Boisson B - Search Results

1

Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module.

Koss M, Bolze A, Brendolan A, Saggese M, Capellini TD, Bojilova E, Boisson B, Prall OW, Elliott DA, Solloway M, Lenti E, Hidaka C, Chang CP, Mahlaoui N, Harvey RP, Casanova JL, Selleri L. Koss M, et al. Among authors: boisson b. Dev Cell. 2012 May 15;22(5):913-26. doi: 10.1016/j.devcel.2012.02.009. Epub 2012 May 3. Dev Cell. 2012. PMID: 22560297 Free PMC article.

2

Phenotypes of 126 Moroccan HIES patients according to NIH Score.

Fadil I, Benhsaien I, El Bakkouri J, Jeddane L, Benaajiba N, Rada N, Hbibi M, Amenzoui N, Ben Miloud S, Hida M, Bouskraoui M, El Fetoiki FZ, Hali F, Chiheb S, Admou B, Casanova JL, Puel A, Boisson B, Beziat V, Ailal F, Bousfiha AA. Fadil I, et al. Among authors: boisson b. Tunis Med. 2024 Oct 5;102(10):696-701. doi: 10.62438/tunismed.v102i10.5148. Tunis Med. 2024. PMID: 39441153 Free PMC article. English.

3

Hyperimmunoglobulinemia E and hereditary immune deficiencies.

Fadil I, Ailal F, Beziat V, Casanova JL, Boisson B, Bousfiha AA. Fadil I, et al. Among authors: boisson b. Tunis Med. 2023 Dec 5;101(12):862-870. Tunis Med. 2023. PMID: 38477192 Free PMC article. French.

4

Whole-exome sequencing-based discovery of STIM1 deficiency in a child with fatal classic Kaposi sarcoma.

Byun M, Abhyankar A, Lelarge V, Plancoulaine S, Palanduz A, Telhan L, Boisson B, Picard C, Dewell S, Zhao C, Jouanguy E, Feske S, Abel L, Casanova JL. Byun M, et al. Among authors: boisson b. J Exp Med. 2010 Oct 25;207(11):2307-12. doi: 10.1084/jem.20101597. Epub 2010 Sep 27. J Exp Med. 2010. PMID: 20876309 Free PMC article.

5

An ACT1 mutation selectively abolishes interleukin-17 responses in humans with chronic mucocutaneous candidiasis.

Boisson B, Wang C, Pedergnana V, Wu L, Cypowyj S, Rybojad M, Belkadi A, Picard C, Abel L, Fieschi C, Puel A, Li X, Casanova JL. Boisson B, et al. Immunity. 2013 Oct 17;39(4):676-86. doi: 10.1016/j.immuni.2013.09.002. Epub 2013 Oct 10. Immunity. 2013. PMID: 24120361 Free PMC article.

6

A recurrent dominant negative E47 mutation causes agammaglobulinemia and BCR(-) B cells.

Boisson B, Wang YD, Bosompem A, Ma CS, Lim A, Kochetkov T, Tangye SG, Casanova JL, Conley ME. Boisson B, et al. J Clin Invest. 2013 Nov;123(11):4781-5. doi: 10.1172/JCI71927. J Clin Invest. 2013. PMID: 24216514 Free PMC article.

7

LUBAC: A new function in immunity.

Boisson B, Casanova JL. Boisson B, et al. J Exp Med. 2014 Jun 30;211(7):1272. doi: 10.1084/jem.2117insight3. J Exp Med. 2014. PMID: 24980746 Free PMC article. No abstract available.

8

The differential regulation of human ACT1 isoforms by Hsp90 in IL-17 signaling.

Wu L, Wang C, Boisson B, Misra S, Rayman P, Finke JH, Puel A, Casanova JL, Li X. Wu L, et al. Among authors: boisson b. J Immunol. 2014 Aug 15;193(4):1590-9. doi: 10.4049/jimmunol.1400715. Epub 2014 Jul 14. J Immunol. 2014. PMID: 25024377 Free PMC article.

9

Immunological loss-of-function due to genetic gain-of-function in humans: autosomal dominance of the third kind.

Boisson B, Quartier P, Casanova JL. Boisson B, et al. Curr Opin Immunol. 2015 Feb;32:90-105. doi: 10.1016/j.coi.2015.01.005. Epub 2015 Jan 31. Curr Opin Immunol. 2015. PMID: 25645939 Free PMC article. Review.

10

Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants.

Belkadi A, Bolze A, Itan Y, Cobat A, Vincent QB, Antipenko A, Shang L, Boisson B, Casanova JL, Abel L. Belkadi A, et al. Among authors: boisson b. Proc Natl Acad Sci U S A. 2015 Apr 28;112(17):5473-8. doi: 10.1073/pnas.1418631112. Epub 2015 Mar 31. Proc Natl Acad Sci U S A. 2015. PMID: 25827230 Free PMC article.

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