These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
189 related articles for article (PubMed ID: 24973446)
21. Not All SCID Pigs Are Created Equally: Two Independent Mutations in the Artemis Gene Cause SCID in Pigs. Waide EH; Dekkers JC; Ross JW; Rowland RR; Wyatt CR; Ewen CL; Evans AB; Thekkoot DM; Boddicker NJ; Serão NV; Ellinwood NM; Tuggle CK J Immunol; 2015 Oct; 195(7):3171-9. PubMed ID: 26320255 [TBL] [Abstract][Full Text] [Related]
22. IL7R and RAG1/2 genes mutations/polymorphisms in patients with SCID. Safaei S; Pourpak Z; Moin M; Houshmand M Iran J Allergy Asthma Immunol; 2011 Jun; 10(2):129-32. PubMed ID: 21625022 [TBL] [Abstract][Full Text] [Related]
23. Detection of RAG mutations and prenatal diagnosis in families presenting with either T-B- severe combined immunodeficiency or Omenn's syndrome. Tabori U; Mark Z; Amariglio N; Etzioni A; Golan H; Biloray B; Toren A; Rechavi G; Dalal I Clin Genet; 2004 Apr; 65(4):322-6. PubMed ID: 15025726 [TBL] [Abstract][Full Text] [Related]
24. Similar recombination-activating gene (RAG) mutations result in similar immunobiological effects but in different clinical phenotypes. IJspeert H; Driessen GJ; Moorhouse MJ; Hartwig NG; Wolska-Kusnierz B; Kalwak K; Pituch-Noworolska A; Kondratenko I; van Montfrans JM; Mejstrikova E; Lankester AC; Langerak AW; van Gent DC; Stubbs AP; van Dongen JJ; van der Burg M J Allergy Clin Immunol; 2014 Apr; 133(4):1124-33. PubMed ID: 24418478 [TBL] [Abstract][Full Text] [Related]
25. The immunophenotypic and immunogenotypic B-cell differentiation arrest in bone marrow of RAG-deficient SCID patients corresponds to residual recombination activities of mutated RAG proteins. Noordzij JG; de Bruin-Versteeg S; Verkaik NS; Vossen JM; de Groot R; Bernatowska E; Langerak AW; van Gent DC; van Dongen JJ Blood; 2002 Sep; 100(6):2145-52. PubMed ID: 12200379 [TBL] [Abstract][Full Text] [Related]
26. Fetal bone engraftment reconstitutes the immune system in pigs with severe combined immunodeficiency. Monarch K; Yoon J; Uh K; Reese E; Restrepo DC; de Carvalho Madrid DM; Touchard L; Spate LD; Samuel MS; Driver JP; Lim JH; Schlink S; Whitworth KM; Wells KD; Prather RS; Chen PR; Lee K Lab Anim (NY); 2024 Oct; 53(10):276-286. PubMed ID: 39289566 [TBL] [Abstract][Full Text] [Related]
27. Development of Zhao H; Ye W; Guo J; Wang J; Jiao D; Xu K; Yang C; Chen S; Jamal MA; Bai Z; Wei T; Cai J; Nguyen TD; Qing Y; Cheng W; Jia B; Li H; Zhao HY; Chen Q; Wei HJ Front Immunol; 2022; 13():950194. PubMed ID: 36032112 [TBL] [Abstract][Full Text] [Related]
28. [Omenn Syndrome and DNA recombination defects]. Yachie A Nihon Rinsho Meneki Gakkai Kaishi; 2017; 40(3):179-189. PubMed ID: 28747605 [TBL] [Abstract][Full Text] [Related]
29. Recombination-activating gene 1 (Rag1)-deficient mice with severe combined immunodeficiency treated with lentiviral gene therapy demonstrate autoimmune Omenn-like syndrome. van Til NP; Sarwari R; Visser TP; Hauer J; Lagresle-Peyrou C; van der Velden G; Malshetty V; Cortes P; Jollet A; Danos O; Cassani B; Zhang F; Thrasher AJ; Fontana E; Poliani PL; Cavazzana M; Verstegen MM; Villa A; Wagemaker G J Allergy Clin Immunol; 2014 Apr; 133(4):1116-23. PubMed ID: 24332219 [TBL] [Abstract][Full Text] [Related]
30. Long-Term Health Outcome and Quality of Life Post-HSCT for IL7Rα-, Artemis-, RAG1- and RAG2-Deficient Severe Combined Immunodeficiency: a Single Center Report. Abd Hamid IJ; Slatter MA; McKendrick F; Pearce MS; Gennery AR J Clin Immunol; 2018 Aug; 38(6):727-732. PubMed ID: 30105620 [TBL] [Abstract][Full Text] [Related]
31. Efficient production of biallelic GGTA1 knockout pigs by cytoplasmic microinjection of CRISPR/Cas9 into zygotes. Petersen B; Frenzel A; Lucas-Hahn A; Herrmann D; Hassel P; Klein S; Ziegler M; Hadeler KG; Niemann H Xenotransplantation; 2016 Sep; 23(5):338-46. PubMed ID: 27610605 [TBL] [Abstract][Full Text] [Related]
32. Immune dysregulation in patients with RAG deficiency and other forms of combined immune deficiency. Delmonte OM; Villa A; Notarangelo LD Blood; 2020 Feb; 135(9):610-619. PubMed ID: 31942628 [TBL] [Abstract][Full Text] [Related]
33. Increased and prolonged human norovirus infection in RAG2/IL2RG deficient gnotobiotic pigs with severe combined immunodeficiency. Lei S; Ryu J; Wen K; Twitchell E; Bui T; Ramesh A; Weiss M; Li G; Samuel H; Clark-Deener S; Jiang X; Lee K; Yuan L Sci Rep; 2016 Apr; 6():25222. PubMed ID: 27118081 [TBL] [Abstract][Full Text] [Related]
34. Signal joint formation is inhibited in murine scid preB cells and fibroblasts in substrates with homopolymeric coding ends. Sun T; Ezekiel UR; Erskine L; Agulo R; Bozek G; Roth D; Storb U Mol Immunol; 1999 Jun; 36(8):551-8. PubMed ID: 10475610 [TBL] [Abstract][Full Text] [Related]
35. Novel RAG1 mutation and the occurrence of mycobacterial and Chromobacterium violaceum infections in a case of leaky SCID. Khan TA; Iqbal A; Rahman H; Cabral-Marques O; Ishfaq M; Muhammad N Microb Pathog; 2017 Aug; 109():114-119. PubMed ID: 28552805 [TBL] [Abstract][Full Text] [Related]
36. Collaboration of RAG2 with RAG1-like proteins during the evolution of V(D)J recombination. Carmona LM; Fugmann SD; Schatz DG Genes Dev; 2016 Apr; 30(8):909-17. PubMed ID: 27056670 [TBL] [Abstract][Full Text] [Related]
37. Correction of murine Rag1 deficiency by self-inactivating lentiviral vector-mediated gene transfer. Pike-Overzet K; Rodijk M; Ng YY; Baert MR; Lagresle-Peyrou C; Schambach A; Zhang F; Hoeben RC; Hacein-Bey-Abina S; Lankester AC; Bredius RG; Driessen GJ; Thrasher AJ; Baum C; Cavazzana-Calvo M; van Dongen JJ; Staal FJ Leukemia; 2011 Sep; 25(9):1471-83. PubMed ID: 21617701 [TBL] [Abstract][Full Text] [Related]
38. [Clinical phenotype and gene diagnostic analysis of Omenn syndrome]. Wang YQ; Cui YX; Feng J Zhonghua Er Ke Za Zhi; 2013 Jan; 51(1):64-8. PubMed ID: 23527934 [TBL] [Abstract][Full Text] [Related]
39. Homozygous deletion of RAG1, RAG2 and 5' region TRAF6 causes severe immune suppression and atypical osteopetrosis. Weisz Hubshman M; Basel-Vanagaite L; Krauss A; Konen O; Levy Y; Garty BZ; Smirin-Yosef P; Maya I; Lagovsky I; Taub E; Marom D; Gaash D; Shichrur K; Avigad S; Hayman-Manzur L; Villa A; Sobacchi C; Shohat M; Yaniv I; Stein J Clin Genet; 2017 Jun; 91(6):902-907. PubMed ID: 27808398 [TBL] [Abstract][Full Text] [Related]