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1. Full Text Cracking the Estrogen Receptor's Posttranslational Code in Breast Tumors
by Le Romancer, Muriel and Poulard, Coralie and Cohen, Pascale and Sentis, Stéphanie and Renoir, Jack-Michel and Corbo, Laura
Endocrine Reviews, ISSN 0163-769X, 10/2011, Volume 32, Issue 5, pp. 597 - 622
Estrogen signaling pathways, because of their central role in regulating the growth and survival of breast tumor cells, have been identified as suitable and... 
O-GLYCOSYLATION/O-PHOSPHORYLATION | GROWTH-FACTOR RECEPTOR | LIGAND-INDEPENDENT ACTIVATION | TRANSCRIPTIONAL ACTIVITY | ENDOCRINOLOGY & METABOLISM | CREB-BINDING-PROTEIN | ALPHA HINGE-REGION | CANCER-CELL-PROLIFERATION | NF-KAPPA-B | STEROID-RECEPTOR | ER-ALPHA | Estrogens - physiology | Antineoplastic Agents, Hormonal | Estrogen Receptor beta - physiology | Phosphorylation | Receptors, Estrogen - genetics | Signal Transduction | Humans | Breast Neoplasms - drug therapy | Protein Processing, Post-Translational - physiology | Breast Neoplasms - chemistry | Estrogen Receptor Modulators - therapeutic use | Ubiquitination | Animals | Estrogen Receptor alpha - genetics | Estrogen Receptor beta - genetics | Receptors, Estrogen - chemistry | Protein Processing, Post-Translational - drug effects | Estrogen Receptor alpha - analysis | Female | Acetylation | Estrogen Receptor alpha - physiology | Mutation | Methylation | Receptors, Estrogen - physiology | Receptors, Estrogen | Estrogens | Estrogen Receptor Modulators | Breast Neoplasms | Life Sciences | Estrogen Receptor alpha | Protein Processing, Post-Translational | Estrogen Receptor beta | Cancer
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2. Full Text The Relationship Among HOXA10, Estrogen Receptor α, Progesterone Receptor, and Progesterone Receptor B Proteins in Rectosigmoid Endometriosis
: A Tissue Microarray Study
by Zanatta, Alysson and Pereira, Ricardo Mendes Alves and Rocha, André Monteiro da and Cogliati, Bruno and Baracat, Edmund Chada and Taylor, Hugh S and Motta, Eduardo Leme Alves da and Serafini, Paulo Cesar
Reproductive Sciences, ISSN 1933-7191, 1/2015, Volume 22, Issue 1, pp. 31 - 37
Background: Very few studies have evaluated the expression of homeobox A10 (HOXA10) and steroid (estrogen and progesterone) receptors exclusively in deep... 
HOXA10 | deep endometriosis pathogenesis | estrogen receptor | progesterone receptor | rectosigmoid endometriosis | MOUSE | ESTABLISHMENT | HOMEOBOX GENES | OBSTETRICS & GYNECOLOGY | RESPONSE ELEMENT | NODULES | REPRODUCTIVE BIOLOGY | DISEASE | ERE | CLUSTER | EXPRESSION | EXPOSURE | Immunohistochemistry | Sigmoid Diseases - pathology | Epithelial Cells - chemistry | Sigmoid Diseases - physiopathology | Tissue Array Analysis | Humans | Rectal Diseases - physiopathology | Stromal Cells - chemistry | Menstrual Cycle | Rectal Diseases - pathology | Endometriosis - pathology | Endometrium - chemistry | Receptors, Progesterone - analysis | Homeodomain Proteins - analysis | Endometriosis - metabolism | Endometrium - physiopathology | Estrogen Receptor alpha - analysis | Adult | Female | Sigmoid Diseases - metabolism | Rectal Diseases - metabolism | Endometrium - pathology | Endometriosis - physiopathology | Original
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3. Full Text Genome-Wide Analysis of Estrogen Receptor α DNA Binding and Tethering Mechanisms Identifies Runx1 as a Novel Tethering Factor in Receptor-Mediated Transcriptional Activation
by Joshua D. Stender and Kyuri Kim and Tze Howe Charn and Barry Komm and Ken C. N. Chang and W. Lee Kraus and Christopher Benner and Christopher K. Glass and Benita S. Katzenellenbogen
Molecular and Cellular Biology, ISSN 0270-7306, 08/2010, Volume 30, Issue 16, pp. 3943 - 3955
Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley... 
