scholarly article | Q13442814 |
P2093 | author name string | J. Cai | |
L. Zimmer-Nechemias | |||
K. D. Setchell | |||
J. E. Heubi | |||
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Genistein, daidzein, and their .beta.-glycoside conjugates: antitumor isoflavones in soybean foods from American and Asian diets | Q29396585 | ||
Genistein, a specific inhibitor of tyrosine-specific protein kinases | Q29618097 | ||
Analysis of plasma isoflavones by reversed-phase HPLC-multiple reaction ion monitoring-mass spectrometry | Q33486332 | ||
A specific breeding problem of sheep on subterranean clover pastures in Western Australia | Q34146541 | ||
Nonsteroidal estrogens of dietary origin: possible roles in hormone-dependent disease | Q34258149 | ||
Phytoestrogens: epidemiology and a possible role in cancer protection | Q34831826 | ||
Soy intake and cancer risk: a review of the in vitro and in vivo data | Q36737007 | ||
Biochemical targets of the isoflavone genistein in tumor cell lines | Q40613426 | ||
Rapid HPLC analysis of dietary phytoestrogens from legumes and from human urine | Q41003406 | ||
Urinary lignan and isoflavonoid excretion in men and women consuming vegetable and soy diets | Q42474858 | ||
Dietary effects on breast-cancer risk in Singapore | Q45047583 | ||
Neonatal genistein chemoprevents mammary cancer. | Q53467264 | ||
Pituitary-Gonadal Relations in Infancy: 2. Patterns of Serum Gonadal Steroid Concentrations in Man from Birth to Two Years of Age | Q67444659 | ||
Identification of the phyto-oestrogen 3',7-dihydroxyisoflavan, an isomer of equol, in human urine and cow's milk | Q67988764 | ||
High-performance liquid chromatographic analysis of phytoestrogens in soy protein preparations with ultraviolet, electrochemical and thermospray mass spectrometric detection | Q68963265 | ||
Isoflavone intakes by Japanese were overestimated | Q72026186 | ||
Essential fatty acids and USDA's Food Guide Pyramid | Q72026189 | ||
A urinary profile study of dietary phytoestrogens. The identification and mode of metabolism of new isoflavonoids | Q72030104 | ||
Biological effects of a diet of soy protein rich in isoflavones on the menstrual cycle of premenopausal women | Q72158316 | ||
Effects of infant nutrition on cholesterol synthesis rates | Q72379850 | ||
Plasma concentrations of phyto-oestrogens in Japanese men | Q72656995 | ||
Determination of lignans and isoflavonoids in human female plasma following dietary supplementation | Q72728418 | ||
Determination of isoflavones in soybean flours, protein concentrates, and isolates | Q104384994 | ||
P433 | issue | 9070 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 23-27 | |
P577 | publication date | 1997-07-01 | |
1997-07-05 | |||
P1433 | published in | The Lancet | Q939416 |
P1476 | title | Exposure of infants to phyto-oestrogens from soy-based infant formula | |
P478 | volume | 350 |
Q26748994 | A Mouse Model for Studying Nutritional Programming: Effects of Early Life Exposure to Soy Isoflavones on Bone and Reproductive Health |
Q24815119 | A critical review of methods for comparing estrogenic activity of endogenous and exogenous chemicals in human milk and infant formula |
Q34125778 | A hypothesis regarding the molecular mechanism underlying dietary soy-induced effects on seizure propensity |
Q44612675 | A model to estimate the oestrogen receptor mediated effects from exposure to soy isoflavones in food |
Q36064982 | A phytoestrogen-rich diet increases energy expenditure and decreases adiposity in mice |
Q33889203 | Absolute bioavailability of isoflavones from soy protein isolate-containing food in female BALB/c mice |
Q28396342 | Acute and chronic effects of oral genistein administration in neonatal mice |
Q43751829 | Altered sexually dimorphic nucleus of the preoptic area (SDN-POA) volume in adult Long-Evans rats by dietary soy phytoestrogens |
Q38945934 | Analysis of Naturally Occurring Steroid Hormones in Infant Formulas by HPLC-MS/MS and Contribution to Dietary Intake |
Q35119162 | Analysis of phyto-oestrogens in biological matrices |
