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小組
乳腺癌
乳腺癌
發起討論
乳腺癌
26 個討論
只看精華帖
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有大神幫忙分析結果么？
微胖的TUSC3基因
? 最后回復
微胖的TUSC3基因
?
2016-10-26 08:24
3443
2
? 來自相關小組
不解：為什么直接查看乳腺癌的結果，和分享到微信的結果，不太一樣？
flatfoosie
? 最后回復
不羈的PKP2基因
?
2016-09-29 12:26
3945
3
? 來自相關小組
我的報告乳腺癌風險高于平均風險，而我又高齡未育，就更危險了吧，該如何預防哪？
Tgerbear
? 最后回復
安靜的NEB基因
?
2016-08-05 08:12
4310
5
? 來自相關小組
乳腺癌 BRCA2 rs11571746 相同人數百分比只有0.45%
ww2272
? 2016-05-15 11:31
3895
0
? 來自相關小組
乳腺癌基因
nasreddin
? 最后回復
flyboyleo
?
2016-03-25 11:12
6974
4
? 來自相關小組
脂聯素分泌水平對乳腺癌的影響
zhengqiang
? 最后回復
wq
?
2015-01-17 23:31
5180
1
? 來自相關小組
<
1
2
發起討論
乳腺癌
26 個討論
相關基因
BRCA1
位點：I4000377
位點：I4000378
位點：RS16942
位點：RS1799950
位點：RS1799966
位點：RS2227945
位點：RS4986850
位點：RS55770810
BRCA2
位點：I4000379
位點：RS11571833
位點：RS144848
位點：RS28897756
位點：RS4987117
位點：RS766173
TP53
位點：RS1042522
CASP8
位點：RS1045485
ZNF276
位點：RS1061646
VTCN1
位點：RS10754339
位點：RS10801935
位點：RS3738414
FGFR2
位點：RS11200014
位點：RS1219648
位點：RS2420946
位點：RS2981578
位點：RS2981579
位點：RS3750817
位點：RS7895676
EPCAM
位點：RS1126497
TNFSF10
位點：RS1131532
DMBT1
位點：RS11523871
位點：RS2981745
PALB2
位點：RS118203997
位點：RS118203998
位點：RS180177083
位點：RS180177084
位點：RS180177091
位點：RS180177092
位點：RS180177097
位點：RS180177098
位點：RS180177099
位點：RS180177100
位點：RS180177102
位點：RS180177103
位點：RS180177110
位點：RS180177111
位點：RS180177112
位點：RS180177116
位點：RS180177121
位點：RS180177122
位點：RS180177124
位點：RS180177126
位點：RS180177127
位點：RS249954
CYP2C19
位點：RS12248560
TCF7L2
位點：RS12255372
BMPR1B
位點：RS1434536
THEMIS2
位點：RS1467465
ADIPOQ-AS1
位點：RS1501299
CHEK2
位點：RS17879961
ICAM1
位點：RS1799969
ATM
位點：RS1800054
位點：RS1800056
位點：RS1800057
位點：RS1800058
位點：RS4986761
CXCL12
位點：RS1801157
NCOA3
位點：RS2230782
ADIPOQ
位點：RS2241766
LUM
位點：RS2268578
SIPA1
位點：RS2448490
XRCC1
位點：RS25489
BARD1
位點：RS28997576
CDKN1A
位點：RS3176336
CDKN2B-AS1
位點：RS3218005
XRCC2
位點：RS3218536
CDKN1B
位點：RS34330
CDKN2A
位點：RS3731239
CASC16
位點：RS3803662
SLC4A7
位點：RS4973768
CCND1
位點：RS603965
ADIPOR1
位點：RS7539542
RRP1B
位點：RS9306160
CCNE1
位點：RS997669
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Bojesen SE, et al. The common germline Arg72Pro polymorphism of p53 and increased longevity in humans. 2008
Han JY, et al. Association of p53 codon 72 polymorphism and MDM2 SNP309 with clinical outcome of advanced nonsmall cell lung cancer. 2008
Kim JG, et al. TP53 codon 72 polymorphism associated with prognosis in patients with advanced gastric cancer treated with paclitaxel and cisplatin. 2009
Onel KB, et al. Lack of association of the TP53 Arg72Pro SNP and the MDM2 SNP309 with systemic lupus erythematosus in Caucasian, African American, and Asian children and adults. 2009
Gaulton KJ, et al. Comprehensive association study of type 2 diabetes and related quantitative traits with 222 candidate genes. 2008
Ashton KA, et al. Polymorphisms in TP53 and MDM2 combined are associated with high grade endometrial cancer. 2009
Chang-Claude J, et al. Genetic polymorphisms in DNA repair and damage response genes and late normal tissue complications of radiotherapy for breast cancer. 2009
Koshiol J, et al. Common genetic variation in TP53 and risk of human papillomavirus persistence and progression to CIN3/cancer revisited. 2009
Mabuchi F, et al. Lack of association between p53 gene polymorphisms and primary open angle glaucoma in the Japanese population. 2009
Sun P, et al. Association of genetic polymorphisms, mRNA expression of p53 and p21 with chronic benzene poisoning in a chinese occupational population. 2009
Hancox RJ, et al. Accelerated decline in lung function in cigarette smokers is associated with TP53/MDM2 polymorphisms. 2009
Akulevich NM, et al. Polymorphisms of DNA damage response genes in radiation-related and sporadic papillary thyroid carcinoma. 2009
Sinilnikova OM, et al. The TP53 Arg72Pro and MDM2 309G>T polymorphisms are not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers. 2009
Xian W, et al. The Li-Fraumeni syndrome (LFS): a model for the initiation of p53 signatures in the distal Fallopian tube. 2010
