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Paper Details

NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease.
Mucosal Immunol
61
2018
Genetic defects, IBD, Mendelian disorder, NAPDH oxidase 1, NOX1, NOX1 SNP, NOX1 mutations, R287Q, VEOIBD, Y470H, cell lines, colonic crypts, inflammatory bowel disease, oxygen, p, patient, patient-derived colonic organoid cultures, patients, ulcerative colitis
Author NameAffiliation
Christopher G MathewKing's College London School of Medicine, Guy's Hospital London
Davis J McCarthy
Jennifer SambrookUniversity of Cambridge
Jennifer SambrookUniversity of Cambridge
Willem H OuwehandNIHR Blood and Transplant Research Unit in Donor Health and Genomics, University of Cambridge
Willem H OuwehandWellcome Trust Sanger Institute
Willem H Ouwehand
Willem H OuwehandUniversity of Cambridge
Willem H OuwehandNIHR Blood and Transplant Research Unit in Donor Health and Genomics, University of Cambridge
Willem H OuwehandUniversity of Cambridge
Willem H Ouwehand
Willem H OuwehandWellcome Trust Sanger Institute
John DaneshNIHR Blood and Transplant Research Unit in Donor Health and Genomics, University of Cambridge
John DaneshWellcome Trust Sanger Institute
John DaneshUniversity of Cambridge
Carl A AndersonWellcome Trust Sanger Institute
Richard H DuerrUniversity of Pittsburgh School of Medicine
Richard H DuerrUniversity of Pittsburgh Graduate School of Public Health
Dermot P B McGovernF. Widjaja Foundation Inflammatory Bowel and Immunobiology Research Institute, Cedars-Sinai Medical Center
Dermot P B McGovernF. Widjaja Foundation Inflammatory Bowel and Immunobiology Research Institute, Cedars-Sinai Medical Center
Judy H ChoIcahn School of Medicine, Mount Sinai Hospital
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