P. Oliver

发表

Mouse genomic variation and its effect on phenotypes and gene regulation

Thomas M. Keane, R. Durbin, E. Birney, 2011, Nature.

A functional genetic link between distinct developmental language disorders.

D. Geschwind, B. Abrahams, A. Monaco, 2008, The New England journal of medicine.

Limitations to adaptive homeostasis in an hyperoxia-induced model of accelerated ageing

K. Davies, P. Oliver, K. Davies, 2019, Redox biology.

Evolution and Functions of Long Noncoding RNAs

C. Ponting, P. Oliver, W. Reik, 2009, Cell.

Evaluating the links between schizophrenia and sleep and circadian rhythm disruption

Paul J. Harrison, K. Davies, D. Bannerman, 2012, Journal of Neural Transmission.

Genomic and Transcriptional Co-Localization of Protein-Coding and Long Non-Coding RNA Pairs in the Developing Brain

C. Ponting, P. Oliver, G. Lunter, 2009, PLoS genetics.

Long noncoding RNA genes: conservation of sequence and brain expression among diverse amniotes

C. Ponting, E. Green, K. Davies, 2010, Genome Biology.

Crosstalking noncoding RNAs contribute to cell-specific neurodegeneration in SCA7

Keith W. Vance, C. Ponting, N. Brockdorff, 2014, Nature Structural &Molecular Biology.

Erratum: Cross-talking noncoding RNAs contribute to cell-specific neurodegeneration in SCA7 (Nature Structural and Molecular Biology (2014) 21 (955-961))

Keith W. Vance, C. Ponting, N. Brockdorff, 2015 .

Foxp2 Regulates Gene Networks Implicated in Neurite Outgrowth in the Developing Brain

Kay E. Davies, Jean-Baptiste Cazier, Jiannis Ragoussis, 2011, PLoS genetics.

Accelerated Evolution of the Prdm9 Speciation Gene across Diverse Metazoan Taxa

C. Ponting, L. Goodstadt, S. Beatson, 2009, PLoS genetics.

Single-copy expression of an amyotrophic lateral sclerosis-linked TDP-43 mutation (M337V) in BAC transgenic mice leads to altered stress granule dynamics and progressive motor dysfunction

P. Oliver, D. Biggs, B. Davies, 2019, Neurobiology of Disease.

Early microgliosis precedes neuronal loss and behavioural impairment in mice with a frontotemporal dementia-causing CHMP2B mutation

Holly E. Holmes, M. Lythgoe, J. Collinge, 2017, Human molecular genetics.

Absent sleep EEG spindle activity in GluA1 (Gria1) knockout mice: relevance to neuropsychiatric disorders

Paul J. Harrison, R. Sprengel, K. Davies, 2018, Translational Psychiatry.

Neuron-specific antioxidant OXR1 extends survival of a mouse model of amyotrophic lateral sclerosis

K. Davies, P. Oliver, B. Davies, 2015, Brain : a journal of neurology.

Increased 4R tau expression and behavioural changes in a novel MAPT-N296H genomic mouse model of tauopathy

D. Bannerman, P. Oliver, R. Wade-Martins, 2017, Scientific Reports.

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

Steve D. M. Brown, K. Davies, P. Oliver, 2002, Molecular and Cellular Neuroscience.

Chronic Activation of γ 2 AMPK Induces Obesity and Reduces Beta Cell Function

Robin J. W. Willows, Jonathan, Parvathy E. Harikumar, 2016 .

Genetic Analysis of Gv1, a Gene Controlling Transcription of Endogenous Murine Polytropic Proviruses

P. Oliver, J. Stoye, 1999, Journal of Virology.

Crosstalking noncoding RNAs contribute to cell-specific neurodegeneration in SCA7

Keith W. Vance, C. Ponting, N. Brockdorff, 2014, Nature Structural &Molecular Biology.

Explorer Mouse genomic variation and its effect on phenotypes and gene regulation

Thomas M. Keane, Wei-yuan, R. Durbin, 2017 .

Early microgliosis precedes neuronal loss and behavioural impairment in mice with a frontotemporal dementia-causing CHMP2B mutation.

Holly E. Holmes, M. Lythgoe, J. Collinge, 2017, Human molecular genetics.

Behavioural characterization of neuregulin 1 type I overexpressing transgenic mice

Paul J. Harrison, D. Bannerman, P. Oliver, 2009, Neuroreport.

