Jacqueline S. De Belleroche
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 17 publications
d-Amino acids: new clinical pathways for brain diseases.
Journal: Trends in molecular medicine
Published: July 20, 2023
Variants in the zinc transporter-3 encoding gene (SLC30A3) in schizophrenia and bipolar disorder: Effects on brain glutamate-A pilot study.
Journal: Frontiers in psychiatry
Published: April 26, 2022
Tissue-selective regulation of protein homeostasis and unfolded protein response signalling in sporadic ALS.
Journal: Journal of cellular and molecular medicine
Published: January 22, 2020
ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function.
Journal: Neurobiology of aging
Published: April 18, 2018
Focus on the Role of D-serine and D-amino Acid Oxidase in Amyotrophic Lateral Sclerosis/Motor Neuron Disease (ALS).
Journal: Frontiers in molecular biosciences
Published: November 29, 2017
Characterisation of the pathogenic effects of the in vivo expression of an ALS-linked mutation in D-amino acid oxidase: Phenotype and loss of spinal cord motor neurons.
Journal: PloS one
Published: September 20, 2017
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis.
Journal: Nature genetics
Published: February 25, 2016
Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis.
Journal: Science translational medicine
Published: November 26, 2015
CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia.
Journal: Nature communications
Published: August 10, 2015
The CHCHD10 P34S variant is not associated with ALS in a UK cohort of familial and sporadic patients.
Journal: Neurobiology of aging
Published: June 30, 2015
Last Updated: 09/26/2026