de Chasseval R - Search Results

1

Severe combined immunodeficiency and microcephaly in siblings with hypomorphic mutations in DNA ligase IV.

Buck D, Moshous D, de Chasseval R, Ma Y, le Deist F, Cavazzana-Calvo M, Fischer A, Casanova JL, Lieber MR, de Villartay JP. Buck D, et al. Among authors: de chasseval r. Eur J Immunol. 2006 Jan;36(1):224-35. doi: 10.1002/eji.200535401. Eur J Immunol. 2006. PMID: 16358361 Free article.

2

Human and animal models of V(D)J recombination deficiency.

de Villartay JP, Poinsignon C, de Chasseval R, Buck D, Le Guyader G, Villey I. de Villartay JP, et al. Among authors: de chasseval r. Curr Opin Immunol. 2003 Oct;15(5):592-8. doi: 10.1016/s0952-7915(03)00101-8. Curr Opin Immunol. 2003. PMID: 14499270 Review.

3

Phosphorylation of Artemis following irradiation-induced DNA damage.

Poinsignon C, de Chasseval R, Soubeyrand S, Moshous D, Fischer A, Haché RJ, de Villartay JP. Poinsignon C, et al. Among authors: de chasseval r. Eur J Immunol. 2004 Nov;34(11):3146-55. doi: 10.1002/eji.200425455. Eur J Immunol. 2004. PMID: 15468306 Free article.

4

Cernunnos, a novel nonhomologous end-joining factor, is mutated in human immunodeficiency with microcephaly.

Buck D, Malivert L, de Chasseval R, Barraud A, Fondanèche MC, Sanal O, Plebani A, Stéphan JL, Hufnagel M, le Deist F, Fischer A, Durandy A, de Villartay JP, Revy P. Buck D, et al. Among authors: de chasseval r. Cell. 2006 Jan 27;124(2):287-99. doi: 10.1016/j.cell.2005.12.030. Cell. 2006. PMID: 16439204 Free article.

5

Functional characterization of the promoter for the human germ-line T cell receptor J alpha (TEA) transcript.

de Chasseval R, de Villartay JP. de Chasseval R, et al. Among authors: de villartay jp. Eur J Immunol. 1993 Jun;23(6):1294-8. doi: 10.1002/eji.1830230616. Eur J Immunol. 1993. PMID: 8388796

6

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. Nicolas N, et al. Among authors: de villartay jp, de chasseval r. J Exp Med. 1998 Aug 17;188(4):627-34. doi: 10.1084/jem.188.4.627. J Exp Med. 1998. PMID: 9705945 Free PMC article.

7

Three-dimensional clustering of human RAG2 gene mutations in severe combined immune deficiency.

Corneo B, Moshous D, Callebaut I, de Chasseval R, Fischer A, de Villartay JP. Corneo B, et al. Among authors: de chasseval r. J Biol Chem. 2000 Apr 28;275(17):12672-5. doi: 10.1074/jbc.275.17.12672. J Biol Chem. 2000. PMID: 10777560 Free article.

8

Artemis, a novel DNA double-strand break repair/V(D)J recombination protein, is mutated in human severe combined immune deficiency.

Moshous D, Callebaut I, de Chasseval R, Corneo B, Cavazzana-Calvo M, Le Deist F, Tezcan I, Sanal O, Bertrand Y, Philippe N, Fischer A, de Villartay JP. Moshous D, et al. Among authors: de chasseval r. Cell. 2001 Apr 20;105(2):177-86. doi: 10.1016/s0092-8674(01)00309-9. Cell. 2001. PMID: 11336668 Free article.

9

The V(D)J recombination/DNA repair factor artemis belongs to the metallo-beta-lactamase family and constitutes a critical developmental checkpoint of the lymphoid system.

Moshous D, Callebaut I, de Chasseval R, Poinsignon C, Villey I, Fischer A, de Villartay JP. Moshous D, et al. Among authors: de chasseval r. Ann N Y Acad Sci. 2003 Apr;987:150-7. doi: 10.1111/j.1749-6632.2003.tb06043.x. Ann N Y Acad Sci. 2003. PMID: 12727634 Review.

10

The differentiation of human pro-thymocytes along the TCR-alpha/beta pathway in vitro is accompanied by the site-specific deletion of the TCR-delta locus.

de Villartay JP, Mossalayi D, de Chasseval R, Dalloul A, Debré P. de Villartay JP, et al. Among authors: de chasseval r. Int Immunol. 1991 Dec;3(12):1301-5. doi: 10.1093/intimm/3.12.1301. Int Immunol. 1991. PMID: 1838004

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