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NOBOX gene

Known as: NEWBORN OVARY HOMEOBOX, MOUSE, HOMOLOG OF, Og2x, NOBOX 
 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
A homozygous NOBOX truncating variant causes defective transcriptional activation and leads to primary ovarian insufficiency
STUDY QUESTION Does a novel homozygous NOBOX truncating variant, identified in whole exome sequencing (WES) of patients with… Expand
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2010
2010
The Interactions Between the Stimulatory Effect of Follicle-Stimulating Hormone and the Inhibitory Effect of Estrogen on Mouse Primordial Folliculogenesis1
Abstract The murine primordial follicle pool develops largely within 3 days after birth through germline nest breakdown and… Expand
Highly Cited
2008
Highly Cited
2008
Lim Homeobox Gene, Lhx8, Is Essential for Mouse Oocyte Differentiation and Survival1
Abstract Lhx8 is a member of the LIM-homeobox transcription factor family and preferentially expressed in oocytes and germ cells… Expand
Highly Cited
2007
Highly Cited
2007
NOBOX homeobox mutation causes premature ovarian failure.
NOBOX (newborn ovary homeobox gene) is an oocyte-specific homeobox gene that plays a critical role in early folliculogenesis and… Expand
Highly Cited
2006
Highly Cited
2006
Characterization of NOBOX DNA Binding Specificity and Its Regulation of Gdf9 and Pou5f1 Promoters*
Nobox (newborn ovary homeobox gene) deficiency disrupts early folliculogenesis and the expression of oocyte-specific genes in… Expand
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Highly Cited
2004
Highly Cited
2004
NOBOX Deficiency Disrupts Early Folliculogenesis and Oocyte-Specific Gene Expression
Primordial ovarian follicles in mice form when somatic cells surround individual oocytes. We show that lack of Nobox, an oocyte… Expand
Highly Cited
2002
Highly Cited
2002
Nobox is a homeobox-encoding gene preferentially expressed in primordial and growing oocytes
To identify novel genes involved in early mammalian folliculogenesis, we used the Unigene collection of mouse cDNA libraries to… Expand
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Highly Cited
2002
Highly Cited
2002
Overexpression of Phex in Osteoblasts Fails to Rescue the Hyp Mouse Phenotype*
Inactivating mutations of Phex, a phosphate-regulating endopeptidase, cause hypophosphatemia and impaired mineralization in X… Expand
Highly Cited
1999
Highly Cited
1999
Characterization of Osf1, an Osteoblast-specific Transcription Factor Binding to a Critical cis-acting Element in the MouseOsteocalcin Promoters*
To elucidate the mechanisms of osteoblast-specific gene expression we are studying the regulation ofosteocalcin, the most… Expand
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Highly Cited
1997
Highly Cited
1997
1,25-Dihydroxyvitamin D3 Inhibits Osteocalcin Expression in Mouse through an Indirect Mechanism*
1,25-Dihydroxyvitamin D3 (1,25-(OH)2D3), a key regulator of mineral metabolism, regulates the expression of several genes that… Expand
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