-
1
-
-
0242319568
-
An overview of commercially used brominated flame retardants, their applications, their use patterns in different countries/regions and possible modes of release
-
M. Alaee, P. Arias, A. Sjodin, and A. Bergman, An overview of commercially used brominated flame retardants, their applications, their use patterns in different countries/regions and possible modes of release, Environ. Int. 29 (2003), pp. 683-689.
-
(2003)
Environ. Int
, vol.29
, pp. 683-689
-
-
Alaee, M.1
Arias, P.2
Sjodin, A.3
Bergman, A.4
-
2
-
-
0242382566
-
Polybrominated diphenyl ether flame retardants in the North American environment
-
R.C. Hale, M. Alaee, J.B. Manchester-Neesvig, H.M. Stapleton, and M.G. Ikonomou, Polybrominated diphenyl ether flame retardants in the North American environment, Environ. Int. 29 (2003), pp. 771-779.
-
(2003)
Environ. Int
, vol.29
, pp. 771-779
-
-
Hale, R.C.1
Alaee, M.2
Manchester-Neesvig, J.B.3
Stapleton, H.M.4
Ikonomou, M.G.5
-
3
-
-
1242297693
-
Polybrominated diphenyl ethers in the environment and in people: A meta-analysis of concentrations
-
R.A. Hites, Polybrominated diphenyl ethers in the environment and in people: A meta-analysis of concentrations, Environ. Sci. Technol. 38 (2004), pp. 945-956.
-
(2004)
Environ. Sci. Technol
, vol.38
, pp. 945-956
-
-
Hites, R.A.1
-
4
-
-
0035050751
-
Polybrominated diphenyl ethers: Occurrence, dietary exposure, and toxicology
-
P.O. Darnerud, G.S. Eriksen, T. Johannesson, P.B. Larsen, and M. Viluksela, Polybrominated diphenyl ethers: Occurrence, dietary exposure, and toxicology, Environ. Health Perspect. 109(Suppl. 1) (2001), pp. 49-68.
-
(2001)
Environ. Health Perspect
, vol.109
, Issue.SUPPL. 1
, pp. 49-68
-
-
Darnerud, P.O.1
Eriksen, G.S.2
Johannesson, T.3
Larsen, P.B.4
Viluksela, M.5
-
5
-
-
0346495994
-
Brominated flame retardants: Cause for concern?
-
L.S. Birnbaum and D.F. Staskal, Brominated flame retardants: Cause for concern? Environ. Health Perspect. 112 (2004), pp. 9-17.
-
(2004)
Environ. Health Perspect
, vol.112
, pp. 9-17
-
-
Birnbaum, L.S.1
Staskal, D.F.2
-
6
-
-
33744913861
-
Highest PBDE levels (max 63 ppm) yet found in biota measured in seabird eggs from San Francisco Bay
-
J. She, A. Holden, M. Tanner, M. Sharp, T. Adelsbach, and K. Hooper, Highest PBDE levels (max 63 ppm) yet found in biota measured in seabird eggs from San Francisco Bay, Organohalogen Compd. 66 (2004), pp. 3939-3944.
-
(2004)
Organohalogen Compd
, vol.66
, pp. 3939-3944
-
-
She, J.1
Holden, A.2
Tanner, M.3
Sharp, M.4
Adelsbach, T.5
Hooper, K.6
-
7
-
-
14944370042
-
Polybrominated diphenyl ether flame retardants in the U.S. population: Current levels, temporal trends, and comparison with dioxins, dibenzofurans, and polychlorinated biphenyls
-
A. Schecter, O. Papke, K.C. Tung, J. Joseph, T.R. Harris, and J. Dahlgreen, Polybrominated diphenyl ether flame retardants in the U.S. population: Current levels, temporal trends, and comparison with dioxins, dibenzofurans, and polychlorinated biphenyls, J. Occup. Environ. Med. 47 (2005), pp. 199-211.
