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Dylan Lawless

Showing results (11-20 of 21) with videos related to

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Elife|December 15, 2021
Biallelic mutations in <i>calcium release activated channel regulator 2A (CRACR2A</i>) cause a primary immunodeficiency disorderBeibei Wu, Laura Rice, Jennifer Shrimpton, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|September 24, 2020
A Novel RELA Truncating Mutation in a Familial Behçet's Disease-like Mucocutaneous Ulcerative ConditionFahd Adeeb, Emma R Dorris, Niamh E Morgan, et al.
Journal of Clinical Immunology|December 21, 2019
Expanding Clinical Phenotype and Novel Insights into the Pathogenesis of ICOS DeficiencyHassan Abolhassani, Yasser M El-Sherbiny, Gururaj Arumugakani, et al.
The Journal of Infectious Diseases|November 14, 2022
Viral Genetic Determinants of Prolonged Respiratory Syncytial Virus Infection Among Infants in a Healthy Term Birth CohortDylan Lawless, Christopher G McKennan, Suman R Das, et al.
Scientific Reports|April 21, 2021
Author Correction: The influence of human genetic variation on Epstein-Barr virus sequence diversitySina Rüeger, Christian Hammer, Alexis Loetscher, et al.
Scientific Reports|February 26, 2021
The influence of human genetic variation on Epstein-Barr virus sequence diversitySina Rüeger, Christian Hammer, Alexis Loetscher, et al.
American Journal of Human Genetics|May 15, 2024
Joint host-pathogen genomic analysis identifies hepatitis B virus mutations associated with human NTCP and HLA class I variationZhi Ming Xu, Gnimah Eva Gnouamozi, Sina Rüeger, et al.
Ebiomedicine|June 4, 2026
Genome-wide association study of paediatric bacteraemia and sepsisDylan Lawless, Flavia Aurelia Hodel, Christian W Thorball, et al.
Blood|June 11, 2020
Germline TET2 loss of function causes childhood immunodeficiency and lymphomaJarmila Stremenova Spegarova, Dylan Lawless, Siti Mardhiana Binti Mohamad, et al.
Science Translational Medicine|April 1, 2016
Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activationSeth L Masters, Vasiliki Lagou, Isabelle Jéru, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Elife|December 15, 2021
Biallelic mutations in <i>calcium release activated channel regulator 2A (CRACR2A</i>) cause a primary immunodeficiency disorderBeibei Wu, Laura Rice, Jennifer Shrimpton, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|September 24, 2020
A Novel RELA Truncating Mutation in a Familial Behçet's Disease-like Mucocutaneous Ulcerative ConditionFahd Adeeb, Emma R Dorris, Niamh E Morgan, et al.
Journal of Clinical Immunology|December 21, 2019
Expanding Clinical Phenotype and Novel Insights into the Pathogenesis of ICOS DeficiencyHassan Abolhassani, Yasser M El-Sherbiny, Gururaj Arumugakani, et al.
The Journal of Infectious Diseases|November 14, 2022
Viral Genetic Determinants of Prolonged Respiratory Syncytial Virus Infection Among Infants in a Healthy Term Birth CohortDylan Lawless, Christopher G McKennan, Suman R Das, et al.
Scientific Reports|April 21, 2021
Author Correction: The influence of human genetic variation on Epstein-Barr virus sequence diversitySina Rüeger, Christian Hammer, Alexis Loetscher, et al.
Scientific Reports|February 26, 2021
The influence of human genetic variation on Epstein-Barr virus sequence diversitySina Rüeger, Christian Hammer, Alexis Loetscher, et al.
American Journal of Human Genetics|May 15, 2024
Joint host-pathogen genomic analysis identifies hepatitis B virus mutations associated with human NTCP and HLA class I variationZhi Ming Xu, Gnimah Eva Gnouamozi, Sina Rüeger, et al.
Ebiomedicine|June 4, 2026
Genome-wide association study of paediatric bacteraemia and sepsisDylan Lawless, Flavia Aurelia Hodel, Christian W Thorball, et al.
Blood|June 11, 2020
Germline TET2 loss of function causes childhood immunodeficiency and lymphomaJarmila Stremenova Spegarova, Dylan Lawless, Siti Mardhiana Binti Mohamad, et al.
Science Translational Medicine|April 1, 2016
Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activationSeth L Masters, Vasiliki Lagou, Isabelle Jéru, et al.
Pageof 3