Long-term depression links amyloid-β to the pathological hyperphosphorylation of tau.
Journal article
Taylor HBC. et al, (2021), Cell Rep, 36
Homeostatic Presynaptic Plasticity Is Specifically Regulated by P/Q-type Ca2+ Channels at Mammalian Hippocampal Synapses.
Journal article
Jeans AF. et al, (2017), Cell Rep, 21, 341 - 350
Is Parkinson's disease truly a prion-like disorder? An appraisal of current evidence.
Journal article
Chauhan A. and Jeans AF., (2015), Neurol Res Int, 2015
Imaging synaptic vesicles using VGLUT1-venus knock-in mice: insights into the dynamic nature of intersynaptic vesicle exchange.
Journal article
Padamsey Z. and Jeans A., (2012), J Neurosci, 32, 3284 - 3286
Increased expression of dysbindin-1A leads to a selective deficit in NMDA receptor signaling in the hippocampus.
Journal article
Jeans A. et al, (2011), Neuropharmacology, 61, 1345 - 1353
Cerebellopontine angle arachnoid cyst containing ectopic choroid plexus--case report.
Journal article
Singleton WGB. et al, (2010), Acta Neurochir (Wien), 152, 881 - 883
Cerebral primitive neuroectodermal tumor in an adult with a heterozygous MSH2 mutation.
Journal article
Jeans AF. et al, (2009), Nat Rev Clin Oncol, 6, 295 - 299
Primary angiitis of the CNS mimicking a spinal cord tumour.
Journal article
Baumer D. et al, (2008), J Neurol, 255, 1970 - 1972
Muscle hemorrhage in a paraplegic adult with neurofibromatosis type 1 and an associated vasculopathy.
Journal article
Matthews PC. et al, (2008), Am J Med Genet A, 146A, 2424 - 2426
A case of bilateral recurrent haemorrhages in the lower limbs due to neurofibromatosis type 1
Conference paper
Jeans AF. et al, (2007), NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 33, 269 - 269
A dominant mutation in Snap25 causes impaired vesicle trafficking, sensorimotor gating, and ataxia in the blind-drunk mouse.
Journal article
Jeans AF. et al, (2007), Proc Natl Acad Sci U S A, 104, 2431 - 2436
Functional studies of Af4 in the robotic mouse.
Conference paper
Davies KE. et al, (2003), AMERICAN JOURNAL OF HUMAN GENETICS, 73, 179 - 179
A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse.
Journal article
Isaacs AM. et al, (2003), J Neurosci, 23, 1631 - 1637
Identification of a new Pmp22 mouse mutant and trafficking analysis of a Pmp22 allelic series suggesting that protein aggregates may be protective in Pmp22-associated peripheral neuropathy.
Journal article
Isaacs AM. et al, (2002), Mol Cell Neurosci, 21, 114 - 125