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Joshua D Milner

Showing results (161-170 of 183) with videos related to

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The New England Journal of Medicine|May 31, 2023
Variant <i>STAT4</i> and Response to Ruxolitinib in an Autoinflammatory SyndromeHratch Baghdassarian, Sarah A Blackstone, Owen S Clay, et al.
Blood Advances|September 28, 2022
Genetically defined individual reference ranges for tryptase limit unnecessary procedures and unmask myeloid neoplasmsJack Chovanec, Ilker Tunc, Jason Hughes, et al.
Blood|November 1, 2014
Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutationsJoshua D Milner, Tiphanie P Vogel, Lisa Forbes, et al.
JAMA|October 24, 2024
Expanded Newborn Screening Using Genome Sequencing for Early Actionable ConditionsAlban Ziegler, Carrie Koval-Burt, Denise M Kay, et al.
Medrxiv : the Preprint Server for Health Sciences|August 6, 2025
The polygenic architecture of hidradenitis suppurativa reveals signaling mechanisms that implicate epithelial remodelingAtlas Khan, Poppy A Gould, Yiming Luo, et al.
The Journal of Allergy and Clinical Immunology|April 30, 2026
Clinical features, genetics, treatment, and long-term outcomes of STAT3 hyper-IgE syndrome: a single-center cohort analysisAlexandra F Freeman, Chen Wang, Amanda Urban, et al.
Blood Advances|December 11, 2025
Systematic functional validation of IKAROS variants from patients and laboratory-generated mutationsHye Sun Kuehn, Agustin Alejandro Gil Silva, Natchanun Klangkalya, et al.
The Journal of Allergy and Clinical Immunology|September 1, 2018
Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic diseaseBatsukh Dorjbal, Jeffrey R Stinson, Chi A Ma, et al.
The Journal of Experimental Medicine|June 10, 2020
Correction: Dominant-negative mutations in human IL6ST underlie hyper-IgE syndromeVivien Béziat, Simon J Tavernier, Yin-Huai Chen, et al.
The Journal of Experimental Medicine|March 25, 2020
Dominant-negative mutations in human IL6ST underlie hyper-IgE syndromeVivien Béziat, Simon J Tavernier, Yin-Huai Chen, et al.
Pageof 19

Showing results (161-170 of 183) with videos related to

Sort By:
Pageof 19
The New England Journal of Medicine|May 31, 2023
Variant <i>STAT4</i> and Response to Ruxolitinib in an Autoinflammatory SyndromeHratch Baghdassarian, Sarah A Blackstone, Owen S Clay, et al.
Blood Advances|September 28, 2022
Genetically defined individual reference ranges for tryptase limit unnecessary procedures and unmask myeloid neoplasmsJack Chovanec, Ilker Tunc, Jason Hughes, et al.
Blood|November 1, 2014
Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutationsJoshua D Milner, Tiphanie P Vogel, Lisa Forbes, et al.
JAMA|October 24, 2024
Expanded Newborn Screening Using Genome Sequencing for Early Actionable ConditionsAlban Ziegler, Carrie Koval-Burt, Denise M Kay, et al.
Medrxiv : the Preprint Server for Health Sciences|August 6, 2025
The polygenic architecture of hidradenitis suppurativa reveals signaling mechanisms that implicate epithelial remodelingAtlas Khan, Poppy A Gould, Yiming Luo, et al.
The Journal of Allergy and Clinical Immunology|April 30, 2026
Clinical features, genetics, treatment, and long-term outcomes of STAT3 hyper-IgE syndrome: a single-center cohort analysisAlexandra F Freeman, Chen Wang, Amanda Urban, et al.
Blood Advances|December 11, 2025
Systematic functional validation of IKAROS variants from patients and laboratory-generated mutationsHye Sun Kuehn, Agustin Alejandro Gil Silva, Natchanun Klangkalya, et al.
The Journal of Allergy and Clinical Immunology|September 1, 2018
Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic diseaseBatsukh Dorjbal, Jeffrey R Stinson, Chi A Ma, et al.
The Journal of Experimental Medicine|June 10, 2020
Correction: Dominant-negative mutations in human IL6ST underlie hyper-IgE syndromeVivien Béziat, Simon J Tavernier, Yin-Huai Chen, et al.
The Journal of Experimental Medicine|March 25, 2020
Dominant-negative mutations in human IL6ST underlie hyper-IgE syndromeVivien Béziat, Simon J Tavernier, Yin-Huai Chen, et al.
Pageof 19