BREAST-CANCER CELLS | TARGET GENES | SELECTIVE LIGANDS | DOMAIN | REGULATED GENE-EXPRESSION | NUCLEAR RECEPTORS | BIOCHEMISTRY & MOLECULAR BIOLOGY | RESPONSE ELEMENTS | IN-VIVO | SITES | ER-ALPHA | CELL BIOLOGY | DNA, Neoplasm - metabolism | Vesicular Transport Proteins - metabolism | Humans | Transcriptional Activation | DNA Primers - genetics | Breast Neoplasms - metabolism | Base Sequence | Estrogen Receptor alpha - metabolism | Female | Estradiol - pharmacology | Protein Structure, Tertiary | Genome-Wide Association Study | Estrogen Receptor alpha - chemistry | Core Binding Factor Alpha 2 Subunit - metabolism | Vesicular Transport Proteins - genetics | Mutant Proteins - genetics | Mutant Proteins - metabolism | Vesicular Transport Proteins - chemistry | Binding Sites - genetics | DNA - metabolism | DNA - genetics | Point Mutation | Breast Neoplasms - genetics | Estrogen Receptor alpha - genetics | Mutant Proteins - chemistry | Cell Line, Tumor | DNA, Neoplasm - genetics
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4. Full Text Methyl donor deficiency impairs fatty acid oxidation through PGC-1α hypomethylation and decreased ER-α, ERR-α, and HNF-4α in the rat liver
by Pooya, Shabnam and Blaise, Sébastien and Moreno Garcia, Maira and Giudicelli, Jean and Alberto, Jean-Marc and Guéant-Rodriguez, Rosa-Maria and Jeannesson, Elise and Gueguen, Naig and Bressenot, Aude and Nicolas, Bénédicte and Malthiery, Yves and Daval, Jean-Luc and Peyrin-Biroulet, Laurent and Bronowicki, Jean-Pierre and Guéant, Jean-Louis
Journal of Hepatology, ISSN 0168-8278, 2012, Volume 57, Issue 2, pp. 344 - 351
Background & Aims Folate and cobalamin are methyl donors needed for the synthesis of methionine, which is the precursor of S-adenosylmethionine, the substrate... 
Gastroenterology and Hepatology | Fatty acid oxidation | Cobalamin | Epigenomics | PGC-1α | Vitamin B12 | Methylation | Folate | Liver steatosis | FIBROSIS | METABOLIC SYNDROME | PGC-1 alpha | MICE DEFICIENT | NONALCOHOLIC STEATOHEPATITIS | ENDOPLASMIC-RETICULUM STRESS | MATERNAL NUTRITION | ACTIVATED-RECEPTOR-ALPHA | INSULIN-RESISTANCE | DISEASE | GASTROENTEROLOGY & HEPATOLOGY | HEPATIC STEATOSIS | Electron Transport | Oxidation-Reduction | Oxidative Stress | Rats, Wistar | Liver - metabolism | Rats | Receptors, Estrogen - analysis | Vitamin B 12 - blood | Hepatocyte Nuclear Factor 4 - physiology | Transcription Factors - metabolism | Animals | Hepatocyte Nuclear Factor 4 - analysis | Energy Metabolism | Endoplasmic Reticulum Stress | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Folic Acid - blood | Estrogen Receptor alpha - analysis | Estrogen Receptor alpha - physiology | Fatty Acids - metabolism | RNA-Binding Proteins - metabolism | Fatty Liver - etiology | Receptors, Estrogen - physiology
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5. Full Text Expression of the tumor suppressor miR-206 is associated with cellular proliferative inhibition and impairs invasion in ERα-positive endometrioid adenocarcinoma
by Chen, Xiaoyue and Yan, Qin and Li, Shuangdi and Zhou, Long and Yang, Huajing and Yang, Yixia and Liu, Xuelian and Wan, Xiaoping
Cancer Letters, ISSN 0304-3835, 2011, Volume 314, Issue 1, pp. 41 - 53
Abstract This study investigated the role of miR-206 in estrogen receptor-α (ERα)-positive endometrial endometrioid adenocarcinoma (EEC). We profiled miR-206... 
