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TBX19 gene

Known as: T-BOX 19, dj747L4.1, TBX19 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1966-2017
012319662017

Papers overview

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2015
2015
The Complementary Role of Transcription Factors in the Accurate Diagnosis of Clinically Nonfunctioning Pituitary Adenomas.
Clinically nonfunctioning pituitary adenomas (NFAs) may be hormonally inactive tumors of differentiated cells, mainly not only… (More)
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2012
2012
Identification of TPIT and other novel autoantigens in lymphocytic hypophysitis; immunoscreening of a pituitary cDNA library and development of immunoprecipitation assays
BACKGROUND Lymphocytic hypophysitis is an organ-specific autoimmune disease of the pituitary gland. A specific and sensitive… (More)
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2012
2012
Phenotypic homogeneity and genotypic variability in a large series of congenital isolated ACTH-deficiency patients with TPIT gene mutations.
CONTEXT Congenital isolated ACTH deficiency (IAD) is a rare disease characterized by low plasma ACTH and cortisol levels and… (More)
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2010
2010
Clinical, hormonal and molecular characterization of pituitary ACTH adenomas without (silent corticotroph adenomas) and with Cushing's disease.
OBJECTIVE Silent corticotroph adenomas (SCAs) are rare pituitary tumours immunoreactive for ACTH, but without clinical evidence… (More)
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2007
2007
The TPIT gene mutation M86R associated with isolated adrenocorticotropin deficiency interferes with protein: protein interactions.
CONTEXT Tpit is a T-box transcription factor important for terminal differentiation of pituitary proopiomelanocortin-expressing… (More)
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2006
2006
Low estriol levels in the maternal triple-marker screen as a predictor of isolated adrenocorticotropic hormone deficiency caused by a new mutation in the TPIT gene.
Isolated adrenocorticotropic hormone (ACTH) deficiency (IAD) is a rare cause of adrenocortical insufficiency, especially in… (More)
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2005
2005
Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutations.
Tpit is a T box transcription factor important for terminal differentiation of pituitary proopiomelanocortin-expressing cells. We… (More)
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2004
2004
TPIT mutations are associated with early-onset, but not late-onset isolated ACTH deficiency.
OBJECTIVE Congenital isolated ACTH deficiency (IAD) is a rare inherited disorder that is clinically and genetically heterogeneous… (More)
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2003
2003
Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency.
Tpit is a highly cell-restricted transcription factor that is required for expression of the pro-opiomelanocortin (POMC) gene and… (More)
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2003
2003
Differential regulation of proopiomelanocortin and pituitary-restricted transcription factor (TPIT), a new marker of normal and adenomatous human corticotrophs.
Since the identification of the pituitary-restricted transcription factor Tpit, a novel T-box factor that is only present in… (More)
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