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Stephen F Kingsmore

Showing results (71-80 of 171) with videos related to

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Annals of Neurology|February 3, 2004
Cerebral palsy is characterized by protein mediators in cord serumTuula Kaukola, Ebenezer Satyaraj, Dhavalkumar D Patel, et al.
Clinical Immunology (Orlando, Fla.)|March 29, 2014
Expansion of CCR4+ activated T cells is associated with memory B cell reduction in DOCK8-deficient patientsSonia Caracciolo, Daniele Moratto, Mauro Giacomelli, et al.
Pediatric Pulmonology|March 11, 2014
Polymorphisms of the gene encoding Kit ligand are associated with bronchopulmonary dysplasiaJohanna M Huusko, Mari Mahlman, Minna K Karjalainen, et al.
NPJ Genomic Medicine|April 23, 2021
Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart diseaseNathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury, et al.
NPJ Genomic Medicine|March 28, 2024
Advancing access to genome sequencing for rare genetic disorders: recent progress and call to actionVaidehi Jobanputra, Brock Schroeder, Heidi L Rehm, et al.
NPJ Genomic Medicine|May 27, 2021
Publisher Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart diseaseNathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury, et al.
NPJ Genomic Medicine|May 27, 2021
Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart diseaseNathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury, et al.
The Journal of Emergency Medicine|November 8, 2011
Discriminative value of inflammatory biomarkers for suspected sepsisEphraim L Tsalik, L Brett Jaggers, Seth W Glickman, et al.
Genome Medicine|March 17, 2023
Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learningBennet Peterson, Edgar Javier Hernandez, Charlotte Hobbs, et al.
Human Mutation|April 8, 2015
Alström Syndrome: Mutation Spectrum of ALMS1Jan D Marshall, Jean Muller, Gayle B Collin, et al.
Pageof 18

Showing results (71-80 of 171) with videos related to

Sort By:
Pageof 18
Annals of Neurology|February 3, 2004
Cerebral palsy is characterized by protein mediators in cord serumTuula Kaukola, Ebenezer Satyaraj, Dhavalkumar D Patel, et al.
Clinical Immunology (Orlando, Fla.)|March 29, 2014
Expansion of CCR4+ activated T cells is associated with memory B cell reduction in DOCK8-deficient patientsSonia Caracciolo, Daniele Moratto, Mauro Giacomelli, et al.
Pediatric Pulmonology|March 11, 2014
Polymorphisms of the gene encoding Kit ligand are associated with bronchopulmonary dysplasiaJohanna M Huusko, Mari Mahlman, Minna K Karjalainen, et al.
NPJ Genomic Medicine|April 23, 2021
Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart diseaseNathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury, et al.
NPJ Genomic Medicine|March 28, 2024
Advancing access to genome sequencing for rare genetic disorders: recent progress and call to actionVaidehi Jobanputra, Brock Schroeder, Heidi L Rehm, et al.
NPJ Genomic Medicine|May 27, 2021
Publisher Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart diseaseNathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury, et al.
NPJ Genomic Medicine|May 27, 2021
Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart diseaseNathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury, et al.
The Journal of Emergency Medicine|November 8, 2011
Discriminative value of inflammatory biomarkers for suspected sepsisEphraim L Tsalik, L Brett Jaggers, Seth W Glickman, et al.
Genome Medicine|March 17, 2023
Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learningBennet Peterson, Edgar Javier Hernandez, Charlotte Hobbs, et al.
Human Mutation|April 8, 2015
Alström Syndrome: Mutation Spectrum of ALMS1Jan D Marshall, Jean Muller, Gayle B Collin, et al.
Pageof 18