Hematology, Oncology and Palliative Medicine | Endometrial endometrioid adenocarcinoma (EEC) | Estrogen receptor alpha (ERα) | MicroRNA-206 (miR-206) | PROMOTING PROLIFERATION | CANCER | MESSENGER-RNA | MMP-2 | ONCOLOGY | Estrogen receptor alpha (ER alpha) | ESTROGEN-RECEPTOR-ALPHA | GRADE | CARCINOMA | ESR1 AMPLIFICATION | MICRORNA | Cell Proliferation | Endometrial Neoplasms - chemistry | Neoplasm Invasiveness | Humans | Middle Aged | Carcinoma, Endometrioid - chemistry | Estrogen Receptor alpha - genetics | Cell Line, Tumor | Estrogen Receptor alpha - analysis | Adult | Endometrial Neoplasms - pathology | Female | Estrogen Receptor alpha - physiology | MicroRNAs - physiology | Carcinoma, Endometrioid - pathology
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6. Full Text Hormone signaling and fatty liver in females: Analysis of estrogen receptor α mutant mice
by Hart-Unger, S and Arao, Y and Hamilton, K.J and Lierz, S.L and Malarkey, D.E and Hewitt, S.C and Freemark, M and Korach, K.S
International Journal of Obesity, ISSN 0307-0565, 06/2017, Volume 41, Issue 6, pp. 945 - 954
BACKGROUND: Treatment with estrogen in early menopausal women protects against development of hepatic steatosis and nonalcoholic fatty liver disease but... 
REPLACEMENT | METABOLIC SYNDROME | NUTRITION & DIETETICS | AROMATASE KNOCKOUT MOUSE | PATHWAY | IN-VIVO | MUTATION | ENDOCRINOLOGY & METABOLISM | RESISTANCE | US ADULTS | HEPATIC STEATOSIS | INSULIN SENSITIVITY | Estrogens - pharmacology | DNA-Binding Proteins - drug effects | Diet, High-Fat - adverse effects | Blotting, Western | Mice, Knockout | Non-alcoholic Fatty Liver Disease - drug therapy | Transcription Factors - drug effects | Animals | Estrogen Receptor alpha - genetics | Adiposity | Signal Transduction - drug effects | Female | Mice | Estrogens - administration & dosage | Disease Models, Animal | Index Medicus
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7. Full Text Prognostic impact of the combination of recurrence score and quantitative estrogen receptor expression (ESR1) on predicting late distant recurrence risk in estrogen receptor-positive breast cancer after 5 years of tamoxifen: Results from NRG oncology/national surgical adjuvant breast and bowel project B-28 and B-14
by Wolmark, Norman and Mamounas, Eleftherios P and Baehner, Frederick L and Butler, Steven M and Tang, Gong and Jamshidian, Farid and Sing, Amy P and Shak, Steven and Paik, Soonmyung
Journal of Clinical Oncology, ISSN 0732-183X, 07/2016, Volume 34, Issue 20, pp. 2350 - 2358
Purpose We determined the utility of the 21-Gene Recurrence Score (RS) in predicting late (. 5 years) distant recurrence (LDR) in stage I and II breast cancer... 
