Hasil Pencarian - Gavin Hudson

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  1. 1
    Circulating cell-free mitochondrial DNA levels in Parkinson’s disease are influenced by treatment

    Circulating cell-free mitochondrial DNA levels in Parkinson’s disease are influenced by treatment oleh Hannah Lowes, Angela Pyle, Mauro Santibanez-Koref, Gavin Hudson

    Diterbitkan 2020-02-01
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  2. 2
    Background sequence characteristics influence the occurrence and severity of disease-causing mtDNA mutations.

    Background sequence characteristics influence the occurrence and severity of disease-causing mtDNA mutations. oleh Wei Wei, Aurora Gomez-Duran, Gavin Hudson, Patrick F Chinnery

    Diterbitkan 2017-12-01
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  3. 3
    Correction: Background sequence characteristics influence the occurrence and severity of disease-causing mtDNA mutations.

    Correction: Background sequence characteristics influence the occurrence and severity of disease-causing mtDNA mutations. oleh Wei Wei, Aurora Gomez-Duran, Gavin Hudson, Patrick F Chinnery

    Diterbitkan 2018-05-01
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  4. 4
    Nanobiopsy investigation of the subcellular mtDNA heteroplasmy in human tissues

    Nanobiopsy investigation of the subcellular mtDNA heteroplasmy in human tissues oleh Alexander Bury, Angela Pyle, Amy E. Vincent, Paolo Actis, Gavin Hudson

    Diterbitkan 2024-06-01
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  5. 5
    Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases.

    Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases. oleh Gavin Hudson, Aurora Gomez-Duran, Ian J Wilson, Patrick F Chinnery

    Diterbitkan 2014-05-01
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  6. 6
    Mitochondrial isolation: when size matters [version 2; peer review: 2 approved]

    Mitochondrial isolation: when size matters [version 2; peer review: 2 approved] oleh Alexander G. Bury, Amy E. Vincent, Doug M. Turnbull, Paolo Actis, Gavin Hudson

    Diterbitkan 2020-12-01
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  7. 7
    Raised intraocular pressure as a potential risk factor for visual loss in Leber Hereditary Optic Neuropathy.

    Raised intraocular pressure as a potential risk factor for visual loss in Leber Hereditary Optic Neuropathy. oleh Anais Thouin, Philip G Griffiths, Gavin Hudson, Patrick F Chinnery, Patrick Yu-Wai-Man

    Diterbitkan 2013-01-01
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  8. 8
    The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism

    The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism oleh Charley Xia, Sarah J. Pickett, David C. M. Liewald, Alexander Weiss, Gavin Hudson, W. David Hill

    Diterbitkan 2023-05-01
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  9. 9
    Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in Humans.

    Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in Humans. oleh Angela Pyle, Gavin Hudson, Ian J Wilson, Jonathan Coxhead, Tania Smertenko, Mary Herbert, Mauro Santibanez-Koref, Patrick F Chinnery

    Diterbitkan 2015-05-01
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  10. 10
    Cell-specific expression of key mitochondrial enzymes limits OXPHOS in astrocytes of the adult human neocortex and hippocampal formation

    Cell-specific expression of key mitochondrial enzymes limits OXPHOS in astrocytes of the adult human neocortex and hippocampal formation oleh Arpád Dobolyi, Melinda Cservenák, Attila G. Bagó, Chun Chen, Anna Stepanova, Krisztina Paal, Jeonghyoun Lee, Miklós Palkovits, Gavin Hudson, Christos Chinopoulos

    Diterbitkan 2024-08-01
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  11. 11
    Variant load of mitochondrial DNA in single human mesenchymal stem cells

    Variant load of mitochondrial DNA in single human mesenchymal stem cells oleh Daniel Hipps, Angela Pyle, Anna L. R. Porter, Philip F. Dobson, Helen Tuppen, Conor Lawless, Oliver M. Russell, Doug M. Turnbull, David J. Deehan, Gavin Hudson

    Diterbitkan 2024-09-01
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  12. 12
    Early-stage idiopathic Parkinson’s disease is associated with reduced circular RNA expression

    Early-stage idiopathic Parkinson’s disease is associated with reduced circular RNA expression oleh Benjamin J. Whittle, Osagie G. Izuogu, Hannah Lowes, Dasha Deen, Angela Pyle, Jon Coxhead, Rachael A. Lawson, Alison J. Yarnall, Michael S. Jackson, Mauro Santibanez-Koref, Gavin Hudson

    Diterbitkan 2024-01-01
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  13. 13
    Imaging mass cytometry reveals generalised deficiency in OXPHOS complexes in Parkinson’s disease

    Imaging mass cytometry reveals generalised deficiency in OXPHOS complexes in Parkinson’s disease oleh Chun Chen, David McDonald, Alasdair Blain, Ashwin Sachdeva, Laura Bone, Anna L. M. Smith, Charlotte Warren, Sarah J. Pickett, Gavin Hudson, Andrew Filby, Amy E. Vincent, Doug M. Turnbull, Amy K. Reeve

    Diterbitkan 2021-05-01
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  14. 14
    Parkinson’s disease neurons exhibit alterations in mitochondrial quality control proteins

    Parkinson’s disease neurons exhibit alterations in mitochondrial quality control proteins oleh Chun Chen, David McDonald, Alasdair Blain, Emily Mossman, Kiera Atkin, Michael F. Marusich, Roderick Capaldi, Laura Bone, Anna Smith, Andrew Filby, Daniel Erskine, Oliver Russell, Gavin Hudson, Amy E. Vincent, Amy K. Reeve

    Diterbitkan 2023-08-01
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  15. 15
    A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts

    A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts oleh Anna L. Guyatt, Rebecca R. Brennan, Kimberley Burrows, Philip A. I. Guthrie, Raimondo Ascione, Susan M. Ring, Tom R. Gaunt, Angela Pyle, Heather J. Cordell, Debbie A. Lawlor, Patrick F. Chinnery, Gavin Hudson, Santiago Rodriguez

    Diterbitkan 2019-01-01
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  16. 16
    Heteroplasmic mitochondrial DNA variants in cardiovascular diseases.

    Heteroplasmic mitochondrial DNA variants in cardiovascular diseases. oleh Claudia Calabrese, Angela Pyle, Helen Griffin, Jonathan Coxhead, Rafiqul Hussain, Peter S Braund, Linxin Li, Annette Burgess, Patricia B Munroe, Louis Little, Helen R Warren, Claudia Cabrera, Alistair Hall, Mark J Caulfield, Peter M Rothwell, Nilesh J Samani, Gavin Hudson, Patrick F Chinnery

    Diterbitkan 2022-04-01
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  17. 17
    Mutations in mitochondrial DNA causing tubulointerstitial kidney disease.

    Mutations in mitochondrial DNA causing tubulointerstitial kidney disease. oleh Thomas M Connor, Simon Hoer, Andrew Mallett, Daniel P Gale, Aurora Gomez-Duran, Viktor Posse, Robin Antrobus, Pablo Moreno, Marco Sciacovelli, Christian Frezza, Jennifer Duff, Neil S Sheerin, John A Sayer, Margaret Ashcroft, Michael S Wiesener, Gavin Hudson, Claes M Gustafsson, Patrick F Chinnery, Patrick H Maxwell

    Diterbitkan 2017-03-01
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