Publications by authors named "Alex Morris"

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The class-IIa HDAC inhibitor TMP269 promotes BMP-Smad signalling and is neuroprotective in in vitro and in vivo 6-hydroxydopamine models of Parkinson's disease.
Adam G O'Mahony, Martina Mazzocchi, Alex Morris, Noelia Morales-Prieto, Caitriona Guinane

Neuropharmacology· May 2025

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A retinoic acid:YAP1 signaling axis controls atrial lineage commitment.
Elizabeth Abraham, Aleksandra Kostina, Brett Volmert, Thomas Roule, Ling Huang, Alex Morris

Cell Rep· May 2025

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A Retinoic Acid:YAP1 signaling axis controls atrial lineage commitment.
Elizabeth Abraham, Brett Volmert, Thomas Roule, Ling Huang, Jingting Yu, Alex Morris

bioRxiv· July 2024

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Animal Behaviour Packs a Punch: From Parasitism to Production, Pollution and Prevention in Grazing Livestock.
Lesley A Smith, Naomi J Fox, Glenn Marion, Naomi J Booth, Alex M M Morris

Animals (Basel)· June 2024

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Effect of intravenous magnesium on post-operative pain following Latarjet shoulder reconstruction.
Paul Soeding, Alex Morris, Adam Soeding, Gregory Hoy

Shoulder Elbow· February 2024

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Based on 0.35 T magnetic resonance-guided radiotherapy, what are the nonisotropic PTV margins required for conventional prostate radiotherapy?
Joseph Drabble, Prantik Das, Ben George, Philip Camilleri, Alex Morris

Med Dosim· November 2022

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Variants in the zinc transporter-3 encoding gene (SLC30A3) in schizophrenia and bipolar disorder: Effects on brain glutamate-A pilot study.
Luke A Jelen, Mark S Green, Sinead King, Alex G Morris, Xinyuan Zhang

Front Psychiatry· September 2022

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Further insights into the molecular complexity of the human sinus node - The role of 'novel' transcription factors and microRNAs.
Abimbola J Aminu, Maria Petkova, Andrew J Atkinson, Joseph Yanni, Alex D Morris

Prog Biophys Mol Biol· November 2021

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A nematode that can manipulate the behaviour of slugs.
Alex Morris, Michael Green, Hayley Martin, Katie Crossland, William T Swaney

Behav Processes· June 2018

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VCP mutations are not a major cause of familial amyotrophic lateral sclerosis in the UK.
Chun Tak Kwok, Hsiang-Ya Wang, Alex G Morris, Bradley Smith, Christopher Shaw

J Neurol Sci· February 2015

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Sequestosome-1 (SQSTM1) sequence variants in ALS cases in the UK: prevalence and coexistence of SQSTM1 mutations in ALS kindred with PDB.
Chun T Kwok, Alex Morris, Jacqueline S de Belleroche

Eur J Hum Genet· April 2014

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Association studies indicate that protein disulfide isomerase is a risk factor in amyotrophic lateral sclerosis.
Chun Tak Kwok, Alex G Morris, Jenny Frampton, Bradley Smith, Christopher E Shaw

Free Radic Biol Med· May 2013

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High prevalence of posterior polymorphous corneal dystrophy in the Czech Republic; linkage disequilibrium mapping and dating an ancestral mutation.
Petra Liskova, Rhian Gwilliam, Martin Filipec, Katerina Jirsova, Stanislava Reinstein Merjava, Alex G Morris

PLoS One· April 2013

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The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder.
Bradley N Smith, Stephen Newhouse, Aleksey Shatunov, Caroline Vance, Simon Topp, Karen E Morrison, Alex Morris

Eur J Hum Genet· January 2013

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Characterization of the properties of a novel mutation in VAPB in familial amyotrophic lateral sclerosis.
Han-Jou Chen, Georgia Anagnostou, Andrea Chai, James Withers, Alex Morris

J Biol Chem· December 2010

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Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase.
John Mitchell, Praveen Paul, Han-Jou Chen, Alex Morris, Miles Payling

Proc Natl Acad Sci U S A· April 2010

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Thioredoxin reductase 1 haplotypes modify familial amyotrophic lateral sclerosis onset.
John Mitchell, Alex Morris, Jacqueline de Belleroche

Free Radic Biol Med· January 2009

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Genomic organisation and alternative splicing of human RIM1, a gene implicated in autosomal dominant cone-rod dystrophy (CORD7).
Samantha Johnson, Stephanie Halford, Alex G Morris, Reshma J Patel, Susan E Wilkie

Genomics· March 2003

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Early development and unstable genes in schizophrenia: preliminary results.
Agnes Ayton, Alex G Morris, Philip J Tyson, David Hunt, Ann M Mortimer

Eur Psychiatry· October 2002

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Investigating the association between OPA1 polymorphisms and glaucoma: comparison between normal tension and high tension primary open angle glaucoma.
Tin Aung, Louise Ocaka, Neil D Ebenezer, Alex G Morris, Glen Brice

Hum Genet· May 2002

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A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene.
Tin Aung, Louise Ocaka, Neil D Ebenezer, Alex G Morris, Michael Krawczak

Hum Genet· January 2002

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