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TBX19 gene
Known as:
T-box 19
, dj747L4.1
, TBX19
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National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2012
Highly Cited
2012
Self-powered microscale pumps based on analyte-initiated depolymerization reactions.
Hua Zhang
,
K. Yeung
,
+5 authors
S. T. Phillips
Angewandte Chemie
2012
Corpus ID: 8645905
1) those that are turned on and off byinput from the user; and 2) single-use pumps that are turnedon autonomously by exposure to…
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Review
2007
Review
2007
Of old and new diseases: genetics of pituitary ACTH excess (Cushing) and deficiency
J. Drouin
,
S. Bilodeau
,
S. Vallette
Clinical genetics
2007
Corpus ID: 25671033
The pituitary gland orchestrates our endocrine environment: it produces hormones in response to hypothalamic factors that…
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Highly Cited
2005
Highly Cited
2005
Bone morphogenic protein (Smad)-mediated repression of proopiomelanocortin transcription by interference with Pitx/Tpit activity.
M. Nudi
,
Jean-François Ouimette
,
J. Drouin
Molecular endocrinology
2005
Corpus ID: 44471045
The signaling molecules bone morphogenic protein (BMP) 4 and 2 have been implicated in early organogenesis and cell…
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Highly Cited
2004
Highly Cited
2004
Tpit-independent function of NeuroD1(BETA2) in pituitary corticotroph differentiation.
B. Lamolet
,
G. Poulin
,
K. Chu
,
F. Guillemot
,
M. Tsai
,
J. Drouin
Molecular endocrinology
2004
Corpus ID: 25565416
NeuroD1(BETA2) and Tpit are cell-specific activators of pituitary proopiomelanocortin (POMC) gene transcription. Expression of…
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2004
2004
TPIT mutations are associated with early-onset, but not late-onset isolated ACTH deficiency.
L. Metherell
,
M. Savage
,
+4 authors
A. Clark
European journal of endocrinology
2004
Corpus ID: 2974080
OBJECTIVE Congenital isolated ACTH deficiency (IAD) is a rare inherited disorder that is clinically and genetically heterogeneous…
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Highly Cited
2003
Highly Cited
2003
Tpit determines alternate fates during pituitary cell differentiation.
A. Pulichino
,
S. Vallette-Kasic
,
Judy Tsai
,
C. Couture
,
Y. Gauthier
,
J. Drouin
Genes & development
2003
Corpus ID: 29236514
The T-box transcription factor Tpit was identified as a cell-specific factor for expression of the pituitary proopiomelanocortin…
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Highly Cited
2003
Highly Cited
2003
Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency.
A. Pulichino
,
S. Vallette-Kasic
,
+13 authors
J. Drouin
Genes & development
2003
Corpus ID: 8401628
Tpit is a highly cell-restricted transcription factor that is required for expression of the pro-opiomelanocortin (POMC) gene and…
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Highly Cited
2003
Highly Cited
2003
Differential regulation of proopiomelanocortin and pituitary-restricted transcription factor (TPIT), a new marker of normal and adenomatous human corticotrophs.
S. Vallette-Kasic
,
D. Figarella-Branger
,
+6 authors
T. Brue
The Journal of clinical endocrinology and…
2003
Corpus ID: 24207546
Since the identification of the pituitary-restricted transcription factor Tpit, a novel T-box factor that is only present in…
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Highly Cited
2001
Highly Cited
2001
Tbx19, a tissue-selective regulator of POMC gene expression
J. Liu
,
C. Lin
,
+5 authors
M. Rosenfeld
Proceedings of the National Academy of Sciences…
2001
Corpus ID: 27020285
Pituitary cell types arise in a temporally and spatially specific fashion, in response to combinatorial actions of transcription…
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Highly Cited
1999
Highly Cited
1999
Identification, mapping, and phylogenomic analysis of four new human members of the T-box gene family: EOMES, TBX6, TBX18, and TBX19.
C. Yi
,
J. Terrett
,
+6 authors
J. Brook
Genomics
1999
Corpus ID: 29143916
Brachyury(T) is a mouse mutation, first described over 70 years ago, that causes defects in mesoderm formation. Recently several…
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