Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Wyszukujesz frazę ""Elson, Joanna"" wg kryterium: Autor


Wyświetlanie 1-9 z 9
Tytuł:
A broad comparative genomics approach to understanding the pathogenicity of Complex I mutations.
Autorzy:
Klink GV; Sector of Molecular Evolution, Institute for Information Transmission Problems (Kharkevich Institute) of the Russian Academy of Sciences, Moscow, Russian Federation.
O'Keefe H; Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.
Gogna A; Biosciences Institute, Newcastle University, Newcastle upon Tyne, UK.
Bazykin GA; Sector of Molecular Evolution, Institute for Information Transmission Problems (Kharkevich Institute) of the Russian Academy of Sciences, Moscow, Russian Federation. .; Center of Life Sciences, Skolkovo Institute of Science and Technology, Skolkovo, Russian Federation. .
Elson JL; Biosciences Institute, Newcastle University, Newcastle upon Tyne, UK. J.l.Elson@ncl.ac.uk.; Human Metabolomics, North-West University, Potchefstroom, South Africa. J.l.Elson@ncl.ac.uk.
Pokaż więcej
Źródło:
Scientific reports [Sci Rep] 2021 Oct 01; Vol. 11 (1), pp. 19578. Date of Electronic Publication: 2021 Oct 01.
Typ publikacji:
Journal Article; Meta-Analysis
MeSH Terms:
Genetic Predisposition to Disease*
Genomics*/methods
Mutation*
Electron Transport Complex I/*genetics
Mitochondria/*genetics
Alleles ; Amino Acid Substitution ; Electron Transport Complex I/metabolism ; Genome-Wide Association Study ; Humans ; Mitochondria/metabolism ; Phylogeny ; Selection, Genetic
Czasopismo naukowe
Tytuł:
MtDNA population variation in Myalgic encephalomyelitis/Chronic fatigue syndrome in two populations: a study of mildly deleterious variants.
Autorzy:
Venter M; Human Metabolomics, North-West University, Potchefstroom, South Africa.
Tomas C; Institute of Cellular Medicine & NIHR Biomedical Research Centre in Ageing and Chronic Disease, Newcastle University, Newcastle-upon-Tyne, United Kingdom.
Pienaar IS; School of Life Sciences, University of Sussex, Falmer, BN1 9PH, United Kingdom.; Centre for Neuroinflammation and Neurodegeneration, Imperial College London, London, United Kingdom.
Strassheim V; Institute of Cellular Medicine & NIHR Biomedical Research Centre in Ageing and Chronic Disease, Newcastle University, Newcastle-upon-Tyne, United Kingdom.; Centre for Neuroinflammation and Neurodegeneration, Imperial College London, London, United Kingdom.
Erasmus E; Human Metabolomics, North-West University, Potchefstroom, South Africa.
Ng WF; Institute of Cellular Medicine & NIHR Biomedical Research Centre in Ageing and Chronic Disease, Newcastle University, Newcastle-upon-Tyne, United Kingdom.; Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle, United Kingdom.
Howell N; Department of Radiation Therapy, UTMB, Galveston, Texas, USA.
Newton JL; Centre for Neuroinflammation and Neurodegeneration, Imperial College London, London, United Kingdom.; Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle, United Kingdom.
Van der Westhuizen FH; Human Metabolomics, North-West University, Potchefstroom, South Africa.
Elson JL; Human Metabolomics, North-West University, Potchefstroom, South Africa. j.l.elson@ncl.ac.uk.; Institute of Genetic Medicine, Newcastle University, Newcastle-upon-Tyne, United Kingdom. j.l.elson@ncl.ac.uk.
Pokaż więcej
Źródło:
Scientific reports [Sci Rep] 2019 Feb 27; Vol. 9 (1), pp. 2914. Date of Electronic Publication: 2019 Feb 27.
Typ publikacji:
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genotype*
Population Groups*
DNA, Mitochondrial/*genetics
Fatigue Syndrome, Chronic/*genetics
Mutation/*genetics
Cimicifuga ; Disease Progression ; Fatigue Syndrome, Chronic/epidemiology ; Gene Frequency ; Gene Regulatory Networks ; Haplotypes ; Humans ; Phenotype ; Polymorphism, Genetic ; South Africa/epidemiology ; United Kingdom/epidemiology
Czasopismo naukowe
Tytuł:
Haplogroup Context is Less Important in the Penetrance of Mitochondrial DNA Complex I Mutations Compared to mt-tRNA Mutations.
Autorzy:
O'Keefe H; Institute of Genetic Medicine, Newcastle University, Newcastle-upon-Tyne, NE1 3BZ, UK.; School of Computing, Newcastle University, Newcastle-upon-Tyne, NE4 5TG, UK.
Queen RA; Institute of Genetic Medicine, Newcastle University, Newcastle-upon-Tyne, NE1 3BZ, UK.
