Filtros de búsqueda

Lista de obras de Barbara Burwinkel

11q13 is a susceptibility locus for hormone receptor positive breast cancer

artículo científico publicado en 2012

19p13.1 is a triple-negative-specific breast cancer susceptibility locus

artículo científico publicado en 2012

7q21-rs6964587 and breast cancer risk: an extended case-control study by the Breast Cancer Association Consortium

artículo científico publicado en 2011

9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: evidence from the Breast Cancer Association Consortium

artículo científico publicado en 2012

A BRCA1 promoter variant (rs11655505) and breast cancer risk

artículo científico publicado en 2010

A bias in genotyping the ERBB2 (HER2) Ile655Val variant

artículo científico publicado en 2005

A breast cancer risk haplotype in the caspase-8 gene

artículo científico publicado en 2009

A genetic variant in the pre-miR-27a oncogene is associated with a reduced familial breast cancer risk

scientific article published on 18 November 2009

A genome-wide association scan (GWAS) for mean telomere length within the COGS project: identified loci show little association with hormone-related cancer risk

scientific article published on 29 July 2013

A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium

artículo científico publicado en 2013

A mutation in the canalicular phospholipid transporter gene, ABCB4, is associated with cholestasis, ductopenia, and cirrhosis in adults

artículo científico publicado en 2008

A network analysis to identify mediators of germline-driven differences in breast cancer prognosis

artículo científico publicado en 2020

A prognostic CpG score derived from epigenome-wide profiling of tumor tissue was independently associated with colorectal cancer survival

artículo científico publicado en 2019

A serum microRNA signature predicts tumor relapse and survival in triple-negative breast cancer patients.

artículo científico publicado en 2014

A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

artículo científico publicado en 2018

A variant affecting a putative miRNA target site in estrogen receptor (ESR) 1 is associated with breast cancer risk in premenopausal women.

artículo científico publicado en 2008

A variant affecting miRNAs binding in the circadian gene Neuronal PAS domain protein 2 (NPAS2) is not associated with breast cancer risk.

artículo científico publicado en 2010

ARLTS1 variants and melanoma risk

artículo científico publicado en 2006

ARLTS1 variants and risk of colorectal cancer

Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers

artículo científico publicado en 2016

Allelotyping of pooled DNA with 250 K SNP microarrays

artículo científico publicado en 2007

Arthrogryposis multiplex with deafness, inguinal hernias, and early death: a family report of a probably autosomal recessive trait.

artículo científico publicado en 2005

Association Between Functional FABP2 Promoter Haplotype and Type 2 Diabetes

Association analysis identifies 65 new breast cancer risk loci.

artículo científico publicado en 2017

Association of () polymorphisms with breast cancer risk

Association of ESR1 gene tagging SNPs with breast cancer risk

artículo científico publicado en 2009

Association of NCOA3 polymorphisms with breast cancer risk

artículo científico publicado en 2005

Association of a common AKAP9 variant with breast cancer risk: a collaborative analysis

artículo científico publicado en 2008

Association of acyl-CoA-binding protein (ACBP) single nucleotide polymorphisms and type 2 diabetes in two German study populations

artículo científico publicado en 2007

Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.

scientific article published on 21 October 2016

Association of death receptor 4 haplotype 626C-683C with an increased breast cancer risk.

artículo científico publicado en 2005

Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry

artículo científico publicado en 2016

Association of genetic variants in the Rho guanine nucleotide exchange factor AKAP13 with familial breast cancer.

artículo científico publicado en 2005

Association of prolactin and its receptor gene regions with familial breast cancer.

artículo científico publicado en 2006

Association of the CASP10 V410I variant with reduced familial breast cancer risk and interaction with the CASP8 D302H variant.

artículo científico publicado en 2005

Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium

artículo científico publicado en 2011

Associations of genetic variants in the estrogen receptor coactivators PPARGC1A, PPARGC1B and EP300 with familial breast cancer

artículo científico publicado en 2006

Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis

article by Xiang Shu et al published 1 October 2018 in International Journal of Epidemiology

BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers

artículo científico publicado en 2015

BRIP1 (BACH1) variants and familial breast cancer risk: a case-control study

artículo científico publicado en 2007

Body mass index and breast cancer survival: a Mendelian randomization analysis

artículo científico publicado en 2017

Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk

artículo científico publicado en 2020

Breast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2

artículo científico publicado en 2012

Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.

