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List of works by Christopher J Carroll

A urinary biosignature for mitochondrial myopathy, encephalopathy, lactic acidosis and stroke like episodes (MELAS).

scientific article published on 19 February 2018

Absence of Hikeshi, a nuclear transporter for heat-shock protein HSP70, causes infantile hypomyelinating leukoencephalopathy

scientific article published on 21 December 2016

Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy

scientific article published on 17 August 2016

BAG-1 proteins protect cardiac myocytes from simulated ischemia/reperfusion-induced apoptosis via an alternate mechanism of cell survival independent of the proteasome.

scientific article published on 20 February 2004

Cardioprotection mediated by urocortin is dependent on PKCepsilon activation.

scientific article published on 10 March 2005

Defective mitochondrial ATPase due to rare mtDNA m.8969G>A mutation-causing lactic acidosis, intellectual disability, and poor growth

scientific article

Defective mitochondrial RNA processing due to PNPT1 variants causes Leigh syndrome.

scientific article published on 22 June 2017

Effects of polyclonal IgG derived from patients with different clinical types of the antiphospholipid syndrome on monocyte signaling pathways.

scientific article

Exploring open access coverage of Wikipedia-cited research across the White Rose Universities

article

GAA repeat instability in Friedreich ataxia YAC transgenic mice.

scientific article

Genetic Basis of Severe Childhood-Onset Cardiomyopathies

scientific article published on 01 November 2018

Genetic background of ataxia in children younger than 5 years in Finland

scientific article published on 05 June 2020

Ketogenic diet slows down mitochondrial myopathy progression in mice

scientific article published on 17 February 2010

Metabolomes of mitochondrial diseases and inclusion body myositis patients: treatment targets and biomarkers

scientific article published on 01 December 2018

Mitochondrial DNA Replication Defects Disturb Cellular dNTP Pools and Remodel One-Carbon Metabolism

scientific article

Mitochondrial myopathy induces a starvation-like response

scientific article published on 23 July 2010

Mitochondrial phenylalanyl-tRNA synthetase mutations underlie fatal infantile Alpers encephalopathy

scientific article published on 23 July 2012

Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia ⬇️

scientific article

Next-generation sequencing for mitochondrial disorders

scientific article published on April 2014

Regulation of myocardial interleukin-6 expression by p53 and STAT1.

scientific article published on 15 May 2013

Reply to 'Letter to Editor by Finsterer J and Zarrouk-Mahjoub S: Phenotypic manifestations of the m.8969G>A variant'

scientific article published on 26 February 2018

Rescue of the Friedreich's ataxia knockout mouse by human YAC transgenesis

scientific article published on 01 October 2001

STAT1 regulates p73-mediated Bax gene expression

scientific article published on 01 March 2007

Supernumerary proteins of the human mitochondrial ribosomal small subunit are integral for assembly and translation

scientific article published in 2024

Transgenic overexpression of HSP56 does not result in cardiac hypertrophy nor protect from ischaemia/reperfusion injury

scientific article published on 29 October 2010

Urocortin inhibits Beclin1-mediated autophagic cell death in cardiac myocytes exposed to ischaemia/reperfusion injury

scientific journal article

Urocortin prevents mitochondrial permeability transition in response to reperfusion injury indirectly by reducing oxidative stress

scientific article

Urocortin protects cardiac myocytes from ischemia/reperfusion injury by attenuating calcium-insensitive phospholipase A2 gene expression

scientific journal article

Whole-exome sequencing identifies a mutation in the mitochondrial ribosome protein MRPL44 to underlie mitochondrial infantile cardiomyopathy

scientific article

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