about
Impact of polychlorinated biphenyls contamination on estrogenic activity in human male serum.The potential for chemical mixtures from the environment to enable the cancer hallmark of sustained proliferative signallingA unique co-culture model for fundamental and applied studies of human fetoplacental steroidogenesis and interference by environmental chemicalsAssessing the carcinogenic potential of low-dose exposures to chemical mixtures in the environment: the challenge aheadRing-substituted analogs of 3,3'-diindolylmethane (DIM) induce apoptosis and necrosis in androgen-dependent and -independent prostate cancer cells.The steroid hormone biosynthesis pathway as a target for endocrine-disrupting chemicals.Challenges for research on polyphenols from foods in Alzheimer's disease: bioavailability, metabolism, and cellular and molecular mechanisms.Lithocholic acid induces endoplasmic reticulum stress, autophagy and mitochondrial dysfunction in human prostate cancer cells.Effects of Neonicotinoids on Promoter-Specific Expression and Activity of Aromatase (CYP19) in Human Adrenocortical Carcinoma (H295R) and Primary Umbilical Vein Endothelial (HUVEC) Cells.Antiandrogenic mechanisms of pesticides in human LNCaP prostate and H295R adrenocortical carcinoma cells.Antiproliferative, antiandrogenic and cytotoxic effects of novel caffeic acid derivatives in LNCaP human androgen-dependent prostate cancer cells.Antiandrogenic and growth inhibitory effects of ring-substituted analogs of 3,3'-diindolylmethane (ring-DIMs) in hormone-responsive LNCaP human prostate cancer cells.The 5-HT 2A serotonin receptor enhances cell viability, affects cell cycle progression and activates MEK-ERK1/2 and JAK2-STAT3 signalling pathways in human choriocarcinoma cell lines.Mixture effects of estrogenic compounds on proliferation and pS2 expression of MCF-7 human breast cancer cells.Quantitative RT-PCR methods for evaluating toxicant-induced effects on steroidogenesis using the H295R cell line.Effects of polybrominated diphenyl ethers on basal and TCDD-induced ethoxyresorufin activity and cytochrome P450-1A1 expression in MCF-7, HepG2, and H4IIE cells.Induction and inhibition of aromatase (CYP19) activity by natural and synthetic flavonoid compounds in H295R human adrenocortical carcinoma cells.2,3,7,8-Tetrachlorodibenzo-p-dioxin and diindolylmethanes differentially induce cytochrome P450 1A1, 1B1, and 19 in H295R human adrenocortical carcinoma cells.Bile acids induce apoptosis selectively in androgen-dependent and -independent prostate cancer cells2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) induces hepatic cytochrome P450-dependent arachidonic acid epoxygenation in diverse avian orders: regioisomer selectivity and immunochemical comparison of the TCDD-induced P450s to CYP1A4 and 1A5.Evaluation of a bioluminescent mouse model expressing aromatase PII-promoter-controlled luciferase as a tool for the study of endocrine disrupting chemicals.Induction and inhibition of aromatase (CYP19) activity by various classes of pesticides in H295R human adrenocortical carcinoma cells.Effects of natural and synthetic estrogens and various environmental contaminants on vitellogenesis in fish primary hepatocytes: comparison of bream (Abramis brama) and carp (Cyprinus carpio).Inhibition of aromatase activity by methyl sulfonyl PCB metabolites in primary culture of human mammary fibroblasts.Effects of environmental and natural estrogens on vitellogenin production in hepatocytes of the brown frog (Rana temporaria).Cytochrome P450 1A1 and 1B1 in human blood lymphocytes are not suitable as biomarkers of exposure to dioxin-like compounds: polymorphisms and interindividual variation in expression and inducibility.Placental and fetal steroidogenesis.Induction of ethoxy-resorufin-O-deethylase activity by halogenated aromatic hydrocarbons and polycyclic aromatic hydrocarbons in primary hepatocytes of the green frog (Rana esculenta).Diindolylmethane and its halogenated derivatives