Robotic Mouse

P. Oliver, E. Bitoun, Kay E. Davies, 2021, Handbook of the Cerebellum and Cerebellar Disorders.

Mediation of Af4 protein function in the cerebellum by Siah proteins.

K. Davies, P. Oliver, E. Bitoun, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Identification and Characterization of Murine SCARA5, a Novel Class A Scavenger Receptor That Is Expressed by Populations of Epithelial Cells*

K. Davies, P. Oliver, Yanyan Jiang, 2006, Journal of Biological Chemistry.

Expression profiling in spinal muscular atrophy reveals an RNA binding protein deficit

K. Davies, P. Oliver, D. Baban, 2004, Neuromuscular Disorders.

Chronic Activation of g 2 AMPK Induces Obesity and Reduces b Cell Function

Robin J. W. Willows, Parvathy E. Harikumar, Nathan R. Qi, 2016 .

Neuronal over-expression of Oxr1 is protective against ALS-associated mutant TDP-43 mislocalisation in motor neurons and neuromuscular defects in vivo

K. Davies, P. Oliver, K. Talbot, 2019, Human molecular genetics.

TLDc proteins: new players in the oxidative stress response and neurological disease

P. Oliver, Mattéa J. Finelli, M. Finelli, 2017, Mammalian Genome.

Behavioural Characterisation of Macrod1 and Macrod2 Knockout Mice

P. Oliver, I. Ahel, Kerryanne Crawford, 2021, Cells.

Targeted deletion of the Ncoa7 gene results in incomplete distal renal tubular acidosis in mice.

P. Oliver, Dennis Brown, Diane E. Capen, 2018, American journal of physiology. Renal physiology.

AF4 Is a Critical Regulator of the IGF-1 Signaling Pathway during Purkinje Cell Development

K. Davies, P. Oliver, E. Bitoun, 2009, The Journal of Neuroscience.

The cardiovascular and platelet actions of 9β‐methyl carbacyclin (ciprostene), a chemically stable analogue of prostacyclin, in the dog and monkey

P. Oliver, B. Whittle, G. Allan, 1985, British journal of pharmacology.

ROS Generation in Microglia: Understanding Oxidative Stress and Inflammation in Neurodegenerative Disease

P. Oliver, Dominic S A Simpson, 2020, Antioxidants.

Temporal transcriptomics suggest that twin-peaking genes reset the clock

Chris P Ponting, C. Ponting, K. Davies, 2015, eLife.

Gv1, a Zinc Finger Gene Controlling Endogenous MLV Expression

P. Oliver, J. Stoye, G. Young, 2021, Molecular biology and evolution.

Disruption of Visc-2, a Brain-Expressed Conserved Long Noncoding RNA, Does Not Elicit an Overt Anatomical or Behavioral Phenotype

C. Ponting, E. Green, Z. Molnár, 2014, Cerebral cortex.

A Transcriptomic Atlas of Mouse Neocortical Layers

Chris P. Ponting, Elliott H. Margulies, T. Grant Belgard, 2011, Neuron.

The mixed-lineage leukemia fusion partner AF4 stimulates RNA polymerase II transcriptional elongation and mediates coordinated chromatin remodeling.

K. Davies, P. Oliver, E. Bitoun, 2007, Human molecular genetics.

The long non-coding RNA Paupar regulates the expression of both local and distal genes

Keith W. Vance, C. Ponting, P. Oliver, 2014, The EMBO journal.

Oxidation Resistance 1 Modulates Glycolytic Pathways in the Cerebellum via an Interaction with Glucose-6-Phosphate Isomerase

P. Biggin, P. Oliver, R. Wade-Martins, 2018, Molecular Neurobiology.

Identification and characterisation of a Maf1/Macoco protein complex that interacts with GABAA receptors in neurons

P. Oliver, N. Brandon, S. Moss, 2010, Molecular and Cellular Neuroscience.

Sexual selection and the adaptive evolution of mammalian ejaculate proteins.

Chris P Ponting, Richard D Emes, Paula Stockley, 2007, Molecular biology and evolution.

Mutations in α-Tubulin Cause Abnormal Neuronal Migration in Mice and Lissencephaly in Humans

Steve D. M. Brown, D. Keays, J. Flint, 2007, Cell.

