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K Chinn

Showing results (91-100 of 135) with videos related to

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The Journal of Allergy and Clinical Immunology|January 3, 2017
Update on the use of immunoglobulin in human disease: A review of evidenceElena E Perez, Jordan S Orange, Francisco Bonilla, et al.
The Journal of Allergy and Clinical Immunology. in Practice|September 15, 2019
Immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome with NK dysfunction and EBV-driven malignancy treated with stem cell transplantationCaitlin M Burk, Kara E Coffey, Emily M Mace, et al.
Blood|October 28, 2010
First use of thymus transplantation therapy for FOXN1 deficiency (nude/SCID): a report of 2 casesM Louise Markert, José G Marques, Bénédicte Neven, et al.
Biorxiv : the Preprint Server for Biology|November 18, 2024
VizCNV: An integrated platform for concurrent phased BAF and CNV analysis with trio genome sequencing dataHaowei Du, Ming Yin Lun, Lidiia Gagarina, et al.
Journal of Clinical Immunology|January 17, 2023
Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic DevelopmentPeter J Mustillo, Kathleen E Sullivan, Ivan K Chinn, et al.
Journal of Clinical Immunology|January 22, 2024
Correction to: Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic DevelopmentPeter J Mustillo, Kathleen E Sullivan, Ivan K Chinn, et al.
The Journal of Allergy and Clinical Immunology. in Practice|July 1, 2020
Intralesional Corticosteroids as Adjunctive Therapy for Refractory Cutaneous Lesions in Chronic Granulomatous DiseaseMichelle Joseph, Wai-Tim Chew, Filiz Seeborg, et al.
American Journal of Human Genetics|July 24, 2018
Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function AllelesZeynep Coban-Akdemir, Janson J White, Xiaofei Song, et al.
Science Signaling|July 28, 2021
Short stature and combined immunodeficiency associated with mutations in RGS10Ivan K Chinn, Zhihui Xie, Eunice C Chan, et al.
The Journal of Allergy and Clinical Immunology|January 14, 2018
Mutations in PI3K110δ cause impaired natural killer cell function partially rescued by rapamycin treatmentRaquel Ruiz-García, Alexander Vargas-Hernández, Ivan K Chinn, et al.
Pageof 14

Showing results (91-100 of 135) with videos related to

Sort By:
Pageof 14
The Journal of Allergy and Clinical Immunology|January 3, 2017
Update on the use of immunoglobulin in human disease: A review of evidenceElena E Perez, Jordan S Orange, Francisco Bonilla, et al.
The Journal of Allergy and Clinical Immunology. in Practice|September 15, 2019
Immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome with NK dysfunction and EBV-driven malignancy treated with stem cell transplantationCaitlin M Burk, Kara E Coffey, Emily M Mace, et al.
Blood|October 28, 2010
First use of thymus transplantation therapy for FOXN1 deficiency (nude/SCID): a report of 2 casesM Louise Markert, José G Marques, Bénédicte Neven, et al.
Biorxiv : the Preprint Server for Biology|November 18, 2024
VizCNV: An integrated platform for concurrent phased BAF and CNV analysis with trio genome sequencing dataHaowei Du, Ming Yin Lun, Lidiia Gagarina, et al.
Journal of Clinical Immunology|January 17, 2023
Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic DevelopmentPeter J Mustillo, Kathleen E Sullivan, Ivan K Chinn, et al.
Journal of Clinical Immunology|January 22, 2024
Correction to: Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic DevelopmentPeter J Mustillo, Kathleen E Sullivan, Ivan K Chinn, et al.
The Journal of Allergy and Clinical Immunology. in Practice|July 1, 2020
Intralesional Corticosteroids as Adjunctive Therapy for Refractory Cutaneous Lesions in Chronic Granulomatous DiseaseMichelle Joseph, Wai-Tim Chew, Filiz Seeborg, et al.
American Journal of Human Genetics|July 24, 2018
Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function AllelesZeynep Coban-Akdemir, Janson J White, Xiaofei Song, et al.
Science Signaling|July 28, 2021
Short stature and combined immunodeficiency associated with mutations in RGS10Ivan K Chinn, Zhihui Xie, Eunice C Chan, et al.
The Journal of Allergy and Clinical Immunology|January 14, 2018
Mutations in PI3K110δ cause impaired natural killer cell function partially rescued by rapamycin treatmentRaquel Ruiz-García, Alexander Vargas-Hernández, Ivan K Chinn, et al.
Pageof 14