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Publications by E.E. Coffey

Lysosomal Alkalization and Dysfunction in Human Fibroblasts With the Alzheimer’s Disease-Linked Presenilin 1 A246E Mutation Can Be Reversed With cAMP

English

Related publications

Mental Disorders in Young Adults From Families With the Presenilin-1 Gene Mutation E280A in the Preclinical Stage of Alzheimer’s Disease

Journal of Alzheimer's Disease Reports

English

Variant Alzheimer Disease With Spastic Paraparesis: A Rare Presenilin-1 Mutation

Canadian Journal of Neurological Sciences

English

Neuronal Localization of Presenilin-1 and Association With Amyloid Plaques and Neurofibrillary Tangles in Alzheimer’s Disease

Journal of Neuroscience

English

Wide Range of Disease Onset in a Family With Alzheimer Disease and a His163Tyr Mutation in the Presenilin-1 Gene

Archives of Neurology

English

Homozygosity of the Autosomal Dominant Alzheimer Disease Presenilin 1 E280A Mutation

English

Novel Presenilin 1 Mutation (S170F) Causing Alzheimer Disease With Lewy Bodies in the Third Decade of Life

Archives of Neurology

English

Presenilin-1 280Glu→Ala Mutation Alters C-Terminal APP Processing Yielding Longer Aβ Peptides: Implications for Alzheimer’s Disease

Molecular Medicine

Molecular Medicine

Molecular Biology

English

Regulation of Brain G-Protein Goby Alzheimer’s Disease Gene Presenilin-1

Journal of Biological Chemistry

Molecular Biology

English

Can Arginase Inhibitors Be the Answer to Therapeutic Challenges in Alzheimer’s Disease?

Neurotherapeutics

English