-
(2005)
J. Occup. Environ. Med
, vol.47
, pp. 199-211
-
-
Schecter, A.1
Papke, O.2
Tung, K.C.3
Joseph, J.4
Harris, T.R.5
Dahlgreen, J.6
-
8
-
-
33744943769
-
Levels and trends of brominated flame retardants in the European environment
-
R.J. Law, C.R. Allchin, J. de Boer, A. Covaci, D. Herzke, P. Lepom, S. Morris, J. Tronczynski, and C.A. de Wit, Levels and trends of brominated flame retardants in the European environment, Chemosphere 64 (2006), pp. 187-208.
-
(2006)
Chemosphere
, vol.64
, pp. 187-208
-
-
Law, R.J.1
Allchin, C.R.2
de Boer, J.3
Covaci, A.4
Herzke, D.5
Lepom, P.6
Morris, S.7
Tronczynski, J.8
de Wit, C.A.9
-
9
-
-
0035025255
-
In vitro estrogenicity of polybrominated diphenyl ethers, hydroxylated PDBEs, and polybrominated bisphenol A compounds
-
I.A. Meerts, R.J. Letcher, S. Hoving, G. Marsh, A. Bergman, J.G. Lemmen, B. van der Burg, and A. Brouwer, In vitro estrogenicity of polybrominated diphenyl ethers, hydroxylated PDBEs, and polybrominated bisphenol A compounds, Environ. Health Perspect. 109 (2001), pp. 399-407.
-
(2001)
Environ. Health Perspect
, vol.109
, pp. 399-407
-
-
Meerts, I.A.1
Letcher, R.J.2
Hoving, S.3
Marsh, G.4
Bergman, A.5
Lemmen, J.G.6
van der Burg, B.7
Brouwer, A.8
-
10
-
-
33745591889
-
In vitro profiling of the endocrine-disrupting potency of brominated flame retardants
-
T. Hamers, J.H. Kamstra, E. Sonneveld, A.J. Murk, M.H.A. Kester, P.L. Andersson, J. Legler, and A. Brouwer, In vitro profiling of the endocrine-disrupting potency of brominated flame retardants, Toxicol. Sci. 92 (2006), pp. 157-173.
-
(2006)
Toxicol. Sci
, vol.92
, pp. 157-173
-
-
Hamers, T.1
Kamstra, J.H.2
Sonneveld, E.3
Murk, A.J.4
Kester, M.H.A.5
Andersson, P.L.6
Legler, J.7
Brouwer, A.8
-
11
-
-
23044442687
-
In vivo and in vitro anti-androgenic effects of DE-71, a commercial polybrominated diphenyl ether (PBDE) mixture
-
T.E. Stoker, R.L. Cooper, C.S. Lambright, V.S. Wilson, J. Furr, and L.E. Gray, In vivo and in vitro anti-androgenic effects of DE-71, a commercial polybrominated diphenyl ether (PBDE) mixture, Toxicol. Appl. Pharmacol. 207 (2005), pp. 78-88.
-
(2005)
Toxicol. Appl. Pharmacol
, vol.207
, pp. 78-88
-
-
Stoker, T.E.1
Cooper, R.L.2
Lambright, C.S.3
Wilson, V.S.4
Furr, J.5
Gray, L.E.6
-
12
-
-
55949090982
-
Hydroxylated metabolites of the polybrominated diphenyl ether mixture DE-71 are weak estrogen receptor - a ligands
-
M. Mercado-Feliciano and R.M. Bigsby, Hydroxylated metabolites of the polybrominated diphenyl ether mixture DE-71 are weak estrogen receptor - a ligands, Environ. Health Perspect. 116 (2008), pp. 1315-1321.
-
(2008)
Environ. Health Perspect
, vol.116
, pp. 1315-1321
-
-
Mercado-Feliciano, M.1
Bigsby, R.M.2
-
13
-
-
33747802475
-
SAR and QSAR modeling of endocrine disruptors
-
J. Devillers, N. Marchand-Geneste, A. Carpy, and J.M. Porcher, SAR and QSAR modeling of endocrine disruptors, SAR QSAR Environ. Res. 17 (2006), pp. 393-412.