Do TN, et al. TP53 R72P and MDM2 SNP309 polymorphisms in modification of childhood acute lymphoblastic leukemia susceptibility. 2009
Naccarati A, et al. Genotype and haplotype analysis of TP53 gene and the risk of pancreatic cancer: an association study in the Czech Republic. 2010
Ebner F, et al. The role of TP53 and p21 gene polymorphisms in breast cancer biology in a well specified and characterized German cohort. 2010
Fan BJ, et al. Association of polymorphisms of tumor necrosis factor and tumor protein p53 with primary open-angle glaucoma. 2010
Litviakov NV, et al. Association between TP53 gene ARG72PRO polymorphism and chromosome aberrations in human cancers. 2010
Tsuchiya Y, et al. Evidence that genetic variants of metabolic detoxication and cell cycle control are not related to gallbladder cancer risk in Chilean women. 2010
Ricks-Santi L, et al. p53 Pro72Arg polymorphism and prostate cancer in men of African descent. 2010
Dahabreh IJ, et al. TP53 Arg72Pro polymorphism and colorectal cancer risk: a systematic review and meta-analysis. 2010
Ucisik-Akkaya E, et al. Examination of genetic polymorphisms in newborns for signatures of sex-specific prenatal selection. 2010
Shi JY, et al. Genetic variations of DNA repair genes and their prognostic significance in patients with acute myeloid leukemia. 2011
Yoshimoto N, et al. Genetic and environmental predictors, endogenous hormones and growth factors, and risk of estrogen receptor-positive breast cancer in Japanese women. 2011
Di Vuolo V, et al. TP53 and MDM2 gene polymorphisms and risk of hepatocellular carcinoma among Italian patients. 2011
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Reiling E, et al. Codon 72 polymorphism (rs1042522) of TP53 is associated with changes in diastolic blood pressure over time. 2012
Leander K, et al. NAMPT (visfatin) and AKT1 genetic variants associate with myocardial infarction. 2012
Cotignola J, et al. Investigation of the effect of MDM2 SNP309 and TP53 Arg72Pro polymorphisms on the age of onset of cutaneous melanoma. 2012
Heitzer E, et al. Infrequent p53 gene mutation but UV gradient-like p53 protein positivity in keloids. 2012
Naccarati A, et al. Mutations and polymorphisms in TP53 gene--an overview on the role in colorectal cancer. 2012
Cherdyntseva NV, et al. Crosstalk between the FGFR2 and TP53 genes in breast cancer: data from an association study and epistatic interaction analysis. 2012
Corbo RM, et al. How contemporary human reproductive behaviors influence the role of fertility-related genes: the example of the p53 gene. 2012
Azad AK, et al. Validation of genetic sequence variants as prognostic factors in early-stage head and neck squamous cell cancer survival. 2012
Yang Y, et al. Tumor suppressor gene TP53 is genetically associated with schizophrenia in the Chinese population. 2004
Mechanic LE, et al. Polymorphisms in XPD and TP53 and mutation in human lung cancer. 2005
Zhang X, et al. Genetic polymorphisms in cell cycle regulatory genes MDM2 and TP53 are associated with susceptibility to lung cancer. 2006
Wu X, et al. Bladder cancer predisposition: a multigenic approach to DNA-repair and cell-cycle-control genes. 2006
Hill DA, et al. Risk of non-Hodgkin lymphoma (NHL) in relation to germline variation in DNA repair and related genes. 2006
Savage SA, et al. Germ-line genetic variation of TP53 in osteosarcoma. 2007
Mechanic LE, et al. Common genetic variation in TP53 is associated with lung cancer risk and prognosis in African Americans and somatic mutations in lung tumors. 2007
Baynes C, et al. Common variants in the ATM, BRCA1, BRCA2, CHEK2 and TP53 cancer susceptibility genes are unlikely to increase breast cancer risk. 2015
Sprague BL, et al. Genetic variation in TP53 and risk of breast cancer in a population-based case control study. 2007
Toyama T, et al. Association of TP53 codon 72 polymorphism and the outcome of adjuvant therapy in breast cancer patients. 2015
Gaudet MM, et al. Genetic variation of TP53, polycyclic aromatic hydrocarbon-related exposures, and breast cancer risk among women on Long Island, New York. 2008
