Fischer A - Search Results

1

Lymphopoiesis in transgenic mice over-expressing Artemis.

Rivera-Munoz P, Abramowski V, Jacquot S, André P, Charrier S, Lipson-Ruffert K, Fischer A, Galy A, Cavazzana M, de Villartay JP. Rivera-Munoz P, et al. Among authors: fischer a. Gene Ther. 2016 Feb;23(2):176-86. doi: 10.1038/gt.2015.95. Epub 2015 Oct 1. Gene Ther. 2016. PMID: 26361272

2

Variable correction of Artemis deficiency by I-Sce1-meganuclease-assisted homologous recombination in murine hematopoietic stem cells.

Rivière J, Hauer J, Poirot L, Brochet J, Souque P, Mollier K, Gouble A, Charneau P, Fischer A, Pâques F, de Villartay JP, Cavazzana M. Rivière J, et al. Among authors: fischer a. Gene Ther. 2014 May;21(5):529-32. doi: 10.1038/gt.2014.20. Epub 2014 Mar 13. Gene Ther. 2014. PMID: 24622732

3

Gene therapy of severe combined immunodeficiencies.

Cavazzana-Calvo M, Hacein-Bey S, Yates F, de Villartay JP, Le Deist F, Fischer A. Cavazzana-Calvo M, et al. Among authors: fischer a. J Gene Med. 2001 May-Jun;3(3):201-6. doi: 10.1002/1521-2254(200105/06)3:3<201::AID-JGM195>3.0.CO;2-Z. J Gene Med. 2001. PMID: 11437325 Review.

4

Gene therapy for primary immunodeficiencies.

Fischer A, Hacein-Bey Abina S, Touzot F, Cavazzana M. Fischer A, et al. Clin Genet. 2015 Dec;88(6):507-15. doi: 10.1111/cge.12576. Epub 2015 Mar 23. Clin Genet. 2015. PMID: 25708106 Review.

5

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.

6

Naturally occurring primary deficiencies of the immune system.

Fischer A, Cavazzana-Calvo M, De Saint Basile G, DeVillartay JP, Di Santo JP, Hivroz C, Rieux-Laucat F, Le Deist F. Fischer A, et al. Annu Rev Immunol. 1997;15:93-124. doi: 10.1146/annurev.immunol.15.1.93. Annu Rev Immunol. 1997. PMID: 9143683 Review.

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

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.

9

A new gene involved in DNA double-strand break repair and V(D)J recombination is located on human chromosome 10p.

Moshous D, Li L, Chasseval R, Philippe N, Jabado N, Cowan MJ, Fischer A, de Villartay JP. Moshous D, et al. Among authors: fischer a. Hum Mol Genet. 2000 Mar 1;9(4):583-8. doi: 10.1093/hmg/9.4.583. Hum Mol Genet. 2000. PMID: 10699181

10

Increased radiosensitivity of granulocyte macrophage colony-forming units and skin fibroblasts in human autosomal recessive severe combined immunodeficiency.

Cavazzana-Calvo M, Le Deist F, De Saint Basile G, Papadopoulo D, De Villartay JP, Fischer A. Cavazzana-Calvo M, et al. Among authors: fischer a. J Clin Invest. 1993 Mar;91(3):1214-8. doi: 10.1172/JCI116282. J Clin Invest. 1993. PMID: 8450050 Free PMC article.

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