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Deepak S. Lala

Researcher at Duke University

Publications -  12
Citations -  2475

Deepak S. Lala is an academic researcher from Duke University. The author has contributed to research in topics: Steroidogenic factor 1 & Nuclear receptor. The author has an hindex of 11, co-authored 12 publications receiving 2414 citations. Previous affiliations of Deepak S. Lala include University of Texas Southwestern Medical Center & Howard Hughes Medical Institute.

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Journal ArticleDOI

Steroidogenic factor I, a key regulator of steroidogenic enzyme expression, is the mouse homolog of fushi tarazu-factor I.

TL;DR: The model that a steroidogenic cell-selective protein interacts with related promoter elements from three steroidogenic enzymes to regulate their coordinate expression is supported and a cDNA is isolate and characterize that very likely encodes this protein.
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The nuclear receptor steroidogenic factor 1 acts at multiple levels of the reproductive axis.

TL;DR: Novel roles are established in reproductive function of Steroidogenic factor 1 at other levels of the hypothalamic/pituitary/gonadal axis and a possible mechanism for the impaired gonadotropin expression in Ftz-F1-disrupted mice is established.
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Characterization of the mouse FTZ-F1 gene, which encodes a key regulator of steroid hydroxylase gene expression

TL;DR: It is shown thatSF-1 is selectively expressed in steroidogenic cells, that an antiserum against its protein product specifically abolishes the SF-1-related gel-shift complex, and that its coexpression increases promoter activity of the 21-hydroxylase 5'-flanking region in transfection experiments.
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Steroidogenic factor 1: an essential mediator of endocrine development.

TL;DR: This chapter will review the experiments that established SF-1 as a pivotal, global determinant of endocrine differentiation and function, as well as the current status of research aimed at delineating its roles in specific tissues.
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Activation of the orphan nuclear receptor steroidogenic factor 1 by oxysterols

TL;DR: It is shown that 25, 26, or 27-hydroxycholesterol, known suppressors of cholesterol biosynthesis, enhance SF-1-dependent transcriptional activity and this results suggest that specific oxysterols may mediate transcriptional activation via different intracellular receptors.