Zhu Y, et al. Correlating observed odds ratios from lung cancer case-control studies to SNP functional scores predicted by bioinformatic tools. 2008
Rosenberger A, et al. Do genetic factors protect for early onset lung cancer? A case control study before the age of 50 years. 2008
Bittenbring J, et al. MDM2 gene SNP309 T/G and p53 gene SNP72 G/C do not influence diffuse large B-cell non-Hodgkin lymphoma onset or survival in central European Caucasians. 2008
Dai Z, et al. Genotyping panel for assessing response to cancer chemotherapy. 2008
Israni AK, et al. Association of donor inflammation- and apoptosis-related genotypes and delayed allograft function after kidney transplantation. 2008
Shi J, et al. Genetic associations with schizophrenia: meta-analyses of 12 candidate genes. 2008
Pangilinan F, et al. Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation in TP53 and neural tube defect risk in an Irish population. 2008
Tempfer CB, et al. Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis. 2009
Hamaguchi M, et al. Possible difference in frequencies of genetic polymorphisms of estrogen receptor alpha, estrogen metabolism and P53 genes between estrogen receptor-positive and -negative breast cancers. 2008
Wu X, et al. Germline genetic variations in drug action pathways predict clinical outcomes in advanced lung cancer treated with platinum-based chemotherapy. 2008
Lan Q, et al. Large-scale evaluation of candidate genes identifies associations between DNA repair and genomic maintenance and development of benzene hematotoxicity. 2009
Hung RJ, et al. International Lung Cancer Consortium: pooled analysis of sequence variants in DNA repair and cell cycle pathways. 2008
Polakova V, et al. Genotype and haplotype analysis of cell cycle genes in sporadic colorectal cancer in the Czech Republic. 2009
Hirata H, et al. Bcl2 -938C/A polymorphism carries increased risk of biochemical recurrence after radical prostatectomy. 2009
Schildkraut JM, et al. Single nucleotide polymorphisms in the TP53 region and susceptibility to invasive epithelial ovarian cancer. 2009
Gallì P, et al. A case-control study on the combined effects of p53 and p73 polymorphisms on head and neck cancer risk in an Italian population. 2009
Kang HJ, et al. Single-nucleotide polymorphisms in the p53 pathway regulate fertility in humans. 2009
Zhou X, et al. Polymorphisms in HPV E6/E7 protein interacted genes and risk of cervical cancer in Chinese women: a case-control analysis. 2009
Marcel V, et al. TP53 PIN3 and MDM2 SNP309 polymorphisms as genetic modifiers in the Li-Fraumeni syndrome: impact on age at first diagnosis. 2009
Klug SJ, et al. TP53 codon 72 polymorphism and cervical cancer: a pooled analysis of individual data from 49 studies. 2009
Scacchi R, et al. Association study between P53 and P73 gene polymorphisms and the sporadic late-onset form of Alzheimer's disease. 2009
Imboden M, et al. Decreased PM10 exposure attenuates age-related lung function decline: genetic variants in p53, p21, and CCND1 modify this effect. 2009
Daugherty CL, et al. Primary open angle glaucoma in a Caucasian population is associated with the p53 codon 72 polymorphism. 2009
Zhu F, et al. Genetic factors associated with intestinal metaplasia in a high risk Singapore-Chinese population: a cohort study. 2009
Doi N, et al. Persistence criteria for susceptibility genes for schizophrenia: a discussion from an evolutionary viewpoint. 2009
Maia AT, et al. Extent of differential allelic expression of candidate breast cancer genes is similar in blood and breast. 2009
Lee EB, et al. TP53 mutations in Korean patients with non-small cell lung cancer. 2010
Grochola LF, et al. Single-nucleotide polymorphisms in the p53 signaling pathway. 2010
Robertson LB, et al. Survey of familial glioma and role of germline p16INK4A/p14ARF and p53 mutation. 2010
Huang YJ, et al. A novel functional DEC1 promoter polymorphism -249T>C reduces risk of squamous cell carcinoma of the head and neck. 2010
