Revy P - Search Results

1

Whole-exome sequencing identifies Coronin-1A deficiency in 3 siblings with immunodeficiency and EBV-associated B-cell lymphoproliferation.

Moshous D, Martin E, Carpentier W, Lim A, Callebaut I, Canioni D, Hauck F, Majewski J, Schwartzentruber J, Nitschke P, Sirvent N, Frange P, Picard C, Blanche S, Revy P, Fischer A, Latour S, Jabado N, de Villartay JP. Moshous D, et al. Among authors: revy p. J Allergy Clin Immunol. 2013 Jun;131(6):1594-603. doi: 10.1016/j.jaci.2013.01.042. Epub 2013 Mar 21. J Allergy Clin Immunol. 2013. PMID: 23522482

2

Interferon-gamma-receptor deficiency in an infant with fatal bacille Calmette-Guérin infection.

Jouanguy E, Altare F, Lamhamedi S, Revy P, Emile JF, Newport M, Levin M, Blanche S, Seboun E, Fischer A, Casanova JL. Jouanguy E, et al. Among authors: revy p. N Engl J Med. 1996 Dec 26;335(26):1956-61. doi: 10.1056/NEJM199612263352604. N Engl J Med. 1996. PMID: 8960475 Free article. No abstract available.

3

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.

4

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.

5

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.

6

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

7

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

8

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.

9

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.

10

Hyper-immunoglobulin M syndromes caused by intrinsic B-lymphocyte defects.

Durandy A, Revy P, Imai K, Fischer A. Durandy A, et al. Among authors: revy p. Immunol Rev. 2005 Feb;203:67-79. doi: 10.1111/j.0105-2896.2005.00222.x. Immunol Rev. 2005. PMID: 15661022 Review.

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