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MicroRNA Regulation of DNA Repair Gene Expression in Hypoxic Stress

Cancer research (Chicago, Ill.), 2009-02, Vol.69 (3), p.1221-1229

2009

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Pan-cancer Analysis of Homologous Recombination Repair-associated Gene Alterations and Genome-wide Loss-of-Heterozygosity Score

Clinical cancer research, 2022-04, Vol.28 (7), p.1412-1421

2022

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ZC3H13-mediated N6-methyladenosine modification of PHF10 is impaired by fisetin which inhibits the DNA damage response in pancreatic cancer

Cancer letters, 2022-04, Vol.530, p.16-28

2022

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RAD51 as a potential surrogate marker for DNA repair capacity in solid malignancies

International journal of cancer, 2017-10, Vol.141 (7), p.1286-1294

2017

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Immune Checkpoint Inhibitors in Tumors Harboring Homologous Recombination Deficiency: Challenges in Attaining Efficacy

Frontiers in immunology, 2022-02, Vol.13, p.826577

2022

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DNA-repair defects in pancreatic neuroendocrine tumors and potential clinical applications

Cancer treatment reviews, 2016-03, Vol.44, p.1-9

2016

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Hereditary breast and ovarian cancer: new genes in confined pathways

Nature reviews. Cancer, 2016-09, Vol.16 (9), p.599-612

2016

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Impact of DNA damage repair defects on response to radium-223 and overall survival in metastatic castration-resistant prostate cancer

European journal of cancer (1990), 2020-09, Vol.136, p.16-24

2020

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MYB regulates the DNA damage response and components of the homology-directed repair pathway in human estrogen receptor-positive breast cancer cells

Oncogene, 2019-06, Vol.38 (26), p.5239-5249

2019

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EGFRvIII upregulates DNA mismatch repair resulting in increased temozolomide sensitivity of MGMT promoter methylated glioblastoma

Oncogene, 2020-04, Vol.39 (15), p.3041-3055

2020

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Recommendations for Childhood Cancer Screening and Surveillance in DNA Repair Disorders

Clinical cancer research, 2017-06, Vol.23 (11), p.e23-e31

2017

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DNA Repair Pathways and Their Association With Lethal Prostate Cancer in African American and European American Men

JNCI cancer spectrum, 2022-02, Vol.6 (1)

2022

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DNA repair and cancer in colon and rectum: Novel players in genetic susceptibility

International journal of cancer, 2020-01, Vol.146 (2), p.363-372

2020

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The clinical value of aberrant epigenetic changes of DNA damage repair genes in human cancer

Oncotarget, 2016-06, Vol.7 (24), p.37331-37346

2016

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Identification of germline genetic mutations in patients with pancreatic cancer

Cancer, 2015-12, Vol.121 (24), p.4382-4388

2015

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Modeling cancer genomic data in yeast reveals selection against ATM function during tumorigenesis

PLoS genetics, 2020-03, Vol.16 (3), p.e1008422

2020

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Clinical effect of temozolomide‐based chemotherapy in poorly differentiated endocrine carcinoma after progression on first‐line chemotherapy

Cancer, 2011-10, Vol.117 (20), p.4617-4622

2011

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Rare key functional domain missense substitutions in MRE11A, RAD50, and NBN contribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study

Breast cancer research : BCR, 2014-06, Vol.16 (3), p.R58-R58

2014

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IGF-1R inhibition enhances radiosensitivity and delays double-strand break repair by both non-homologous end-joining and homologous recombination

Oncogene, 2014-11, Vol.33 (45), p.5262-5273

2014

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Combined Microsatellite Instability, MLH1 Methylation Analysis, and Immunohistochemistry for Lynch Syndrome Screening in Endometrial Cancers From GOG210: An NRG Oncology and Gynecologic Oncology Group Study

Journal of clinical oncology, 2015-12, Vol.33 (36), p.4301-4308

2015

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Promoter methylation and expression of MGMT and the DNA mismatch repair genes MLH1, MSH2, MSH6 and PMS2 in paired primary and recurrent glioblastomas

International journal of cancer, 2011-08, Vol.129 (3), p.659-670

2011

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Feasibility of Screening for Lynch Syndrome Among Patients With Colorectal Cancer

Journal of clinical oncology, 2008-12, Vol.26 (35), p.5783-5788

2008

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RAD50 germline mutations are associated with poor survival in BRCA1/2–negative breast cancer patients

International journal of cancer, 2018-10, Vol.143 (8), p.1935-1942

2018

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Genetic and clinical determinants of constitutional mismatch repair deficiency syndrome: Report from the constitutional mismatch repair deficiency consortium

European journal of cancer (1990), 2014-03, Vol.50 (5), p.987-996

2014

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Defects in homologous recombination repair behind the human diseases: FA and HBOC

Endocrine-related cancer, 2016-10, Vol.23 (10), p.T19-T37

2016

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MicroRNA Regulation of DNA Repair Gene Expression in Hypoxic Stress

Pan-cancer Analysis of Homologous Recombination Repair-associated Gene Alterations and Genome-wide Loss-of-Heterozygosity Score

ZC3H13-mediated N6-methyladenosine modification of PHF10 is impaired by fisetin which inhibits the DNA damage response in pancreatic cancer

RAD51 as a potential surrogate marker for DNA repair capacity in solid malignancies

Immune Checkpoint Inhibitors in Tumors Harboring Homologous Recombination Deficiency: Challenges in Attaining Efficacy

DNA-repair defects in pancreatic neuroendocrine tumors and potential clinical applications

Hereditary breast and ovarian cancer: new genes in confined pathways

Impact of DNA damage repair defects on response to radium-223 and overall survival in metastatic castration-resistant prostate cancer

MYB regulates the DNA damage response and components of the homology-directed repair pathway in human estrogen receptor-positive breast cancer cells

EGFRvIII upregulates DNA mismatch repair resulting in increased temozolomide sensitivity of MGMT promoter methylated glioblastoma

Recommendations for Childhood Cancer Screening and Surveillance in DNA Repair Disorders

DNA Repair Pathways and Their Association With Lethal Prostate Cancer in African American and European American Men

DNA repair and cancer in colon and rectum: Novel players in genetic susceptibility

The clinical value of aberrant epigenetic changes of DNA damage repair genes in human cancer

Identification of germline genetic mutations in patients with pancreatic cancer

Modeling cancer genomic data in yeast reveals selection against ATM function during tumorigenesis

Clinical effect of temozolomide‐based chemotherapy in poorly differentiated endocrine carcinoma after progression on first‐line chemotherapy

Rare key functional domain missense substitutions in MRE11A, RAD50, and NBN contribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study

IGF-1R inhibition enhances radiosensitivity and delays double-strand break repair by both non-homologous end-joining and homologous recombination

Combined Microsatellite Instability, MLH1 Methylation Analysis, and Immunohistochemistry for Lynch Syndrome Screening in Endometrial Cancers From GOG210: An NRG Oncology and Gynecologic Oncology Group Study

Promoter methylation and expression of MGMT and the DNA mismatch repair genes MLH1, MSH2, MSH6 and PMS2 in paired primary and recurrent glioblastomas

Feasibility of Screening for Lynch Syndrome Among Patients With Colorectal Cancer

RAD50 germline mutations are associated with poor survival in BRCA1/2–negative breast cancer patients

Genetic and clinical determinants of constitutional mismatch repair deficiency syndrome: Report from the constitutional mismatch repair deficiency consortium

Defects in homologous recombination repair behind the human diseases: FA and HBOC

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