Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Infection and RAG1[original query] |
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| Mutations in genes required for T-cell development: IL7R, CD45, IL2RG, JAK3, RAG1, RAG2, ARTEMIS, and ADA and severe combined immunodeficiency: HuGE review. Genetics in medicine : official journal of the American College of Medical Genetics 0 6 (1): 16-26. Kalman Lisa, Lindegren Mary Lou, Kobrynski Lisa, Vogt Robert, Hannon Harry, Howard Joelyn Tonkin, Buckley Rebec |
| GvHD-associated cytokine polymorphisms do not associate with Omenn syndrome rather than T-B- SCID in patients with defects in RAG genes. Clinical immunology (Orlando, Fla.) 2007 Aug 124 (2): 165-9. Haq Iram J, Steinberg Laura J, Hoenig Manfred, van der Burg Mirjam, Villa Anna, Cant Andrew J, Middleton Peter G, Gennery Andrew |
| Clinical and Laboratory Factors Affecting the Prognosis of Severe Combined Immunodeficiency. Journal of clinical immunology 2022 4 42 (5): 1036-1050. Ozturk Elif, Catak Mehmet Cihangir, Kiykim Ayca, Baser Dilek, Bilgic Eltan Sevgi, Yalcin Koray, Kasap Nurhan, Nain Ercan, Bulutoglu Alper, Akgun Gamze, Can Yasemin, Sefer Asena Pinar, Babayeva Royala, Caki-Kilic Suar, Tezcan Karasu Gulsun, Yesilipek Akif, Ozen Ahmet, Karakoc-Aydiner Elif, Baris Sa |
| Hypomorphic RAG deficiency: impact of disease burden on survival and thymic recovery argues for early diagnosis and HSCT. Blood 2022 10 . Schuetz C, Gerke J, Ege M, Walter J, Kusters M, Worth A, Kanakry J A, Dimitrova D, Wolska-Ku?nierz B, Chen K, Unal E, Karakukcu M, Pashchenko O, Leiding J, Kawai T, Amrolia P J, Berghuis D, Buechner J, Buchbinder D, Cowan M J, Gennery A R, Güngör T, Heimall J, Miano M, Meyts I, Morris E C, Rivière J, Sharapova S O, Shaw P J, Slatter M, Honig M, Veys P, Fischer A, Cavazzana M, Moshous D, Schulz A, Albert M H, Puck J M, Lankester A C, Notarangelo L D, Neven |
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