Oxr1 improves pathogenic cellular features of ALS-associated FUS and TDP-43 mutations

K. Davies, P. Oliver, Mattéa J. Finelli, 2015, Human molecular genetics.

Investigating TDP43 biological dysfunction through the characterisation of Tardbp ENU mouse mutants: implications for neurodegeneration

P. Oliver, A. Acevedo-Arozena, H. Oliveira, 2014 .

Interaction between environmental and genetic factors modulates schizophrenic endophenotypes in the Snap-25 mouse mutant blind-drunk

K. Davies, P. Oliver, 2009, Human Molecular Genetics.

Analysis of the mouse mutant Cloth-ears shows a role for the voltage-gated sodium channel Scn8a in peripheral neural hearing loss

P. Oliver, F. Mackenzie, N. Parkinson, 2009, Genes, brain, and behavior.

TBC1D24 genotype–phenotype correlation

J. Rosenfeld, I. Scheffer, J. Gécz, 2016, Neurology.

The epilepsy-associated protein TBC1D24 is required for normal development, survival and vesicle trafficking in mammalian neurons

Andrew R. Bassett, F. Benfenati, P. Oliver, 2018, Human molecular genetics.

The Evolutionarily Conserved Tre2/Bub2/Cdc16 (TBC), Lysin Motif (LysM), Domain Catalytic (TLDc) Domain Is Neuroprotective against Oxidative Stress*

K. Davies, P. Oliver, L. Sánchez-Pulido, 2015, The Journal of Biological Chemistry.

The antioxidant protein Oxr1 influences aspects of mitochondrial morphology

K. Davies, P. Oliver, Yixing Wu, 2016, Free radical biology & medicine.

Oxr1 Is Essential for Protection against Oxidative Stress-Induced Neurodegeneration

K. Davies, P. Oliver, Esther B. E. Becker, 2011, PLoS genetics.

The mutant Moonwalker TRPC3 channel links calcium signaling to lipid metabolism in the developing cerebellum

K. Davies, P. Oliver, Esther B. E. Becker, 2015, Human molecular genetics.

The Ncoa7 locus regulates V-ATPase formation and function, neurodevelopment and behaviour

Andrew R. Bassett, P. Oliver, B. Davies, 2020, Cellular and Molecular Life Sciences.

Oxidation resistance 1 regulates post-translational modifications of peroxiredoxin 2 in the cerebellum

P. Oliver, M. Crabtree, W. Yue, 2018, Free radical biology & medicine.

Comparative genetic analysis: the utility of mouse genetic systems for studying human monogenic disease

K. Davies, P. Oliver, E. Bitoun, 2007, Mammalian Genome.

Genomic and Post-Genomic Tools for Studying Synapse Biology

Josef T. Kittler, Peter L. Oliver, J. Kittler, 2006 .

Human-Mouse Quantitative Trait Locus Concordance and the Dissection of a Human Neuroticism Locus

Janice M. Fullerton, R. Copley, R. Mott, 2008, Biological Psychiatry.

SNARE proteins and schizophrenia: linking synaptic and neurodevelopmental hypotheses.

K. Davies, P. Oliver, Reuben D. Johnson, 2008, Acta biochimica Polonica.

Transcription linked to recombination: a gene-internal promoter coincides with the recombination hot spot II of the human MLL gene

P. Oliver, T. Dingermann, R. Marschalek, 2007, Oncogene.

The Regulatory Factor ZFHX3 Modifies Circadian Function in SCN via an AT Motif-Driven Axis

A. Mallon, S. Wells, R. Satija, 2015, Cell.

Deletion of AMPA receptor GluA1 subunit gene (Gria1) causes circadian rhythm disruption and aberrant responses to environmental cues

R. Sprengel, K. Davies, V. Vyazovskiy, 2021, Translational Psychiatry.

A dominant mutation in Snap25 causes impaired vesicle trafficking, sensorimotor gating, and ataxia in the blind-drunk mouse

Marco Capogna, Lena Eliasson, Zoltán Molnár, 2007, Proceedings of the National Academy of Sciences.

Challenges of Analysing Gene-Environment Interactions in Mouse Models of Schizophrenia

P. Oliver, 2011, TheScientificWorldJournal.

Analysis of human neurological disorders using mutagenesis in the mouse.

