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Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium.
Smahi A, Courtois G, Vabres P, Yamaoka S, Heuertz S, Munnich A, Israël A, Heiss NS, Klauck SM, Kioschis P, Wiemann S, Poustka A, Esposito T, Bardaro T, Gianfrancesco F, Ciccodicola A, D'Urso M, Woffendin H, Jakins T, Donnai D, Stewart H, Kenwrick SJ, Aradhya S, Yamagata T, Levy M, Lewis RA, Nelson DL. Smahi A, et al. Among authors: israel a. Nature. 2000 May 25;405(6785):466-72. doi: 10.1038/35013114. Nature. 2000. PMID: 10839543
IKK regulation and human genetics.
Courtois G, Israël A. Courtois G, et al. Among authors: israel a. Curr Top Microbiol Immunol. 2011;349:73-95. doi: 10.1007/82_2010_98. Curr Top Microbiol Immunol. 2011. PMID: 20845108 Review.
NEMO/IKK gamma-deficient mice model incontinentia pigmenti.
Schmidt-Supprian M, Bloch W, Courtois G, Addicks K, Israël A, Rajewsky K, Pasparakis M. Schmidt-Supprian M, et al. Among authors: israel a. Mol Cell. 2000 Jun;5(6):981-92. doi: 10.1016/s1097-2765(00)80263-4. Mol Cell. 2000. PMID: 10911992 Free article.
NF-kappa B defects in humans: the NEMO/incontinentia pigmenti connection.
Courtois G, Israël A. Courtois G, et al. Among authors: israel a. Sci STKE. 2000 Nov 14;2000(58):pe1. doi: 10.1126/stke.2000.58.pe1. Sci STKE. 2000. PMID: 11752619 Review.
The components of the nuclear factor-kappaB (NF-kappaB) family of transcription factors are critical for regulating the response to immune challenges. Recently, a role for NF-kappaB in skin biology has been revealed. Within the cascade of proteins whose activities impinge …
The components of the nuclear factor-kappaB (NF-kappaB) family of transcription factors are critical for regulating the response to immune c …
NEMO/IKK gamma: linking NF-kappa B to human disease.
Courtois G, Smahi A, Israël A. Courtois G, et al. Among authors: israel a. Trends Mol Med. 2001 Oct;7(10):427-30. doi: 10.1016/s1471-4914(01)02154-2. Trends Mol Med. 2001. PMID: 11597506 No abstract available.
X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling.
Döffinger R, Smahi A, Bessia C, Geissmann F, Feinberg J, Durandy A, Bodemer C, Kenwrick S, Dupuis-Girod S, Blanche S, Wood P, Rabia SH, Headon DJ, Overbeek PA, Le Deist F, Holland SM, Belani K, Kumararatne DS, Fischer A, Shapiro R, Conley ME, Reimund E, Kalhoff H, Abinun M, Munnich A, Israël A, Courtois G, Casanova JL. Döffinger R, et al. Among authors: israel a. Nat Genet. 2001 Mar;27(3):277-85. doi: 10.1038/85837. Nat Genet. 2001. PMID: 11242109
503 results