Incontinentia pigmenti (Bloch–Sulzberger syndrome)
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Elsevier
Reference86 articles.
1. A recurrent deletion in the ubiquitously expressed NEMO (IKK-gamma) gene accounts for the vast majority of incontinentia pigmenti mutations;Aradhya;Hum Mol Genet,2001
2. Atypical forms of incontinentia pigmenti in male individuals result from mutations of a cytosine tract in exon 10 of NEMO (IKK-gamma);Aradhya;Am J Hum Genet,2001
3. Hsp70 stimulates cytokine production through a CD14-dependant pathway, demonstrating its dual role as a chaperone and cytokine;Asea;Nat Med,2000
4. Pro-inflammatory signaling: last pieces in the NF-κB puzzle?;Baeuerle;Curr Biol,1998
5. Incontinentia pigmenti: (Bloch–Sulzberger syndrome);Bambridge;Pediatrics,1953
Cited by 18 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. NEMO reshapes the α-Synuclein aggregate interface and acts as an autophagy adapter by co-condensation with p62;Nature Communications;2023-12-19
2. A case report of neonatal incontinentia pigmenti complicated by severe cerebrovascular lesions in one of the male monozygotic twins;2023-09-11
3. Oral Rehabilitation as Part of a Multidisciplinary Treatment in a Case Study of Pigmentary Incontinence;Children;2023-09-04
4. NEMO reshapes the protein aggregate interface and promotes aggrephagy by co-condensation with p62;2023-06-06
5. Uncovering incontinentia pigmenti: From DNA sequence to pathophysiology;Frontiers in Pediatrics;2022-09-06
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