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Brett H Graham

Showing results (11-20 of 92) with videos related to

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Biophysical Journal|December 26, 2003
The physiological properties of a novel family of VDAC-like proteins from Drosophila melanogasterAlexander G Komarov, Brett H Graham, William J Craigen, et al.
American Journal of Medical Genetics. Part A|March 31, 2007
Fine-Lubinsky syndrome: sibling pair suggests possible autosomal recessive inheritanceAshley M Holder, Brett H Graham, Brendan Lee, et al.
Molecular Genetics and Metabolism|April 3, 2010
Current molecular diagnostic algorithm for mitochondrial disordersLee-Jun C Wong, Fernando Scaglia, Brett H Graham, et al.
Pediatrics in Review|September 30, 2023
Pancytopenia, Hepatomegaly, and Neurologic Abnormalities in Two Pediatric PatientsOlufunke Y Martin, Deborah K Hamby, Brett H Graham, et al.
Cytotherapy|September 25, 2023
Survey of genetic counselors identifies a knowledge gap discerning properly regulated cell and gene therapy trialsLily A Geiselman, Leah Wetherill, Brett H Graham, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|September 14, 2019
Rapid quantification of underivatized alloisoleucine and argininosuccinate using mixed-mode chromatography with tandem mass spectrometryChandler Griffin, Zineb Ammous, Gail H Vance, et al.
Developmental Disabilities Research Reviews|September 7, 2010
Bacteria, yeast, worms, and flies: exploiting simple model organisms to investigate human mitochondrial diseasesShane L Rea, Brett H Graham, Eiko Nakamaru-Ogiso, et al.
Molecular Genetics and Metabolism|August 4, 2016
Expanding the phenotypic spectrum of Succinyl-CoA ligase deficiency through functional validation of a new SUCLG1 variantTaraka R Donti, Ruchi Masand, Daryl A Scott, et al.
Cytogenetic and Genome Research|February 9, 2022
Girl-Boy Twins with Developmental Delay from 16p11.2 Triplication due to Biparental Inheritance from Two Parents with 16p11.2 DuplicationSidrah A Badar, Amy M Breman, Celanie K Christensen, et al.
Disease Models & Mechanisms|November 26, 2013
Screen for abnormal mitochondrial phenotypes in mouse embryonic stem cells identifies a model for succinyl-CoA ligase deficiency and mtDNA depletionTaraka R Donti, Carmen Stromberger, Ming Ge, et al.
Pageof 10

Showing results (11-20 of 92) with videos related to

Sort By:
Pageof 10
Biophysical Journal|December 26, 2003
The physiological properties of a novel family of VDAC-like proteins from Drosophila melanogasterAlexander G Komarov, Brett H Graham, William J Craigen, et al.
American Journal of Medical Genetics. Part A|March 31, 2007
Fine-Lubinsky syndrome: sibling pair suggests possible autosomal recessive inheritanceAshley M Holder, Brett H Graham, Brendan Lee, et al.
Molecular Genetics and Metabolism|April 3, 2010
Current molecular diagnostic algorithm for mitochondrial disordersLee-Jun C Wong, Fernando Scaglia, Brett H Graham, et al.
Pediatrics in Review|September 30, 2023
Pancytopenia, Hepatomegaly, and Neurologic Abnormalities in Two Pediatric PatientsOlufunke Y Martin, Deborah K Hamby, Brett H Graham, et al.
Cytotherapy|September 25, 2023
Survey of genetic counselors identifies a knowledge gap discerning properly regulated cell and gene therapy trialsLily A Geiselman, Leah Wetherill, Brett H Graham, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|September 14, 2019
Rapid quantification of underivatized alloisoleucine and argininosuccinate using mixed-mode chromatography with tandem mass spectrometryChandler Griffin, Zineb Ammous, Gail H Vance, et al.
Developmental Disabilities Research Reviews|September 7, 2010
Bacteria, yeast, worms, and flies: exploiting simple model organisms to investigate human mitochondrial diseasesShane L Rea, Brett H Graham, Eiko Nakamaru-Ogiso, et al.
Molecular Genetics and Metabolism|August 4, 2016
Expanding the phenotypic spectrum of Succinyl-CoA ligase deficiency through functional validation of a new SUCLG1 variantTaraka R Donti, Ruchi Masand, Daryl A Scott, et al.
Cytogenetic and Genome Research|February 9, 2022
Girl-Boy Twins with Developmental Delay from 16p11.2 Triplication due to Biparental Inheritance from Two Parents with 16p11.2 DuplicationSidrah A Badar, Amy M Breman, Celanie K Christensen, et al.
Disease Models & Mechanisms|November 26, 2013
Screen for abnormal mitochondrial phenotypes in mouse embryonic stem cells identifies a model for succinyl-CoA ligase deficiency and mtDNA depletionTaraka R Donti, Carmen Stromberger, Ming Ge, et al.
Pageof 10