-
(2006)
SAR QSAR Environ. Res
, vol.17
, pp. 393-412
-
-
Devillers, J.1
Marchand-Geneste, N.2
Carpy, A.3
Porcher, J.M.4
-
14
-
-
67650097331
-
Comparison of several molecular docking programs: Pose prediction and virtual screening accuracy
-
J.B. Cross, D.C. Thompson, B.K. Rai, J. Christian Baber, K.Y. Fan, Y.B. Hu, and C. Humblet, Comparison of several molecular docking programs: Pose prediction and virtual screening accuracy, J. Chem. Inf. Model. 49 (2009), pp. 1455-1474.
-
(2009)
J. Chem. Inf. Model
, vol.49
, pp. 1455-1474
-
-
Cross, J.B.1
Thompson, D.C.2
Rai, B.K.3
Christian Baber, J.4
Fan, K.Y.5
Hu, Y.B.6
Humblet, C.7
-
15
-
-
56849085011
-
An efficient tool for identifying inhibitors based on 3D-QSAR and docking using feature-shape pharmacophore of biologically active conformation: A case study with CDK2/CyclinA
-
N.M. Mascarenhas and N. Ghoshal, An efficient tool for identifying inhibitors based on 3D-QSAR and docking using feature-shape pharmacophore of biologically active conformation: A case study with CDK2/CyclinA, Eur. J. Med. Chem. 43 (2008), pp. 2807-2818.
-
(2008)
Eur. J. Med. Chem
, vol.43
, pp. 2807-2818
-
-
Mascarenhas, N.M.1
Ghoshal, N.2
-
16
-
-
4544367743
-
Comparative evaluation of eight docking tools for docking and virtual screening accuracy
-
E. Kellenberger, J. Rodrigo, P. Muller, and D. Rognan, Comparative evaluation of eight docking tools for docking and virtual screening accuracy, Proteins 57 (2004), pp. 225-242.
-
(2004)
Proteins
, vol.57
, pp. 225-242
-
-
Kellenberger, E.1
Rodrigo, J.2
Muller, P.3
Rognan, D.4
-
17
-
-
0037434582
-
Surflex: Fully automatic flexible molecular docking using a molecular similarity-based search engine
-
A.N. Jain, Surflex: Fully automatic flexible molecular docking using a molecular similarity-based search engine, J. Med. Chem. 46 (2003), pp. 499-511.
-
(2003)
J. Med. Chem
, vol.46
, pp. 499-511
-
-
Jain, A.N.1
-
18
-
-
64249113960
-
Molecular design, synthesis and docking study of benz[b]oxepines and 12-oxobenzo[c] phenanthridinones as topoisomerase 1 inhibitors
-
S.H. Lee, H.T.M. Van, S.H. Yang, K.T. Lee, Y. Kwon, and W.J. Cho, Molecular design, synthesis and docking study of benz[b]oxepines and 12-oxobenzo[c] phenanthridinones as topoisomerase 1 inhibitors, Bioorg. Med. Chem. Lett. 19 (2009), pp. 2444-2447.
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, pp. 2444-2447
-
-
Lee, S.H.1
Van, H.T.M.2
Yang, S.H.3
Lee, K.T.4
Kwon, Y.5
Cho, W.J.6
-
19
-
-
64249172205
-
Structural modification of 3-arylisoquinolines to isoindolo[2,1-b]isoquino- linones for the development of novel topoisomerase 1 inhibitors with molecular docking study
-
H. Van and W. Cho, Structural modification of 3-arylisoquinolines to isoindolo[2,1-b]isoquino- linones for the development of novel topoisomerase 1 inhibitors with molecular docking study, Bioorg. Med. Chem. Lett. 19 (2009), pp. 2551-2554.
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, pp. 2551-2554
-
-
Van, H.1
Cho, W.2
-
20
-
-
52049120609
-
Molecular docking of intercalators and groove-binders to nucleic acids using Autodock and Surflex
-
P.A. Holt, J.B. Chaires, and J.O. Trent, Molecular docking of intercalators and groove-binders to nucleic acids using Autodock and Surflex, J. Chem. Inf. Model. 48 (2008), pp. 1602-1615.
-
(2008)
J. Chem. Inf. Model
, vol.48
, pp. 1602-1615
-
-
Holt, P.A.1
Chaires, J.B.2
Trent, J.O.3
-
21
-
-
67349261359
-
Effects of protein conformation in docking: Improved pose prediction through protein pocket adaptation
-
A.N. Jain, Effects of protein conformation in docking: improved pose prediction through protein pocket adaptation, J. Comput. Aid. Mol. Design 23 (2009), pp. 355-374.
