Associated Papers
Rare Tumor-Normal Matched Whole Exome Sequencing Identifies Novel Genomic Pathogenic Germline and Somatic Aberrations.
Sprissler R et al.
Cancers, 2020
32570879 (PubMed )
Supplement: cancers-12-01618-s001.zip › cancers-817200-Supplementary_Materials3 › Supplementary_table_S1.xlsx › TSG
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 › HOXB13_Homology_Modelling___SNP.xlsx › PANTHER
Identification of Two Novel HOXB13 Germline Mutations in Portuguese Prostate Cancer Patients.
Maia S et al.
Plos One, 2015
Association between germline HOXB13 G84E mutation and risk of prostate cancer.
Akbari MR et al.
Journal of the National Cancer Institute, 2012
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