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Andrew J Duncan

Showing results (21-30 of 43) with videos related to

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Frontiers in Veterinary Science|May 1, 2023
Corrigendum: Evaluations of the disease surveillance centre network in Scotland: what parts has it reached?Andrew J Duncan, Jude I Eze, Franz Brülisauer, et al.
Clinical Chemistry|November 25, 2005
Determination of coenzyme Q10 status in blood mononuclear cells, skeletal muscle, and plasma by HPLC with di-propoxy-coenzyme Q10 as an internal standardAndrew J Duncan, Simon J R Heales, Kevin Mills, et al.
Nature|April 23, 2011
Optically healable supramolecular polymersMark Burnworth, Liming Tang, Justin R Kumpfer, et al.
Molecular and Cellular Endocrinology|January 14, 2012
Analysis of LIN28A in early human ovary development and as a candidate gene for primary ovarian insufficiencyRanna El-Khairi, Rahul Parnaik, Andrew J Duncan, et al.
BMJ Open|January 7, 2012
Hearing in 44-45 year olds with m.1555A>G, a genetic mutation predisposing to aminoglycoside-induced deafness: a population based cohort studyShamima Rahman, Russell Ecob, Harry Costello, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|May 6, 2006
Effect of risk-adjusted, non-dialysis-dependent renal dysfunction on mortality and morbidity following coronary artery bypass surgery: a multi-centre studyMohan P Devbhandari, Andrew J Duncan, Antony D Grayson, et al.
Epilepsia|December 5, 2008
Status epilepticus in children with Alpers' disease caused by POLG1 mutations: EEG and MRI featuresNicole I Wolf, Shamima Rahman, Bernhard Schmitt, et al.
Wellcome Open Research|May 2, 2017
A genomic atlas of human adrenal and gonad developmentIgnacio Del Valle, Federica Buonocore, Andrew J Duncan, et al.
Molecular Genetics and Metabolism|June 27, 2006
Phenotypic variability of mitochondrial disease caused by a nuclear mutation in complex IIAlistair T Pagnamenta, Iain P Hargreaves, Andrew J Duncan, et al.
American Journal of Human Genetics|March 27, 2012
Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weightMiho Ishida, David Monk, Andrew J Duncan, et al.
Pageof 5

Showing results (21-30 of 43) with videos related to

Sort By:
Pageof 5
Frontiers in Veterinary Science|May 1, 2023
Corrigendum: Evaluations of the disease surveillance centre network in Scotland: what parts has it reached?Andrew J Duncan, Jude I Eze, Franz Brülisauer, et al.
Clinical Chemistry|November 25, 2005
Determination of coenzyme Q10 status in blood mononuclear cells, skeletal muscle, and plasma by HPLC with di-propoxy-coenzyme Q10 as an internal standardAndrew J Duncan, Simon J R Heales, Kevin Mills, et al.
Nature|April 23, 2011
Optically healable supramolecular polymersMark Burnworth, Liming Tang, Justin R Kumpfer, et al.
Molecular and Cellular Endocrinology|January 14, 2012
Analysis of LIN28A in early human ovary development and as a candidate gene for primary ovarian insufficiencyRanna El-Khairi, Rahul Parnaik, Andrew J Duncan, et al.
BMJ Open|January 7, 2012
Hearing in 44-45 year olds with m.1555A>G, a genetic mutation predisposing to aminoglycoside-induced deafness: a population based cohort studyShamima Rahman, Russell Ecob, Harry Costello, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|May 6, 2006
Effect of risk-adjusted, non-dialysis-dependent renal dysfunction on mortality and morbidity following coronary artery bypass surgery: a multi-centre studyMohan P Devbhandari, Andrew J Duncan, Antony D Grayson, et al.
Epilepsia|December 5, 2008
Status epilepticus in children with Alpers' disease caused by POLG1 mutations: EEG and MRI featuresNicole I Wolf, Shamima Rahman, Bernhard Schmitt, et al.
Wellcome Open Research|May 2, 2017
A genomic atlas of human adrenal and gonad developmentIgnacio Del Valle, Federica Buonocore, Andrew J Duncan, et al.
Molecular Genetics and Metabolism|June 27, 2006
Phenotypic variability of mitochondrial disease caused by a nuclear mutation in complex IIAlistair T Pagnamenta, Iain P Hargreaves, Andrew J Duncan, et al.
American Journal of Human Genetics|March 27, 2012
Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weightMiho Ishida, David Monk, Andrew J Duncan, et al.
Pageof 5