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NR0B1 gene

Known as: nuclear receptor subfamily 0 group B member 1, Nuclear Receptor Subfamily 0, Group B, Member 1 Gene, NR0B1 
This gene plays a role in both modulation of receptor signaling and transcription.
National Institutes of Health

Related topics

Related topics

15 relations
Biologic DevelopmentCell Differentiation processCell ProliferationDAX-1 Orphan Nuclear Receptor

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NR0B1 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
NOVEL DAX-1 (NR0B1) MUTATION IN A THAI BOY WITH X-LINKED ADRENAL HYPOPLASIA CONGENITA (AHC): A FIRST REPORT
Background:Adrenal hypoplasia congenita (AHC) is a rare inherited disorder of adrenal development resulting in hypoplasia of… 
2017
2017
The role of orphan nuclear receptor DAX-1 (NR0B1) in human breast cancer cells: expression, proliferation and metastasis
Review
2015
Review
2015
[DAX1-unusual member of nuclear receptors superfamily with diverse functions].
Nuclear receptors (NRs) are ligand-activated transcription factors that play an important role in metabolism, homeostasis… 
Review
2015
Review
2015
Identification of Novel Drug Targets and Lead Compounds for 5 a . CONTRACT NUMBER Advanced Prostate Cancer through Genomic and Cheminformatic Analyses
Nuclear receptors (NRs), a family of 48 transcriptional factors, have been studied intensively for their roles in cancer… 
2014
2014
Clinical and Biochemical Function of Polymorphic NR0B1 GGAA-Microsatellites in Ewing Sarcoma: A Report from the Children's Oncology Group
Background The genetics involved in Ewing sarcoma susceptibility and prognosis are poorly understood. EWS/FLI and related EWS/ETS… 
2012
2012
Long-Term Evaluation and Clinical Spectrum of the Pubertal Abnormalities of Two Siblings Harboring NR0B1 Inactivating Mutation
2011
2011
マウスES細胞の自己複製維持における Dax1 と Esrrb の相互作用
2010
2010
Tumorigenic role of orphan nuclear receptor NR0B1 in lung adenocarcinoma
2009
2009
The Testatin/Cres subgroup of family 2 cystatins in sexual development
The genetic sex in mammals is established at fertilization, where an XX chromosome complement will lead to female development and… 
2004
2004
Congenital Adrenal Hypoplasia and Male Pseudohermaphroditism Due to DAX1 Mutation, SF1 Mutation or Neither: A Patient Report
A 15 year-old African American phenotypic female with congenital adrenal hypoplasia and intra-abdominal testes is described; she… 
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