نتایج جستجو برای: esr1 gene

تعداد نتایج: 1141824  

Journal: :The International journal of eating disorders 2014
Margarita C T Slof-Op 't Landt Eric F van Furth Ingrid Meulenbelt Meike Bartels Jouke Jan Hottenga P Eline Slagboom Dorret I Boomsma

OBJECTIVE The female preponderance and onset around puberty in the majority of eating disorders (EDs) suggest that sex hormones, like estrogens, may be involved in the onset of these disorders. An eight-SNP haplotype at the estrogen receptor I (ESR1) gene was found to be associated with anorexia nervosa (AN) (Versini et al., Neuropsychopharmacology, 35, 1818-1825, 2010) and three SNPs from this...

Journal: :Hypertension 2007
Inga Peter Gordon S Huggins Amanda M Shearman Arthur Pollak Christopher H Schmid L Adrienne Cupples Serkalem Demissie Richard D Patten Richard H Karas David E Housman Michael E Mendelsohn Ramachandran S Vasan Emelia J Benjamin

Left ventricular (LV) mass and other LV measures have been shown to be heritable. In this study we hypothesized that functional variation in the gene coding for estrogen receptor-alpha (ESR1), known for mediating the effect of estrogens on myocardium, is associated with age-related changes in LV structure. Four genetic markers (ESR1 TA repeat; rs2077647, or +30T>C; rs2234693, or PvuII; and rs93...

Journal: :American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008
Jonathan Mill Eniko Kiss Ildiko Baji Krisztina Kapornai Gabriella Daróczy Agnes Vetró James Kennedy Maria Kovacs Cathy Barr

Depressive disorders are heterogeneous psychiatric disorders involving deficits in cognitive, psychomotor, and emotional processing. Depressive disorders have a significant genetic component, with severe, recurrent and early-onset forms demonstrating elevated heritability. In this study we genotyped eleven single nucleotide polymorphisms (SNPs) spanning the estrogen receptor alpha gene (ESR1) i...

Journal: :Cell reports 2013
Shunqiang Li Dong Shen Jieya Shao Robert Crowder Wenbin Liu Aleix Prat Xiaping He Shuying Liu Jeremy Hoog Charles Lu Li Ding Obi L Griffith Christopher Miller Dave Larson Robert S Fulton Michelle Harrison Tom Mooney Joshua F McMichael Jingqin Luo Yu Tao Rodrigo Goncalves Christopher Schlosberg Jeffrey F Hiken Laila Saied Cesar Sanchez Therese Giuntoli Caroline Bumb Crystal Cooper Robert T Kitchens Austin Lin Chanpheng Phommaly Sherri R Davies Jin Zhang Megha Shyam Kavuri Donna McEachern Yi Yu Dong Cynthia Ma Timothy Pluard Michael Naughton Ron Bose Rama Suresh Reida McDowell Loren Michel Rebecca Aft William Gillanders Katherine DeSchryver Richard K Wilson Shaomeng Wang Gordon B Mills Ana Gonzalez-Angulo John R Edwards Christopher Maher Charles M Perou Elaine R Mardis Matthew J Ellis

To characterize patient-derived xenografts (PDXs) for functional studies, we made whole-genome comparisons with originating breast cancers representative of the major intrinsic subtypes. Structural and copy number aberrations were found to be retained with high fidelity. However, at the single-nucleotide level, variable numbers of PDX-specific somatic events were documented, although they were ...

Journal: :Acta neurologica Scandinavica 2008
L Lazaros S Markoula N Xita S Giannopoulos P Gogou G Lagos A P Kyritsis I Georgiou

OBJECTIVE The vascular protective effects of estrogens are mediated by their binding to the two known estrogen receptors. In this study, we examine the association of stroke with two common polymorphisms of the ESR1 gene in patients with metabolic syndrome. MATERIALS AND METHODS DNA from 130 patients hospitalized for ischemic stroke and 240 healthy controls were genotyped for ESR1 PvuII and X...

Journal: :Archives of otolaryngology--head & neck surgery 2006
Maria J Worsham Kang Mei Chen Venkata Meduri Anders O H Nygren Abdellatif Errami Jan P Schouten Michael S Benninger

OBJECTIVE To examine the promoter methylation status of the 22 cancer genes and their contribution to disease progression in 6 head and neck squamous cell carcinoma (HNSCC) cell lines. DESIGN A panel of 41 gene probes, designed to interrogate 35 unique genes with known associations to cancer including HNSCC, was interrogated for alterations in gene copy number and aberrant methylation status ...

2013
Xiaoming Wu Shuzhang Guo Guanghao Shen Xing Ma Chi Tang Kangning Xie Juan Liu Wei Guo Yili Yan Erping Luo

BACKGROUND Osteoporosis affects 200 million people worldwide and places an enormous economic burden on society. We aim to identify the feature genes that are related to osteoprotegerin in osteoporosis and to perform function analysis with DNA microarray from human bone marrow. METHODS We downloaded the gene expression profile GSE35957 from Gene Expression Omnibus database including nine gene ...

Journal: :Cancer research 2004
Martin Widschwendter Kimberly D Siegmund Hannes M Müller Heidi Fiegl Christian Marth Elisabeth Müller-Holzner Peter A Jones Peter W Laird

We have generated DNA methylation profiles of 148 human breast tumors and found significant differences in hormone receptor (HR) status between clusters of DNA methylation profiles. Of 35 DNA methylation markers analyzed, the ESR1 gene, encoding estrogen receptor alpha, proved to be the best predictor of progesterone receptor status, whereas methylation of the PGR gene, encoding progesterone re...

2012
Jirong Long Qiuyin Cai Hyuna Sung Jiajun Shi Ben Zhang Ji-Yeob Choi Wanqing Wen Ryan J. Delahanty Wei Lu Yu-Tang Gao Hongbing Shen Sue K. Park Kexin Chen Chen-Yang Shen Zefang Ren Christopher A. Haiman Keitaro Matsuo Mi Kyung Kim Ui Soon Khoo Motoki Iwasaki Ying Zheng Yong-Bing Xiang Kai Gu Nathaniel Rothman Wenjing Wang Zhibin Hu Yao Liu Keun-Young Yoo Dong-Young Noh Bok-Ghee Han Min Hyuk Lee Hong Zheng Lina Zhang Pei-Ei Wu Ya-Lan Shieh Sum Yin Chan Shenming Wang Xiaoming Xie Sung-Won Kim Brian E. Henderson Loic Le Marchand Hidemi Ito Yoshio Kasuga Sei-Hyun Ahn Han Sung Kang Kelvin Y. K. Chan Hiroji Iwata Shoichiro Tsugane Chun Li Xiao-Ou Shu Dae-Hee Kang Wei Zheng

Genetic factors play an important role in the etiology of both sporadic and familial breast cancer. We aimed to discover novel genetic susceptibility loci for breast cancer. We conducted a four-stage genome-wide association study (GWAS) in 19,091 cases and 20,606 controls of East-Asian descent including Chinese, Korean, and Japanese women. After analyzing 690,947 SNPs in 2,918 cases and 2,324 c...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید