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Christopher Barnett

Showing results (11-20 of 72) with videos related to

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Molecular Pharmaceutics|February 21, 2023
Photochemical Internalization Using Natural Anticancer Drugs, Antimetabolites, and Nanoformulations: A Systematic Study against Breast and Pancreatic Cancer Cell LinesChristopher Barnett, Fanny Joubert, Alexandra Iliopoulou, et al.
Case Reports in Cardiology|March 5, 2020
Plaque Rupture-Induced Myocardial Infarction and Mechanical Circulatory Support in Alpha-Gal AllergySohab S Radwan, Gauravpal Gill, Amre Ghazzal, et al.
Molecular Syndromology|June 22, 2018
Atypical Skin Manifestations in <i>FGFR2</i>-Related Craniosynostosis Syndromes Broaden the Phenotypic SpectrumShannon LeBlanc, David David, Alison Colley, et al.
Journal of Pediatric Surgery|July 4, 2009
Looking past the lump: genetic aspects of inguinal hernia in childrenChristopher Barnett, Jacob C Langer, Aleksander Hinek, et al.
Clinical Imaging|March 7, 2022
Metastatic melanoma in the breast and axilla: A case reportChristopher Barnett, Nishi Mehta, William S Towne, et al.
American Journal of Medical Genetics. Part A|April 18, 2020
CDH1-related blepharocheilodontic syndrome is associated with diffuse gastric cancer riskShannon LeBlanc, Dildeepa Naveen, Eric Haan, et al.
Experimental Gerontology|March 31, 2004
Effects of a reduced oxygen tension culture system on human T cell clones as a function of in vitro ageOrla Duggan, Paul Hyland, Kathryn Annett, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 22, 2004
Elimination of an immunodominant CD4+ T cell epitope in human IFN-beta does not result in an in vivo response directed at the subdominant epitopeV Peter Yeung, Judy Chang, Jeff Miller, et al.
Pediatric Dermatology|September 10, 2019
Novel KIT mutation presenting as marked lentiginosisAlain K Tran, Annette Pearce, Marcos López-Sánchez, et al.
The Journal of Craniofacial Surgery|September 21, 2020
Severe Cloverleaf Skull Deformity in c.1061C>G (p.Ser354Cys) Mutated Fibroblast Growth Factor Receptor 2 Gene in Crouzon SyndromeSarut Chaisrisawadisuk, Elie Hammam, Cindy J Molloy, et al.
Pageof 8

Showing results (11-20 of 72) with videos related to

Sort By:
Pageof 8
Molecular Pharmaceutics|February 21, 2023
Photochemical Internalization Using Natural Anticancer Drugs, Antimetabolites, and Nanoformulations: A Systematic Study against Breast and Pancreatic Cancer Cell LinesChristopher Barnett, Fanny Joubert, Alexandra Iliopoulou, et al.
Case Reports in Cardiology|March 5, 2020
Plaque Rupture-Induced Myocardial Infarction and Mechanical Circulatory Support in Alpha-Gal AllergySohab S Radwan, Gauravpal Gill, Amre Ghazzal, et al.
Molecular Syndromology|June 22, 2018
Atypical Skin Manifestations in <i>FGFR2</i>-Related Craniosynostosis Syndromes Broaden the Phenotypic SpectrumShannon LeBlanc, David David, Alison Colley, et al.
Journal of Pediatric Surgery|July 4, 2009
Looking past the lump: genetic aspects of inguinal hernia in childrenChristopher Barnett, Jacob C Langer, Aleksander Hinek, et al.
Clinical Imaging|March 7, 2022
Metastatic melanoma in the breast and axilla: A case reportChristopher Barnett, Nishi Mehta, William S Towne, et al.
American Journal of Medical Genetics. Part A|April 18, 2020
CDH1-related blepharocheilodontic syndrome is associated with diffuse gastric cancer riskShannon LeBlanc, Dildeepa Naveen, Eric Haan, et al.
Experimental Gerontology|March 31, 2004
Effects of a reduced oxygen tension culture system on human T cell clones as a function of in vitro ageOrla Duggan, Paul Hyland, Kathryn Annett, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 22, 2004
Elimination of an immunodominant CD4+ T cell epitope in human IFN-beta does not result in an in vivo response directed at the subdominant epitopeV Peter Yeung, Judy Chang, Jeff Miller, et al.
Pediatric Dermatology|September 10, 2019
Novel KIT mutation presenting as marked lentiginosisAlain K Tran, Annette Pearce, Marcos López-Sánchez, et al.
The Journal of Craniofacial Surgery|September 21, 2020
Severe Cloverleaf Skull Deformity in c.1061C>G (p.Ser354Cys) Mutated Fibroblast Growth Factor Receptor 2 Gene in Crouzon SyndromeSarut Chaisrisawadisuk, Elie Hammam, Cindy J Molloy, et al.
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