Related references
Note: Only part of the references are listed.Copy number amplification of ENSA promotes the progression of triple-negative breast cancer via cholesterol biosynthesis
Yi-Yu Chen et al.
NATURE COMMUNICATIONS (2022)
Exome sequencing reveals a distinct somatic genomic landscape in breast cancer from women with germline PTEN variants
Takae Brewer et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2022)
Association of clock-like mutational signature with immune checkpoint inhibitor outcome in patients with melanoma and NSCLC
Wei Chong et al.
MOLECULAR THERAPY-NUCLEIC ACIDS (2021)
Cancer testis antigen PRAME: An anti-cancer target with immunomodulatory potential
Adviti Naik et al.
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE (2021)
The context-specific role of germline pathogenicity in tumorigenesis
Preethi Srinivasan et al.
NATURE GENETICS (2021)
Highly heterogeneous-related genes of triple-negative breast cancer: potential diagnostic and prognostic biomarkers
Yiduo Liu et al.
BMC CANCER (2021)
The role of the cancer testis antigen PRAME in tumorigenesis and immunotherapy in human cancer
Yichi Xu et al.
CELL PROLIFERATION (2020)
Ovarian and Breast Cancer Risks Associated With Pathogenic Variants in RAD51C and RAD51D
Xin Yang et al.
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE (2020)
Emerging role of PTEN loss in evasion of the immune response to tumours
Thiago Vidotto et al.
BRITISH JOURNAL OF CANCER (2020)
COX6B2 drives metabolic reprogramming toward oxidative phosphorylation to promote metastasis in pancreatic ductal cancer cells
Ke Nie et al.
ONCOGENESIS (2020)
Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer Patients
Jesus del Valle et al.
CANCERS (2020)
WWP1 Gain-of-Function Inactivation of PTEN in Cancer Predisposition
Yu-Ru Lee et al.
NEW ENGLAND JOURNAL OF MEDICINE (2020)
Fanconi Anemia Pathway: Mechanisms of Breast Cancer Predisposition Development and Potential Therapeutic Targets
Can-Bin Fang et al.
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY (2020)
PTEN hamartoma tumour syndrome: what happens when there is no PTEN germline mutation?
Lamis Yehia et al.
HUMAN MOLECULAR GENETICS (2020)
Five Decades of Research on Opioid Peptides: Current Knowledge and Unanswered Questions
Lloyd D. Fricker et al.
MOLECULAR PHARMACOLOGY (2020)
Bex1 significantly contributes to the proliferation and invasiveness of malignant tumor cells
Takefumi Doi et al.
ONCOLOGY LETTERS (2020)
Sperm-specific COX6B2 enhances oxidative phosphorylation, proliferation, and survival in human lung adenocarcinoma
Chun-Chun Cheng et al.
ELIFE (2020)
Rbm24 modulates adult skeletal muscle regeneration via regulation of alternative splicing
Mengkai Zhang et al.
THERANOSTICS (2020)
Age-related mutational signature negatively associated with immune activity and survival outcome in triple-negative breast cancer
Hao Chen et al.
ONCOIMMUNOLOGY (2020)
PTEN Mutations Trigger Resistance to Immunotherapy
Feixiong Cheng et al.
TRENDS IN MOLECULAR MEDICINE (2019)
Comparison of TCGA and GENIE genomic datasets for the detection of clinically actionable alterations in breast cancer
Pushpinder Kaur et al.
SCIENTIFIC REPORTS (2019)
Inherited variants in XRCC2 and the risk of breast cancer
Wojciech Kluzniak et al.
BREAST CANCER RESEARCH AND TREATMENT (2019)
Homo Sapiens Circular RNA 0079993 (hsa_circ_0079993) of the POLR2J4 Gene Acts as an Oncogene in Colorectal Cancer Through the microRNA-203a-3p.1 and CREB1 Axis
Xiaohong Lu et al.
MEDICAL SCIENCE MONITOR (2019)
Gene expression signature of atypical breast hyperplasia and regulation by SFRP1
Kelly J. Gregory et al.
BREAST CANCER RESEARCH (2019)
Pathogenic Germline Variants in 10,389 Adult Cancers
Kuan-lin Huang et al.
CELL (2018)
Maftools: efficient and comprehensive analysis of somatic variants in cancer
Anand Mayakonda et al.
GENOME RESEARCH (2018)
Signatures of positive selection reveal a universal role of chromatin modifiers as cancer driver genes
Luis Zapata et al.
SCIENTIFIC REPORTS (2017)
Association Between Loss-of-Function Mutations Within the FANCM Gene and Early-Onset Familial Breast Cancer
Guido Neidhardt et al.
JAMA ONCOLOGY (2017)
TCGAbiolinks: an R/Bioconductor package for integrative analysis of TCGA data
Antonio Colaprico et al.
NUCLEIC ACIDS RESEARCH (2016)
Exome genotyping arrays to identify rare and low frequency variants associated with epithelial ovarian cancer risk
Jennifer B. Permuth et al.
HUMAN MOLECULAR GENETICS (2016)
FACETS: allele-specific copy number and clonal heterogeneity analysis tool for high-throughput DNA sequencing
Ronglai Shen et al.
NUCLEIC ACIDS RESEARCH (2016)
Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21
Yosr Hamdi et al.
ONCOTARGET (2016)
Mutational Profile of Metastatic Breast Cancers: A Retrospective Analysis
Celine Lefebvre et al.