Di Pietro F, et al. Genomic DNA extraction from whole blood stored from 15- to 30-years at -20 °C by rapid phenol-chloroform protocol: a useful tool for genetic epidemiology studies. 2011
Jha P, et al. TP53 polymorphisms in gliomas from Indian patients: Study of codon 72 genotype, rs1642785, rs1800370 and 16 base pair insertion in intron-3. 2011
Qu L, et al. Association between polymorphisms in RAPGEF1, TP53, NRF1 and type 2 diabetes in Chinese Han population. 2011
Caama?o J, et al. TP53 codon 72 polymorphism is associated with coronary artery disease in Chilean subjects. 2011
Burgdorf KS, et al. Studies of the association of Arg72Pro of tumor suppressor protein p53 with type 2 diabetes in a combined analysis of 55,521 Europeans. 2011
Savage SA, et al. Using epidemiology and genomics to understand osteosarcoma etiology. 2011
Srivastava K, et al. Candidate gene studies in gallbladder cancer: a systematic review and meta-analysis. 2011
Ergul E, et al. TP53 Arg72Pro polymorphism in Turkish patients with sporadic amyotrophic lateral sclerosis. 2011
Denisov EV, et al. Coordination of TP53 abnormalities in breast cancer: data from analysis of TP53 polymorphisms, loss of heterozygosity, methylation, and mutations. 2011
Liu L, et al. Combined effect of genetic polymorphisms in P53, P73, and MDM2 on non-small cell lung cancer survival. 2011
von Keyserling H, et al. Analysis of 4 single-nucleotide polymorphisms in relation to cervical dysplasia and cancer development using a high-throughput ligation-detection reaction procedure. 2011
Lin HY, et al. Polymorphisms of TP53 are markers of bladder cancer vulnerability and prognosis. 2013
M?drek K, et al. Association of common WRAP 53 variant with ovarian cancer risk in the Polish population. 2013
Pastor-Idoate S, et al. The p53 codon 72 polymorphism (rs1042522) is associated with proliferative vitreoretinopathy: the Retina 4 Project. 2013
Singhal P, et al. Association of MDM2 and p53 polymorphisms with the advancement of cervical carcinoma. 2013
Bonfigli AR, et al. The p53 codon 72 (Arg72Pro) polymorphism is associated with the degree of insulin resistance in type 2 diabetic subjects: a cross-sectional study. 2013
Walter SD, et al. Accuracy of p53 codon 72 polymorphism status determined by multiple laboratory methods: a latent class model analysis. 2013
Chansaenroj J, et al. Polymorphisms in TP53 (rs1042522), p16 (rs11515 and rs3088440) and NQO1 (rs1800566) genes in Thai cervical cancer patients with HPV 16 infection. 2015
Son MS, et al. Promoter polymorphisms of pri-miR-34b/c are associated with hepatocellular carcinoma. 2013
de Lourdes Perim A, et al. CXCL12 and TP53 genetic polymorphisms as markers of susceptibility in a Brazilian children population with acute lymphoblastic leukemia (ALL). 2013
Huang Y, et al. [Association of P53 gene polymorphisms with susceptibility to endometriosis]. 2013
Lajin B, et al. Association between polymorphisms in the genes for tumor suppressor protein p53 and its regulator NAD(P)H: quinone oxidoreductase 1 (NQO1) and schizophrenia in a Syrian study cohort. 2013
Yang J, et al. Association of p53 and MDM2 polymorphisms with risk of human papillomavirus (HPV)-related esophageal squamous cell carcinoma (ESCC). 2013
Ye H, et al. Genetic associations with coronary heart disease: meta-analyses of 12 candidate genetic variants. 2013
Henríquez-Hernández LA, et al. Polymorphisms in DNA-repair genes in a cohort of prostate cancer patients from different areas in Spain: heterogeneity between populations as a confounding factor in association studies. 2013
Molina E, et al. The GSTM1null (deletion) and MGMT84 rs12917 (Phe/Phe) haplotype are associated with bulky DNA adduct levels in human leukocytes. 2013
Gomes CC, et al. TP53 single nucleotide polymorphism rs1042522 in salivary gland neoplasms. 2014
Ren YW, et al. P53 Arg72Pro and MDM2 SNP309 polymorphisms cooperate to increase lung adenocarcinoma risk in Chinese female non-smokers: a case control study. 2015
