(Q24813419)

English

Assessment of prediction confidence and domain extrapolation of two structure-activity relationship models for predicting estrogen receptor binding activity

scientific article

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scholarly article

1 reference

Europe PubMed Central

5 July 2017

Assessment of prediction confidence and domain extrapolation of two structure-activity relationship models for predicting estrogen receptor binding activity (English)

1 reference

Europe PubMed Central

5 July 2017

1 reference

based on heuristic

inferred from title

1

object named as

Weida Tong

1 reference

Europe PubMed Central

5 July 2017

4

object named as

Leming Shi

1 reference

Europe PubMed Central

5 July 2017

3

object named as

Huixiao Hong

1 reference

Europe PubMed Central

5 July 2017

author name string

Qian Xie

2

1 reference

Europe PubMed Central

5 July 2017

Hong Fang

5

1 reference

Europe PubMed Central

5 July 2017

Roger Perkins

6

1 reference

Europe PubMed Central

5 July 2017

language of work or name

0 references

publication date

1 August 2004

1 reference

Europe PubMed Central

5 July 2017

number of pages

6

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inferred from page(s)

Environmental Health Perspectives

1 reference

Europe PubMed Central

5 July 2017

112

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Europe PubMed Central

5 July 2017

12

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Europe PubMed Central

5 July 2017

1249-1254

1 reference

Europe PubMed Central

5 July 2017

Methods for reliability and uncertainty assessment and for applicability evaluations of classification- and regression-based QSARs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1277118

7 April 2017

Prediction of estrogen receptor binding for 58,000 chemicals using an integrated system of a tree-based model with structural alerts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1277118

7 April 2017

Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1277118

7 April 2017

Structure-activity relationship approaches and applications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1277118

28 September 2017

Decision forest: combining the predictions of multiple independent decision tree models

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1277118

28 September 2017

QSAR models using a large diverse set of estrogens

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1277118

28 September 2017

Health-effects related structure-toxicity relationships: a paradigm for the first decade of the new millennium

1 reference

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28 September 2017

Induction of the estrogen specific mitogenic response of MCF-7 cells by selected analogues of estradiol-17 beta: a 3D QSAR study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1277118

28 September 2017

Quantitative structure-activity relationships (QSARs) for estrogen binding to the estrogen receptor: predictions across species

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1277118

28 September 2017

Predicting modes of toxic action from chemical structure: an overview

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1277118

28 September 2017

Comparative QSAR in toxicology: examples from teratology and cancer chemotherapy of aniline mustards

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1277118

28 September 2017

The expanding role of quantitative structure-activity relationships (QSAR) in toxicology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1277118

28 September 2017

Quantitative structure-based modeling applied to characterization and prediction of chemical toxicity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1277118

30 May 2018

Ligand-based identification of environmental estrogens.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1277118

30 May 2018

Use of knowledge bases and QSARs to estimate the relative ecological risk of agrichemicals: a problem formulation exercise.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1277118

30 May 2018

Study of 202 Natural, Synthetic, and Environmental Chemicals for Binding to the Androgen Receptor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1277118

28 November 2018

An integrated "4-phase" approach for setting endocrine disruption screening priorities--phase I and II predictions of estrogen receptor binding affinity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1277118

28 November 2018

The estrogen receptor relative binding affinities of 188 natural and xenochemicals: structural diversity of ligands.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1277118

28 November 2018

Novel variable selection quantitative structure--property relationship approach based on the k-nearest-neighbor principle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1277118

28 November 2018

Comparison of estrogen receptor alpha and beta subtypes based on comparative molecular field analysis (CoMFA).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1277118

28 November 2018

Evaluation of quantitative structure-activity relationship methods for large-scale prediction of chemicals binding to the estrogen receptor.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1277118

28 November 2018

Three-dimensional quantitative structure-activity relationship study of nonsteroidal estrogen receptor ligands using the comparative molecular field analysis/cross-validated r2-guided region selection approach.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1277118

28 November 2018

QSAR models for binding of estrogenic compounds to estrogen receptor alpha and beta subtypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15345371

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phytoestrogens and mycoestrogens bind to the rat uterine estrogen receptor

1 reference

https://pubmed.ncbi.nlm.nih.gov/15345371

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings

1 reference

https://api.crossref.org/works/10.1289%2FEHP.7125

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1289/EHP.7125

1 reference

Europe PubMed Central

5 July 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Europe PubMed Central

5 July 2017

1 reference

Europe PubMed Central

5 July 2017

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