PLOS MEDICINE (2016)
Landscape of Phosphatidylinositol-3-Kinase Pathway Alterations Across 19 784 Diverse Solid Tumors
Sherri Z. Millis et al.
JAMA ONCOLOGY (2016)
Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid Cancer
Lamis Yehia et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2015)
Nuclear PTEN tumor-suppressor functions through maintaining heterochromatin structure
Lili Gong et al.
CELL CYCLE (2015)
PTEN Is a Negative Regulator of NK Cell Cytolytic Function
Edward L. Briercheck et al.
JOURNAL OF IMMUNOLOGY (2015)
Robust enumeration of cell subsets from tissue expression profiles
Aaron M. Newman et al.
NATURE METHODS (2015)
Mutations in RECQL Gene Are Associated with Predisposition to Breast Cancer
Jie Sun et al.
PLOS GENETICS (2015)
Breast Cancer in a RAD51D Mutation Carrier: Case Report and Review of the Literature
Jennifer L. Baker et al.
Clinical Breast Cancer (2014)
Trimmomatic: a flexible trimmer for Illumina sequence data
Anthony M. Bolger et al.
BIOINFORMATICS (2014)
Second Malignant Neoplasms in Patients With Cowden Syndrome With Underlying Germline PTEN Mutations
Joanne Ngeow et al.
JOURNAL OF CLINICAL ONCOLOGY (2014)
DNA Double-Strand Break Repair Genes and Oxidative Damage in Brain Metastasis of Breast Cancer
Stephan Woditschka et al.
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE (2014)
svaseq: removing batch effects and other unwanted noise from sequencing data
Jeffrey T. Leek
NUCLEIC ACIDS RESEARCH (2014)
Integrated Genomic and Epigenomic Analysis of Breast Cancer Brain Metastasis
Bodour Salhia et al.
PLOS ONE (2014)
Rare Mutations in RINT1 Predispose Carriers to Breast and Lynch Syndrome-Spectrum Cancers
Daniel J. Park et al.
CANCER DISCOVERY (2014)
PTEN Interacts with Histone H1 and Controls Chromatin Condensation
Zhu Hong Chen et al.
CELL REPORTS (2014)
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
Michael I. Love et al.
GENOME BIOLOGY (2014)
STAR: ultrafast universal RNA-seq aligner
Alexander Dobin et al.
BIOINFORMATICS (2013)
Germline and somatic KLLN alterations in breast cancer dysregulate G2 arrest
Emily A. Nizialek et al.
HUMAN MOLECULAR GENETICS (2013)
Pan-cancer patterns of somatic copy number alteration
Travis I. Zack et al.
NATURE GENETICS (2013)
The Cancer Genome Atlas Pan-Cancer analysis project
John N. Weinstein et al.
NATURE GENETICS (2013)
Vitamin E Protects against Lipid Peroxidation and Rescues Tumorigenic Phenotypes in Cowden/Cowden-like Patient-Derived Lymphoblast Cells with Germline SDHx Variants
Ying Ni et al.
CLINICAL CANCER RESEARCH (2012)
Lifetime Cancer Risks in Individuals with Germline PTEN Mutations
Min-Han Tan et al.
CLINICAL CANCER RESEARCH (2012)
Comprehensive molecular portraits of human breast tumours
Daniel C. Koboldt et al.
NATURE (2012)
MUC5B Leads to Aggressive Behavior of Breast Cancer MCF7 Cells
Helene Valque et al.
PLOS ONE (2012)
Genetic variants associated with breast-cancer risk: comprehensive research synopsis, meta-analysis, and epidemiological evidence
Ben Zhang et al.
LANCET ONCOLOGY (2011)
GISTIC2.0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers
Craig H. Mermel et al.
GENOME BIOLOGY (2011)
Identification of a Z-band associated protein complex involving KY, FLNC and IGFN1
Jane Baker et al.
EXPERIMENTAL CELL RESEARCH (2010)
Identification of glycine N-acyltransferase-like 2 (GLYATL2) as a transferase that produces N-acyl glycines in humans
Dominik P. Waluk et al.
FASEB JOURNAL (2010)
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
Aaron McKenna et al.
GENOME RESEARCH (2010)
Fast and accurate short read alignment with Burrows-Wheeler transform
Heng Li et al.
BIOINFORMATICS (2009)
PRAME expression and clinical outcome of breast cancer
M. T. Epping et al.
BRITISH JOURNAL OF CANCER (2008)
Aberrations of the MRE11-RAD50-NBS1 DNA damage sensor complex in human breast cancer: MRE11 as a candidate familial cancer-predisposing gene
Jirina Bartkova et al.
MOLECULAR ONCOLOGY (2008)
Vitamin E, antioxidant and nothing more
Maret G. Traber et al.
FREE RADICAL BIOLOGY AND MEDICINE (2007)
RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability
Katri Heikkinen et al.
CARCINOGENESIS (2006)
Immunohistochemical analysis of MUC5B apomucin expression in breast cancer and non-malignant breast tissues
C Sóñora et al.
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY (2006)
Expression of mucins (MUC1, MUC2, MUC3, MUC4, MUC5AC and MUC6) and their prognostic significance in human breast cancer
EA Rakha et al.
MODERN PATHOLOGY (2005)
cDNA cloning and expression of CYP4F12, a novel human cytochrome P450
J Bylund et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2001)