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Jonathan A Bernstein

Showing results (511-520 of 606) with videos related to

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Science Immunology|September 16, 2022
DPP9 deficiency: An inflammasomopathy that can be rescued by lowering NLRP1/IL-1 signalingCassandra R Harapas, Kim S Robinson, Kenneth Lay, et al.
Human Mutation|January 14, 2018
Genotype-phenotype correlations in individuals with pathogenic RERE variantsValerie K Jordan, Brieana Fregeau, Xiaoyan Ge, et al.
The Journal of Allergy and Clinical Immunology|March 27, 2021
Functional and structural analysis of cytokine-selective IL6ST defects that cause recessive hyper-IgE syndromeYin-Huai Chen, Diane B Zastrow, Riley D Metcalfe, et al.
Medrxiv : the Preprint Server for Health Sciences|July 16, 2025
Domain specific phenotypic expansion associated with variants in <i>MACF1</i>Nikhita Gogate, Angad Jolly, Jill A Rosenfeld, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2021
Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delayUirá Souto Melo, Devon Bonner, Kevin C Kent Lloyd, et al.
The Journal of Allergy and Clinical Immunology|July 25, 2020
Rhinitis 2020: A practice parameter updateMark S Dykewicz, Dana V Wallace, David J Amrol, et al.
JAMA|March 13, 2014
Clinical interpretation and implications of whole-genome sequencingFrederick E Dewey, Megan E Grove, Cuiping Pan, et al.
The Journal of Allergy and Clinical Immunology|June 9, 2024
Leukotriene receptor antagonists as add-on therapy to antihistamines for urticaria: Systematic review and meta-analysis of randomized clinical trialsDaniel G Rayner, Ming Liu, Alexandro W L Chu, et al.
European Heart Journal|October 12, 2017
New insights into mitral valve dystrophy: a Filamin-A genotype-phenotype and outcome studyThierry Le Tourneau, Solena Le Scouarnec, Caroline Cueff, et al.
Brain : a Journal of Neurology|October 4, 2017
Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephalyDiana Alcantara, Andrew E Timms, Karen Gripp, et al.
Pageof 61

Showing results (511-520 of 606) with videos related to

Sort By:
Pageof 61
Science Immunology|September 16, 2022
DPP9 deficiency: An inflammasomopathy that can be rescued by lowering NLRP1/IL-1 signalingCassandra R Harapas, Kim S Robinson, Kenneth Lay, et al.
Human Mutation|January 14, 2018
Genotype-phenotype correlations in individuals with pathogenic RERE variantsValerie K Jordan, Brieana Fregeau, Xiaoyan Ge, et al.
The Journal of Allergy and Clinical Immunology|March 27, 2021
Functional and structural analysis of cytokine-selective IL6ST defects that cause recessive hyper-IgE syndromeYin-Huai Chen, Diane B Zastrow, Riley D Metcalfe, et al.
Medrxiv : the Preprint Server for Health Sciences|July 16, 2025
Domain specific phenotypic expansion associated with variants in <i>MACF1</i>Nikhita Gogate, Angad Jolly, Jill A Rosenfeld, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2021
Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delayUirá Souto Melo, Devon Bonner, Kevin C Kent Lloyd, et al.
The Journal of Allergy and Clinical Immunology|July 25, 2020
Rhinitis 2020: A practice parameter updateMark S Dykewicz, Dana V Wallace, David J Amrol, et al.
JAMA|March 13, 2014
Clinical interpretation and implications of whole-genome sequencingFrederick E Dewey, Megan E Grove, Cuiping Pan, et al.
The Journal of Allergy and Clinical Immunology|June 9, 2024
Leukotriene receptor antagonists as add-on therapy to antihistamines for urticaria: Systematic review and meta-analysis of randomized clinical trialsDaniel G Rayner, Ming Liu, Alexandro W L Chu, et al.
European Heart Journal|October 12, 2017
New insights into mitral valve dystrophy: a Filamin-A genotype-phenotype and outcome studyThierry Le Tourneau, Solena Le Scouarnec, Caroline Cueff, et al.
Brain : a Journal of Neurology|October 4, 2017
Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephalyDiana Alcantara, Andrew E Timms, Karen Gripp, et al.
Pageof 61