artículo científico publicado en 2016

CD24 Ala57Val polymorphism predicts pathologic complete response to sequential anthracycline- and taxane-based neoadjuvant chemotherapy for primary breast cancer

artículo científico publicado en 2011

CHEK2*1100delC heterozygosity in women with breast cancer associated with early death, breast cancer-specific death, and increased risk of a second breast cancer

artículo científico publicado en 2012

CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancer

artículo científico publicado en 2015

Cancer diagnosis and prognosis decoded by blood-based circulating microRNA signatures

artículo científico publicado en 2013

Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk

artículo científico publicado en 2015

Capture and Amplification by Tailing and Switching (CATS). An ultrasensitive ligation-independent method for generation of DNA libraries for deep sequencing from picogram amounts of DNA and RNA

artículo científico publicado en 2014

Cell-free DNA in breast cancer: a long way to go.

artículo científico publicado en 2018

Cell-free circulating DNA Integrity based on peripheral blood as a biomarker for diagnosis of cancer: a systematic review

artículo científico publicado en 2017

Cell-free circulating DNA integrity is an independent predictor of impending breast cancer recurrence

artículo científico publicado en 2017

Characterization of extracellular circulating microRNA ⬇️

artículo científico publicado en 2011

Check and mate to exosomal extracellular miRNA: new lesson from a new approach

artículo científico publicado en 2015

Circulating free DNA integrity and concentration as independent prognostic markers in metastatic breast cancer

artículo científico publicado en 2018

Circulating miRNAs as surrogate markers for circulating tumor cells and prognostic markers in metastatic breast cancer

artículo científico publicado en 2012

Circulating miRNAs with prognostic value in metastatic breast cancer and for early detection of metastasis

artículo científico publicado en 2016

Circulating microRNAs in plasma as early detection markers for breast cancer.

artículo científico publicado en 2012

Combined genetic and splicing analysis of BRCA1 c.[594-2A>C; 641A>G] highlights the relevance of naturally occurring in-frame transcripts for developing disease gene variant classification algorithms

scientific article published on 23 March 2016

Common germline polymorphisms associated with breast cancer-specific survival

artículo científico publicado en 2015

Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium

artículo científico publicado en 2014

Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

artículo científico publicado en 2012

Comprehensive genetic assessment of the ESR1 locus identifies a risk region for endometrial cancer

artículo científico publicado en 2015

Confirmation of 5p12 as a susceptibility locus for progesterone-receptor-positive, lower grade breast cancer

artículo científico publicado en 2011

Copy number variant in the candidate tumor suppressor gene MTUS1 and familial breast cancer risk

artículo científico publicado en 2007

Copy number variation in patients with cervical artery dissection

artículo científico publicado en 2012

Correction: Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

artículo científico publicado en 2012

DNA methylation array analyses identified breast cancer-associatedHYAL2methylation in peripheral blood

DNA methylation array analysis identifies breast cancer associated RPTOR, MGRN1 and RAPSN hypomethylation in peripheral blood DNA.

artículo científico publicado en 2016

Death receptor 4 variants and colorectal cancer risk.

artículo científico publicado en 2006

Distinct AGO1 and AGO2 associated miRNA profiles in human cells and blood plasma

artículo científico publicado en 2012

Evaluation of Promoter Methylation of RASSF1A and ATM in Peripheral Blood of Breast Cancer Patients and Healthy Control Individuals.

artículo científico publicado en 2018

Evaluation of SNPs in miR-146a, miR196a2 and miR-499 as low-penetrance alleles in German and Italian familial breast cancer cases

artículo científico publicado en 2010

Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk

artículo científico publicado en 2011

Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation

artículo científico publicado en 2014

Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation

scientific article published on 03 September 2016

Exploring the genetics of irritable bowel syndrome: a GWA study in the general population and replication in multinational case-control cohorts

artículo científico publicado en 2014

Extracellular miRNA: A Collision of Two Paradigms

artículo científico publicado en 2016

Extracellular miRNAs: the mystery of their origin and function

artículo científico publicado en 2012

F2RL3 methylation as a biomarker of current and lifetime smoking exposures

artículo científico publicado en 2013

F2RL3 methylation in blood DNA is a strong predictor of mortality

artículo científico publicado en 2014

F2RL3 methylation, lung cancer incidence and mortality

artículo científico publicado en 2015

FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor

artículo científico publicado en 2015

FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium

artículo científico publicado en 2014

FGFR4 Arg388 genotype is associated with pathological complete response to neoadjuvant chemotherapy for primary breast cancer

artículo científico publicado en 2010

Fatal congenital heart glycogenosis caused by a recurrent activating R531Q mutation in the gamma 2-subunit of AMP-activated protein kinase (PRKAG2), not by phosphorylase kinase deficiency

artículo científico publicado en 2005

Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs).