induce protective autophagy in human prostate cancer cells via induction of the oncogenic protein AEG-1 and activation of AMP-activated protein kinase (AMPK).The use of a unique co-culture model of fetoplacental steroidogenesis as a screening tool for endocrine disruptors: The effects of neonicotinoids on aromatase activity and hormone production.Human placenta expresses both peripheral and neuronal isoform of tryptophan hydroxylase.Suppression of aromatase activity in populations of bream (Abramis brama) from the river Elbe, Germany.Hepatic microsomal ethoxyresorufin O-deethylase-inducing potency in ovo and cytosolic Ah receptor binding affinity of 2,3,7,8-tetrachlorodibenzo-p-dioxin: comparison of four avian species.Monitoring biological effects of polychlorinated dibenzo-p-dioxins, dibenzofurans, and biphenyls in great blue heron chicks (Ardea herodias) in British Columbia.Biological effects of polychlorinated dibenzo-p-dioxins, dibenzofurans, and biphenyls in double-crested cormorant chicks (Phalacrocorax auritus).Fluoxetine and its active metabolite norfluoxetine disrupt estrogen synthesis in a co-culture model of the feto-placental unit.Human Primary Trophoblast Cell Culture Model to Study the Protective Effects of Melatonin Against Hypoxia/reoxygenation-induced Disruption.Effects of selective serotonin-reuptake inhibitors (SSRIs) on human villous trophoblasts syncytialization.Estrogenic effects of mixtures of phyto- and synthetic chemicals on uterine growth of prepubertal ratsNo effect of CYP1B1 Val432Leu polymorphism on CYP1B1 messenger RNA levels in an organochlorine-exposed population in Slovakia
P50
Q24815918-EF66259E-5921-4B63-AC74-6FE47491C5AEQ28087571-4B87FE82-6778-4E63-8549-2C695A50D868Q28383904-8F1B27A7-F55D-4E47-B1A7-61D8C471F95EQ28397132-FB321228-1905-4E3A-A845-30698A36BB11Q34741141-B9E81E0A-D49C-4878-955E-E5FB4CE616C8Q36522635-E0E55A6D-CA36-40F5-9420-125E7047E130Q37192480-E1ADCD4D-0E1F-4A48-B179-B21A2AFB1630Q37428836-6FBADAE4-1A73-41A2-A2FD-25970F024055Q38828135-96B267B1-80D2-4BED-A4C6-F0C54E78AA61Q38946999-6D2D7EC0-FC6A-4C57-8F43-7013E876D256Q39089869-4352E249-5B9E-49A3-92E4-D2BBB305D01AQ39591992-3A13DD79-CBE4-418F-88C8-0D1E749B0DFCQ39722714-351F766B-BD0E-4F27-8877-4DA5F08CC51CQ40102909-03626B2D-A812-409C-90FD-2BA16C15ABE1Q40424621-39B18740-D1E0-44D9-A996-44BD9AD6CE69Q40509264-C404EBAD-E0BD-4783-A8C2-8E41F13B5C71Q40523962-04A6FE08-933A-41FA-9844-C999CD5DA000Q40813823-A17E7768-FB81-4AAC-8AF7-54FB10CE48ECQ42149700-5564C328-A8E3-4D9F-9472-6E48F18058D1Q42541617-A79CA60C-6869-43CC-9391-FE4D6A1834E1Q42932288-7FE3CDE2-E325-4465-A91C-F2CDE3CA9E22Q44070940-A40DBB78-77E8-4720-95A7-F82C7EAEFB4FQ44907962-04AB424B-412F-455D-8489-A396332F4C67Q45181730-6DA1BF29-6E03-4681-970C-D2F7BD0AA5E7Q45218743-E99EFCD8-E5CB-43F8-98DF-93963BE30F24Q45230617-4AC813E7-339F-4F83-83AB-04770CBE5E52Q45983417-2DA5094E-8A63-4002-AF0E-37F0765376ABQ46664939-4E401B4D-0F72-4D94-B569-4DF76CBA0CD2Q47783102-6D01A07D-E85E-426B-A30D-D494EC3FBA66Q47954254-CC5ADC70-4C22-412E-A628-D25DEF304451Q48019577-D409EAB0-9EA0-4F65-BECF-213C633823A8Q48465045-157FC308-2913-4CE9-9358-643E5F4CD278Q50761911-72CA4F70-EBA2-4071-AB49-43D2E8880A16Q50773886-AC6235EA-B345-4FD8-92D9-1921EA12B843Q50775265-6DAF8F60-4B99-4615-A92C-1A55A730BB7AQ51301591-97E595B7-A624-4892-89A6-8EAD8DD95D2AQ51474538-76550678-7A31-49C3-974C-6BD1ED2A64F7Q52717784-659F911A-FB21-4EBC-B0C3-14BCFFE3D34EQ80146373-AC05893C-1A3A-4370-B9F6-433AC191A88CQ81521841-277E0FCA-A827-4B2A-9403-B887351D0325
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Thomas Sanderson
@ast
Thomas Sanderson
@en
Thomas Sanderson
@es
Thomas Sanderson
@nl
Thomas Sanderson
@sl
type
label
Thomas Sanderson
@ast
Thomas Sanderson
@en
Thomas Sanderson
@es
Thomas Sanderson
@nl
Thomas Sanderson
@sl
altLabel
T. Sanderson
@nl
prefLabel
Thomas Sanderson
@ast
Thomas Sanderson
@en
Thomas Sanderson
@es
Thomas Sanderson
@nl
Thomas Sanderson
@sl
P1053
H-7272-2015
P106
P1153
7004489858
P21
P31
P3829
P496
0000-0002-3190-2811
P569
2000-01-01T00:00:00Z