Zhang H, et al. Common genetic variants in 53BP1 associated with nonsmall-cell lung cancer risk in Han Chinese. 2014
Cintra HS, et al. Investigation of genetic polymorphisms related to the outcome of radiotherapy for prostate cancer patients. 2013
Hu S, et al. The association between polymorphism of P53 Codon72 Arg/Pro and hepatocellular carcinoma susceptibility: evidence from a meta-analysis of 15 studies with 3,704 cases. 2014
Pastor-Idoate S, et al. The T309G MDM2 gene polymorphism is a novel risk factor for proliferative vitreoretinopathy. 2013
Li Y, et al. TP53 genetic polymorphisms, interactions with lifestyle factors and lung cancer risk: a case control study in a Chinese population. 2013
Brunotto M, et al. Risk genes in head and neck cancer: a systematic review and meta-analysis of last 5 years. 2014
Huang C, et al. Genetic variants in TP53 and MDM2 associated with male infertility in Chinese population. 2012
Akba? H, et al. Role of p53 codon 72 polymorphism in chromosomal aberrations and mitotic index in patients with chronic hepatitis B. 2012
Hao XD, et al. Correlation of telomere length shortening with TP53 somatic mutations, polymorphisms and allelic loss in breast tumors and esophageal cancer. 2013
Di Pietro F, et al. TP53*P72 allele influences negatively female life expectancy in a population of central Italy: cross-sectional study and genetic-demographic approach analysis. 2013
Thun GA, et al. The association of a variant in the cell cycle control gene CCND1 and obesity on the development of asthma in the Swiss SAPALDIA study. 2013
Wang S, et al. Effect of TP53 codon 72 and MDM2 SNP309 polymorphisms on survival of gastric cancer among patients who receiving 5-fluorouracil-based postoperative adjuvant chemotherapy. 2013
Dahabreh IJ, et al. Genotype misclassification in genetic association studies of the rs1042522 TP53 (Arg72Pro) polymorphism: a systematic review of studies of breast, lung, colorectal, ovarian, and endometrial cancer. 2013
Pineda S, et al. Genetic variation in the TP53 pathway and bladder cancer risk. a comprehensive analysis. 2014
Mandal RK, et al. No evidence of correlation between p53 codon 72 G?>?C gene polymorphism and cancer risk in Indian population: a meta-analysis. 2014
Khan MH, et al. Association of the rs1042522 polymorphism with increased risk of prostate adenocarcinoma in the Pakistani population and its HuGE review. 2015
Wu GC, et al. Genetic association of single nucleotide polymorphisms in P53 pathway with gastric cancer risk in a Chinese Han population. 2015
Nowak A, et al. The relationship of TP53 and GRIN2B gene polymorphisms with risk of occurrence and progression of primary open-angle glaucoma in a Polish population. 2014
Hori Y, et al. Impact of TP53 codon 72 and MDM2 SNP 309 polymorphisms in pancreatic ductal adenocarcinoma. 2015
Cox A, et al. A common coding variant in CASP8 is associated with breast cancer risk. 2007
Shephard ND, et al. A breast cancer risk haplotype in the caspase-8 gene. 2009
Enjuanes A, et al. Genetic variants in apoptosis and immunoregulation-related genes are associated with risk of chronic lymphocytic leukemia. 2008
Ramus SJ, et al. Consortium analysis of 7 candidate SNPs for ovarian cancer. 2008
Pittman AM, et al. CASP8 variants D302H and -652 6N ins/del do not influence the risk of colorectal cancer in the United Kingdom population. 2008
Couch FJ, et al. Association of breast cancer susceptibility variants with risk of pancreatic cancer. 2009
Lubahn J, et al. Association of CASP8 D302H polymorphism with reduced risk of aggressive prostate carcinoma. 2010
Srivastava K, et al. Caspase-8 polymorphisms and risk of gallbladder cancer in a northern Indian population. 2010
Campa D, et al. Interactions between genetic variants and breast cancer risk factors in the breast and prostate cancer cohort consortium. 2011
Abnet CC, et al. Genotypic variants at 2q33 and risk of esophageal squamous cell carcinoma in China: a meta-analysis of genome-wide association studies. 2012
