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B Spector

Showing results (61-70 of 82) with videos related to

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Molecular and Cellular Biochemistry|January 1, 1983
Regulation of expression of genes for enzymes of the mammalian urea cycle in permanent cell-culture lines of hepatic and non-hepatic originD F Haggerty, E B Spector, M Lynch, et al.
Prenatal Diagnosis|November 1, 1990
Dystrophin protein and RFLP analysis for fetal diagnosis and carrier confirmation of Duchenne muscular dystrophyW D Boelter, B A Burt, E B Spector, et al.
The Journal of Biological Chemistry|March 10, 1982
Regulation of glucocorticoids of arginase and argininosuccinate synthetase in cultured rat hepatoma cellsD F Haggerty, E B Spector, M Lynch, et al.
Pediatric Neurology|December 15, 2017
Comment on Late-Onset Nonketotic Hyperglycinemia With a Heterozygous Novel Point Mutation of the GLDC GeneCurtis R Coughlin, Michael A Swanson, Elaine B Spector, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 10, 2018
Venous thromboembolism laboratory testing (factor V Leiden and factor II c.*97G>A), 2018 update: a technical standard of the American College of Medical Genetics and Genomics (ACMG)Shulin Zhang, Annette K Taylor, Xuan Huang, et al.
Pediatric Research|July 1, 1979
Hyperargininemia with arginase deficiencyS D Cederbaum, K N Shaw, E B Spector, et al.
American Journal of Medical Genetics. Part A|February 10, 2017
Mild achondroplasia/hypochondroplasia with acanthosis nigricans, normal development, and a p.Ser348Cys FGFR3 mutationNatario L Couser, Chetna K Pande, Christie M Turcott, et al.
Journal of Child Neurology|December 22, 2009
Diagnosis, treatment, and long-term outcomes of late-onset (type III) multiple acyl-CoA dehydrogenase deficiencyLaura M Pollard, Nolan R Williams, Lesby Espinoza, et al.
JIMD Reports|June 5, 2013
Metabolic profiling of total homocysteine and related compounds in hyperhomocysteinemia: utility and limitations in diagnosing the cause of puzzling thrombophilia in a familySally P Stabler, Mark Korson, Reena Jethva, et al.
The Journal of Clinical Investigation|February 1, 1989
Differential expression of the two human arginase genes in hyperargininemia. Enzymatic, pathologic, and molecular analysisW W Grody, C Argyle, R M Kern, et al.
Pageof 9

Showing results (61-70 of 82) with videos related to

Sort By:
Pageof 9
Molecular and Cellular Biochemistry|January 1, 1983
Regulation of expression of genes for enzymes of the mammalian urea cycle in permanent cell-culture lines of hepatic and non-hepatic originD F Haggerty, E B Spector, M Lynch, et al.
Prenatal Diagnosis|November 1, 1990
Dystrophin protein and RFLP analysis for fetal diagnosis and carrier confirmation of Duchenne muscular dystrophyW D Boelter, B A Burt, E B Spector, et al.
The Journal of Biological Chemistry|March 10, 1982
Regulation of glucocorticoids of arginase and argininosuccinate synthetase in cultured rat hepatoma cellsD F Haggerty, E B Spector, M Lynch, et al.
Pediatric Neurology|December 15, 2017
Comment on Late-Onset Nonketotic Hyperglycinemia With a Heterozygous Novel Point Mutation of the GLDC GeneCurtis R Coughlin, Michael A Swanson, Elaine B Spector, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 10, 2018
Venous thromboembolism laboratory testing (factor V Leiden and factor II c.*97G>A), 2018 update: a technical standard of the American College of Medical Genetics and Genomics (ACMG)Shulin Zhang, Annette K Taylor, Xuan Huang, et al.
Pediatric Research|July 1, 1979
Hyperargininemia with arginase deficiencyS D Cederbaum, K N Shaw, E B Spector, et al.
American Journal of Medical Genetics. Part A|February 10, 2017
Mild achondroplasia/hypochondroplasia with acanthosis nigricans, normal development, and a p.Ser348Cys FGFR3 mutationNatario L Couser, Chetna K Pande, Christie M Turcott, et al.
Journal of Child Neurology|December 22, 2009
Diagnosis, treatment, and long-term outcomes of late-onset (type III) multiple acyl-CoA dehydrogenase deficiencyLaura M Pollard, Nolan R Williams, Lesby Espinoza, et al.
JIMD Reports|June 5, 2013
Metabolic profiling of total homocysteine and related compounds in hyperhomocysteinemia: utility and limitations in diagnosing the cause of puzzling thrombophilia in a familySally P Stabler, Mark Korson, Reena Jethva, et al.
The Journal of Clinical Investigation|February 1, 1989
Differential expression of the two human arginase genes in hyperargininemia. Enzymatic, pathologic, and molecular analysisW W Grody, C Argyle, R M Kern, et al.
Pageof 9