D-003 does not possess oestrogenic potential in-vivo: findings of the uterotrophic assay.

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Metabolomics approach to risk assessment: methoxyclor exposure in rats.

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D-003 does not possess oestrogenic potential in-vivo: findings of the uterotrophic assay.

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2007 nî lūn-bûn

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2007年の論文

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2007年学术文章

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D-003 does not possess oestrogenic potential in-vivo: findings of the uterotrophic assay.

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D-003 does not possess oestrogenic potential in-vivo: findings of the uterotrophic assay.

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type

Item

label

D-003 does not possess oestrogenic potential in-vivo: findings of the uterotrophic assay.

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D-003 does not possess oestrogenic potential in-vivo: findings of the uterotrophic assay.

@nl

prefLabel

D-003 does not possess oestrogenic potential in-vivo: findings of the uterotrophic assay.

@en

D-003 does not possess oestrogenic potential in-vivo: findings of the uterotrophic assay.

@nl

P1476

D-003 does not possess oestrogenic potential in-vivo: findings of the uterotrophic assay.

@en

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Ariadne Gutiérrez

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Balia Pardo

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Maikel Valle

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Miriam Noa

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Nilda Mendoza

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Rafael Gámez

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Rosa Mas

http://www.w3.org/2001/XMLSchema#string

Sarahí Mendoza

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P2860

The OECD program to validate the rat uterotrophic bioassay to screen compounds for in vivo estrogenic responses: phase 1.

Apoptosis and osteoporosis.

Estradiol-type activity of coumestrol in mature and immature ovariectomized rat uterotrophic assays.

Bone quality--the material and structural basis of bone strength and fragility.

A prospective study of endogenous estrogens and breast cancer in postmenopausal women.

Osteoporosis intervention following distal forearm fractures: a missed opportunity?

Nitrogen-containing bisphosphonates inhibit the mevalonate pathway and prevent post-translational prenylation of GTP-binding proteins, including Ras.

Inhibition of cholesterol biosynthesis in cultured fibroblasts by D003, a mixture of very long chain saturated fatty acids.

Inhibition of rat lipoprotein lipid peroxidation by the oral administration of D003, a mixture of very long-chain saturated fatty acids.

The ability of statins to inhibit bone resorption is directly related to their inhibitory effect on HMG-CoA reductase activity.

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1433-1437

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scholarly article

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10.1211/JPP.59.10.0015

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2007-10-01T00:00:00Z

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P698

17910820

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D-003 does not possess oestrogenic potential in-vivo: findings of the uterotrophic assay.

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P2860

D-003 does not possess oestrogenic potential in-vivo: findings of the uterotrophic assay.

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P1433

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P2093

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P1433

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P698