artículo científico publicado en 2016

Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus

artículo científico publicado en 2016

Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2.

artículo científico publicado en 2015

Fine-mapping of 150 breast cancer risk regions identifies 178 high confidence target genes

article

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

artículo científico publicado en 2020

Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk

artículo científico publicado en 2014

Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer

artículo científico publicado en 2016

Fine-scale mapping of the 4q24 locus identifies two independent loci associated with breast cancer risk

artículo científico publicado en 2015

Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1.

artículo científico publicado en 2014

Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1.

artículo científico publicado en 2013

First evidence for an association of a functional variant in the microRNA-510 target site of the serotonin receptor-type 3E gene with diarrhea predominant irritable bowel syndrome

artículo científico publicado en 2008

Five endometrial cancer risk loci identified through genome-wide association analysis

artículo científico publicado en 2016

Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium

artículo científico publicado en 2009

Folate metabolic gene polymorphisms and childhood acute lymphoblastic leukemia: a case-control study.

artículo científico publicado en 2006

Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

artículo científico publicado en 2016

Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers

artículo científico publicado en 2013

Genetic Risk Score Mendelian Randomization Shows that Obesity Measured as Body Mass Index, but not Waist:Hip Ratio, Is Causal for Endometrial Cancer

artículo científico publicado en 2016

Genetic Variants in the Vitamin D Pathway, 25(OH)D Levels, and Mortality in a Large Population-Based Cohort Study

artículo científico publicado en 2016

Genetic modifiers of CHEK2*1100delC-associated breast cancer risk

scientific article published on 06 October 2016

Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses.

artículo científico publicado en 2018

Genetic predisposition to ductal carcinoma in situ of the breast

artículo científico publicado en 2016

Genetic predisposition to in situ and invasive lobular carcinoma of the breast

artículo científico publicado en 2014

Genetic variants in DNA repair genes as potential predictive markers for oxaliplatin chemotherapy in colorectal cancer

artículo científico publicado en 2015

Genetic variants in the regulatory T cell related pathway and colorectal cancer prognosis

artículo científico publicado en 2020

Genetic variants within miR-126 and miR-335 are not associated with breast cancer risk.

artículo científico publicado en 2010

Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study

artículo científico publicado en 2014

Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade

artículo científico publicado en 2014

Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium

artículo científico publicado en 2015

Genetic variation in the major mitotic checkpoint genes does not affect familial breast cancer risk

artículo científico publicado en 2007

Genetic variations in the vitamin D binding protein and season-specific levels of vitamin D among older adults

artículo científico publicado en 2013

Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent

artículo científico publicado en 2016

Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types

artículo científico publicado en 2016

Genome-wide DNA methylation analysis reveals a prognostic classifier for non-metastatic colorectal cancer (ProMCol classifier).

artículo científico publicado en 2017

Genome-wide DNA methylation differences according to oestrogen receptor beta status in colorectal cancer

scientific article published on 30 March 2019

Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3.

artículo científico publicado en 2013

Genome-wide association analysis identifies three new breast cancer susceptibility loci

artículo científico publicado en 2012

Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

artículo científico publicado en 2015

Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

article

Genome-wide association studies identify four ER negative-specific breast cancer risk loci

artículo científico publicado en 2013

Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility.

artículo científico publicado en 2010

Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

scientific article published on 18 May 2020

Genome-wide association study of germline variants and breast cancer-specific mortality

artículo científico publicado en 2019

Genomic instability and myelodysplasia with monosomy 7 consequent to EVI1 activation after gene therapy for chronic granulomatous disease

artículo científico publicado en 2010

Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk

artículo científico publicado en 2020

Germline variants of base excision repair genes and breast cancer: A polymorphism in DNA polymerase gamma modifies gene expression and breast cancer risk.

artículo científico publicado en 2012

HYAL2 methylation in peripheral blood as a potential marker for the detection of pancreatic cancer: a case control study

artículo científico publicado en 2017

Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization

artículo científico publicado en 2015

Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk

artículo científico publicado en 2014

Identification and evaluation of plasma microRNAs for early detection of colorectal cancer

artículo científico publicado en 2013

Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk

artículo científico publicado en 2013

Identification of a DMBT1 polymorphism associated with increased breast cancer risk and decreased promoter activity

artículo científico publicado en 2010

Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

artículo científico publicado en 2016

Identification of frequent chromosome copy-number polymorphisms by use of high-resolution single-nucleotide-polymorphism arrays

