Pages that link to "Q34329529"

The following pages link to Understanding missense mutations in the BRCA1 gene: an evolutionary approach (Q34329529):

Displaying 50 items.

• Pervasive adaptive evolution in primate seminal proteins (Q21145283) (← links)
• Cancer as an evolutionary and ecological process (Q22122026) (← links)
• Comparative analysis of cancer genes in the human and chimpanzee genomes (Q24541311) (← links)
• Mapping of Mcs30, a new mammary carcinoma susceptibility quantitative trait locus (QTL30) on rat chromosome 12: identification of fry as a candidate Mcs gene (Q27309935) (← links)
• Functional impact of missense variants in BRCA1 predicted by supervised learning (Q28469139) (← links)
• The emergence of human-evolutionary medical genomics (Q28729955) (← links)
• Evolutionary genomics of human intellectual disability (Q28729961) (← links)
• Analysis of missense variation in human BRCA1 in the context of interspecific sequence variation (Q28764361) (← links)
• In silico whole-genome scanning of cancer-associated nonsynonymous SNPs and molecular characterization of a dynein light chain tumour variant. (Q30350727) (← links)
• Effects of natural selection on interpopulation divergence at polymorphic sites in human protein-coding Loci (Q30350759) (← links)
• Disease Risk of Missense Mutations Using Structural Inference from Predicted Function (Q30394373) (← links)
• Reassessment of the TP53 mutation database in human disease by data mining with a library of TP53 missense mutations (Q30977773) (← links)
• Predicting the phenotypic effects of non-synonymous single nucleotide polymorphisms based on support vector machines (Q33305726) (← links)
• Exhaustive prediction of disease susceptibility to coding base changes in the human genome (Q33369619) (← links)
• Disease-associated mitochondrial mutations and the evolution of primate mitogenomes. (Q33693717) (← links)
• Mutation scanning by meltMADGE: validations using BRCA1 and LDLR, and demonstration of the potential to identify severe, moderate, silent, rare, and paucimorphic mutations in the general population (Q33891865) (← links)
• Integrated evaluation of DNA sequence variants of unknown clinical significance: application to BRCA1 and BRCA2 (Q33910123) (← links)
• Rapid evolution of BRCA1 and BRCA2 in humans and other primates (Q33930642) (← links)
• Determination of cancer risk associated with germ line BRCA1 missense variants by functional analysis (Q34116553) (← links)
• TCOF1 mutation database: novel mutation in the alternatively spliced exon 6A and update in mutation nomenclature. (Q34411726) (← links)
• Identification of I411K, a novel missense EYA4 mutation causing autosomal dominant non‑syndromic hearing loss (Q34426824) (← links)
• PARP1-driven poly-ADP-ribosylation regulates BRCA1 function in homologous recombination-mediated DNA repair. (Q34644116) (← links)
• Missense variants of uncertain significance (VUS) altering the phosphorylation patterns of BRCA1 and BRCA2. (Q34737253) (← links)
• Widespread purifying selection at polymorphic sites in human protein-coding loci (Q34791432) (← links)
• Common variation in the BRCA1 gene and prostate cancer risk. (Q34857410) (← links)
• Phylogeny estimation: traditional and Bayesian approaches (Q35097343) (← links)
• Classification of BRCA1 missense variants of unknown clinical significance (Q35447780) (← links)
• Description and analysis of genetic variants in French hereditary breast and ovarian cancer families recorded in the UMD-BRCA1/BRCA2 databases (Q35630889) (← links)
• Comparative genomics at the vertebrate extremes (Q35778678) (← links)
• Assessing the function of genetic variants in candidate gene association studies (Q35842159) (← links)
• Rapid detection of positive selection in genes and genomes through variation clusters (Q35945777) (← links)
• Positive selection in the evolution of cancer (Q36500617) (← links)
• Genetics of hereditary diffuse gastric cancer: progress and future challenges. (Q36512515) (← links)
• Novel BRCA1 and BRCA2 pathogenic mutations in Slovene hereditary breast and ovarian cancer families (Q36642880) (← links)
• Evaluation of unclassified variants in the breast cancer susceptibility genes BRCA1 and BRCA2 using five methods: results from a population-based study of young breast cancer patients (Q36643111) (← links)
• Programmed genetic instability: a tumor-permissive mechanism for maintaining the evolvability of higher species through methylation-dependent mutation of DNA repair genes in the male germ line (Q36766892) (← links)
• Mammalian evolution and biomedicine: new views from phylogeny (Q36877395) (← links)
• The impact of natural selection on health and disease: uses of the population genetics approach in humans (Q36935092) (← links)
• Clinically applicable models to characterize BRCA1 and BRCA2 variants of uncertain significance (Q37117082) (← links)
• A method to assess the clinical significance of unclassified variants in the BRCA1 and BRCA2 genes based on cancer family history (Q37205554) (← links)
• The Clinical Significance of Unknown Sequence Variants in BRCA Genes. (Q37334266) (← links)
• Epidemiology of Patients with Ovarian Cancer with and Without a BRCA1/2 Mutation (Q38609944) (← links)
• UniPrime: a workflow-based platform for improved universal primer design (Q39089243) (← links)
• In silico identification of functional protein interfaces (Q39774320) (← links)
• Selection and the Cell Cycle: Positive Darwinian Selection in a Well-Known DNA Damage Response Pathway (Q39819704) (← links)
• The CDKN2A database: Integrating allelic variants with evolution, structure, function, and disease association (Q40483208) (← links)
• Fidelity of DNA double-strand break repair in heterozygous cell lines harbouring BRCA1 missense mutations (Q40612623) (← links)
• The Evolution, Functions and Applications of the Breast Cancer Genes BRCA1 and BRCA2. (Q41664074) (← links)
• Natural selection and mammalian BRCA1 sequences: elucidating functionally important sites relevant to breast cancer susceptibility in humans (Q43648036) (← links)
• A mutation analysis of the BRCA1 gene in 140 families from southeast France with a history of breast and/or ovarian cancer (Q44492096) (← links)