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C Gallagher

Showing results (521-530 of 572) with videos related to

Pageof 58
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Human Mutation|June 5, 2010
Positive newborn screen for methylmalonic aciduria identifies the first mutation in TCblR/CD320, the gene for cellular uptake of transcobalamin-bound vitamin B(12)Edward V Quadros, Shao-Chiang Lai, Yasumi Nakayama, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|April 9, 2005
High dose chemotherapy and autologous stem cell transplantation as adjuvant therapy for primary breast cancer patients with four or more lymph nodes involved: long-term results of an international randomised trialR C Coombes, A Howell, M Emson, et al.
Nanoscale|September 20, 2019
Temperature-induced molecular reorganization on Au(111) driven by oligomeric defectsF De Marchi, G Galeotti, M Simenas, et al.
Cancer|May 18, 1999
Treatment of nondysgerminomatous ovarian germ cell tumors: an analysis of 69 casesP L Mitchell, N Al-Nasiri, R A'Hern, et al.
Infection Control and Hospital Epidemiology|February 2, 2022
Poor outcomes in both infection and colonization with carbapenem-resistant EnterobacteralesJessica R Howard-Anderson, Michelle Earley, Lauren Komarow, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 15, 2021
Differential diagnosis of vitamin D-related hypercalcemia using serum vitamin D metabolite profilingMartin Kaufmann, Karl-Peter Schlingmann, Linor Berezin, et al.
Connecticut Medicine|October 27, 2001
A comparison of ON-PUMP vs OFF-PUMP coronary artery bypass surgery among low, intermediate, and high-risk patients: the Hartford Hospital experienceR G McKay, R A Mennett, R C Gallagher, et al.
Molecular Genetics and Metabolism|June 9, 2009
Mutation detection in DNA isolated from cerebrospinal fluid and urine: Clinical utility and pitfalls of multiple displacement amplificationEfraim H Rosenberg, Eduard A Struys, Keith Hyland, et al.
Molecular Pharmacology|August 26, 2006
Functional genetic diversity in the high-affinity carnitine transporter OCTN2 (SLC22A5)Thomas J Urban, Renata C Gallagher, Chaline Brown, et al.
Molecular Genetics and Metabolism|June 1, 2015
Triple therapy with pyridoxine, arginine supplementation and dietary lysine restriction in pyridoxine-dependent epilepsy: Neurodevelopmental outcomeCurtis R Coughlin, Clara D M van Karnebeek, Walla Al-Hertani, et al.
Pageof 58

Showing results (521-530 of 572) with videos related to

Sort By:
Pageof 58
Human Mutation|June 5, 2010
Positive newborn screen for methylmalonic aciduria identifies the first mutation in TCblR/CD320, the gene for cellular uptake of transcobalamin-bound vitamin B(12)Edward V Quadros, Shao-Chiang Lai, Yasumi Nakayama, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|April 9, 2005
High dose chemotherapy and autologous stem cell transplantation as adjuvant therapy for primary breast cancer patients with four or more lymph nodes involved: long-term results of an international randomised trialR C Coombes, A Howell, M Emson, et al.
Nanoscale|September 20, 2019
Temperature-induced molecular reorganization on Au(111) driven by oligomeric defectsF De Marchi, G Galeotti, M Simenas, et al.
Cancer|May 18, 1999
Treatment of nondysgerminomatous ovarian germ cell tumors: an analysis of 69 casesP L Mitchell, N Al-Nasiri, R A'Hern, et al.
Infection Control and Hospital Epidemiology|February 2, 2022
Poor outcomes in both infection and colonization with carbapenem-resistant EnterobacteralesJessica R Howard-Anderson, Michelle Earley, Lauren Komarow, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 15, 2021
Differential diagnosis of vitamin D-related hypercalcemia using serum vitamin D metabolite profilingMartin Kaufmann, Karl-Peter Schlingmann, Linor Berezin, et al.
Connecticut Medicine|October 27, 2001
A comparison of ON-PUMP vs OFF-PUMP coronary artery bypass surgery among low, intermediate, and high-risk patients: the Hartford Hospital experienceR G McKay, R A Mennett, R C Gallagher, et al.
Molecular Genetics and Metabolism|June 9, 2009
Mutation detection in DNA isolated from cerebrospinal fluid and urine: Clinical utility and pitfalls of multiple displacement amplificationEfraim H Rosenberg, Eduard A Struys, Keith Hyland, et al.
Molecular Pharmacology|August 26, 2006
Functional genetic diversity in the high-affinity carnitine transporter OCTN2 (SLC22A5)Thomas J Urban, Renata C Gallagher, Chaline Brown, et al.
Molecular Genetics and Metabolism|June 1, 2015
Triple therapy with pyridoxine, arginine supplementation and dietary lysine restriction in pyridoxine-dependent epilepsy: Neurodevelopmental outcomeCurtis R Coughlin, Clara D M van Karnebeek, Walla Al-Hertani, et al.
Pageof 58