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1دورية أكاديمية
المؤلفون: Ghareyazi, Amin, Mohseni, Amir, Dashti, Hamed, Beheshti, Amin, Dehzangi, Abdollah, Rabiee, Hamid R., Alinejad-Rokny, Hamid
المصدر: Ghareyazi , A , Mohseni , A , Dashti , H , Beheshti , A , Dehzangi , A , Rabiee , H R & Alinejad-Rokny , H 2021 , ' Whole-genome analysis of de novo somatic point mutations reveals novel mutational biomarkers in pancreatic cancer ' , Cancers , vol. 13 , no. 17 , 4376 , pp. 1-22 . https://doi.org/10.3390/cancers13174376Test
مصطلحات موضوعية: Cancer subtype identification, Genotype and phenotype characterization, Pancreatic cancer, Personalized medicine, Somatic point mutations, Therapeutic targets
وصف الملف: application/pdf
الإتاحة: https://doi.org/10.3390/cancers13174376Test
https://researchers.mq.edu.au/en/publications/cdc5e6ab-e84f-47a9-9a07-4ad978132198Test
https://research-management.mq.edu.au/ws/files/175230150/175176805.pdfTest
http://www.scopus.com/inward/record.url?scp=85113892145&partnerID=8YFLogxKTest
http://purl.org/au-research/grants/arc/DE220101210Test -
2دورية أكاديمية
المؤلفون: Pitceathly, Robert D. S., McFarland, Robert
المصدر: Pitceathly , R D S & McFarland , R 2014 , ' Mitochondrial myopathies in adults and children : management and therapy development ' , Current Opinion in Neurology , vol. 27 , no. 5 , pp. 576-582 . https://doi.org/10.1097/WCO.0000000000000126Test
مصطلحات موضوعية: biomarkers, genotype or phenotype, mitochondrial disease, neurodegeneration, treatment, GROWTH-FACTOR 21, POINT MUTATIONS, MERRF MUTATION, DNA DELETIONS, DISEASE, PREVALENCE, POPULATION, A3243G, EPIDEMIOLOGY, DYSFUNCTION
الإتاحة: https://doi.org/10.1097/WCO.0000000000000126Test
https://kclpure.kcl.ac.uk/portal/en/publications/8f2b4c15-cec0-4937-b19f-5b4f007491f3Test -
3دورية أكاديمية
المؤلفون: Pitceathly, Robert D. S., McFarland, Robert
المصدر: Pitceathly , R D S & McFarland , R 2014 , ' Mitochondrial myopathies in adults and children : management and therapy development ' , Current Opinion in Neurology , vol. 27 , no. 5 , pp. 576-582 . https://doi.org/10.1097/WCO.0000000000000126Test
مصطلحات موضوعية: biomarkers, genotype or phenotype, mitochondrial disease, neurodegeneration, treatment, GROWTH-FACTOR 21, POINT MUTATIONS, MERRF MUTATION, DNA DELETIONS, DISEASE, PREVALENCE, POPULATION, A3243G, EPIDEMIOLOGY, DYSFUNCTION
الإتاحة: https://doi.org/10.1097/WCO.0000000000000126Test
https://kclpure.kcl.ac.uk/portal/en/publications/mitochondrial-myopathies-in-adults-and-childrenTest(8f2b4c15-cec0-4937-b19f-5b4f007491f3).html