Fischer A - Search Results

1

Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B-severe combined immune deficiency or Omenn syndrome.

Corneo B, Moshous D, Güngör T, Wulffraat N, Philippet P, Le Deist FL, Fischer A, de Villartay JP. Corneo B, et al. Among authors: fischer a. Blood. 2001 May 1;97(9):2772-6. doi: 10.1182/blood.v97.9.2772. Blood. 2001. PMID: 11313270 Free article.

2

Around the V(D)J recombinase machinery.

de Villartay JP, Rieux-Laucat F, Fischer A. de Villartay JP, et al. Among authors: fischer a. Res Immunol. 1994 Feb;145(2):151-4; discussion 155-8. doi: 10.1016/s0923-2494(94)80030-8. Res Immunol. 1994. PMID: 8079049 Review. No abstract available.

3

Highly restricted human T cell repertoire in peripheral blood and tissue-infiltrating lymphocytes in Omenn's syndrome.

Rieux-Laucat F, Bahadoran P, Brousse N, Selz F, Fischer A, Le Deist F, De Villartay JP. Rieux-Laucat F, et al. Among authors: fischer a. J Clin Invest. 1998 Jul 15;102(2):312-21. doi: 10.1172/JCI332. J Clin Invest. 1998. PMID: 9664072 Free PMC article.

4

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: fischer a. 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.

5

Lymphoproliferative syndrome with autoimmunity: A possible genetic basis for dominant expression of the clinical manifestations.

Rieux-Laucat F, Blachère S, Danielan S, De Villartay JP, Oleastro M, Solary E, Bader-Meunier B, Arkwright P, Pondaré C, Bernaudin F, Chapel H, Nielsen S, Berrah M, Fischer A, Le Deist F. Rieux-Laucat F, et al. Among authors: fischer a. Blood. 1999 Oct 15;94(8):2575-82. Blood. 1999. PMID: 10515860 Free article.

6

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: fischer a. 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.

7

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: fischer a. Cell. 2001 Apr 20;105(2):177-86. doi: 10.1016/s0092-8674(01)00309-9. Cell. 2001. PMID: 11336668 Free article.

8

Restricted heterogeneity of T lymphocytes in combined immunodeficiency with hypereosinophilia (Omenn's syndrome).

de Saint-Basile G, Le Deist F, de Villartay JP, Cerf-Bensussan N, Journet O, Brousse N, Griscelli C, Fischer A. de Saint-Basile G, et al. Among authors: fischer a. J Clin Invest. 1991 Apr;87(4):1352-9. doi: 10.1172/JCI115139. J Clin Invest. 1991. PMID: 2010548 Free PMC article.

9

Successful HLA nonidentical bone marrow transplantation in three patients with the leukocyte adhesion deficiency.

Le Deist F, Blanche S, Keable H, Gaud C, Pham H, Descamp-Latscha B, Wahn V, Griscelli C, Fischer A. Le Deist F, et al. Among authors: fischer a. Blood. 1989 Jul;74(1):512-6. Blood. 1989. PMID: 2665844 Free article.

10

Development of immunologic functions after bone marrow transplantation in 33 patients with severe combined immunodeficiency.

Wijnaendts L, Le Deist F, Griscelli C, Fischer A. Wijnaendts L, et al. Among authors: fischer a. Blood. 1989 Nov 1;74(6):2212-9. Blood. 1989. PMID: 2804359 Free article.

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