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H Robinson

Showing results (1221-1230 of 1,631) with videos related to

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Clinical Endocrinology|December 1, 1977
Measurement of whole body calcium in chronic renal failure: effects of 1alpha-hydroxyvitamin D3 and parathyroidectomyR B Naik, J T Dabek, G Heynen, et al.
Vaccine|September 15, 2004
Attenuated Salmonella typhimurium htrA mutants cause fatal infections in mice deficient in NADPH oxidase and destroy NADPH oxidase-deficient macrophage monolayersMbithe Mutunga, Sarah Graham, Raquel Demarco De Hormaeche, et al.
Molecular Genetics and Metabolism|July 15, 2018
Detection of mucopolysaccharidosis III-A (Sanfilippo Syndrome-A) in dried blood spots (DBS) by tandem mass spectrometryFan Yi, Xinying Hong, Arun Babu Kumar, et al.
American Journal of Medical Genetics. Part A|September 7, 2006
Novel mitochondrial DNA mutations associated with myopathy, cardiomyopathy, renal failure, and deafnessAnnette Feigenbaum, Ren-Kui Bai, Emily S Doherty, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 25, 2015
Absence of keratin 8 or 18 promotes antimitochondrial autoantibody formation in aging male miceDiana M Toivola, Aida Habtezion, Julia O Misiorek, et al.
British Medical Journal|July 28, 1973
Serial estimation of urinary fibrin fibrinogen degradation products in kidney transplantationC L Hall, N Pejhan, R W Thomson, et al.
The Journal of Trauma and Acute Care Surgery|October 24, 2023
Predicting high-intensity resuscitation needs in injured patients in the post-hemostasis phase of care following interventionMichael B Weykamp, Catherine E Beni, Katherine E Stern, et al.
Acta Paediatrica Scandinavica|January 1, 1982
Congenital lactic acidosis, alpha-ketoglutaric aciduria and variant form of maple syrup urine disease due to a single enzyme defect: dihydrolipoyl dehydrogenase deficiencyA Munnich, J M Saudubray, J Taylor, et al.
Pharmacology|January 1, 1988
Absorption of nicotine from a cigarette that does not burn tobaccoJ D deBethizy, J H Robinson, R A Davis, et al.
Journal of Medicinal Chemistry|August 7, 1992
Design and synthesis of some substrate analogue inhibitors of phospholipase A2 and investigations by NMR and molecular modeling into the binding interactions in the enzyme-inhibitor complexC Bennion, S Connolly, N P Gensmantel, et al.
Pageof 164

Showing results (1221-1230 of 1,631) with videos related to

Sort By:
Pageof 164
Clinical Endocrinology|December 1, 1977
Measurement of whole body calcium in chronic renal failure: effects of 1alpha-hydroxyvitamin D3 and parathyroidectomyR B Naik, J T Dabek, G Heynen, et al.
Vaccine|September 15, 2004
Attenuated Salmonella typhimurium htrA mutants cause fatal infections in mice deficient in NADPH oxidase and destroy NADPH oxidase-deficient macrophage monolayersMbithe Mutunga, Sarah Graham, Raquel Demarco De Hormaeche, et al.
Molecular Genetics and Metabolism|July 15, 2018
Detection of mucopolysaccharidosis III-A (Sanfilippo Syndrome-A) in dried blood spots (DBS) by tandem mass spectrometryFan Yi, Xinying Hong, Arun Babu Kumar, et al.
American Journal of Medical Genetics. Part A|September 7, 2006
Novel mitochondrial DNA mutations associated with myopathy, cardiomyopathy, renal failure, and deafnessAnnette Feigenbaum, Ren-Kui Bai, Emily S Doherty, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 25, 2015
Absence of keratin 8 or 18 promotes antimitochondrial autoantibody formation in aging male miceDiana M Toivola, Aida Habtezion, Julia O Misiorek, et al.
British Medical Journal|July 28, 1973
Serial estimation of urinary fibrin fibrinogen degradation products in kidney transplantationC L Hall, N Pejhan, R W Thomson, et al.
The Journal of Trauma and Acute Care Surgery|October 24, 2023
Predicting high-intensity resuscitation needs in injured patients in the post-hemostasis phase of care following interventionMichael B Weykamp, Catherine E Beni, Katherine E Stern, et al.
Acta Paediatrica Scandinavica|January 1, 1982
Congenital lactic acidosis, alpha-ketoglutaric aciduria and variant form of maple syrup urine disease due to a single enzyme defect: dihydrolipoyl dehydrogenase deficiencyA Munnich, J M Saudubray, J Taylor, et al.
Pharmacology|January 1, 1988
Absorption of nicotine from a cigarette that does not burn tobaccoJ D deBethizy, J H Robinson, R A Davis, et al.
Journal of Medicinal Chemistry|August 7, 1992
Design and synthesis of some substrate analogue inhibitors of phospholipase A2 and investigations by NMR and molecular modeling into the binding interactions in the enzyme-inhibitor complexC Bennion, S Connolly, N P Gensmantel, et al.
Pageof 164