Jabado N - Search Results

1

Human RTEL1 deficiency causes Hoyeraal-Hreidarsson syndrome with short telomeres and genome instability.

Le Guen T, Jullien L, Touzot F, Schertzer M, Gaillard L, Perderiset M, Carpentier W, Nitschke P, Picard C, Couillault G, Soulier J, Fischer A, Callebaut I, Jabado N, Londono-Vallejo A, de Villartay JP, Revy P. Le Guen T, et al. Among authors: jabado n. Hum Mol Genet. 2013 Aug 15;22(16):3239-49. doi: 10.1093/hmg/ddt178. Epub 2013 Apr 15. Hum Mol Genet. 2013. PMID: 23591994

2

CD4 ligands inhibit the formation of multifunctional transduction complexes involved in T cell activation.

Jabado N, Pallier A, Le Deist F, Bernard F, Fischer A, Hivroz C. Jabado N, et al. J Immunol. 1997 Jan 1;158(1):94-103. J Immunol. 1997. PMID: 8977179

3

Frequency and severity of central nervous system lesions in hemophagocytic lymphohistiocytosis.

Haddad E, Sulis ML, Jabado N, Blanche S, Fischer A, Tardieu M. Haddad E, et al. Among authors: jabado n. Blood. 1997 Feb 1;89(3):794-800. Blood. 1997. PMID: 9028310 Free article.

4

gp160 of HIV or anti-CD4 monoclonal antibody ligation of CD4 induces inhibition of JNK and ERK-2 activities in human peripheral CD4+ T lymphocytes.

Jabado N, Pallier A, Jauliac S, Fischer A, Hivroz C. Jabado N, et al. Eur J Immunol. 1997 Feb;27(2):397-404. doi: 10.1002/eji.1830270209. Eur J Immunol. 1997. PMID: 9045910

5

Griscelli disease maps to chromosome 15q21 and is associated with mutations in the myosin-Va gene.

Pastural E, Barrat FJ, Dufourcq-Lagelouse R, Certain S, Sanal O, Jabado N, Seger R, Griscelli C, Fischer A, de Saint Basile G. Pastural E, et al. Among authors: jabado n. Nat Genet. 1997 Jul;16(3):289-92. doi: 10.1038/ng0797-289. Nat Genet. 1997. PMID: 9207796

6

Correction of Fas (CD95) deficiency by haploidentical bone marrow transplantation.

Benkerrou M, Le Deist F, de Villartay JP, Caillat-Zucman S, Rieux-Laucat F, Jabado N, Cavazzana-Calvo M, Fischer A. Benkerrou M, et al. Among authors: jabado n. Eur J Immunol. 1997 Aug;27(8):2043-7. doi: 10.1002/eji.1830270831. Eur J Immunol. 1997. PMID: 9295043

7

Linkage of familial hemophagocytic lymphohistiocytosis to 10q21-22 and evidence for heterogeneity.

Dufourcq-Lagelouse R, Jabado N, Le Deist F, Stéphan JL, Souillet G, Bruin M, Vilmer E, Schneider M, Janka G, Fischer A, de Saint Basile G. Dufourcq-Lagelouse R, et al. Among authors: jabado n. Am J Hum Genet. 1999 Jan;64(1):172-9. doi: 10.1086/302194. Am J Hum Genet. 1999. PMID: 9915956 Free PMC article.

8

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: jabado n. Hum Mol Genet. 2000 Mar 1;9(4):583-8. doi: 10.1093/hmg/9.4.583. Hum Mol Genet. 2000. PMID: 10699181

9

Severe combined immunodeficiency caused by deficiency in either the delta or the epsilon subunit of CD3.

de Saint Basile G, Geissmann F, Flori E, Uring-Lambert B, Soudais C, Cavazzana-Calvo M, Durandy A, Jabado N, Fischer A, Le Deist F. de Saint Basile G, et al. Among authors: jabado n. J Clin Invest. 2004 Nov;114(10):1512-7. doi: 10.1172/JCI22588. J Clin Invest. 2004. PMID: 15546002 Free PMC article.

10

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: jabado n. 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

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