K. Davies, P. Oliver, 2005, Clinical science.

Region-specific deficits in dopamine, but not norepinephrine, signaling in a novel A30P α-synuclein BAC transgenic mouse

S. Cragg, K. Davies, D. Bannerman, 2014, Neurobiology of Disease.

A Novel Mouse Model of a Patient Mucolipidosis II Mutation Recapitulates Disease Pathology

K. Davies, P. Oliver, J. Kenyon, 2014, The Journal of Biological Chemistry.

New insights into behaviour using mouse ENU mutagenesis

K. Davies, P. Oliver, 2012, Human molecular genetics.

Wild-Type, but Not Mutant N296H, Human Tau Restores Aβ-Mediated Inhibition of LTP in Tau−/− mice

O. Paulsen, M. Vargas-Caballero, P. Oliver, 2017, Front. Neurosci..

TLDc proteins: new players in the oxidative stress response and neurological disease

P. Oliver, Mattéa J. Finelli, 2017, Mammalian Genome.

The Interconnected Mechanisms of Oxidative Stress and Neuroinflammation in Epilepsy

P. Oliver, Tânia R P Soares, D. Rial, 2022, Antioxidants.

A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice

E. Fisher, K. Davies, P. Oliver, 2009, Proceedings of the National Academy of Sciences.

Cytoarchitectural disruption of the superior colliculus and an enlarged acoustic startle response in the Tuba1a mutant mouse

Martin W. Breuss, D. Keays, J. Flint, 2011, Neuroscience.

Chronic Activation of γ2 AMPK Induces Obesity and Reduces β Cell Function

Robin J. W. Willows, Parvathy E. Harikumar, Nathan R. Qi, 2016, Cell Metabolism.

Chronic Activation of γ2 AMPK Induces Obesity and Reduces β Cell Function

Robin J. W. Willows, Parvathy E. Harikumar, Nathan R. Qi, 2016, Cell Metabolism.

Loss of Frrs1l disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalities

S. Wells, D. Kullmann, P. Oliver, 2018, Disease Models & Mechanisms.

Chondrolectin affects cell survival and neuronal outgrowth in in vitro and in vivo models of spinal muscular atrophy.

K. Davies, P. Oliver, K. Talbot, 2014, Human molecular genetics.

Stereotypic wheel running decreases cortical activity in mice

Laura E. McKillop, Vladyslav V. Vyazovskiy, Jessica Gemignani, 2016, Nature Communications.

A Mutation in Af4 Is Predicted to Cause Cerebellar Ataxia and Cataracts in the Robotic Mouse

Steve D. M. Brown, K. Davies, P. Oliver, 2003, The Journal of Neuroscience.

Impairment of Macroautophagy in Dopamine Neurons Has Opposing Effects on Parkinsonian Pathology and Behavior

S. Cragg, D. Bannerman, P. Oliver, 2019, Cell reports.

HspB8 mutation causing hereditary distal motor neuropathy impairs lysosomal delivery of autophagosomes

P. Oliver, K. Talbot, V. R. Agashe, 2011, Journal of neurochemistry.

Disrupted Circadian Rhythms in a Mouse Model of Schizophrenia

K. Davies, P. Oliver, E. Maywood, 2012, Current Biology.

Report s in a Mouse Model of Schizophrenia

K. Davies, P. Oliver, E. Maywood, 2012 .

Laf4/Aff3, a Gene Involved in Intellectual Disability, Is Required for Cellular Migration in the Mouse Cerebral Cortex

K. Davies, Z. Molnár, P. Oliver, 2014, PloS one.

Behavioural characterisation of the robotic mouse mutant

D. Keays, K. Davies, P. Oliver, 2007, Behavioural Brain Research.

SNAP25 mutation disrupts metabolic homeostasis, steroid hormone production and central neurobehavior.

P. Oliver, F. Kraemer, W. Shen, 2021, Biochimica et biophysica acta. Molecular basis of disease.

Zfhx3-mediated genetic ablation of the SCN abolishes light entrainable circadian activity while sparing food anticipatory activity

P. Oliver, E. Maywood, M. Hastings, 2021, iScience.

Circadian profiling in two mouse models of lysosomal storage disorders; Niemann Pick type-C and Sandhoff disease

L. Brown, P. Oliver, S. Peirson, 2016, Behavioural Brain Research SreeTestContent1.

Mutations in α-Tubulin Cause Abnormal Neuronal Migration in Mice and Lissencephaly in Humans

Steve D. M. Brown, D. Keays, J. Flint, 2007, Cell.

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.

Steve D. M. Brown, K. Davies, P. Oliver, 2003, Molecular and cellular neurosciences.

Chronic Activation of γ2 AMPK Induces Obesity and Reduces β Cell Function

Robin J. W. Willows, Parvathy E. Harikumar, Nathan R. Qi, 2016, Cell metabolism.