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L Alston

Showing results (61-70 of 174) with videos related to

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AIDS (London, England)|March 4, 2006
Pharmacokinetic interaction between nelfinavir and pravastatin in HIV-seronegative volunteers: ACTG Study A5108Judith A Aberg, Susan L Rosenkranz, Carl J Fichtenbaum, et al.
Human Mutation|September 2, 2011
A comparative analysis approach to determining the pathogenicity of mitochondrial tRNA mutationsJohn W Yarham, Mazhor Al-Dosary, Emma L Blakely, et al.
Forensic Science International|June 11, 2018
Bayesian modeling predicts age and sex are not required for accurate stature estimation from femoral lengthMikaela S Reynolds, Donna M MacGregor, Clair L Alston-Knox, et al.
Developmental Medicine and Child Neurology|February 28, 2012
The clinical spectrum of the m.10191T>C mutation in complex I-deficient Leigh syndromeVictoria Nesbitt, Patrick J Morrison, Ellen Crushell, et al.
JAMA Neurology|October 16, 2013
Near-identical segregation of mtDNA heteroplasmy in blood, muscle, urinary epithelium, and hair follicles in twins with optic atrophy, ptosis, and intractable epilepsyAchilles Spyropoulos, Mark Manford, Rita Horvath, et al.
Journal of Forensic Sciences|November 26, 2016
Apophyseal Ossification of the Iliac Crest in Forensic Age Estimation: Computed Tomography Standards for Modern Australian SubadultsNicolene Lottering, Clair L Alston-Knox, Donna M MacGregor, et al.
European Journal of Human Genetics : EJHG|June 30, 2011
Maternally inherited mitochondrial DNA disease in consanguineous familiesCharlotte L Alston, Langping He, Andrew A Morris, et al.
BBA Clinical|June 23, 2016
Three families with 'de novo' m.3243A > G mutationPaul de Laat, Mirian C H Janssen, Charlotte L Alston, et al.
Bioorganic & Medicinal Chemistry|March 28, 2007
A kit method for the high level synthesis of [211At]MABGGanesan Vaidyanathan, Donna J Affleck, Kevin L Alston, et al.
Neuromuscular Disorders : NMD|May 18, 2010
The pathogenic m.3243A>T mitochondrial DNA mutation is associated with a variable neurological phenotypeCharlotte L Alston, Andreas Bender, Iain P Hargreaves, et al.
Pageof 18

Showing results (61-70 of 174) with videos related to

Sort By:
Pageof 18
AIDS (London, England)|March 4, 2006
Pharmacokinetic interaction between nelfinavir and pravastatin in HIV-seronegative volunteers: ACTG Study A5108Judith A Aberg, Susan L Rosenkranz, Carl J Fichtenbaum, et al.
Human Mutation|September 2, 2011
A comparative analysis approach to determining the pathogenicity of mitochondrial tRNA mutationsJohn W Yarham, Mazhor Al-Dosary, Emma L Blakely, et al.
Forensic Science International|June 11, 2018
Bayesian modeling predicts age and sex are not required for accurate stature estimation from femoral lengthMikaela S Reynolds, Donna M MacGregor, Clair L Alston-Knox, et al.
Developmental Medicine and Child Neurology|February 28, 2012
The clinical spectrum of the m.10191T>C mutation in complex I-deficient Leigh syndromeVictoria Nesbitt, Patrick J Morrison, Ellen Crushell, et al.
JAMA Neurology|October 16, 2013
Near-identical segregation of mtDNA heteroplasmy in blood, muscle, urinary epithelium, and hair follicles in twins with optic atrophy, ptosis, and intractable epilepsyAchilles Spyropoulos, Mark Manford, Rita Horvath, et al.
Journal of Forensic Sciences|November 26, 2016
Apophyseal Ossification of the Iliac Crest in Forensic Age Estimation: Computed Tomography Standards for Modern Australian SubadultsNicolene Lottering, Clair L Alston-Knox, Donna M MacGregor, et al.
European Journal of Human Genetics : EJHG|June 30, 2011
Maternally inherited mitochondrial DNA disease in consanguineous familiesCharlotte L Alston, Langping He, Andrew A Morris, et al.
BBA Clinical|June 23, 2016
Three families with 'de novo' m.3243A > G mutationPaul de Laat, Mirian C H Janssen, Charlotte L Alston, et al.
Bioorganic & Medicinal Chemistry|March 28, 2007
A kit method for the high level synthesis of [211At]MABGGanesan Vaidyanathan, Donna J Affleck, Kevin L Alston, et al.
Neuromuscular Disorders : NMD|May 18, 2010
The pathogenic m.3243A>T mitochondrial DNA mutation is associated with a variable neurological phenotypeCharlotte L Alston, Andreas Bender, Iain P Hargreaves, et al.
Pageof 18