Revy P - Search Results

1

Extended clinical and genetic spectrum associated with biallelic RTEL1 mutations.

Touzot F, Kermasson L, Jullien L, Moshous D, Ménard C, Ikincioğullari A, Doğu F, Sari S, Giacobbi-Milet V, Etzioni A, Soulier J, Londono-Vallejo A, Fischer A, Callebaut I, de Villartay JP, Leblanc T, Kannengiesser C, Revy P. Touzot F, et al. Among authors: revy p. Blood Adv. 2016 Nov 22;1(1):36-46. doi: 10.1182/bloodadvances.2016001313. eCollection 2016 Nov 29. Blood Adv. 2016. PMID: 29296694 Free PMC article.

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

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

4

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

5

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.

6

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.

7

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.

8

Analysis of class switch recombination and somatic hypermutation in patients affected with autosomal dominant hyper-IgM syndrome type 2.

Imai K, Zhu Y, Revy P, Morio T, Mizutani S, Fischer A, Nonoyama S, Durandy A. Imai K, et al. Among authors: revy p. Clin Immunol. 2005 Jun;115(3):277-85. doi: 10.1016/j.clim.2005.02.003. Clin Immunol. 2005. PMID: 15893695

9

The repair of DNA damages/modifications during the maturation of the immune system: lessons from human primary immunodeficiency disorders and animal models.

Revy P, Buck D, le Deist F, de Villartay JP. Revy P, et al. Adv Immunol. 2005;87:237-95. doi: 10.1016/S0065-2776(05)87007-5. Adv Immunol. 2005. PMID: 16102576 Review.

10

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: revy p. Cell. 2006 Jan 27;124(2):287-99. doi: 10.1016/j.cell.2005.12.030. Cell. 2006. PMID: 16439204 Free article.

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