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G A Mitchell

Showing results (31-40 of 110) with videos related to

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The Journal of Biological Chemistry|October 4, 1996
Modeling of a mutation responsible for human 3-hydroxy-3-methylglutaryl-CoA lyase deficiency implicates histidine 233 as an active site residueJ R Roberts, G A Mitchell, H M Miziorko
The American Review of Respiratory Disease|October 1, 1970
Studies of chronic nontuberculous lung disease in New Guinea Populations. The prevalence of Hemophilus influenzae precipitinsC R Blackburn, W F Green, G A Mitchell
Thrombosis Research|February 1, 1979
A sensitive fluorescent assay for determining alpha2-plasmin inhibitor using a synthetic substrateD E Lawson, G A Mitchell, R M Huseby
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|May 24, 2001
Tyrosinemia: a reviewP A Russo, G A Mitchell, R M Tanguay
Canadian Journal of Comparative Medicine : Revue Canadienne De Medecine Comparee|January 1, 1971
Antibody production in milk serum after virus instillation of goat mammary gland. IV. Experiments with protective properties of specific influenza antibody associated with lactogammaglobulinG A Mitchell, L F Guerin, A E Pasieka
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1994
[Hyperornithinemia and gyrate atrophy: ornithine aminotransferase gene error causing a Finnish disease]I Sipilä, D Valle, G A Mitchell, et al.
Medical Laboratory Sciences|March 1, 1981
Sister chromatid exchange assays: pre-scanning of chemicals for subtoxic levelsG A Mitchell, K M Meher-Homji, R S Baker
Environmental Mutagenesis|January 1, 1982
Sister chromatid exchange induction in two cell linesG A Mitchell, K M Meher-Homji, R S Baker
Methods in Enzymology|September 16, 2000
Molecular and enzymatic methods for detection of genetic defects in distal pathways of branched-chain amino acid metabolismK M Gibson, M Ugarte, T Fukao, et al.
The British Veterinary Journal|March 19, 2010
A study of isolation in fowl paralysis (lymphomatosis)S T HARRISS, J W JOHNSTON, S G A MITCHELL
Pageof 11

Showing results (31-40 of 110) with videos related to

Sort By:
Pageof 11
The Journal of Biological Chemistry|October 4, 1996
Modeling of a mutation responsible for human 3-hydroxy-3-methylglutaryl-CoA lyase deficiency implicates histidine 233 as an active site residueJ R Roberts, G A Mitchell, H M Miziorko
The American Review of Respiratory Disease|October 1, 1970
Studies of chronic nontuberculous lung disease in New Guinea Populations. The prevalence of Hemophilus influenzae precipitinsC R Blackburn, W F Green, G A Mitchell
Thrombosis Research|February 1, 1979
A sensitive fluorescent assay for determining alpha2-plasmin inhibitor using a synthetic substrateD E Lawson, G A Mitchell, R M Huseby
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|May 24, 2001
Tyrosinemia: a reviewP A Russo, G A Mitchell, R M Tanguay
Canadian Journal of Comparative Medicine : Revue Canadienne De Medecine Comparee|January 1, 1971
Antibody production in milk serum after virus instillation of goat mammary gland. IV. Experiments with protective properties of specific influenza antibody associated with lactogammaglobulinG A Mitchell, L F Guerin, A E Pasieka
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1994
[Hyperornithinemia and gyrate atrophy: ornithine aminotransferase gene error causing a Finnish disease]I Sipilä, D Valle, G A Mitchell, et al.
Medical Laboratory Sciences|March 1, 1981
Sister chromatid exchange assays: pre-scanning of chemicals for subtoxic levelsG A Mitchell, K M Meher-Homji, R S Baker
Environmental Mutagenesis|January 1, 1982
Sister chromatid exchange induction in two cell linesG A Mitchell, K M Meher-Homji, R S Baker
Methods in Enzymology|September 16, 2000
Molecular and enzymatic methods for detection of genetic defects in distal pathways of branched-chain amino acid metabolismK M Gibson, M Ugarte, T Fukao, et al.
The British Veterinary Journal|March 19, 2010
A study of isolation in fowl paralysis (lymphomatosis)S T HARRISS, J W JOHNSTON, S G A MITCHELL
Pageof 11