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Showing results (881-890 of 1,220) with videos related to

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Gene Therapy|April 1, 2011
The hyperactive Sleeping Beauty transposase SB100X improves the genetic modification of T cells to express a chimeric antigen receptorZ Jin, S Maiti, H Huls, et al.
Oncoimmunology|April 9, 2016
The beneficial effects of a gas-permeable flask for expansion of Tumor-Infiltrating lymphocytes as reflected in their mitochondrial function and respiration capacityMarie-Andrée Forget, Cara Haymaker, Jennifer B Dennison, et al.
Human Molecular Genetics|September 1, 1993
Detection of missense mutations by single-strand conformational polymorphism (SSCP) analysis in five dysfunctional variants of coagulation factor VIIO Takamiya, G Kemball-Cook, D M Martin, et al.
International Journal of Pediatric Otorhinolaryngology|June 7, 2017
The effect of perioperative dexamethasone dosing on post-tonsillectomy hemorrhage riskYin Yiu, Justin B Mahida, Jennifer N Cooper, et al.
Human Mutation|September 11, 2014
Identification of large NF1 duplications reciprocal to NAHR-mediated type-1 NF1 deletionsHildegard Kehrer-Sawatzki, Kathrin Bengesser, Tom Callens, et al.
Nature Communications|November 28, 2025
Expanding the utility of variant effect predictions with phenotype-specific modelsDavid Stein, Meltem Ece Kars, Baptiste Milisavljevic, et al.
JAMA Surgery|December 18, 2015
Effectiveness of Patient Choice in Nonoperative vs Surgical Management of Pediatric Uncomplicated Acute AppendicitisPeter C Minneci, Justin B Mahida, Daniel L Lodwick, et al.
Pediatric Surgery International|December 22, 2015
A comparison of pediatric gastrostomy tube placement techniquesJason P Sulkowski, Ana C De Roo, Jason Nielsen, et al.
Human Mutation|February 4, 2016
mutation3D: Cancer Gene Prediction Through Atomic Clustering of Coding Variants in the Structural ProteomeMichael J Meyer, Ryan Lapcevic, Alfonso E Romero, et al.
Neurology|July 23, 2003
D4F104S1 deletion in facioscapulohumeral muscular dystrophy: phenotype, size, and detectionR J L F Lemmers, M Osborn, T Haaf, et al.
Pageof 122

Showing results (881-890 of 1,220) with videos related to

Sort By:
Pageof 122
Gene Therapy|April 1, 2011
The hyperactive Sleeping Beauty transposase SB100X improves the genetic modification of T cells to express a chimeric antigen receptorZ Jin, S Maiti, H Huls, et al.
Oncoimmunology|April 9, 2016
The beneficial effects of a gas-permeable flask for expansion of Tumor-Infiltrating lymphocytes as reflected in their mitochondrial function and respiration capacityMarie-Andrée Forget, Cara Haymaker, Jennifer B Dennison, et al.
Human Molecular Genetics|September 1, 1993
Detection of missense mutations by single-strand conformational polymorphism (SSCP) analysis in five dysfunctional variants of coagulation factor VIIO Takamiya, G Kemball-Cook, D M Martin, et al.
International Journal of Pediatric Otorhinolaryngology|June 7, 2017
The effect of perioperative dexamethasone dosing on post-tonsillectomy hemorrhage riskYin Yiu, Justin B Mahida, Jennifer N Cooper, et al.
Human Mutation|September 11, 2014
Identification of large NF1 duplications reciprocal to NAHR-mediated type-1 NF1 deletionsHildegard Kehrer-Sawatzki, Kathrin Bengesser, Tom Callens, et al.
Nature Communications|November 28, 2025
Expanding the utility of variant effect predictions with phenotype-specific modelsDavid Stein, Meltem Ece Kars, Baptiste Milisavljevic, et al.
JAMA Surgery|December 18, 2015
Effectiveness of Patient Choice in Nonoperative vs Surgical Management of Pediatric Uncomplicated Acute AppendicitisPeter C Minneci, Justin B Mahida, Daniel L Lodwick, et al.
Pediatric Surgery International|December 22, 2015
A comparison of pediatric gastrostomy tube placement techniquesJason P Sulkowski, Ana C De Roo, Jason Nielsen, et al.
Human Mutation|February 4, 2016
mutation3D: Cancer Gene Prediction Through Atomic Clustering of Coding Variants in the Structural ProteomeMichael J Meyer, Ryan Lapcevic, Alfonso E Romero, et al.
Neurology|July 23, 2003
D4F104S1 deletion in facioscapulohumeral muscular dystrophy: phenotype, size, and detectionR J L F Lemmers, M Osborn, T Haaf, et al.
Pageof 122