Q43606362 | Animal models impacted by phytoestrogens in commercial chow: implications for pathways influenced by hormones |
Q36918173 | Anti-diabetic functions of soy isoflavone genistein: mechanisms underlying its effects on pancreatic β-cell function |
Q27321724 | Anxiogenic effects of developmental bisphenol A exposure are associated with gene expression changes in the juvenile rat amygdala and mitigated by soy |
Q42406722 | Assessing risks and benefits of genistein and soy. |
Q41680654 | Assessment of safety and efficacy of perinatal or peripubertal exposure to daidzein on bone development in rats |
Q33789925 | Association of intrauterine and early-life exposures with diagnosis of uterine leiomyomata by 35 years of age in the Sister Study |
Q40653893 | Cell‐transforming activity and mutagenicity of 5 phytoestrogens in cultured mammalian cells |
Q61940353 | Changes in Isoflavone Concentration with 58 Years of Genetic Improvement of Short-Season Soybean Cultivars in Canada |
Q35334938 | Circulating levels of genistein in the neonate, apart from dose and route, predict future adverse female reproductive outcomes |
Q37595210 | Coexposure to phytoestrogens and bisphenol a mimics estrogenic effects in an additive manner |
Q51896888 | Combined developmental toxicity of bisphenol A and genistein in micromass cultures of rat embryonic limb bud and midbrain cells |
Q42694450 | Comparative Developmental Toxicity of Flavonoids Using an Integrative Zebrafish System |
Q28369392 | Comparative estrogenic activity of wine extracts and organochlorine pesticide residues in food |
Q35458175 | Comparative metabolomics in vegans and omnivores reveal constraints on diet-dependent gut microbiota metabolite production. |
Q43960748 | Comparison of the oestrogenic effects of infant milk formulae, oestradiol and the phytoestrogen coumestrol delivered continuously in the drinking water to ovariectomised mice |
Q28387994 | Concerns for the use of soy-based formulas in infant nutrition |
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Q35021742 | Criteria for chemical selection for programs on human milk surveillance and research for environmental chemicals |
Q24814058 | Cross-species and interassay comparisons of phytoestrogen action |
Q24816122 | Cumulative dietary energy intake determines the onset of puberty in female rats |
Q51612396 | Daidzein supplementation prevents non-alcoholic fatty liver disease through alternation of hepatic gene expression profiles and adipocyte metabolism. |
Q46420971 | Developmental and reproductive toxicity of soybean isoflavones to immature SD rats. |
Q43016801 | Developmental exposures of male rats to soy isoflavones impact Leydig cell differentiation. |
Q34119212 | Diet and the aetiology of temporal advances in human and rodent sexual development |
Q37307326 | Dietary factors influence production of the soy isoflavone metabolite s-(-)equol in healthy adults |
Q46867150 | Dietary phyto-oestrogens and the risk of ovarian and endometrial cancers: findings from two Australian case-control studies |
Q44032245 | Dietary soy phytoestrogens and ERalpha signalling modulate interferon gamma production in response to bacterial infection |
Q48798615 | Dietary soy phytoestrogens produce anxiolytic effects in the elevated plus-maze |
Q37108482 | Disrupted female reproductive physiology following neonatal exposure to phytoestrogens or estrogen specific ligands is associated with decreased GnRH activation and kisspeptin fiber density in the hypothalamus |
Q21284799 | Diverse effects of phytoestrogens on the reproductive performance: cow as a model |
Q30774468 | Dose- and Time-Dependent Transcriptional Response of Ishikawa Cells Exposed to Genistein |
Q44484816 | Drug interaction potential of soy extract and Panax ginseng |
Q88679101 | EB 2017 Article: Soy protein isolate feeding does not result in reproductive toxicity in the pre-pubertal rat testis |
Q34247954 | Early exposure to soy isoflavones and effects on reproductive health: a review of human and animal studies |
Q36238701 | Early-life soy exposure and age at menarche |
