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P Venditti

Showing results (131-140 of 178) with videos related to

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Behavior Genetics|March 1, 1994
DNA markers associated with high versus low IQ: the IQ Quantitative Trait Loci (QTL) ProjectR Plomin, G E McClearn, D L Smith, et al.
JIMD Reports|February 20, 2020
High-dose hydroxocobalamin achieves biochemical correction and improvement of neuropsychiatric deficits in adults with late onset cobalamin C deficiencyTomoyasu Higashimoto, Alexander Y Kim, Jessica T Ogawa, et al.
Human Molecular Genetics|November 1, 2016
Systemic AAV9 gene therapy improves the lifespan of mice with Niemann-Pick disease, type C1Randy J Chandler, Ian M Williams, Alana L Gibson, et al.
Science Translational Medicine|May 25, 2022
Aberrant methylmalonylation underlies methylmalonic acidemia and is attenuated by an engineered sirtuinPamelaSara E Head, Sangho Myung, Yong Chen, et al.
Molecular Biosystems|December 18, 2015
The proteome of methylmalonic acidemia (MMA): the elucidation of altered pathways in patient liversMarianna Caterino, Randy J Chandler, Jennifer L Sloan, et al.
Journal of Inherited Metabolic Disease|June 26, 2014
A detailed analysis of methylmalonic acid kinetics during hemodialysis and after combined liver/kidney transplantation in a patient with mut (0) methylmalonic acidemiaHilary J Vernon, C John Sperati, Joshua D King, et al.
Molecular Therapy. Methods & Clinical Development|September 25, 2023
Systemic gene therapy using an AAV44.9 vector rescues a neonatal lethal mouse model of propionic acidemiaRandy J Chandler, Giovanni Di Pasquale, Eun-Young Choi, et al.
Journal of Medical Genetics|January 1, 1997
46,XX, inv(6)(p21.1p23) in a pedigree with hereditary haemochromatosisC P Venditti, N K Seese, G S Gerhard, et al.
American Journal of Medical Genetics|July 1, 1993
Clinical and molecular analyses of deletion 3p25-pter syndromeP N Mowrey, M J Chorney, C P Venditti, et al.
Molecular Psychiatry|January 10, 2024
Intellectual disability and autism in propionic acidemia: a biomarker-behavioral investigation implicating dysregulated mitochondrial biologyOleg A Shchelochkov, Cristan A Farmer, Colby Chlebowski, et al.
Pageof 18

Showing results (131-140 of 178) with videos related to

Sort By:
Pageof 18
Behavior Genetics|March 1, 1994
DNA markers associated with high versus low IQ: the IQ Quantitative Trait Loci (QTL) ProjectR Plomin, G E McClearn, D L Smith, et al.
JIMD Reports|February 20, 2020
High-dose hydroxocobalamin achieves biochemical correction and improvement of neuropsychiatric deficits in adults with late onset cobalamin C deficiencyTomoyasu Higashimoto, Alexander Y Kim, Jessica T Ogawa, et al.
Human Molecular Genetics|November 1, 2016
Systemic AAV9 gene therapy improves the lifespan of mice with Niemann-Pick disease, type C1Randy J Chandler, Ian M Williams, Alana L Gibson, et al.
Science Translational Medicine|May 25, 2022
Aberrant methylmalonylation underlies methylmalonic acidemia and is attenuated by an engineered sirtuinPamelaSara E Head, Sangho Myung, Yong Chen, et al.
Molecular Biosystems|December 18, 2015
The proteome of methylmalonic acidemia (MMA): the elucidation of altered pathways in patient liversMarianna Caterino, Randy J Chandler, Jennifer L Sloan, et al.
Journal of Inherited Metabolic Disease|June 26, 2014
A detailed analysis of methylmalonic acid kinetics during hemodialysis and after combined liver/kidney transplantation in a patient with mut (0) methylmalonic acidemiaHilary J Vernon, C John Sperati, Joshua D King, et al.
Molecular Therapy. Methods & Clinical Development|September 25, 2023
Systemic gene therapy using an AAV44.9 vector rescues a neonatal lethal mouse model of propionic acidemiaRandy J Chandler, Giovanni Di Pasquale, Eun-Young Choi, et al.
Journal of Medical Genetics|January 1, 1997
46,XX, inv(6)(p21.1p23) in a pedigree with hereditary haemochromatosisC P Venditti, N K Seese, G S Gerhard, et al.
American Journal of Medical Genetics|July 1, 1993
Clinical and molecular analyses of deletion 3p25-pter syndromeP N Mowrey, M J Chorney, C P Venditti, et al.
Molecular Psychiatry|January 10, 2024
Intellectual disability and autism in propionic acidemia: a biomarker-behavioral investigation implicating dysregulated mitochondrial biologyOleg A Shchelochkov, Cristan A Farmer, Colby Chlebowski, et al.
Pageof 18