Search Results - "GRIFFITHS, Lyn R."
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Advances in genetics of migraine
Published in Journal of headache and pain (21-06-2019)“…Background Migraine is a complex neurovascular disorder with a strong genetic component. There are rare monogenic forms of migraine, as well as more common…”
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Mitochondrial Genome Acquisition Restores Respiratory Function and Tumorigenic Potential of Cancer Cells without Mitochondrial DNA
Published in Cell metabolism (06-01-2015)“…We report that tumor cells without mitochondrial DNA (mtDNA) show delayed tumor growth, and that tumor formation is associated with acquisition of mtDNA from…”
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The impact of APOA5, APOB, APOC3 and ABCA1 gene polymorphisms on ischemic stroke: Evidence from a meta-analysis
Published in Atherosclerosis (01-10-2017)“…Genetic studies have been reported on the association between APOA5, APOB, APOC3 and ABCA1 gene polymorphisms and ischemic stroke, but results remain…”
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Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes
Published in Frontiers in genetics (07-02-2018)“…Epilepsy is a neurological disorder characterized by an increased predisposition for seizures. Although this definition suggests that it is a single disorder,…”
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Human Mesenchymal Stem Cells Retain Multilineage Differentiation Capacity Including Neural Marker Expression after Extended In Vitro Expansion
Published in PloS one (10-09-2015)“…The suitability of human mesenchymal stem cells (hMSCs) in regenerative medicine relies on retention of their proliferative expansion potential in conjunction…”
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Evaluation of a 7-Gene Genetic Profile for Athletic Endurance Phenotype in Ironman Championship Triathletes
Published in PloS one (30-12-2015)“…Polygenic profiling has been proposed for elite endurance performance, using an additive model determining the proportion of optimal alleles in endurance…”
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A causal role for TRESK loss of function in migraine mechanisms
Published in Brain (London, England : 1878) (01-12-2019)“…The two-pore potassium channel, TRESK has been implicated in nociception and pain disorders. We have for the first time investigated TRESK function in human…”
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Can Genetic Markers Predict the Sporadic Form of Alzheimer’s Disease? An Updated Review on Genetic Peripheral Markers
Published in International journal of molecular sciences (01-09-2023)“…Alzheimer’s disease (AD) is the most common form of dementia that affects millions of individuals worldwide. Although the research over the last decades has…”
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Review: Alternative Splicing (AS) of Genes As An Approach for Generating Protein Complexity
Published in Current genomics (01-05-2013)“…Prior to the completion of the human genome project, the human genome was thought to have a greater number of genes as it seemed structurally and functionally…”
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Exploiting Heparan Sulfate Proteoglycans in Human Neurogenesis-Controlling Lineage Specification and Fate
Published in Frontiers in integrative neuroscience (17-10-2017)“…Unspecialized, self-renewing stem cells have extraordinary application to regenerative medicine due to their multilineage differentiation potential. Stem cell…”
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Genome-wide association study reveals three susceptibility loci for common migraine in the general population
Published in Nature genetics (01-07-2011)“…Migraine is a common, heterogeneous and heritable neurological disorder. Its pathophysiology is incompletely understood, and its genetic influences at the…”
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Exonic mutations in cell–cell adhesion may contribute to CADASIL-related CSVD pathology
Published in Human genetics (01-09-2023)“…Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a condition caused by mutations in NOTCH3 and results…”
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The gene SMART study: method, study design, and preliminary findings
Published in BMC genomics (14-11-2017)“…The gene SMART (genes and the Skeletal Muscle Adaptive Response to Training) Study aims to identify genetic variants that predict the response to both a single…”
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The effects of OPRM1 118A>G on methadone response in pain management in advanced cancer at end of life
Published in Scientific reports (10-02-2024)“…Cancer pain is the most feared symptom at end of life. Methadone has advantages over other opioids but is associated with significant variability in clinical…”
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Shared Molecular Genetic Mechanisms Underlie Endometriosis and Migraine Comorbidity
Published in Genes (29-02-2020)“…Observational epidemiological studies indicate that endometriosis and migraine co-occur within individuals more than expected by chance. However, the aetiology…”
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Associations between Cerebrovascular Function and the Expression of Genes Related to Endothelial Function in Hormonal Migraine
Published in International journal of molecular sciences (01-02-2024)“…There is evidence to suggest that hormonal migraine is associated with altered cerebrovascular function. We aimed to investigate whether the expression of…”
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GSTM1 and GSTT1 polymorphisms associated with pain in a chemotherapy-induced peripheral neuropathy cohort
Published in Journal of cancer research and clinical oncology (01-08-2023)“…Purpose Chemotherapy induced peripheral neuropathy (CIPN) is a debilitating condition that is a direct consequence of receiving cancer treatment. The molecular…”
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Association of KCNJ6 rs2070995 and methadone response for pain management in advanced cancer at end-of-life
Published in Scientific reports (19-10-2022)“…Opioids are the therapeutic agents of choice to manage moderate to severe pain in patients with advanced cancer, however the unpredictable inter-individual…”
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An epigenetic clock for human skeletal muscle
Published in Journal of cachexia, sarcopenia and muscle (01-08-2020)“…Background Ageing is associated with DNA methylation changes in all human tissues, and epigenetic markers can estimate chronological age based on DNA…”
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Saliva as a comparable-quality source of DNA for Whole Exome Sequencing on Ion platforms
Published in Genomics (San Diego, Calif.) (01-03-2020)“…Whole Exome Sequencing (WES) utilises overlapping fragments prone to sequencing artefacts. Saliva, a non-invasive source of DNA, has been successfully used in…”
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