Q35682882 | Early-life soy exposure and gender-role play behavior in children |
Q44447376 | Effect of daidzein on CYP1A2 activity and pharmacokinetics of theophylline in healthy volunteers |
Q44341176 | Effect of human dietary exposure levels of genistein during gestation and lactation on long-term reproductive development and sperm quality in mice |
Q36661701 | Effect of sulphation on the oestrogen agonist activity of the phytoestrogens genistein and daidzein in MCF-7 human breast cancer cells |
Q90293374 | Effects of Phytoestrogens on the Developing Brain, Gut Microbiota, and Risk for Neurobehavioral Disorders |
Q43819088 | Effects of dietary genistein exposure during development on male and female CD (Sprague-Dawley) rats |
Q40738940 | Effects of flavonoid phytochemicals on cortisol production and on activities of steroidogenic enzymes in human adrenocortical H295R cells |
Q42141248 | Effects of genistein and equol on human and rat testicular 3beta-hydroxysteroid dehydrogenase and 17beta-hydroxysteroid dehydrogenase 3 activities |
Q36207772 | Effects of phytoestrogen on sexual development |
Q34123754 | Endocrine Disruptors and Leydig Cell Function |
Q38889619 | Endocrine disruption by dietary phyto-oestrogens: impact on dimorphic sexual systems and behaviours |
Q93349801 | Endocrine disruption through membrane estrogen receptors and novel pathways leading to rapid toxicological and epigenetic effects |
Q24670574 | Endocrine disruptors and human health--is there a problem? An update |
Q36655771 | Equol inhibits growth, induces atresia, and inhibits steroidogenesis of mouse antral follicles in vitro |
Q24594674 | Equol: history, chemistry, and formation |
Q44148648 | Estrogen receptor expression in the prostate of rats treated with dietary genistein |
Q43724663 | Estrogenic activity of two standardized red clover extracts (Menoflavon) intended for large scale use in hormone replacement therapy |
Q43899324 | Estrogenic isoflavones in rodent diets |
Q28393495 | Exogenous hormonal regulation in breast cancer cells by phytoestrogens and endocrine disruptors |
Q37511143 | Factors to consider in the association between soy isoflavone intake and breast cancer risk |
Q104389007 | Flavonoids in Sophora Species |
Q61988437 | Food plant toxicants and safety |
Q34313658 | Genistein enhancement of respiratory allergen trimellitic anhydride-induced IgE production by adult B6C3F1 mice following in utero and postnatal exposure |
Q48323215 | Genistein exerts estrogen-like effects in male mouse reproductive tract |
Q37595216 | Genistein exposure during the early postnatal period favors the development of obesity in female, but not male rats |
Q34619801 | Genistein modulation of streptozotocin diabetes in male B6C3F1 mice can be induced by diet |
Q34541665 | Genistein suppresses LPS-induced inflammatory response through inhibiting NF-κB following AMP kinase activation in RAW 264.7 macrophages |
Q24529917 | Goitrogenic and estrogenic activity of soy isoflavones |
Q33849301 | Guidance from an NIH workshop on designing, implementing, and reporting clinical studies of soy interventions |
Q34881409 | Identification and quantification of polyphenol phytoestrogens in foods and human biological fluids |
Q36952300 | Impact of neonatal exposure to the ERalpha agonist PPT, bisphenol-A or phytoestrogens on hypothalamic kisspeptin fiber density in male and female rats |
Q36900894 | In Utero exposure to genistein enhanced intranasal house dust mite allergen-induced respiratory sensitization in young adult B6C3F1 mice |
Q34881523 | Inactivation of thyroid peroxidase by soy isoflavones, in vitro and in vivo |
Q73514104 | Induction of micronuclei, DNA strand breaks and HPRT mutations in cultured Chinese hamster V79 cells by the phytoestrogen coumoestrol |
Q32052146 | Infant formulas and soy protein-based formulas: current data |
Q44808608 | Influence of soya-based infant formula consumption on isoflavone and gut microflora metabolite concentrations in urine and on faecal microflora composition and metabolic activity in infants and children |
