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Catherine M Biggs

Showing results (31-40 of 43) with videos related to

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Journal of Clinical Immunology|April 28, 2025
A Germline Heterozygous Dominant Negative IKZF2 Variant Causing Syndromic Primary Immune Regulatory Disorder and ICHADHenry Y Lu, Maryam Vaseghi-Shanjani, Avery J Lam, et al.
Journal of Medical Genetics|June 14, 2023
Dominant negative variants in <i>IKZF2</i> cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delayArezoo Mohajeri, Maryam Vaseghi-Shanjani, Jill A Rosenfeld, et al.
Pediatric Rheumatology Online Journal|February 16, 2019
Calm in the midst of cytokine storm: a collaborative approach to the diagnosis and treatment of hemophagocytic lymphohistiocytosis and macrophage activation syndromeOlha Halyabar, Margaret H Chang, Michelle L Schoettler, et al.
JCI Insight|December 22, 2022
Human JAK1 gain of function causes dysregulated myelopoeisis and severe allergic inflammationCatherine M Biggs, Anna Cordeiro-Santanach, Sergey V Prykhozhij, et al.
Cell|December 22, 2023
Sensory neurons promote immune homeostasis in the lungMasato Tamari, Kate L Del Bel, Aaron M Ver Heul, et al.
Medrxiv : the Preprint Server for Health Sciences|September 19, 2025
Human germline biallelic loss-of-function <i>OSMR</i> variants cause severe allergic diseaseMehul Sharma, Simran Samra, Yihui Liu, et al.
Journal of Human Immunity|November 26, 2025
Novel genotypes, phenotypes, and triggers in humans with OTULIN haploinsufficiencyTristan J van der Linden, Rob J W Arts, Catherine M Biggs, et al.
The Journal of Experimental Medicine|July 31, 2025
ASXL1 deficiency causes epigenetic dysfunction, combined immunodeficiency, and EBV-associated lymphomaMaggie P Fu, Mehul Sharma, Pariya Yousefi, et al.
Journal of Human Immunity|June 1, 2026
Human germline biallelic loss-of-function <i>OSMR</i> variants cause severe allergic diseaseSimran Samra, Mehul Sharma, Julia Körholz, et al.
The Journal of Experimental Medicine|March 7, 2023
Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumoniaAna García-García, Rebeca Pérez de Diego, Carlos Flores, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Journal of Clinical Immunology|April 28, 2025
A Germline Heterozygous Dominant Negative IKZF2 Variant Causing Syndromic Primary Immune Regulatory Disorder and ICHADHenry Y Lu, Maryam Vaseghi-Shanjani, Avery J Lam, et al.
Journal of Medical Genetics|June 14, 2023
Dominant negative variants in <i>IKZF2</i> cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delayArezoo Mohajeri, Maryam Vaseghi-Shanjani, Jill A Rosenfeld, et al.
Pediatric Rheumatology Online Journal|February 16, 2019
Calm in the midst of cytokine storm: a collaborative approach to the diagnosis and treatment of hemophagocytic lymphohistiocytosis and macrophage activation syndromeOlha Halyabar, Margaret H Chang, Michelle L Schoettler, et al.
JCI Insight|December 22, 2022
Human JAK1 gain of function causes dysregulated myelopoeisis and severe allergic inflammationCatherine M Biggs, Anna Cordeiro-Santanach, Sergey V Prykhozhij, et al.
Cell|December 22, 2023
Sensory neurons promote immune homeostasis in the lungMasato Tamari, Kate L Del Bel, Aaron M Ver Heul, et al.
Medrxiv : the Preprint Server for Health Sciences|September 19, 2025
Human germline biallelic loss-of-function <i>OSMR</i> variants cause severe allergic diseaseMehul Sharma, Simran Samra, Yihui Liu, et al.
Journal of Human Immunity|November 26, 2025
Novel genotypes, phenotypes, and triggers in humans with OTULIN haploinsufficiencyTristan J van der Linden, Rob J W Arts, Catherine M Biggs, et al.
The Journal of Experimental Medicine|July 31, 2025
ASXL1 deficiency causes epigenetic dysfunction, combined immunodeficiency, and EBV-associated lymphomaMaggie P Fu, Mehul Sharma, Pariya Yousefi, et al.
Journal of Human Immunity|June 1, 2026
Human germline biallelic loss-of-function <i>OSMR</i> variants cause severe allergic diseaseSimran Samra, Mehul Sharma, Julia Körholz, et al.
The Journal of Experimental Medicine|March 7, 2023
Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumoniaAna García-García, Rebeca Pérez de Diego, Carlos Flores, et al.
Pageof 5