WOMEN | PAM50 RISK | BENEFIT | ASSAY | RANDOMIZED-TRIALS | ONCOTYPE DX | ONCOLOGY | VALIDATION | ENDOCRINE THERAPY | CHEMOTHERAPY | IMMUNOHISTOCHEMISTRY | Prognosis | Humans | Middle Aged | Risk | Breast Neoplasms - drug therapy | Neoplasm Recurrence, Local - etiology | Breast Neoplasms - chemistry | Breast Neoplasms - pathology | Tamoxifen - therapeutic use | Estrogen Receptor alpha - analysis | Adult | Female | Aged | ORIGINAL REPORTS | Bc8
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8. Effects of Staphylococcus aureus intramammary infection on the expression of estrogen receptor α and progesterone receptor in mammary glands of nonlactating cows administered estradiol and progesterone to stimulate mammary growth
by Enger, B.D and Tucker, H.L.M and Nickerson, S.C and Parsons, C.L.M and Akers, R.M
Journal of Dairy Science, ISSN 0022-0302, 03/2019, Volume 102, Issue 3, pp. 2607 - 2617
Intramammary infections (IMI) are prevalent in nonlactating dairy cattle and are known to alter mammary structure and negatively affect the amount of mammary... 
mammary growth | mastitis | myoepithelial cell | dry cow | heifer | AGRICULTURE, DAIRY & ANIMAL SCIENCE | FOOD SCIENCE & TECHNOLOGY | TISSUE | HEIFERS | PROLIFERATION | PREVALENCE | HISTOLOGY | MYOEPITHELIAL CELLS | rnyoepithelial cell | GENE-EXPRESSION | LACTATION | HORMONES | Milk - chemistry | Progesterone - administration & dosage | Estradiol - administration & dosage | Mastitis, Bovine - metabolism | Mammary Glands, Animal - drug effects | Staphylococcal Infections - veterinary | Mammary Glands, Animal - growth & development | Mastitis, Bovine - microbiology | Receptors, Progesterone - analysis | Animals | Cattle | Cell Count - veterinary | Estrogen Receptor alpha - analysis | Female | Mammary Glands, Animal - chemistry | Staphylococcus aureus
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9. Full Text Hormone signaling and fatty liver in females: analysis of estrogen receptor [alpha] mutant mice
by Hart-Unger, S and Arao, Y and Hamilton, K J and Lierz, S L and Malarkey, D E and Hewitt, S C and Freemark, M and Korach, K S
International Journal of Obesity, ISSN 0307-0565, 06/2017, Volume 41, Issue 6, p. 945
Treatment with estrogen in early menopausal women protects against development of hepatic steatosis and nonalcoholic fatty liver disease but estrogen has... 
Care and treatment | Receptors | Fatty liver | Estrogen | Development and progression | Cellular signal transduction | Health aspects
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10. Full Text Location Analysis of Estrogen Receptor α Target Promoters Reveals That FOXA1 Defines a Domain of the Estrogen Response
by Josée Laganière and Geneviève Deblois and Céline Lefebvre and Alain R. Bataille and François Robert and Vincent Giguère and Ronald M. Evans
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 8/2005, Volume 102, Issue 33, pp. 11651 - 11656
Nuclear receptors can activate diverse biological pathways within a target cell in response to their cognate ligands, but how this compartmentalization is... 