Q61984377 | Is equol production beneficial to health? |
Q43892970 | Isoflavone content of the soy based supplements |
Q51321834 | Isoflavone exposure throughout suckling results in improved adult bone health in mice. |
Q64077130 | Isoflavones |
Q80595020 | Isoflavones from soya foods are more bioavailable in children than adults |
Q31165973 | Isoflavones in urine, saliva, and blood of infants: data from a pilot study on the estrogenic activity of soy formula |
Q34460804 | Isoflavones, genistein and daidzein, regulate mucosal immune response by suppressing dendritic cell function |
Q44843581 | Isoflavonoid biosynthesis and accumulation in developing soybean seeds |
Q37721521 | Long-term effects of chromatin remodeling and DNA damage in stem cells induced by environmental and dietary agents |
Q21129084 | Long-term effects of environmental endocrine disruptors on reproductive physiology and behavior |
Q34084662 | Long-term exposure to dietary sources of genistein induces estrogen-independence in the human breast cancer (MCF-7) xenograft model |
Q35883554 | Low-dose dietary genistein negates the therapeutic effect of tamoxifen in athymic nude mice |
Q30875241 | Management of bovine protein allergy: new perspectives and nutritional aspects |
Q37364535 | Marked individual variation in isoflavone metabolism after a soy challenge can modulate the skeletal effect of isoflavones in premenopausal women |
Q48952765 | Maternal and perinatal brain aromatase: effects of dietary soy phytoestrogens. |
Q34508191 | Maternal genistein alters coat color and protects Avy mouse offspring from obesity by modifying the fetal epigenome |
Q36490858 | Meeting report: batch-to-batch variability in estrogenic activity in commercial animal diets--importance and approaches for laboratory animal research |
Q55034008 | Molecular 'pharming' with plant P450s. |
Q53442755 | Multidimensional chemobehavior analysis of flavonoids and neuroactive compounds in zebrafish. |
Q35046420 | Multiple-targeting and conformational selection in the estrogen receptor: computation and experiment |
Q26155136 | NTP-CERHR expert panel report on the reproductive and developmental toxicity of genistein |
Q23915889 | NTP-CERHR expert panel report on the reproductive and developmental toxicity of soy formula |
Q28829268 | Neonatal exposure of 17β-estradiol has no effects on mutagenicity of 7,12-dimethylbenz [a] anthracene in reproductive tissues of adult mice |
Q44873150 | Neonatal exposure to endocrine active compounds or an ERbeta agonist increases adult anxiety and aggression in gonadally intact male rats |
Q34553920 | Neonatal exposure to genistein adversely impacts the ontogeny of hypothalamic kisspeptin signaling pathways and ovarian development in the peripubertal female rat |
Q83553682 | Neonatal exposure to genistein ameliorates high-fat diet-induced non-alcoholic steatohepatitis in rats |
Q37181654 | Neonatal exposure to genistein disrupts ability of female mouse reproductive tract to support preimplantation embryo development and implantation |
Q58557102 | Neonatal genistein exposure disrupts ovarian and uterine development in the mouse by inhibiting cellular proliferation |
Q45400662 | No difference indicated in electroencephalographic power spectral analysis in 3- and 6-month-old infants fed soy- or milk-based formula |
Q41701691 | Nutrition. From 'whither' to 'wither' micronutrient malnutrition? |
Q28392900 | Oral exposure to genistin, the glycosylated form of genistein, during neonatal life adversely affects the female reproductive system |
Q28389598 | Overlapping but distinct effects of genistein and ethinyl estradiol (EE(2)) in female Sprague-Dawley rats in multigenerational reproductive and chronic toxicity studies |
Q34514602 | PTEN and p53 cross-regulation induced by soy isoflavone genistein promotes mammary epithelial cell cycle arrest and lobuloalveolar differentiation |
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Q44053469 | Pharmacokinetic analysis in serum of genistein administered subcutaneously to neonatal mice |
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