Pharoah PD, et al. Association between common variation in 120 candidate genes and breast cancer risk. 2007
Sigurdson AJ, et al. Polymorphisms in apoptosis- and proliferation-related genes, ionizing radiation exposure, and risk of breast cancer among U.S. Radiologic Technologists. 2007
Loza MJ, et al. Assembly of inflammation-related genes for pathway-focused genetic analysis. 2007
Li C, et al. Genetic variants and haplotypes of the caspase-8 and caspase-10 genes contribute to susceptibility to cutaneous melanoma. 2008
Gail MH, et al. Discriminatory accuracy from single-nucleotide polymorphisms in models to predict breast cancer risk. 2008
Smith AK, et al. Association of polymorphisms in CASP10 and CASP8 with FEV(1)/FVC and bronchial hyperresponsiveness in ethnically diverse asthmatics. 2008
Garcia-Closas M, et al. Genetic susceptibility loci for breast cancer by estrogen receptor status. 2008
Tapper W, et al. The influence of genetic variation in 30 selected genes on the clinical characteristics of early onset breast cancer. 2008
Thomas G, et al. A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). 2009
Lan Q, et al. Genetic variation in caspase genes and risk of non-Hodgkin lymphoma: a pooled analysis of 3 population-based case-control studies. 2009
Gaudet MM, et al. Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium. 2009
Sergentanis TN, et al. Association of two CASP8 polymorphisms with breast cancer risk: a meta-analysis. 2010
Mavaddat N, et al. Familial relative risks for breast cancer by pathological subtype: a population-based cohort study. 2010
Wacholder S, et al. Performance of common genetic variants in breast-cancer risk models. 2010
Grochola LF, et al. Single-nucleotide polymorphisms in the p53 signaling pathway. 2010
Travis RC, et al. Gene-environment interactions in 7610 women with breast cancer: prospective evidence from the Million Women Study. 7610
Srivastava K, et al. Gallbladder cancer predisposition: a multigenic approach to DNA-repair, apoptotic and inflammatory pathway genes. 2011
Broeks A, et al. Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium. 2011
Bye H, et al. Population-specific genetic associations with oesophageal squamous cell carcinoma in South Africa. 2011
Nell EM, et al. The apoptosis pathway and the genetic predisposition to Achilles tendinopathy. 2012
Guan YP, et al. Breast cancer association studies in a Han Chinese population using 10 European-ancestry-associated breast cancer susceptibility SNPs. 1009
Rihani A, et al. CASP8 SNP D302H (rs1045485) is associated with worse survival in MYCN-amplified neuroblastoma patients. 2014
Haiman CA, et al. Comprehensive association testing of common genetic variation in DNA repair pathway genes in relationship with breast cancer risk in multiple populations. 2008
Smith TR, et al. Polygenic model of DNA repair genetic polymorphisms in human breast cancer risk. 2008
Zhang J, et al. B7-H4 gene polymorphisms are associated with sporadic breast cancer in a Chinese Han population. 2009
Liu W, et al. A simple and efficient algorithm for genome-wide homozygosity analysis in disease. 2009
Ozg?z A, et al. An investigation of the effects of FGFR2 and B7-H4 polymorphisms in breast cancer. 2013
Zhang J, et al. B7-H4 gene polymorphisms are associated with sporadic breast cancer in a Chinese Han population. 2009
Ozg?z A, et al. An investigation of the effects of FGFR2 and B7-H4 polymorphisms in breast cancer. 2013
Hunter DJ, et al. A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. 2007
Zhao ZZ, et al. Common variation in the fibroblast growth factor receptor 2 gene is not associated with endometriosis risk. 2008
Udler MS, et al. FGFR2 variants and breast cancer risk: fine-scale mapping using African American studies and analysis of chromatin conformation. 2009
Zhu X, et al. Histone-acetylated control of fibroblast growth factor receptor 2 intron 2 polymorphisms and isoform splicing in breast cancer. 2009
Nan H, et al. Genetic variants in FGFR2 and FGFR4 genes and skin cancer risk in the Nurses' Health Study. 2009