artículo científico publicado en 2006

Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

artículo científico publicado en 2016

Identification of new acyl-CoA binding protein transcripts in human and mouse

artículo científico publicado en 2005

Identification of nine new susceptibility loci for endometrial cancer

artículo científico publicado en 2018

Identification of novel genetic markers of breast cancer survival

artículo científico publicado en 2015

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

artículo científico publicado en 2017

Incorporating progesterone receptor expression into the PREDICT breast prognostic model

artículo científico publicado en 2022

Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer

artículo científico publicado en 2015

Interaction of Werner and Bloom syndrome genes with p53 in familial breast cancer

artículo científico publicado en 2006

Isolation of circulating microRNA associated with RNA-binding protein

artículo científico

Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair

artículo científico publicado en 2015

Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair

artículo científico publicado en 2015

Large-scale genotyping identifies 41 new loci associated with breast cancer risk

artículo científico publicado en 2013

Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium

artículo científico publicado en 2011

Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients

artículo científico publicado en 2010

MTHFR genetic polymorphisms and susceptibility to childhood acute lymphoblastic leukemia

artículo científico publicado en 2005

Mendelian randomisation study of smoking exposure in relation to breast cancer risk

artículo científico publicado en 2021

Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.

artículo científico publicado en 2015

Metabolic shifts in residual breast cancer drive tumor recurrence

artículo científico publicado en 2017

Methylation status at HYAL2 predicts overall and progression-free survival of colon cancer patients under 5-FU chemotherapy

artículo científico publicado en 2015

MicroRNA related polymorphisms and breast cancer risk

artículo científico publicado en 2014

MicroRNA signatures: novel biomarker for colorectal cancer?

artículo científico publicado en 2011

Missense variants in ATM in 26,101 breast cancer cases and 29,842 controls

artículo científico publicado en 2010

Molecular and clinical characterization of an in frame deletion of uncertain clinical significance in the BRCA2 gene

artículo científico publicado en 2012

Molecular genetic analysis of NBS1 in German melanoma patients.

artículo científico publicado en 2007

Multicentre study of CASP8 polymorphisms in breast cancer

artículo científico publicado en 2008

Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

artículo científico publicado en 2013

Muscle glycogenosis with low phosphorylase kinase activity: mutations in PHKA1, PHKG1 or six other candidate genes explain only a minority of cases

artículo científico publicado en 2003

Mutations in ROGDI Cause Kohlschütter-Tönz Syndrome

artículo científico publicado en 2012

Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.

artículo científico publicado en 2009

No Association of Vitamin D Pathway Genetic Variants with Cancer Risks in a Population-Based Cohort of German Older Adults

artículo científico

No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.

artículo científico publicado en 2015

No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing

scientific article published on 26 February 2016

Nuclear receptor coregulator SNP discovery and impact on breast cancer risk

artículo científico publicado en 2009

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

artículo científico publicado en 2016

PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1.

artículo científico publicado en 2017

Pancreatic cancer susceptibility loci and their role in survival

artículo científico publicado en 2011

Pathway analysis of genetic variants in folate-mediated one-carbon metabolism-related genes and survival in a prospectively followed cohort of colorectal cancer patients

artículo científico publicado en 2018

Plasma DNA integrity as a biomarker for primary and metastatic breast cancer and potential marker for early diagnosis

artículo científico publicado en 2014

Plasma S100P level as a novel prognostic marker of metastatic breast cancer

artículo científico publicado en 2016

Plasma hyaluronic acid level as a prognostic and monitoring marker of metastatic breast cancer

artículo científico publicado en 2015

Plasma miR-122 and miR-200 family are prognostic markers in colorectal cancer

artículo científico publicado en 2016

Plasma microRNA panel for minimally invasive detection of breast cancer

artículo científico publicado en 2013

Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

artículo científico publicado en 2019

Polymorphisms in BRCA2 resulting in aberrant codon-usage and their analysis on familial breast cancer risk

artículo científico publicado en 2009

Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression

artículo científico publicado en 2015

Polymorphisms in genes involved in GH1 release and their association with breast cancer risk

artículo científico publicado en 2006

Polymorphisms in the Janus kinase 2 (JAK)/signal transducer and activator of transcription (STAT) genes: putative association of the STAT gene region with familial breast cancer

scientific article published on 01 June 2007

Prediction of breast cancer risk based on profiling with common genetic variants

artículo científico publicado en 2015

Preliminary Evidence of FABP2 A54T Polymorphism Associated with Reduced Risk of Type 2 Diabetes and Obesity in Women from a German Cohort

article

Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.

