TIF2 factor, human

Known as: TIF2, bHLHe75, Class E Basic Helix-Loop-Helix Protein 75 
Nuclear receptor coactivator 2 (1464 aa, ~159 kDa) is encoded by the human NCOA2 gene. This protein plays a role in the regulation of steroid… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1982-2018
05101519822018

Papers overview

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Highly Cited
2010
Highly Cited
2010
Annotation of prostate cancer genomes provides a foundation for discoveries that can impact disease understanding and treatment… (More)
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Highly Cited
2005
Highly Cited
2005
Selective peroxisome proliferator-activated receptor (PPAR) gamma modulation is a new pharmacological approach that, based on… (More)
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Highly Cited
2002
Highly Cited
2002
We have explored the effects of two members of the p160 coregulator family on energy homeostasis. TIF2-/- mice are protected… (More)
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Highly Cited
2002
Highly Cited
2002
Human TIF2 (hTIF2) is a member of the p160 family of nuclear receptor coactivators, which includes SRC-1 and p/CIP. Although the… (More)
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Highly Cited
2000
Highly Cited
2000
Recent studies have indicated that a complex machinery of transactivation of target genes by estrogen or antiestrogen through… (More)
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Highly Cited
1999
Highly Cited
1999
The endocrine system exerts important functions in a multitude of physiological processes including embryogenesis… (More)
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Highly Cited
1998
Highly Cited
1998
The nuclear receptor (NR) coactivator TIF2 possesses a single NR interaction domain (NID) and two autonomous activation domains… (More)
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Highly Cited
1998
Highly Cited
1998
Chromosomal abnormalities of band 8p11 are associated with a distinct subtype of acute myeloid leukemia with French-American… (More)
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Highly Cited
1998
Highly Cited
1998
Previous studies in yeast and mammalian cells showed a functional interaction between the amino-terminal domain and the carboxy… (More)
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Highly Cited
1996
Highly Cited
1996
Nuclear receptors (NRs) act as ligand-inducible transcription factors which regulate the expression of target genes upon binding… (More)
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