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Journal of Child Neurology
|
March 25, 2014
Social communication features in children following moderate to severe acquired brain injury: a cross-sectional pilot study
Lynn M Breau, Brenda Clark, Ori Scott, et al.
Frontiers in Immunology
|
June 5, 2023
The human Stat1 gain-of-function T385M mutation causes expansion of activated T-follicular helper/T-helper 1-like CD4 T cells and sex-biased autoimmunity in specific pathogen-free mice
Ori Scott, Shagana Visuvanathan, Emily Reddy, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
March 28, 2023
Favorable outcome of COVID-19 in pediatric patients with primary immunodeficiency
Jenny Garkaby, Jessica Willett Pachul, Ori Scott, et al.
Frontiers in Immunology
|
February 7, 2022
Case Report: Eosinophilic Esophagitis in a Patient With a Novel STAT1 Gain-of-Function Pathogenic Variant
Ori Scott, Nigel Sharfe, Harjit Dadi, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
November 5, 2021
DNA-Binding domain mutations confer severe outcome at an early age among STAT1 gain-of-function patients
Ori Scott, Harjit Dadi, Linda Vong, et al.
Nature Cell Biology
|
July 12, 2024
Pressure sensing of lysosomes enables control of TFEB responses in macrophages
Ruiqi Cai, Ori Scott, Gang Ye, et al.
Disease Models & Mechanisms
|
August 5, 2024
Generation and characterization of a novel mouse model of Becker Muscular Dystrophy with a deletion of exons 52 to 55
Lucie O M Perillat, Tatianna W Y Wong, Eleonora Maino, et al.
The Journal of Allergy and Clinical Immunology. Global
|
May 27, 2024
Utilization of next-generation sequencing to define the role of heterozygous <i>FOXN1</i> variants in immunodeficiency
Yehonatan Pasternak, Linda Vong, Daniele Merico, et al.
Disease Models & Mechanisms
|
June 17, 2024
An Irak1-Mecp2 tandem duplication mouse model for the study of MECP2 duplication syndrome
Eleonora Maino, Ori Scott, Samar Z Rizvi, et al.
NPJ Genomic Medicine
|
November 19, 2021
Homozygous duplication identified by whole genome sequencing causes LRBA deficiency
Daniele Merico, Yehonatan Pasternak, Mehdi Zarrei, et al.
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Search research articles
Search
Showing results (21-30 of 31) with videos related to
Sort By:
Page
of 4
Journal of Child Neurology
|
March 25, 2014
Social communication features in children following moderate to severe acquired brain injury: a cross-sectional pilot study
Lynn M Breau, Brenda Clark, Ori Scott, et al.
Frontiers in Immunology
|
June 5, 2023
The human Stat1 gain-of-function T385M mutation causes expansion of activated T-follicular helper/T-helper 1-like CD4 T cells and sex-biased autoimmunity in specific pathogen-free mice
Ori Scott, Shagana Visuvanathan, Emily Reddy, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
March 28, 2023
Favorable outcome of COVID-19 in pediatric patients with primary immunodeficiency
Jenny Garkaby, Jessica Willett Pachul, Ori Scott, et al.
Frontiers in Immunology
|
February 7, 2022
Case Report: Eosinophilic Esophagitis in a Patient With a Novel STAT1 Gain-of-Function Pathogenic Variant
Ori Scott, Nigel Sharfe, Harjit Dadi, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
November 5, 2021
DNA-Binding domain mutations confer severe outcome at an early age among STAT1 gain-of-function patients
Ori Scott, Harjit Dadi, Linda Vong, et al.
Nature Cell Biology
|
July 12, 2024
Pressure sensing of lysosomes enables control of TFEB responses in macrophages
Ruiqi Cai, Ori Scott, Gang Ye, et al.
Disease Models & Mechanisms
|
August 5, 2024
Generation and characterization of a novel mouse model of Becker Muscular Dystrophy with a deletion of exons 52 to 55
Lucie O M Perillat, Tatianna W Y Wong, Eleonora Maino, et al.
The Journal of Allergy and Clinical Immunology. Global
|
May 27, 2024
Utilization of next-generation sequencing to define the role of heterozygous <i>FOXN1</i> variants in immunodeficiency
Yehonatan Pasternak, Linda Vong, Daniele Merico, et al.
Disease Models & Mechanisms
|
June 17, 2024
An Irak1-Mecp2 tandem duplication mouse model for the study of MECP2 duplication syndrome
Eleonora Maino, Ori Scott, Samar Z Rizvi, et al.
NPJ Genomic Medicine
|
November 19, 2021
Homozygous duplication identified by whole genome sequencing causes LRBA deficiency
Daniele Merico, Yehonatan Pasternak, Mehdi Zarrei, et al.
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of 4