Generation of multiple farnesoid-X-receptor isoforms through the use of alternative promoters (Q28204305)

1

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Kathleen Murphy

2

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Bowman Miao

3

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John R Link

4

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Mark R Cunningham

5

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Mark J Rupar

6

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Paul L Gunyuzlu

7

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Thomas F Haws

8

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Altaf Kassam

9

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Francoise Powell

10

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Gregory F Hollis

11

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Peter R Young

12

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Ranjan Mukherjee

13

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Timothy C Burn

Autoregulation of glucocorticoid receptor gene expression

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language of work or name

English

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publication date

15 May 2002

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published in

Gene

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volume

290

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issue

1-2

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page(s)

35-43

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A novel method for real time quantitative RT-PCR.

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A regulatory cascade of the nuclear receptors FXR, SHP-1, and LRH-1 represses bile acid biosynthesis

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Multiple androgen response elements and a Myc consensus site in the androgen receptor (AR) coding region are involved in androgen-mediated up-regulation of AR messenger RNA.

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Identification of a bile acid-responsive element in the human ileal bile acid-binding protein gene. Involvement of the farnesoid X receptor/9-cis-retinoic acid receptor heterodimer

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Identification of a thyroid hormone receptor that is pituitary-specific

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Regulation of hepatic 7 alpha-hydroxylase expression and response to dietary cholesterol in the rat and hamster

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Effect of retinoid status on alpha, beta and gamma retinoic acid receptor mRNA levels in various rat tissues

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Initial sequencing and analysis of the human genome

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Multiplicity generates diversity in the retinoic acid signalling pathways

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Molecular basis for feedback regulation of bile acid synthesis by nuclear receptors

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Identification of a nuclear receptor for bile acids

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Thyroid hormone-independent interaction between the thyroid hormone receptor beta2 amino terminus and coactivators

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Bile acids: natural ligands for an orphan nuclear receptor

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Expression of three forms of thyroid hormone receptor in human tissues

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Hepatocyte nuclear factor-1alpha is an essential regulator of bile acid and plasma cholesterol metabolism

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Targeted disruption of the nuclear receptor FXR/BAR impairs bile acid and lipid homeostasis.

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Opposite regulation of PPAR-α and -γ gene expression by both their ligands and retinoic acid in brown adipocytes

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Peroxisome proliferator-activated receptor gene expression in human tissues. Effects of obesity, weight loss, and regulation by insulin and glucocorticoids

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Endogenous bile acids are ligands for the nuclear receptor FXR/BAR

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Activation of the orphan receptor RIP14 by retinoids

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Structural organization of mouse peroxisome proliferator-activated receptor gamma (mPPAR gamma) gene: alternative promoter use and different splicing yield two mPPAR gamma isoforms

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