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K Chinn

Showing results (81-90 of 135) with videos related to

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Frontiers in Immunology|June 13, 2017
Novel Combined Immune Deficiency and Radiation Sensitivity Blended Phenotype in an Adult with Biallelic Variations in <i>ZAP70</i> and <i>RNF168</i>Ivan K Chinn, Robert P Sanders, Asbjørg Stray-Pedersen, et al.
Biorxiv : the Preprint Server for Biology|March 23, 2026
Autosomal dominant CDC45 deficiency with allelic expression bias causes a novel genetic disease of the immune systemNicole C Guilz, Yong-Oon Ahn, Seungmae Seo, et al.
The Journal of Allergy and Clinical Immunology|August 20, 2022
FOXI3 haploinsufficiency contributes to low T-cell receptor excision circles and T-cell lymphopeniaRajarshi Ghosh, Marita Bosticardo, Sunita Singh, et al.
Frontiers in Pediatrics|June 7, 2021
Immune Dysregulation Mimicking Systemic Lupus Erythematosus in a Patient With Lysinuric Protein Intolerance: Case Report and Review of the LiteratureJosefina Longeri Contreras, Mabel A Ladino, Katherine Aránguiz, et al.
Frontiers in Pediatrics|August 17, 2019
Novel Heterozygous Mutation in <i>NFKB2</i> Is Associated With Early Onset CVID and a Functional Defect in NK Cells Complicated by Disseminated CMV Infection and Severe Nephrotic SyndromeAlejandra Aird, Macarena Lagos, Alexander Vargas-Hernández, et al.
JCI Insight|November 8, 2022
Partial loss-of-function mutations in GINS4 lead to NK cell deficiency with neutropeniaMatilde I Conte, M Cecilia Poli, Angelo Taglialatela, et al.
Blood|February 8, 2007
Review of 54 patients with complete DiGeorge anomaly enrolled in protocols for thymus transplantation: outcome of 44 consecutive transplantsM Louise Markert, Blythe H Devlin, Marilyn J Alexieff, et al.
The Journal of Allergy and Clinical Immunology|March 28, 2016
Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorderMichael D Keller, Rahul Pandey, Dong Li, et al.
Cell Reports|January 15, 2025
The Golgi complex governs natural killer cell lytic granule positioning to promote directionality in cytotoxicityLuis A Pedroza, Frederique van den Haak, Alexander Frumovitz, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|March 2, 2025
Accuracy of bead-based epitope assay testing for peanut allergy diagnosis: Real-world pediatric population studyJessica M Palmieri, Vibha Szafron, Melissa Hearrell, et al.
Pageof 14

Showing results (81-90 of 135) with videos related to

Sort By:
Pageof 14
Frontiers in Immunology|June 13, 2017
Novel Combined Immune Deficiency and Radiation Sensitivity Blended Phenotype in an Adult with Biallelic Variations in <i>ZAP70</i> and <i>RNF168</i>Ivan K Chinn, Robert P Sanders, Asbjørg Stray-Pedersen, et al.
Biorxiv : the Preprint Server for Biology|March 23, 2026
Autosomal dominant CDC45 deficiency with allelic expression bias causes a novel genetic disease of the immune systemNicole C Guilz, Yong-Oon Ahn, Seungmae Seo, et al.
The Journal of Allergy and Clinical Immunology|August 20, 2022
FOXI3 haploinsufficiency contributes to low T-cell receptor excision circles and T-cell lymphopeniaRajarshi Ghosh, Marita Bosticardo, Sunita Singh, et al.
Frontiers in Pediatrics|June 7, 2021
Immune Dysregulation Mimicking Systemic Lupus Erythematosus in a Patient With Lysinuric Protein Intolerance: Case Report and Review of the LiteratureJosefina Longeri Contreras, Mabel A Ladino, Katherine Aránguiz, et al.
Frontiers in Pediatrics|August 17, 2019
Novel Heterozygous Mutation in <i>NFKB2</i> Is Associated With Early Onset CVID and a Functional Defect in NK Cells Complicated by Disseminated CMV Infection and Severe Nephrotic SyndromeAlejandra Aird, Macarena Lagos, Alexander Vargas-Hernández, et al.
JCI Insight|November 8, 2022
Partial loss-of-function mutations in GINS4 lead to NK cell deficiency with neutropeniaMatilde I Conte, M Cecilia Poli, Angelo Taglialatela, et al.
Blood|February 8, 2007
Review of 54 patients with complete DiGeorge anomaly enrolled in protocols for thymus transplantation: outcome of 44 consecutive transplantsM Louise Markert, Blythe H Devlin, Marilyn J Alexieff, et al.
The Journal of Allergy and Clinical Immunology|March 28, 2016
Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorderMichael D Keller, Rahul Pandey, Dong Li, et al.
Cell Reports|January 15, 2025
The Golgi complex governs natural killer cell lytic granule positioning to promote directionality in cytotoxicityLuis A Pedroza, Frederique van den Haak, Alexander Frumovitz, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|March 2, 2025
Accuracy of bead-based epitope assay testing for peanut allergy diagnosis: Real-world pediatric population studyJessica M Palmieri, Vibha Szafron, Melissa Hearrell, et al.
Pageof 14