, K Turajane, LC Wong - International Journal of …, 2022 - mdpi.com
Neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS) and Parkinson's
disease (PD) are both characterized by pathogenic protein aggregates that correlate with …
disease (PD) are both characterized by pathogenic protein aggregates that correlate with …
[PDF][PDF] Nucleocytoplasmic mRNA redistribution accompanies RNA binding protein mislocalization in ALS motor neurons and is restored by VCP ATPase inhibition
Amyotrophic lateral sclerosis (ALS) is characterized by nucleocytoplasmic mislocalization of
the RNA-binding protein (RBP) TDP-43. However, emerging evidence suggests more …
the RNA-binding protein (RBP) TDP-43. However, emerging evidence suggests more …
Fall risk, sleep behavior, and sleep-related movement disorders in Young urbanites exposed to air pollution
L Calderón-Garcidueñas, R Kulesza… - Journal of …, 2023 - content.iospress.com
Background: Quadruple aberrant hyperphosphorylated tau, amyloid-ß, α-synuclein, and
TDP-43 pathology had been documented in 202/203 forensic autopsies in Metropolitan …
TDP-43 pathology had been documented in 202/203 forensic autopsies in Metropolitan …
[HTML][HTML] Is Dutasteride a Therapeutic Alternative for Amyotrophic Lateral Sclerosis?
B Proaño, J Casani-Cubel, M Benlloch… - Biomedicines, 2022 - mdpi.com
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that is characterized by
the loss of upper and lower motor neurons (MNs) in the cerebral cortex, brainstem and …
the loss of upper and lower motor neurons (MNs) in the cerebral cortex, brainstem and …
FUS-P525L juvenile amyotrophic lateral sclerosis and intellectual disability: Evidence for association and oligogenic inheritance
O Goldstein, T Inbar, M Kedmi, M Gana-Weisz… - Neurology …, 2022 - AAN Enterprises
Background and Objectives Amyotrophic lateral sclerosis (ALS) is characterized by upper
and lower motor neuron degeneration, with juvenile ALS (jALS) defined as disease with age …
and lower motor neuron degeneration, with juvenile ALS (jALS) defined as disease with age …
[PDF][PDF] Is Dutasteride a Therapeutic Alternative for Amyotrophic Lateral Sclerosis? Biomedicines 2022, 10, 2084
B Proaño, J Casani-Cubel, M Benlloch… - 2022 - researchgate.net
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that is characterized by
the loss of upper and lower motor neurons (MNs) in the cerebral cortex, brainstem and …
the loss of upper and lower motor neurons (MNs) in the cerebral cortex, brainstem and …
[PDF][PDF] ALS associated mutations in ANXA11 cause distal axonopathy, disrupt calcium signalling, and influence RNA dynamics in patient derived motor neurons
E Hedges - 2023 - kclpure.kcl.ac.uk
The neurodegenerative disease amyotrophic lateral sclerosis (ALS) is characteristically
heterogeneous in both genetic causality and cellular pathology. In ALS, the upper and lower …
heterogeneous in both genetic causality and cellular pathology. In ALS, the upper and lower …