Barnholtz-Sloan JS, et al. FGFR2 and other loci identified in genome-wide association studies are associated with breast cancer in African-American and younger women. 2010
Chan M, et al. Association of common genetic variants with breast cancer risk and clinicopathological characteristics in a Chinese population. 2012
Zhou L, et al. Three novel functional polymorphisms in the promoter of FGFR2 gene and breast cancer risk: a HuGE review and meta-analysis. 2012
Jiang L, et al. A non-synonymous polymorphism Thr115Met in the EpCAM gene is associated with an increased risk of breast cancer in Chinese population. 2011
Hu M, et al. Functional polymorphism in the EpCAM gene is associated with occurrence and advanced disease status of cervical cancer in Chinese population. 2012
Yang Y, et al. Polymorphisms of EpCAM gene and prognosis for non-small-cell lung cancer in Han Chinese. 2014
Jung JH, et al. TNF superfamily gene polymorphism as prognostic factor in early breast cancer. 2010
Van Ness B, et al. Genomic variation in myeloma: design, content, and initial application of the Bank On A Cure SNP Panel to detect associations with progression-free survival. 2008
Schnabel RB, et al. The relation of genetic and environmental factors to systemic inflammatory biomarker concentrations. 2009
Tchatchou S, et al. Identification of a DMBT1 polymorphism associated with increased breast cancer risk and decreased promoter activity. 2010
Johnson N, et al. Counting potentially functional variants in BRCA1, BRCA2 and ATM predicts breast cancer susceptibility. 2007
Won HH, et al. Cataloging coding sequence variations in human genome databases. 2008
Garcia-Closas M, et al. Genome-wide association studies identify four ER negative-specific breast cancer risk loci. 2013
Michailidou K, et al. Large-scale genotyping identifies 41 new loci associated with breast cancer risk. 2013
Wang Y, et al. Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer. 2014
Casadei S, et al. Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancer. 2011
Rahman N, et al. PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene. 2007
Hofstatter EW, et al. PALB2 mutations in familial breast and pancreatic cancer. 2011
Hunter DJ, et al. A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. 2007
Zhao ZZ, et al. Common variation in the fibroblast growth factor receptor 2 gene is not associated with endometriosis risk. 2008
Raskin L, et al. FGFR2 is a breast cancer susceptibility gene in Jewish and Arab Israeli populations. 2008
Liang J, et al. Genetic variants in fibroblast growth factor receptor 2 (FGFR2) contribute to susceptibility of breast cancer in Chinese women. 2008
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Rrp1B gene polymorphism (1307T>C) in metastatic progression of breast cancer
Association of single-nucleotide polymorphisms in the cell cycle genes with breast cancer in the British population
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深圳市市場監督管理局企業主體身份公示
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粵ICP備15012185號
| 互聯網藥品信息服務資格證書:（粵）-非經營性-2023-0379
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主站蜘蛛池模板：
西乡县
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汾西县
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绥江县
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特克斯县
|
福鼎市
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华池县
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枝江市
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溧水县
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凤庆县
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乌海市
|
军事
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永兴县
|
安义县
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东兴市
|
阿拉尔市
|
麻栗坡县
|
阿瓦提县
|
弋阳县
|
五寨县
|
石家庄市
|
开远市
|
桂东县
|
进贤县
|
桦甸市
|
丹凤县
|
洱源县
|
太谷县
|
靖远县
|
永靖县
|
郧西县
|
凤山市
|
滁州市
|
遂溪县
|
临桂县
|
应用必备
|
苏尼特左旗
|
五峰
|
泾源县
|
凤山市
|
萨嘎县
|
唐河县
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純合片段分析
姓氏祖源
祖源平均臉
基因關系
基因保險助手
原始數據
深圳市市場監督管理局企業主體身份公示
中文
English