Similar articles for PMID: 8810255

Year	Number of Results
1990	1
1991	2
1992	1
1993	4
1994	4
1995	4
1996	5
1997	3
1998	2
1999	1
2000	6
2001	8
2002	5
2003	2
2004	2
2005	6
2006	2
2007	2
2008	2
2009	5
2010	3
2011	4
2012	2
2013	2
2014	8
2015	4
2016	4
2017	4
2018	5
2019	8
2020	7
2021	2
2023	1
2024	0

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. Schwarz K, et al. Science. 1996 Oct 4;274(5284):97-9. doi: 10.1126/science.274.5284.97. Science. 1996. PMID: 8810255

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. Noordzij JG, et al. Blood. 2002 Sep 15;100(6):2145-52. Blood. 2002. PMID: 12200379 Free article.

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. Li W, et al. Mol Cell Biol. 2001 Jun;21(12):3935-46. doi: 10.1128/MCB.21.12.3935-3946.2001. Mol Cell Biol. 2001. PMID: 11359901 Free PMC article.

4

Recombinase deficiency in mouse and man.

Schwarz K, Hansen-Hagge TE, Bartram CR. Schwarz K, et al. Immunodeficiency. 1993;4(1-4):249-52. Immunodeficiency. 1993. PMID: 8167711 No abstract available.

5

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. Agematsu K, et al. Clin Exp Immunol. 2001 Jun;124(3):461-4. doi: 10.1046/j.1365-2249.2001.01553.x. Clin Exp Immunol. 2001. PMID: 11472408 Free PMC article.

6

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. Meshaal SS, et al. Clin Exp Immunol. 2019 Feb;195(2):202-212. doi: 10.1111/cei.13222. Epub 2018 Nov 4. Clin Exp Immunol. 2019. PMID: 30307608 Free PMC article.

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. Noordzij JG, et al. Blood. 2003 Feb 15;101(4):1446-52. doi: 10.1182/blood-2002-01-0187. Epub 2002 Oct 24. Blood. 2003. PMID: 12406895 Free article.

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. Tabori U, et al. Clin Genet. 2004 Apr;65(4):322-6. doi: 10.1111/j.1399-0004.2004.00227.x. Clin Genet. 2004. PMID: 15025726

9

Omenn syndrome in the context of other B cell-negative severe combined immunodeficiencies.

Villa A, Sobacchi C, Vezzoni P. Villa A, et al. Isr Med Assoc J. 2002 Mar;4(3):218-21. Isr Med Assoc J. 2002. PMID: 11908269 Free article. Review.

10

Human RAG mutations: biochemistry and clinical implications.

Notarangelo LD, Kim MS, Walter JE, Lee YN. Notarangelo LD, et al. Nat Rev Immunol. 2016 Apr;16(4):234-46. doi: 10.1038/nri.2016.28. Epub 2016 Mar 21. Nat Rev Immunol. 2016. PMID: 26996199 Free PMC article. Review.

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