-
(2009)
J. Comput. Aid. Mol. Design
, vol.23
, pp. 355-374
-
-
Jain, A.N.1
-
22
-
-
50549087247
-
Structure-based virtual screening for glycosyltransferase51
-
M. Yang, L. Zhou, Z.L. Zuo, X.Y. Tang, J. Liu, and X. Ma, Structure-based virtual screening for glycosyltransferase51, Mol. Simulat. 34 (2008), pp. 849-856.
-
(2008)
Mol. Simulat
, vol.34
, pp. 849-856
-
-
Yang, M.1
Zhou, L.2
Zuo, Z.L.3
Tang, X.Y.4
Liu, J.5
Ma, X.6
-
23
-
-
0032568931
-
Four amino acid residues are critical for high affinity binding of neuromedin B to the neuromedin B receptor
-
E. Sainz, M. Akeson, S.A. Mantey, R.T. Jensen, and J.F. Battey, Four amino acid residues are critical for high affinity binding of neuromedin B to the neuromedin B receptor, J. Biol. Chem. 273 (1998), pp. 15927-15932.
-
(1998)
J. Biol. Chem
, vol.273
, pp. 15927-15932
-
-
Sainz, E.1
Akeson, M.2
Mantey, S.A.3
Jensen, R.T.4
Battey, J.F.5
-
24
-
-
38649111953
-
Evaluation and QSAR modeling on multiple endpoints of estrogen activity based on different bioassays
-
H.X. Liu, E. Papa, and P. Gramatica, Evaluation and QSAR modeling on multiple endpoints of estrogen activity based on different bioassays, Chemosphere 70 (2008), pp. 1889-1897.
-
(2008)
Chemosphere
, vol.70
, pp. 1889-1897
-
-
Liu, H.X.1
Papa, E.2
Gramatica, P.3
-
25
-
-
0033782755
-
Quantitative comparisons of in vitro assays for estrogenic activities
-
H. Fang, W.D. Tong, R. Perkins, A.M. Soto, N.V. Prechtl, and D.M. Sheehan, Quantitative comparisons of in vitro assays for estrogenic activities, Environ. Health Perspect. 108 (2000), pp. 723-729.
-
(2000)
Environ. Health Perspect
, vol.108
, pp. 723-729
-
-
Fang, H.1
Tong, W.D.2
Perkins, R.3
Soto, A.M.4
Prechtl, N.V.5
Sheehan, D.M.6
-
26
-
-
68949213092
-
Binding orientations, QSAR, and molecular design of thiophene derivative inhibitors
-
S.Y. Liao, T.J. Chen, T.F. Miao, L. Qian, and K.C. Zheng, Binding orientations, QSAR, and molecular design of thiophene derivative inhibitors, Chem. Biol. Drug Des. 74 (2009), pp. 289-296.
-
(2009)
Chem. Biol. Drug Des
, vol.74
, pp. 289-296
-
-
Liao, S.Y.1
Chen, T.J.2
Miao, T.F.3
Qian, L.4
Zheng, K.C.5
-
27
-
-
0030667676
-
Molecular basis of agonism and antagonism in the oestrogen receptor
-
A. Brzozowski, A. Pike, Z. Dauter, R. Hubbard, T. Bonn, O. Engstrom, L. Ohman, G. Greene, J. Gustafsson, and M. Carlquist, Molecular basis of agonism and antagonism in the oestrogen receptor, Nature 389 (1997), pp. 753-758.
-
(1997)
Nature
, vol.389
, pp. 753-758
-
-
Brzozowski, A.1
Pike, A.2
Dauter, Z.3
Hubbard, R.4
Bonn, T.5
Engstrom, O.6
Ohman, L.7
Greene, G.8
Gustafsson, J.9
Carlquist, M.10
-
28
-
-
0032446607
-
The structural basis of estrogen receptor/coactivator recognition and the antagonism of this interaction by tamoxifen
-
A.K. Shiau, D. Barstad, P.M. Loria, L. Cheng, P.J. Kushner, D.A. Agard, and G.L. Greene, The structural basis of estrogen receptor/coactivator recognition and the antagonism of this interaction by tamoxifen, Cell 95 (1998), pp. 927-937.