Biological Sciences | Genes | DNA | Estrogens | Cell cycle | Cell lines | Small interfering RNA | Breast cancer | Gene expression regulation | Nuclear receptors | Binding sites | ChIP-on-chip | Transcription | Forkhead box | transcription | MICROARRAY | cell cycle | MULTIDISCIPLINARY SCIENCES | forkhead box | PROLIFERATION | FACTOR-BINDING SITES | IDENTIFICATION | BREAST-CANCER CELLS | ELEMENTS | GENE-EXPRESSION | CHROMATIN-IMMUNOPRECIPITATION | CYCLE PROGRESSION | ChlP-on-chip | TRANSCRIPTIONAL REGULATION
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11. Full Text Visualisation and characterisation of oestrogen receptor α‐positive neurons expressing green fluorescent protein under the control of the oestrogen receptor α promoter
by Matsuda, Ken Ichi and Yanagisawa, Miho and Sano, Kazuhiro and Ochiai, Ikuo and Musatov, Sergei and Okoshi, Kota and Tsukahara, Shinji and Ogawa, Sonoko and Kawata, Mitsuhiro
European Journal of Neuroscience, ISSN 0953-816X, 07/2013, Volume 38, Issue 2, pp. 2242 - 2249
Oestrogen receptor (ER)α plays important roles in the development and function of various neuronal systems through activation by its ligands, oestrogens. To... 
adeno‐associated virus | green fluorescent protein | small hairpin RNA | transgenic mouse | ovarian steroid hormone | Small hairpin RNA | Transgenic mouse | Adeno-associated virus | Ovarian steroid hormone | Green fluorescent protein | SEXUALLY DIMORPHIC NUCLEUS | adeno-associated virus | PREOPTIC AREA | NEUROSCIENCES | CEREBRAL-CORTEX | MESSENGER-RNA | VENTROMEDIAL NUCLEUS | STEREOLOGICAL EVALUATION | MEDIAL AMYGDALA | EPIGENETIC REGULATION | CENTRAL-NERVOUS-SYSTEM | INSITU HYBRIDIZATION | Green Fluorescent Proteins - metabolism | Promoter Regions, Genetic | Brain - cytology | Ovariectomy | Cells, Cultured | Male | Mice, Transgenic | Green Fluorescent Proteins - genetics | Brain - metabolism | Animals | Estrogen Receptor alpha - genetics | Estrogen Receptor alpha - analysis | Estrogen Receptor alpha - metabolism | Female | Mice | Neurons - metabolism | Genes, Reporter | Amygdala
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12. Full Text Estrogen receptor-alpha isoforms are the main estrogen receptors expressed in non-small cell lung carcinoma
by Pelekanou, Vasiliki and Anastasiou, Eleftheria and Bakogeorgou, Efstathia and Notas, George and Kampa, Marilena and Garcia-Milian, Rolando and Lavredaki, Katerina and Moustou, Eleni and Chinari, Georgia and Arapantoni, Petroula and O'Grady, Anthony and Georgoulias, Vassilios and Tsapis, Andreas and Stathopoulos, Efstathios N and Castanas, Elias
Steroids, ISSN 0039-128X, 02/2019, Volume 142, pp. 65 - 76
The expression profile of estrogen receptors (ER) in Non-Small Cell Lung Carcinoma (NSCLC) remains contradictory. Here we investigated protein and... 
NSCLC | Microarrays | Immunostaining | Estrogen receptor-alpha | Lung | Meta-analysis | ER-ALPHA-36 | ADENOCARCINOMA | BIOCHEMISTRY & MOLECULAR BIOLOGY | RECEPTOR-ALPHA-36 | VARIANT | BETA | BREAST-CANCER CELLS | GROWTH-FACTOR RECEPTOR | FULVESTRANT | ENDOCRINOLOGY & METABOLISM | SEX-DIFFERENCES | GENOME BROWSER | Carcinoma, Non-Small-Cell Lung - pathology | Immunohistochemistry | Humans | Lung Neoplasms - metabolism | Middle Aged | Carcinoma, Non-Small-Cell Lung - metabolism | Lung Neoplasms - pathology | Male | Protein Isoforms - analysis | Protein Isoforms - biosynthesis | Aged, 80 and over | Cell Line, Tumor | Estrogen Receptor alpha - analysis | Adult | Female | Aged | Estrogen Receptor alpha - biosynthesis | Retrospective Studies | Carcinoma | Analysis | Phenols | Lung cancer, Non-small cell | Estradiol | Antigenic determinants | Cancer
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