Revy P - Search Results

1

An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiation.

Le Guen T, Touzot F, André-Schmutz I, Lagresle-Peyrou C, France B, Kermasson L, Lambert N, Picard C, Nitschke P, Carpentier W, Bole-Feysot C, Lim A, Cavazzana M, Callebaut I, Soulier J, Jabado N, Fischer A, de Villartay JP, Revy P. Le Guen T, et al. Among authors: revy p. J Allergy Clin Immunol. 2015 Dec;136(6):1619-1626.e5. doi: 10.1016/j.jaci.2015.06.008. Epub 2015 Jul 26. J Allergy Clin Immunol. 2015. PMID: 26220525

2

Normal CD40-mediated activation of monocytes and dendritic cells from patients with hyper-IgM syndrome due to a CD40 pathway defect in B cells.

Revy P, Geissmann F, Debré M, Fischer A, Durandy A. Revy P, et al. Eur J Immunol. 1998 Nov;28(11):3648-54. doi: 10.1002/(SICI)1521-4141(199811)28:11<3648::AID-IMMU3648>3.0.CO;2-U. Eur J Immunol. 1998. PMID: 9842907 Free article.

3

Activation of the Janus kinase 3-STAT5a pathway after CD40 triggering of human monocytes but not of resting B cells.

Revy P, Hivroz C, Andreu G, Graber P, Martinache C, Fischer A, Durandy A. Revy P, et al. J Immunol. 1999 Jul 15;163(2):787-93. J Immunol. 1999. PMID: 10395671

4

A syndrome involving intrauterine growth retardation, microcephaly, cerebellar hypoplasia, B lymphocyte deficiency, and progressive pancytopenia.

Revy P, Busslinger M, Tashiro K, Arenzana F, Pillet P, Fischer A, Durandy A. Revy P, et al. Pediatrics. 2000 Mar;105(3):E39. doi: 10.1542/peds.105.3.e39. Pediatrics. 2000. PMID: 10699141

5

Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2).

Revy P, Muto T, Levy Y, Geissmann F, Plebani A, Sanal O, Catalan N, Forveille M, Dufourcq-Labelouse R, Gennery A, Tezcan I, Ersoy F, Kayserili H, Ugazio AG, Brousse N, Muramatsu M, Notarangelo LD, Kinoshita K, Honjo T, Fischer A, Durandy A. Revy P, et al. Cell. 2000 Sep 1;102(5):565-75. doi: 10.1016/s0092-8674(00)00079-9. Cell. 2000. PMID: 11007475 Free article.

6

Hyper-IgM syndrome type 4 with a B lymphocyte-intrinsic selective deficiency in Ig class-switch recombination.

Imai K, Catalan N, Plebani A, Maródi L, Sanal O, Kumaki S, Nagendran V, Wood P, Glastre C, Sarrot-Reynauld F, Hermine O, Forveille M, Revy P, Fischer A, Durandy A. Imai K, et al. Among authors: revy p. J Clin Invest. 2003 Jul;112(1):136-42. doi: 10.1172/JCI18161. J Clin Invest. 2003. PMID: 12840068 Free PMC article.

7

The block in immunoglobulin class switch recombination caused by activation-induced cytidine deaminase deficiency occurs prior to the generation of DNA double strand breaks in switch mu region.

Catalan N, Selz F, Imai K, Revy P, Fischer A, Durandy A. Catalan N, et al. Among authors: revy p. J Immunol. 2003 Sep 1;171(5):2504-9. doi: 10.4049/jimmunol.171.5.2504. J Immunol. 2003. PMID: 12928399

8

Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination.

Imai K, Slupphaug G, Lee WI, Revy P, Nonoyama S, Catalan N, Yel L, Forveille M, Kavli B, Krokan HE, Ochs HD, Fischer A, Durandy A. Imai K, et al. Among authors: revy p. Nat Immunol. 2003 Oct;4(10):1023-8. doi: 10.1038/ni974. Epub 2003 Sep 7. Nat Immunol. 2003. PMID: 12958596

9

Hyper-immunoglobulin-M syndromes caused by an intrinsic B cell defect.

Durandy A, Revy P, Fischer A. Durandy A, et al. Among authors: revy p. Curr Opin Allergy Clin Immunol. 2003 Dec;3(6):421-5. doi: 10.1097/00130832-200312000-00002. Curr Opin Allergy Clin Immunol. 2003. PMID: 14612665 Review.

10

Human models of inherited immunoglobulin class switch recombination and somatic hypermutation defects (hyper-IgM syndromes).

Durandy A, Revy P, Fischer A. Durandy A, et al. Among authors: revy p. Adv Immunol. 2004;82:295-330. doi: 10.1016/S0065-2776(04)82007-8. Adv Immunol. 2004. PMID: 14975260 Review. No abstract available.

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