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Science Immunology
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September 16, 2022
DPP9 deficiency: An inflammasomopathy that can be rescued by lowering NLRP1/IL-1 signaling
Cassandra R Harapas, Kim S Robinson, Kenneth Lay, et al.
Human Mutation
|
January 14, 2018
Genotype-phenotype correlations in individuals with pathogenic RERE variants
Valerie 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 syndrome
Yin-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 delay
Uirá 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 update
Mark S Dykewicz, Dana V Wallace, David J Amrol, et al.
JAMA
|
March 13, 2014
Clinical interpretation and implications of whole-genome sequencing
Frederick 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 trials
Daniel 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 study
Thierry 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 megalencephaly
Diana Alcantara, Andrew E Timms, Karen Gripp, et al.
Page
of 61
Search research articles
Search
Showing results (511-520 of 606) with videos related to
Sort By:
Page
of 61
Science Immunology
|
September 16, 2022
DPP9 deficiency: An inflammasomopathy that can be rescued by lowering NLRP1/IL-1 signaling
Cassandra R Harapas, Kim S Robinson, Kenneth Lay, et al.
Human Mutation
|
January 14, 2018
Genotype-phenotype correlations in individuals with pathogenic RERE variants
Valerie 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 syndrome
Yin-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 delay
Uirá 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 update
Mark S Dykewicz, Dana V Wallace, David J Amrol, et al.
JAMA
|
March 13, 2014
Clinical interpretation and implications of whole-genome sequencing
Frederick 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 trials
Daniel 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 study
Thierry 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 megalencephaly
Diana Alcantara, Andrew E Timms, Karen Gripp, et al.
Page
of 61