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Showing results (331-340 of 357) with videos related to

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JAMA Pediatrics|October 12, 2020
Outcomes of Neonates Born to Mothers With Severe Acute Respiratory Syndrome Coronavirus 2 Infection at a Large Medical Center in New York CityDani Dumitriu, Ukachi N Emeruwa, Erin Hanft, et al.
The Journal of Experimental Medicine|April 2, 2024
Individuals with JAK1 variants are affected by syndromic features encompassing autoimmunity, atopy, colitis, and dermatitisMichael E Horesh, Marta Martin-Fernandez, Conor Gruber, et al.
The Journal of Allergy and Clinical Immunology|July 30, 2021
Genetic errors of immunity distinguish pediatric nonmalignant lymphoproliferative disordersLisa R Forbes, Olive S Eckstein, Nitya Gulati, et al.
The Journal of Clinical Investigation|July 19, 2016
Destabilized SMC5/6 complex leads to chromosome breakage syndrome with severe lung diseaseSaskia N van der Crabben, Marije P Hennus, Grant A McGregor, et al.
The Journal of Clinical Investigation|November 29, 2016
Biallelic mutations in IRF8 impair human NK cell maturation and functionEmily M Mace, Venetia Bigley, Justin T Gunesch, et al.
Nature Communications|April 21, 2015
Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cellsJin Li, Silje F Jørgensen, S Melkorka Maggadottir, et al.
Nature Communications|October 4, 2019
Publisher Correction: Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasisNina K Serwas, Birgit Hoeger, Rico C Ardy, et al.
Blood|April 11, 2018
Genetic and mechanistic diversity in pediatric hemophagocytic lymphohistiocytosisIvan K Chinn, Olive S Eckstein, Erin C Peckham-Gregory, et al.
Nature Communications|July 17, 2019
Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasisNina K Serwas, Birgit Hoeger, Rico C Ardy, et al.
Genome Medicine|March 23, 2017
Lessons learned from additional research analyses of unsolved clinical exome casesMohammad K Eldomery, Zeynep Coban-Akdemir, Tamar Harel, et al.
Pageof 36

Showing results (331-340 of 357) with videos related to

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Pageof 36
JAMA Pediatrics|October 12, 2020
Outcomes of Neonates Born to Mothers With Severe Acute Respiratory Syndrome Coronavirus 2 Infection at a Large Medical Center in New York CityDani Dumitriu, Ukachi N Emeruwa, Erin Hanft, et al.
The Journal of Experimental Medicine|April 2, 2024
Individuals with JAK1 variants are affected by syndromic features encompassing autoimmunity, atopy, colitis, and dermatitisMichael E Horesh, Marta Martin-Fernandez, Conor Gruber, et al.
The Journal of Allergy and Clinical Immunology|July 30, 2021
Genetic errors of immunity distinguish pediatric nonmalignant lymphoproliferative disordersLisa R Forbes, Olive S Eckstein, Nitya Gulati, et al.
The Journal of Clinical Investigation|July 19, 2016
Destabilized SMC5/6 complex leads to chromosome breakage syndrome with severe lung diseaseSaskia N van der Crabben, Marije P Hennus, Grant A McGregor, et al.
The Journal of Clinical Investigation|November 29, 2016
Biallelic mutations in IRF8 impair human NK cell maturation and functionEmily M Mace, Venetia Bigley, Justin T Gunesch, et al.
Nature Communications|April 21, 2015
Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cellsJin Li, Silje F Jørgensen, S Melkorka Maggadottir, et al.
Nature Communications|October 4, 2019
Publisher Correction: Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasisNina K Serwas, Birgit Hoeger, Rico C Ardy, et al.
Blood|April 11, 2018
Genetic and mechanistic diversity in pediatric hemophagocytic lymphohistiocytosisIvan K Chinn, Olive S Eckstein, Erin C Peckham-Gregory, et al.
Nature Communications|July 17, 2019
Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasisNina K Serwas, Birgit Hoeger, Rico C Ardy, et al.
Genome Medicine|March 23, 2017
Lessons learned from additional research analyses of unsolved clinical exome casesMohammad K Eldomery, Zeynep Coban-Akdemir, Tamar Harel, et al.
Pageof 36