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Showing results (71-80 of 92) with videos related to

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Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|May 29, 2025
Interferon-γ Therapy in Patients With Refractory Disseminated CoccidioidomycosisChen Wang, Brenna A LaBere, Michell M Lozano Chinga, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|November 17, 2025
IL12RB1 deficiency appearing in North America: expanding the clinical phenotypesChen Wang, Beatriz E Marciano, Annalie J Harris, et al.
The European Respiratory Journal|February 5, 2021
Genome-wide association study in patients with pulmonary <i>Mycobacterium avium</i> complex diseaseHo Namkoong, Yosuke Omae, Takanori Asakura, et al.
Nature Immunology|December 23, 2021
Congenital iRHOM2 deficiency causes ADAM17 dysfunction and environmentally directed immunodysregulatory diseaseSatoshi Kubo, Jill M Fritz, Hayley M Raquer-McKay, et al.
Nature Genetics|November 8, 2016
Elevated basal serum tryptase identifies a multisystem disorder associated with increased TPSAB1 copy numberJonathan J Lyons, Xiaomin Yu, Jason D Hughes, et al.
Frontiers in Immunology|May 22, 2023
Chromosomal microarray analysis supplements exome sequencing to diagnose children with suspected inborn errors of immunityBreanna J Beers, Morgan N Similuk, Rajarshi Ghosh, et al.
The Journal of Allergy and Clinical Immunology|February 22, 2026
Clinical relevance of mosaic variants detected by exome sequencingRajarshi Ghosh, Zeeshan Fazal, Andrew J Oler, et al.
JCI Insight|September 27, 2022
Immunogenetics associated with severe coccidioidomycosisAmy P Hsu, Agnieszka Korzeniowska, Cynthia C Aguilar, et al.
Science (New York, N.Y.)|July 11, 2020
HEM1 deficiency disrupts mTORC2 and F-actin control in inherited immunodysregulatory diseaseSarah A Cook, William A Comrie, M Cecilia Poli, et al.
Science Translational Medicine|September 18, 2024
A deep intronic splice-altering <i>AIRE</i> variant causes APECED syndrome through antisense oligonucleotide-targetable pseudoexon inclusionSebastian Ochoa, Amy P Hsu, Andrew J Oler, et al.
Pageof 10

Showing results (71-80 of 92) with videos related to

Sort By:
Pageof 10
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|May 29, 2025
Interferon-γ Therapy in Patients With Refractory Disseminated CoccidioidomycosisChen Wang, Brenna A LaBere, Michell M Lozano Chinga, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|November 17, 2025
IL12RB1 deficiency appearing in North America: expanding the clinical phenotypesChen Wang, Beatriz E Marciano, Annalie J Harris, et al.
The European Respiratory Journal|February 5, 2021
Genome-wide association study in patients with pulmonary <i>Mycobacterium avium</i> complex diseaseHo Namkoong, Yosuke Omae, Takanori Asakura, et al.
Nature Immunology|December 23, 2021
Congenital iRHOM2 deficiency causes ADAM17 dysfunction and environmentally directed immunodysregulatory diseaseSatoshi Kubo, Jill M Fritz, Hayley M Raquer-McKay, et al.
Nature Genetics|November 8, 2016
Elevated basal serum tryptase identifies a multisystem disorder associated with increased TPSAB1 copy numberJonathan J Lyons, Xiaomin Yu, Jason D Hughes, et al.
Frontiers in Immunology|May 22, 2023
Chromosomal microarray analysis supplements exome sequencing to diagnose children with suspected inborn errors of immunityBreanna J Beers, Morgan N Similuk, Rajarshi Ghosh, et al.
The Journal of Allergy and Clinical Immunology|February 22, 2026
Clinical relevance of mosaic variants detected by exome sequencingRajarshi Ghosh, Zeeshan Fazal, Andrew J Oler, et al.
JCI Insight|September 27, 2022
Immunogenetics associated with severe coccidioidomycosisAmy P Hsu, Agnieszka Korzeniowska, Cynthia C Aguilar, et al.
Science (New York, N.Y.)|July 11, 2020
HEM1 deficiency disrupts mTORC2 and F-actin control in inherited immunodysregulatory diseaseSarah A Cook, William A Comrie, M Cecilia Poli, et al.
Science Translational Medicine|September 18, 2024
A deep intronic splice-altering <i>AIRE</i> variant causes APECED syndrome through antisense oligonucleotide-targetable pseudoexon inclusionSebastian Ochoa, Amy P Hsu, Andrew J Oler, et al.
Pageof 10