NFIX gene

Known as: NF1A, nuclear factor I X, NFIX 
This gene is involved in transcriptional regulation.
National Institutes of Health

Topic mentions per year

Topic mentions per year

2001-2017
02420012017

Papers overview

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Review
2017
Review
2017
Moyamoya angiopathy (MA) is a rare cerebrovascular disorder characterised by the progressive occlusion of the internal carotid… (More)
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Review
2016
Review
2016
BACKGROUND AND AIM Sotos syndrome 2 (MIM #614753), known also as Malan syndrome, is caused by heterozygous mutations/deletions of… (More)
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2016
2016
Nfix belongs to a family of four highly conserved proteins that act as transcriptional activators and/or repressors of cellular… (More)
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2015
2015
Astrocytes play a critical role during the development and the maintenance of the CNS in health and disease. Yet, their lack of… (More)
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2013
2013
The majority of neural stem cells (NSCs) in the adult brain are quiescent, and this fraction increases with aging. Although… (More)
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2013
2013
OBJECTIVE The use of subphenotypes may be an effective approach for genetic studies of complex diseases. Manic episodes with a… (More)
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2012
2012
Neurofibromatosis type 1 (NF1) is a common, dominantly inherited genetic disorder that results from mutations in the… (More)
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2011
2011
Our laboratory has previously cloned and purified an ovarian protein found to be a novel 17β-hydroxysteroid dehydrogenase type 7… (More)
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Highly Cited
2007
Highly Cited
2007
The Nuclear Factor I (NFI) multi-gene family encodes site-specific transcription factors essential for the development of a… (More)
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2001
2001
Vascular disease is an underestimated complication of neurofibromatosis type 1 (NF1). The few studies available on this disease… (More)
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