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David S Sinasac

Showing results (1-10 of 19) with videos related to

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BMC Genomics|November 25, 2014
A novel genetic locus linked to pro-inflammatory cytokines after virulent H5N1 virus infection in miceAdrianus C M Boon, Robert W Williams, David S Sinasac, et al.
Pediatric Neurology|July 1, 2017
A New Patient With Intermediate Severe Salla Disease With Hypomyelination: A Literature Review for Salla DiseaseRebecca Barmherzig, Garrett Bullivant, Dawn Cordeiro, et al.
JIMD Reports|September 10, 2019
Transiently elevated plasma methionine, <i>S</i>-adenosylmethionine and <i>S</i>-adenosylhomocysteine: Unreported laboratory findings in a patient with NGLY1 deficiency, a congenital disorder of deglycosylationCaitlin A Chang, Xing-Chang Wei, Steven R Martin, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|August 24, 2019
Characterization of the C584R variant in the mtDNA depletion syndrome gene FBXL4, reveals a novel role for FBXL4 as a regulator of mitochondrial fusionRasha Sabouny, Rachel Wong, Laurie Lee-Glover, et al.
Diabetes|December 29, 2006
Mice with a deletion in the gene for CCAAT/enhancer-binding protein beta are protected against diet-induced obesityCarrie A Millward, Jason D Heaney, David S Sinasac, et al.
Journal of Hepatology|February 7, 2006
Pyruvate ameliorates the defect in ureogenesis from ammonia in citrin-deficient miceMitsuaki Moriyama, Meng Xian Li, Keiko Kobayashi, et al.
Journal of Inherited Metabolic Disease|March 4, 2025
Altered Fibroblast Glutamine Metabolism Is Linked to the Severity of Cardiac Dysfunction in DCMA, a Mitochondrial CardiomyopathyMelissa A King, Katherine C Heger, Marija Drikic, et al.
Molecular and Cellular Biology|January 1, 2004
Slc25a13-knockout mice harbor metabolic deficits but fail to display hallmarks of adult-onset type II citrullinemiaDavid S Sinasac, Mitsuaki Moriyama, M Abdul Jalil, et al.
Molecular Genetics and Metabolism|September 13, 2011
Metabolomic analysis reveals hepatic metabolite perturbations in citrin/mitochondrial glycerol-3-phosphate dehydrogenase double-knockout mice, a model of human citrin deficiencyTakeyori Saheki, Kanako Inoue, Hiromi Ono, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 5, 2010
Analyzing complex traits with congenic strainsHaifeng Shao, David S Sinasac, Lindsay C Burrage, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
BMC Genomics|November 25, 2014
A novel genetic locus linked to pro-inflammatory cytokines after virulent H5N1 virus infection in miceAdrianus C M Boon, Robert W Williams, David S Sinasac, et al.
Pediatric Neurology|July 1, 2017
A New Patient With Intermediate Severe Salla Disease With Hypomyelination: A Literature Review for Salla DiseaseRebecca Barmherzig, Garrett Bullivant, Dawn Cordeiro, et al.
JIMD Reports|September 10, 2019
Transiently elevated plasma methionine, <i>S</i>-adenosylmethionine and <i>S</i>-adenosylhomocysteine: Unreported laboratory findings in a patient with NGLY1 deficiency, a congenital disorder of deglycosylationCaitlin A Chang, Xing-Chang Wei, Steven R Martin, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|August 24, 2019
Characterization of the C584R variant in the mtDNA depletion syndrome gene FBXL4, reveals a novel role for FBXL4 as a regulator of mitochondrial fusionRasha Sabouny, Rachel Wong, Laurie Lee-Glover, et al.
Diabetes|December 29, 2006
Mice with a deletion in the gene for CCAAT/enhancer-binding protein beta are protected against diet-induced obesityCarrie A Millward, Jason D Heaney, David S Sinasac, et al.
Journal of Hepatology|February 7, 2006
Pyruvate ameliorates the defect in ureogenesis from ammonia in citrin-deficient miceMitsuaki Moriyama, Meng Xian Li, Keiko Kobayashi, et al.
Journal of Inherited Metabolic Disease|March 4, 2025
Altered Fibroblast Glutamine Metabolism Is Linked to the Severity of Cardiac Dysfunction in DCMA, a Mitochondrial CardiomyopathyMelissa A King, Katherine C Heger, Marija Drikic, et al.
Molecular and Cellular Biology|January 1, 2004
Slc25a13-knockout mice harbor metabolic deficits but fail to display hallmarks of adult-onset type II citrullinemiaDavid S Sinasac, Mitsuaki Moriyama, M Abdul Jalil, et al.
Molecular Genetics and Metabolism|September 13, 2011
Metabolomic analysis reveals hepatic metabolite perturbations in citrin/mitochondrial glycerol-3-phosphate dehydrogenase double-knockout mice, a model of human citrin deficiencyTakeyori Saheki, Kanako Inoue, Hiromi Ono, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 5, 2010
Analyzing complex traits with congenic strainsHaifeng Shao, David S Sinasac, Lindsay C Burrage, et al.
Pageof 2