NR0B1 wt Allele

Known as: SRXY22, Nuclear Receptor Subfamily 0, Group B, Member 1 wt Allele, DSS 
Human NR0B1 wild-type allele is located within Xp21.3-p21.2 and is approximately 5 kb in length. This allele, which encodes nuclear receptor… (More)
National Institutes of Health

Papers overview

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Review
2016
Review
2016
Attosecond science offers formidable tools for the investigation of electronic processes at the heart of important physical… (More)
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Highly Cited
2015
Highly Cited
2012
Highly Cited
2012
High-harmonic generation (HHG) traditionally combines ~100 near-infrared laser photons to generate bright, phase-matched, extreme… (More)
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Highly Cited
2011
Highly Cited
2011
Harmonic generation is a general feature of driven nonlinear systems. In particular high-order harmonic generation (HHG) in… (More)
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Highly Cited
2009
Highly Cited
2009
The lightest Non Methane HydroCarbon (NMHC), i.e., acetylene (C 2H2) is found to form secondary organic aerosol (SOA). Contrary… (More)
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Highly Cited
1998
Highly Cited
1998
DAX1, which encodes an unusual member of the nuclear hormone-receptor superfamily, is a gene that may be responsible for a sex… (More)
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Highly Cited
1997
Highly Cited
1997
X-linked adrenal hypoplasia congenita (AHC) with hypogonadotropic hypogonadism was recently shown to be caused by mutations in a… (More)
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Highly Cited
1996
Highly Cited
1996
Mutations of the orphan nuclear receptors, steroidogenic factor 1 (SF-1) and DAX-1, cause complex endocrine phenotypes that… (More)
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Highly Cited
1994
Highly Cited
1994
X-linked adrenal hypoplasia congenita is a developmental disorder of the human adrenal gland that results in profound hormonal… (More)
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Highly Cited
1994
Highly Cited
1994
ADRENAL hypoplasia congenita (AHC) is an X-linked disorder characterized by primary adrenal insufficiency1,2. Hypogonadotropic… (More)
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