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J Keating

Showing results (1081-1090 of 1,115) with videos related to

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Transplant International : Official Journal of the European Society for Organ Transplantation|March 18, 2021
Early detection of SARS-CoV-2 and other infections in solid organ transplant recipients and household members using wearable devicesBrendan J Keating, Eyas H Mukhtar, Eric D Elftmann, et al.
The Journal of Trauma and Acute Care Surgery|March 6, 2021
An Eastern Association for the Surgery of Trauma multicenter trial examining prehospital procedures in penetrating trauma patientsSharven Taghavi, Zoe Maher, Amy J Goldberg, et al.
Science Advances|February 19, 2025
The mutational landscape and functional effects of noncoding ultraconserved elements in human cancersRecep Bayraktar, Yitao Tang, Mihnea P Dragomir, et al.
Plos Genetics|July 9, 2011
Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT)Alexander P Reiner, Guillaume Lettre, Michael A Nalls, et al.
Nature Medicine|May 17, 2024
Integrative multi-omics profiling in human decedents receiving pig heart xenograftsEloi Schmauch, Brian Piening, Maedeh Mohebnasab, et al.
Circulation. Cardiovascular Genetics|November 10, 2012
Novel loci associated with PR interval in a genome-wide association study of 10 African American cohortsAnne M Butler, Xiaoyan Yin, Daniel S Evans, et al.
Biodata Mining|August 4, 2017
Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individualsEmily R Holzinger, Shefali S Verma, Carrie B Moore, et al.
Plos Genetics|February 25, 2011
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe ProjectGuillaume Lettre, Cameron D Palmer, Taylor Young, et al.
Nature Communications|October 10, 2015
Genetic sharing and heritability of paediatric age of onset autoimmune diseasesYun R Li, Sihai D Zhao, Jin Li, et al.
Human Mutation|February 7, 2015
De novo heterozygous mutations in SMC3 cause a range of Cornelia de Lange syndrome-overlapping phenotypesMaría Concepción Gil-Rodríguez, Matthew A Deardorff, Morad Ansari, et al.
Pageof 112

Showing results (1081-1090 of 1,115) with videos related to

Sort By:
Pageof 112
Transplant International : Official Journal of the European Society for Organ Transplantation|March 18, 2021
Early detection of SARS-CoV-2 and other infections in solid organ transplant recipients and household members using wearable devicesBrendan J Keating, Eyas H Mukhtar, Eric D Elftmann, et al.
The Journal of Trauma and Acute Care Surgery|March 6, 2021
An Eastern Association for the Surgery of Trauma multicenter trial examining prehospital procedures in penetrating trauma patientsSharven Taghavi, Zoe Maher, Amy J Goldberg, et al.
Science Advances|February 19, 2025
The mutational landscape and functional effects of noncoding ultraconserved elements in human cancersRecep Bayraktar, Yitao Tang, Mihnea P Dragomir, et al.
Plos Genetics|July 9, 2011
Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT)Alexander P Reiner, Guillaume Lettre, Michael A Nalls, et al.
Nature Medicine|May 17, 2024
Integrative multi-omics profiling in human decedents receiving pig heart xenograftsEloi Schmauch, Brian Piening, Maedeh Mohebnasab, et al.
Circulation. Cardiovascular Genetics|November 10, 2012
Novel loci associated with PR interval in a genome-wide association study of 10 African American cohortsAnne M Butler, Xiaoyan Yin, Daniel S Evans, et al.
Biodata Mining|August 4, 2017
Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individualsEmily R Holzinger, Shefali S Verma, Carrie B Moore, et al.
Plos Genetics|February 25, 2011
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe ProjectGuillaume Lettre, Cameron D Palmer, Taylor Young, et al.
Nature Communications|October 10, 2015
Genetic sharing and heritability of paediatric age of onset autoimmune diseasesYun R Li, Sihai D Zhao, Jin Li, et al.
Human Mutation|February 7, 2015
De novo heterozygous mutations in SMC3 cause a range of Cornelia de Lange syndrome-overlapping phenotypesMaría Concepción Gil-Rodríguez, Matthew A Deardorff, Morad Ansari, et al.
Pageof 112