-
(1998)
Cell
, vol.95
, pp. 927-937
-
-
Shiau, A.K.1
Barstad, D.2
Loria, P.M.3
Cheng, L.4
Kushner, P.J.5
Agard, D.A.6
Greene, G.L.7
-
29
-
-
18044382708
-
QSAR models using a large diverse set of estrogens
-
L.M. Shi, H. Fang, W.D. Tong, J. Wu, R. Perkins, R.M. Blair, W.S. Branham, S.L. Dial, C.L. Moland, and D.M. Sheehan, QSAR models using a large diverse set of estrogens, Chem. Inf. Comput. Sci. 41 (2001), pp. 186-195.
-
(2001)
Chem. Inf. Comput. Sci
, vol.41
, pp. 186-195
-
-
Shi, L.M.1
Fang, H.2
Tong, W.D.3
Wu, J.4
Perkins, R.5
Blair, R.M.6
Branham, W.S.7
Dial, S.L.8
Moland, C.L.9
Sheehan, D.M.10
-
30
-
-
57449086143
-
Exploring interactions of endocrine-disrupting compounds with different conformations of the human estrogen receptor r ligand binding domain: A molecular docking study
-
L. Celik, J. Lund, and B. Schiøtt, Exploring interactions of endocrine-disrupting compounds with different conformations of the human estrogen receptor r ligand binding domain: A molecular docking study, Chem. Res. Toxicol. 21 (2008), pp. 2195-2206.
-
(2008)
Chem. Res. Toxicol
, vol.21
, pp. 2195-2206
-
-
Celik, L.1
Lund, J.2
Schiøtt, B.3
-
31
-
-
17144447462
-
Effect of highly bioaccumulated polychlorinated biphenyl congeners on estrogen and androgen receptor activity
-
E.C. Bonefeld-Jørgensen, H.R. Andersen, T.H. Rasmussen, and A.M. Vinggaard, Effect of highly bioaccumulated polychlorinated biphenyl congeners on estrogen and androgen receptor activity, Toxicology 158 (2001), pp. 141-153.
-
(2001)
Toxicology
, vol.158
, pp. 141-153
-
-
Bonefeld-Jørgensen, E.C.1
Andersen, H.R.2
Rasmussen, T.H.3
Vinggaard, A.M.4
-
32
-
-
0027335891
-
Polychlorinated biphenyls (PCBs), dibenzo-p-dioxins (PCDDs), and dibenzofurans (PCDFs) as antiestrogens in MCF-7 human breast cancer cells: Quantitative structure-activity relationships
-
V. Krishnan and S. Safe, Polychlorinated biphenyls (PCBs), dibenzo-p-dioxins (PCDDs), and dibenzofurans (PCDFs) as antiestrogens in MCF-7 human breast cancer cells: quantitative structure-activity relationships, Toxicol. Appl. Pharmacol. 120 (1993), pp. 55-61.
-
(1993)
Toxicol. Appl. Pharmacol
, vol.120
, pp. 55-61
-
-
Krishnan, V.1
Safe, S.2
-
33
-
-
0035085038
-
Structure-activity relationships for a large diverse set of natural, synthetic, and environmental estrogens
-
H. Fang, W.D. Tong, L.M. Shi, R. Blair, R. Perkins, W. Branham, B.S. Hass, Q. Xie, S.L. Dial, C.L. Moland, and D.M. Sheehan, Structure-activity relationships for a large diverse set of natural, synthetic, and environmental estrogens, Chem. Res. Toxicol. 14 (2001), pp. 280-294.
-
(2001)
Chem. Res. Toxicol
, vol.14
, pp. 280-294
-
-
Fang, H.1
Tong, W.D.2
Shi, L.M.3
Blair, R.4
Perkins, R.5
Branham, W.6
Hass, B.S.7
Xie, Q.8
Dial, S.L.9
Moland, C.L.10
Sheehan, D.M.11
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