Similar articles for PMID: 30913450

Year	Number of Results
2000	4
2001	5
2002	1
2003	1
2004	3
2005	3
2006	4
2007	5
2008	11
2009	4
2010	7
2011	14
2012	8
2013	9
2014	14
2015	12
2016	4
2017	12
2018	9
2019	12
2020	13
2021	8
2022	14
2023	2
2024	0

1

A novel inhibitor of nuclear factor kappa-B kinase subunit gamma mutation identified in an incontinentia pigmenti patient with syndromic tooth agenesis.

Sun S, Li F, Liu Y, Qu H, Wong SW, Zeng L, Yu M, Feng H, Liu H, Han D. Sun S, et al. Arch Oral Biol. 2019 May;101:100-107. doi: 10.1016/j.archoralbio.2019.03.013. Epub 2019 Mar 18. Arch Oral Biol. 2019. PMID: 30913450

2

Lack of interaction between NEMO and SHARPIN impairs linear ubiquitination and NF-κB activation and leads to incontinentia pigmenti.

Bal E, Laplantine E, Hamel Y, Dubosclard V, Boisson B, Pescatore A, Picard C, Hadj-Rabia S, Royer G, Steffann J, Bonnefont JP, Ursini VM, Vabres P, Munnich A, Casanova JL, Bodemer C, Weil R, Agou F, Smahi A. Bal E, et al. J Allergy Clin Immunol. 2017 Dec;140(6):1671-1682.e2. doi: 10.1016/j.jaci.2016.11.056. Epub 2017 Feb 27. J Allergy Clin Immunol. 2017. PMID: 28249776

3

Insight into IKBKG/NEMO locus: report of new mutations and complex genomic rearrangements leading to incontinentia pigmenti disease.

Conte MI, Pescatore A, Paciolla M, Esposito E, Miano MG, Lioi MB, McAleer MA, Giardino G, Pignata C, Irvine AD, Scheuerle AE, Royer G, Hadj-Rabia S, Bodemer C, Bonnefont JP, Munnich A, Smahi A, Steffann J, Fusco F, Ursini MV. Conte MI, et al. Hum Mutat. 2014 Feb;35(2):165-77. doi: 10.1002/humu.22483. Epub 2013 Dec 12. Hum Mutat. 2014. PMID: 24339369

4

Identification of TRAF6-dependent NEMO polyubiquitination sites through analysis of a new NEMO mutation causing incontinentia pigmenti.

Sebban-Benin H, Pescatore A, Fusco F, Pascuale V, Gautheron J, Yamaoka S, Moncla A, Ursini MV, Courtois G. Sebban-Benin H, et al. Hum Mol Genet. 2007 Dec 1;16(23):2805-15. doi: 10.1093/hmg/ddm237. Epub 2007 Aug 29. Hum Mol Genet. 2007. PMID: 17728323

5

Identification of a new NEMO/TRAF6 interface affected in incontinentia pigmenti pathology.

Gautheron J, Pescatore A, Fusco F, Esposito E, Yamaoka S, Agou F, Ursini MV, Courtois G. Gautheron J, et al. Hum Mol Genet. 2010 Aug 15;19(16):3138-49. doi: 10.1093/hmg/ddq222. Epub 2010 Jun 7. Hum Mol Genet. 2010. PMID: 20529958

6

Immunodeficiency in Two Female Patients with Incontinentia Pigmenti with Heterozygous NEMO Mutation Diagnosed by LPS Unresponsiveness.

Ohnishi H, Kishimoto Y, Taguchi T, Kawamoto N, Nakama M, Kawai T, Nakayama M, Ohara O, Orii K, Fukao T. Ohnishi H, et al. J Clin Immunol. 2017 Aug;37(6):529-538. doi: 10.1007/s10875-017-0417-3. Epub 2017 Jul 12. J Clin Immunol. 2017. PMID: 28702714

7

EDA-ID and IP, two faces of the same coin: how the same IKBKG/NEMO mutation affecting the NF-κB pathway can cause immunodeficiency and/or inflammation.

Fusco F, Pescatore A, Conte MI, Mirabelli P, Paciolla M, Esposito E, Lioi MB, Ursini MV. Fusco F, et al. Int Rev Immunol. 2015;34(6):445-59. doi: 10.3109/08830185.2015.1055331. Epub 2015 Aug 13. Int Rev Immunol. 2015. PMID: 26269396 Review.

8

The common NF-κB essential modulator (NEMO) gene rearrangement in Korean patients with incontinentia pigmenti.

Song MJ, Chae JH, Park EA, Ki CS. Song MJ, et al. J Korean Med Sci. 2010 Oct;25(10):1513-7. doi: 10.3346/jkms.2010.25.10.1513. Epub 2010 Sep 20. J Korean Med Sci. 2010. PMID: 20890435 Free PMC article.

9

Unusual Father-to-Daughter Transmission of Incontinentia Pigmenti Due to Mosaicism in IP Males.

Fusco F, Conte MI, Diociaiuti A, Bigoni S, Branda MF, Ferlini A, El Hachem M, Ursini MV. Fusco F, et al. Pediatrics. 2017 Sep;140(3):e20162950. doi: 10.1542/peds.2016-2950. Epub 2017 Aug 9. Pediatrics. 2017. PMID: 28794079

10

Incontinentia pigmenti in a male (XY) infant with long-term follow up over 8 years.

Matsuzaki Y, Rokunohe A, Minakawa S, Nomura K, Nakano H, Ito E, Sawamura D. Matsuzaki Y, et al. J Dermatol. 2018 Jan;45(1):100-103. doi: 10.1111/1346-8138.14002. Epub 2017 Aug 9. J Dermatol. 2018. PMID: 28791733

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