Meldau S; Inherited Metabolic Disease Laboratory, National Health Laboratory Services, Cape Town, South Africa.; Division of Chemical Pathology, University of Cape Town, Cape Town, South Africa.
Lord P; School of Computing, Newcastle University, Newcastle-upon-Tyne, NE4 5TG, UK.
Elson JL; Institute of Genetic Medicine, Newcastle University, Newcastle-upon-Tyne, NE1 3BZ, UK. joanna.elson@newcastle.ac.uk.; Centre for Human Metabonomics, North-West University, Potchefstroom, South Africa. joanna.elson@newcastle.ac.uk.
Pokaż więcej
Źródło:
Journal of molecular evolution [J Mol Evol] 2018 Jul; Vol. 86 (6), pp. 395-403. Date of Electronic Publication: 2018 Jul 09.
Typ publikacji:
Journal Article
MeSH Terms:
Penetrance*
DNA, Mitochondrial/*genetics
Haplotypes/*genetics
Mutation/*genetics
RNA, Transfer/*genetics
Base Sequence ; Consensus Sequence/genetics ; Electron Transport Complex I/genetics ; Genetic Variation ; Humans ; Species Specificity
Czasopismo naukowe
Tytuł:
Clinically proven mtDNA mutations are not common in those with chronic fatigue syndrome.
Autorzy:
Schoeman EM; Centre for Human Metabolomics, North-West University, Potchefstroom, South Africa.
Van Der Westhuizen FH; Centre for Human Metabolomics, North-West University, Potchefstroom, South Africa.
Erasmus E; Centre for Human Metabolomics, North-West University, Potchefstroom, South Africa.
van Dyk E; Centre for Human Metabolomics, North-West University, Potchefstroom, South Africa.
Knowles CV; Wellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience, The Medical School, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK.
Al-Ali S; Institute of Cellular Medicine, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.; Department of Biology, College of Science, University of Basrah, Basrah, Iraq.
Ng WF; Institute of Cellular Medicine, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.; Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Taylor RW; Wellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience, The Medical School, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK.
Newton JL; Institute of Cellular Medicine, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.; Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Elson JL; Centre for Human Metabolomics, North-West University, Potchefstroom, South Africa. Joanna.elson@ncl.ac.uk.; Institute of Genetic Medicine, Newcastle University, Central Parkway, Newcastle upon Tyne, UK. Joanna.elson@ncl.ac.uk.
Pokaż więcej
Źródło:
BMC medical genetics [BMC Med Genet] 2017 Mar 16; Vol. 18 (1), pp. 29. Date of Electronic Publication: 2017 Mar 16.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Mutation*
DNA, Mitochondrial/*genetics
Fatigue Syndrome, Chronic/*genetics
Female ; Genetic Predisposition to Disease ; Humans ; Male ; Sequence Analysis, DNA/methods
Czasopismo naukowe
Tytuł:
Strong purifying selection in transmission of mammalian mitochondrial DNA.
Autorzy:
Stewart JB; Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden. />Freyer C
Elson JL
Wredenberg A
Cansu Z
Trifunovic A
Larsson NG
Pokaż więcej
Źródło:
PLoS biology [PLoS Biol] 2008 Jan; Vol. 6 (1), pp. e10.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Inheritance Patterns*
Mutation*
Selection, Genetic*
DNA, Mitochondrial/*genetics
Animals ; Base Sequence ; DNA-Directed DNA Polymerase ; Female ; Genetic Variation ; Humans ; Mammals ; Mice ; Molecular Sequence Data
Czasopismo naukowe
Tytuł:
Accumulation of mitochondrial DNA mutations in ageing, cancer, and mitochondrial disease: is there a common mechanism?
Autorzy:
Chinnery PF; Departments of Neurology, University of Newcastle upon Tyne, NE2 4HH, Newcastle upon Tyne, UK. />Samuels DC
Elson J
Turnbull DM
Pokaż więcej
Źródło:
Lancet (London, England) [Lancet] 2002 Oct 26; Vol. 360 (9342), pp. 1323-5.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Mutation*
Aging/*genetics
DNA, Mitochondrial/*genetics
Mitochondrial Diseases/*genetics
Neoplasms/*genetics
DNA, Mitochondrial/analysis ; Disease Progression ; Homeostasis/physiology ; Humans ; Models, Theoretical
Czasopismo naukowe
Tytuł:
Mitochondrial DNA sequence context in the penetrance of mitochondrial t-RNA mutations: A study across multiple lineages with diagnostic implications.
Autorzy:
Queen, Rachel A.
Steyn, Jannetta S.
Lord, Phillip
Elson, Joanna L.
Pokaż więcej
Temat:
MITOCHONDRIAL DNA
GENETIC disorders
HETEROGENEITY
GENETIC mutation
MICROBIAL virulence
Źródło:
PLoS ONE; 11/21/2017, Vol. 12 Issue 11, p1-22, 22p
Czasopismo naukowe
    Wyświetlanie 1-9 z 9

    Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies