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.
318 related articles for article (PubMed ID: 8810255)
1. RAG mutations in human B cell-negative SCID. Schwarz K; Gauss GH; Ludwig L; Pannicke U; Li Z; Lindner D; Friedrich W; Seger RA; Hansen-Hagge TE; Desiderio S; Lieber MR; Bartram CR Science; 1996 Oct; 274(5284):97-9. PubMed ID: 8810255 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. Rag-1 mutations associated with B-cell-negative scid dissociate the nicking and transesterification steps of V(D)J recombination. Li W; Chang FC; Desiderio S Mol Cell Biol; 2001 Jun; 21(12):3935-46. PubMed ID: 11359901 [TBL] [Abstract][Full Text] [Related]
4. Phenotypical heterogeneity in RAG-deficient patients from a highly consanguineous population. Meshaal SS; El Hawary RE; Abd Elaziz DS; Eldash A; Alkady R; Lotfy S; Mauracher AA; Opitz L; Pachlopnik Schmid J; van der Burg M; Chou J; Galal NM; Boutros JA; Geha R; Elmarsafy AM Clin Exp Immunol; 2019 Feb; 195(2):202-212. PubMed ID: 30307608 [TBL] [Abstract][Full Text] [Related]
6. Complete arrest from pro- to pre-B cells in a case of B cell-negative severe combined immunodeficiency (SCID) without recombinase activating gene (RAG) mutations. Agematsu K; Nagumo H; Hokibara S; Mori T; Wada T; Yachie A; Kanegane H; Miyawaki T; Sugita K; Karasuyama H; Komiyama A Clin Exp Immunol; 2001 Jun; 124(3):461-4. PubMed ID: 11472408 [TBL] [Abstract][Full Text] [Related]
7. Radiosensitive SCID patients with Artemis gene mutations show a complete B-cell differentiation arrest at the pre-B-cell receptor checkpoint in bone marrow. Noordzij JG; Verkaik NS; van der Burg M; van Veelen LR; de Bruin-Versteeg S; Wiegant W; Vossen JM; Weemaes CM; de Groot R; Zdzienicka MZ; van Gent DC; van Dongen JJ Blood; 2003 Feb; 101(4):1446-52. PubMed ID: 12406895 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Omenn syndrome in the context of other B cell-negative severe combined immunodeficiencies. Villa A; Sobacchi C; Vezzoni P Isr Med Assoc J; 2002 Mar; 4(3):218-21. PubMed ID: 11908269 [TBL] [Abstract][Full Text] [Related]
10. Human RAG mutations: biochemistry and clinical implications. Notarangelo LD; Kim MS; Walter JE; Lee YN Nat Rev Immunol; 2016 Apr; 16(4):234-46. PubMed ID: 26996199 [TBL] [Abstract][Full Text] [Related]
11. Clinical, immunologic, and genetic characteristics of RAG mutations in 15 Chinese patients with SCID and Omenn syndrome. Bai X; Liu J; Zhang Z; Liu C; Zhang Y; Tang W; Dai R; Wu J; Tang X; Zhang Y; Ding Y; Jiang L; Zhao X Immunol Res; 2016 Apr; 64(2):497-507. PubMed ID: 26476733 [TBL] [Abstract][Full Text] [Related]
12. Recent advances in understanding RAG deficiencies. Gennery A F1000Res; 2019; 8():. PubMed ID: 30800289 [TBL] [Abstract][Full Text] [Related]
13. V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations. Villa A; Sobacchi C; Notarangelo LD; Bozzi F; Abinun M; Abrahamsen TG; Arkwright PD; Baniyash M; Brooks EG; Conley ME; Cortes P; Duse M; Fasth A; Filipovich AM; Infante AJ; Jones A; Mazzolari E; Muller SM; Pasic S; Rechavi G; Sacco MG; Santagata S; Schroeder ML; Seger R; Strina D; Ugazio A; Väliaho J; Vihinen M; Vogler LB; Ochs H; Vezzoni P; Friedrich W; Schwarz K Blood; 2001 Jan; 97(1):81-8. PubMed ID: 11133745 [TBL] [Abstract][Full Text] [Related]
14. A human severe combined immunodeficiency (SCID) condition with increased sensitivity to ionizing radiations and impaired V(D)J rearrangements defines a new DNA recombination/repair deficiency. Nicolas N; Moshous D; Cavazzana-Calvo M; Papadopoulo D; de Chasseval R; Le Deist F; Fischer A; de Villartay JP J Exp Med; 1998 Aug; 188(4):627-34. PubMed ID: 9705945 [TBL] [Abstract][Full Text] [Related]
15. Evidence for defects in V(D)J rearrangements in patients with severe combined immunodeficiency. Abe T; Tsuge I; Kamachi Y; Torii S; Utsumi K; Akahori Y; Ichihara Y; Kurosawa Y; Matsuoka H J Immunol; 1994 Jun; 152(11):5504-13. PubMed ID: 8189068 [TBL] [Abstract][Full Text] [Related]
16. Evolution of a T-B- SCID into an Omenn syndrome phenotype following parainfluenza 3 virus infection. Dalal I; Tabori U; Bielorai B; Golan H; Rosenthal E; Amariglio N; Rechavi G; Toren A Clin Immunol; 2005 Apr; 115(1):70-3. PubMed ID: 15870023 [TBL] [Abstract][Full Text] [Related]
17. More than just SCID--the phenotypic range of combined immunodeficiencies associated with mutations in the recombinase activating genes (RAG) 1 and 2. Niehues T; Perez-Becker R; Schuetz C Clin Immunol; 2010 May; 135(2):183-92. PubMed ID: 20172764 [TBL] [Abstract][Full Text] [Related]
18. GvHD-associated cytokine polymorphisms do not associate with Omenn syndrome rather than T-B- SCID in patients with defects in RAG genes. Haq IJ; Steinberg LJ; Hoenig M; van der Burg M; Villa A; Cant AJ; Middleton PG; Gennery AR Clin Immunol; 2007 Aug; 124(2):165-9. PubMed ID: 17572155 [TBL] [Abstract][Full Text] [Related]
19. Generation of recombination activating gene-1-deficient neonatal piglets: a model of T and B cell deficient severe combined immune deficiency. Ito T; Sendai Y; Yamazaki S; Seki-Soma M; Hirose K; Watanabe M; Fukawa K; Nakauchi H PLoS One; 2014; 9(12):e113833. PubMed ID: 25437445 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]