相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Biomarkers for breast cancer immunotherapy: PD-L1, TILs, and beyond
Alessandro Rizzo et al.
EXPERT OPINION ON INVESTIGATIONAL DRUGS (2022)
Therapeutic strategies to overcome cisplatin resistance in ovarian cancer
Mengdi Song et al.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY (2022)
Prevalence of comprehensiveDNAdamage repair gene germline mutations in Chinese prostate cancer patients
Junlong Wu et al.
INTERNATIONAL JOURNAL OF CANCER (2021)
Neoantigen-driven B cell and CD4 T follicular helper cell collaboration promotes anti-tumor CD8 T cell responses
Can Cui et al.
CELL (2021)
Homologous recombination deficiency in breast cancer: Implications for risk, cancer development, and therapy
Rayhaan M. M. Ali et al.
GENES CHROMOSOMES & CANCER (2021)
Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries
Hyuna Sung et al.
CA-A CANCER JOURNAL FOR CLINICIANS (2021)
DNA damage response inhibitors: An avenue for TNBC treatment
Juan Jin et al.
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER (2021)
Cross-oncopanel study reveals high sensitivity and accuracy with overall analytical performance depending on genomic regions
Binsheng Gong et al.
GENOME BIOLOGY (2021)
Basal-like breast cancer with low TGFβ and high TNFα pathway activity is rich in activated memory CD4 T cells and has a good prognosis
Dingxie Liu et al.
INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES (2021)
Comparison of BRCA versus non-BRCA germline mutations and is associated somatic mutation profiles in patients with unselected breast cancer
Bo Chen et al.
AGING-US (2020)
Prevalence and mutational determinants of high tumor mutation burden in breast cancer
R. Barroso-Sousa et al.
ANNALS OF ONCOLOGY (2020)
Germline and somatic DNA repair gene alterations in prostate cancer
Marc A. Dall'Era et al.
CANCER (2020)
KEYNOTE-355: Randomized, double-blind, phase III study of pembrolizumab + chemotherapy versus placebo + chemotherapy for previously untreated locally recurrent inoperable or metastatic triple-negative breast cancer.
Javier Cortes et al.
JOURNAL OF CLINICAL ONCOLOGY (2020)
Breast Cancer Treatment A Review
Adrienne G. Waks et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2019)
Exploiting DNA repair defects in breast cancer: from chemotherapy to immunotherapy
Burak Yasin Aktas et al.
EXPERT REVIEW OF ANTICANCER THERAPY (2019)
Immune Checkpoint Inhibitors: Basics and Challenges
Bin Li et al.
CURRENT MEDICINAL CHEMISTRY (2019)
B Cells and T Follicular Helper Cells Mediate Response to Checkpoint Inhibitors in High Mutation Burden Mouse Models of Breast Cancer
Daniel P. Hollern et al.
CELL (2019)
An Integrated TCGA Pan-Cancer Clinical Data Resource to Drive High-Quality Survival Outcome Analytics
Jianfang Liu et al.
CELL (2018)
Genomic and Molecular Landscape of DNA Damage Repair Deficiency across The Cancer Genome Atlas
Theo A. Knijnenburg et al.
CELL REPORTS (2018)
Association of Germline PALB2 Mutation and Response to Platinum-Based Chemotherapy in Metastatic Breast Cancer: A Case Series
Daniel Isaac et al.
JCO PRECISION ONCOLOGY (2018)
COSMIC: somatic cancer genetics at high-resolution
Simon A. Forbes et al.
NUCLEIC ACIDS RESEARCH (2017)
Antitumor activity and safety of the PARP inhibitor rucaparib in patients with high-grade ovarian carcinoma and a germline or somatic BRCA1 or BRCA2 mutation: Integrated analysis of data from Study 10 and ARIEL2
Amit M. Oza et al.
GYNECOLOGIC ONCOLOGY (2017)
Germline Mutations in DNA Repair Genes in Lung Adenocarcinoma
Erin M. Parry et al.
JOURNAL OF THORACIC ONCOLOGY (2017)
Pan-cancer Immunogenomic Analyses Reveal Genotype-Immunophenotype Relationships and Predictors of Response to Checkpoint Blockade
Pornpimol Charoentong et al.
CELL REPORTS (2017)
The Role of Genetic Testing in Patients With Breast Cancer A Review
Olivia M. Valencia et al.
JAMA SURGERY (2017)
Predictive biomarkers for triple negative breast cancer treated with platinum-based chemotherapy
Juan Jin et al.
CANCER BIOLOGY & THERAPY (2017)
Targeted sequencing of BRCA1 and BRCA2 across a large unselected breast cancer cohort suggests that one-third of mutations are somatic
C. Winter et al.
ANNALS OF ONCOLOGY (2016)
PD-L1 expression, Cancer Genome Atlas (TCGA) subtype, and mutational load as independent predictors of response to atezolizumab (atezo) in metastatic urothelial carcinoma (mUC; IMvigor210)
Jonathan E. Rosenberg et al.
JOURNAL OF CLINICAL ONCOLOGY (2016)
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
Sue Richards et al.
GENETICS IN MEDICINE (2015)
Targeting the DNA Damage Response in Cancer
Mark J. O'Connor
MOLECULAR CELL (2015)
Recommendations for Human Epidermal Growth Factor Receptor 2 Testing in Breast Cancer American Society of Clinical Oncology/College of American Pathologists Clinical Practice Guideline Update
Antonio C. Wolff et al.
ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE (2014)
BRCA1 and BRCA2 - update and implications on the genetics of breast cancer: a clinical perspective
W. D. Foulkes
CLINICAL GENETICS (2014)
Integrated analysis of germline and somatic variants in ovarian cancer
Krishna L. Kanchi et al.
NATURE COMMUNICATIONS (2014)
A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3
Pablo Cingolani et al.
FLY (2012)
VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing
Daniel C. Koboldt et al.
GENOME RESEARCH (2012)
DNA repair dysregulation from cancer driver to therapeutic target
Nicola J. Curtin
NATURE REVIEWS CANCER (2012)
Dual Roles of Immune Cells and Their Factors in Cancer Development and Progression
Brian F. Zamarron et al.
INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES (2011)
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
Aaron McKenna et al.
GENOME RESEARCH (2010)
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
Kai Wang et al.
NUCLEIC ACIDS RESEARCH (2010)
Fast and accurate short read alignment with Burrows-Wheeler transform
Heng Li et al.
BIOINFORMATICS (2009)
分享论文