artículo científico publicado en 2018

Publisher Correction: Shared heritability and functional enrichment across six solid cancers

scientific article published on 23 September 2019

RAD51B in Familial Breast Cancer

artículo científico publicado en 2016

Re: Association of a common variant of the CASP8 gene with reduced risk of breast cancer

artículo científico publicado en 2005

Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia

artículo científico publicado en 2014

Reprogramming of the ERRα and ERα target gene landscape triggers tamoxifen resistance in breast cancer

artículo científico publicado en 2015

Risk of estrogen receptor-positive and -negative breast cancer and single-nucleotide polymorphism 2q35-rs13387042.

artículo científico publicado en 2009

S100P and HYAL2 as prognostic markers for patients with triple-negative breast cancer

artículo científico publicado en 2015

SNP genotyping on a genome-wide amplified DOP-PCR template

artículo científico publicado en 2002

SNP-SNP interaction analysis of NF-κB signaling pathway on breast cancer survival

artículo científico publicado en 2015

SNPs in transporter and metabolizing genes as predictive markers for oxaliplatin treatment in colorectal cancer patients

artículo científico publicado en 2016

SNPs in ultraconserved elements and familial breast cancer risk

scientific article published on 03 January 2008

Serial enumeration of circulating tumor cells predicts treatment response and prognosis in metastatic breast cancer: a prospective study in 393 patients

artículo científico publicado en 2014

Severe phenotype of phosphorylase kinase-deficient liver glycogenosis with mutations in the PHKG2 gene

artículo científico publicado en 2003

Shared heritability and functional enrichment across six solid cancers

artículo científico publicado en 2019

Shared heritability and functional enrichment across six solid cancers

Smoking, F2RL3 methylation, and prognosis in stable coronary heart disease

artículo científico publicado en 2012

TP53-binding protein variants and breast cancer risk: a case-control study

artículo científico publicado en 2005

Targeting Id1 and Id3 by a specific peptide aptamer induces E-box promoter activity, cell cycle arrest, and apoptosis in breast cancer cells

artículo científico publicado en 2010

Ten recently identified associations between nsSNPs and colorectal cancer could not be replicated in German families

article

The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity

artículo científico publicado en 2018

The CASP8 -652 6N del promoter polymorphism and breast cancer risk: a multicenter study

artículo científico publicado en 2007

The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

scientific article published on 01 November 2019

The association between breast cancer and S100P methylation in peripheral blood by multicenter case-control studies

artículo científico publicado en 2017

The associations of DNA methylation alterations in oxidative stress-related genes with cancer incidence and mortality outcomes: a population-based cohort study

article

The functional genetic variant Arg324Gly of frizzled-related protein is associated with colorectal cancer risk

The functional genetic variant Ile646Val located in the kinase binding domain of the A-kinase anchoring protein 10 is associated with familial breast cancer

artículo científico

The rare ERBB2 variant Ile654Val is associated with an increased familial breast cancer risk

artículo científico publicado en 2004

The rare ERBB2 variant Ile654Val is associated with an increased familial breast cancer risk.

artículo científico publicado en 2005

The role of genetic breast cancer susceptibility variants as prognostic factors

artículo científico publicado en 2012

The rs12975333 variant in the miR-125a and breast cancer risk in Germany, Italy, Australia and Spain

article

The single nucleotide polymorphism IVS1+309 in mouse double minute 2 does not affect risk of familial breast cancer.

artículo científico publicado en 2006

Tobacco-smoking-related differential DNA methylation: 27K discovery and replication

artículo científico publicado en 2011

Transcription factor 7-like 2 (TCF7L2) variant is associated with familial breast cancer risk: a case-control study

artículo científico publicado en 2006

Transcriptome-wide association study of breast cancer risk by estrogen-receptor status

artículo científico publicado en 2020

Two truncating variants in FANCC and breast cancer risk

artículo científico publicado en 2019

Vitamin D receptor genotype rs731236 (Taq1) and breast cancer prognosis

artículo científico publicado en 2013

Vitamin D receptor polymorphism and colorectal cancer-specific and all-cause mortality.

artículo científico publicado en 2013

c-MYC Asn11Ser is associated with increased risk for familial breast cancer

artículo científico publicado en 2005

miR-16 and miR-103 impact 5-HT4 receptor signalling and correlate with symptom profile in irritable bowel syndrome. ⬇️

artículo científico publicado en 2017

rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk

artículo científico publicado en 2016

40 EASD Annual Meeting of the European Association for the Study of Diabetes : Munich, Germany, 5-9 September 2004 ⬇️

artículo

Dominio Público Uruguay está sostenido por:

Acerca de Dominio Público Uruguay

Ayuda