Associated Papers
Germline Mutations in Patients With Early-Onset Prostate Cancer.
Tang T et al.
Frontiers in Oncology, 2022
Synergistic Interaction of HOXB13 and CIP2A Predisposes to Aggressive Prostate Cancer.
Sipeky C et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2018
Prostate Cancer Genomics: Recent Advances and the Prevailing Underrepresentation from Racial and Ethnic Minorities.
Tan SH et al.
International Journal of Molecular Sciences, 2018
In silico analysis of the deleterious nsSNPs (missense) in the homeobox domain of human HOXB13 gene responsible for hereditary prostate cancer.
Chandrasekaran G et al.
Chemical Biology & Drug Design, 2017
HOXB13 mutations and binding partners in prostate development and cancer: Function, clinical significance, and future directions.
Brechka H et al.
Genes & Diseases, 2017
Computational Modeling of complete HOXB13 protein for predicting the functional effect of SNPs and the associated role in hereditary prostate cancer.
Chandrasekaran G et al.
Scientific Reports, 2017
28272408 (PubMed )
Supplement: srep43830-s1.zip › SR_Supplementary_Data_Files_Complete › PROVEAN › PROVEAN_results.pdf
Identification of Two Novel HOXB13 Germline Mutations in Portuguese Prostate Cancer Patients.
Maia S et al.
Plos One, 2015
Dysregulation of the homeobox transcription factor gene HOXB13: role in prostate cancer.
Decker B et al.
Pharmacogenomics and Personalized Medicine, 2014
Germline mutations in HOXB13 and prostate-cancer risk.
Ewing CM et al.
The New England Journal of Medicine, 2012
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