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A KEITH

Showing results (501-510 of 1,124) with videos related to

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Microbial Pathogenesis|April 4, 2020
Shell disorder analysis predicts greater resilience of the SARS-CoV-2 (COVID-19) outside the body and in body fluidsGerard Kian-Meng Goh, A Keith Dunker, James A Foster, et al.
Journal of Proteome Research|February 10, 2022
Computational, Experimental, and Clinical Evidence of a Specific but Peculiar Evolutionary Nature of (COVID-19) SARS-CoV-2Gerard Kian-Meng Goh, A Keith Dunker, James A Foster, et al.
Free Radical Biology & Medicine|July 11, 2003
Macrophages as a major source of oxygen radicals in the hyperoxic newborn rat lungRobert P Jankov, Leslie Johnstone, Xiaoping Luo, et al.
American Journal of Respiratory and Critical Care Medicine|May 27, 2006
Fibroblast growth factor-2 and receptor-1alpha(IIIc) regulate postnatal rat lung cell apoptosisMan Yi, Rosetta Belcastro, Samuel Shek, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|January 18, 2011
Long-term failure of alveologenesis after an early short-term exposure to a PDGF-receptor antagonistMandy Lau, Azhar Masood, Man Yi, et al.
Pediatric Research|February 24, 2006
Lgl1 is suppressed in oxygen toxicity animal models of bronchopulmonary dysplasia and normalizes during recovery in airKatia Nadeau, Robert P Jankov, A Keith Tanswell, et al.
The Journal of Prosthetic Dentistry|February 1, 1983
Internal derangements of the temporomandibular joint: an assessment of condylar position in centric occlusionR W Katzberg, D A Keith, W R Ten Eick, et al.
International Journal of Molecular Sciences|September 21, 2017
Mouse Monoclonal Antibodies Generated from Full Length Human Cereblon: Detection of Cereblon Protein in Patients with Multiple MyelomaXiubao Chang, Qinqin Xu, Yuexian Hou, et al.
Neuromuscular Disorders : NMD|January 15, 2013
Homozygous lamin A/C familial lipodystrophy R482Q mutation in autosomal recessive Emery Dreifuss muscular dystrophyKatie M Wiltshire, Robert A Hegele, A Micheil Innes, et al.
Journal of Proteome Research|May 10, 2008
Protein disorder is positively correlated with gene expression in Escherichia coliOleg Paliy, Shawn M Gargac, Yugong Cheng, et al.
Pageof 113

Showing results (501-510 of 1,124) with videos related to

Sort By:
Pageof 113
Microbial Pathogenesis|April 4, 2020
Shell disorder analysis predicts greater resilience of the SARS-CoV-2 (COVID-19) outside the body and in body fluidsGerard Kian-Meng Goh, A Keith Dunker, James A Foster, et al.
Journal of Proteome Research|February 10, 2022
Computational, Experimental, and Clinical Evidence of a Specific but Peculiar Evolutionary Nature of (COVID-19) SARS-CoV-2Gerard Kian-Meng Goh, A Keith Dunker, James A Foster, et al.
Free Radical Biology & Medicine|July 11, 2003
Macrophages as a major source of oxygen radicals in the hyperoxic newborn rat lungRobert P Jankov, Leslie Johnstone, Xiaoping Luo, et al.
American Journal of Respiratory and Critical Care Medicine|May 27, 2006
Fibroblast growth factor-2 and receptor-1alpha(IIIc) regulate postnatal rat lung cell apoptosisMan Yi, Rosetta Belcastro, Samuel Shek, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|January 18, 2011
Long-term failure of alveologenesis after an early short-term exposure to a PDGF-receptor antagonistMandy Lau, Azhar Masood, Man Yi, et al.
Pediatric Research|February 24, 2006
Lgl1 is suppressed in oxygen toxicity animal models of bronchopulmonary dysplasia and normalizes during recovery in airKatia Nadeau, Robert P Jankov, A Keith Tanswell, et al.
The Journal of Prosthetic Dentistry|February 1, 1983
Internal derangements of the temporomandibular joint: an assessment of condylar position in centric occlusionR W Katzberg, D A Keith, W R Ten Eick, et al.
International Journal of Molecular Sciences|September 21, 2017
Mouse Monoclonal Antibodies Generated from Full Length Human Cereblon: Detection of Cereblon Protein in Patients with Multiple MyelomaXiubao Chang, Qinqin Xu, Yuexian Hou, et al.
Neuromuscular Disorders : NMD|January 15, 2013
Homozygous lamin A/C familial lipodystrophy R482Q mutation in autosomal recessive Emery Dreifuss muscular dystrophyKatie M Wiltshire, Robert A Hegele, A Micheil Innes, et al.
Journal of Proteome Research|May 10, 2008
Protein disorder is positively correlated with gene expression in Escherichia coliOleg Paliy, Shawn M Gargac, Yugong Cheng, et al.
Pageof 113