Implementation of next-generation sequencing for molecular diagnosis of hereditary breast and ovarian cancer highlights its genetic heterogeneity. - Test2 - elhamkhani - TriplyDB

Implementation of next-generation sequencing for molecular diagnosis of hereditary breast and ovarian cancer highlights its genetic heterogeneity.

Implementation of next-generation sequencing for molecular diagnosis of hereditary breast and ovarian cancer highlights its genetic heterogeneity.

http://www.wikidata.org/entity/Q49097031

about

Next-Generation Sequencing in Oncology: Genetic Diagnosis, Risk Prediction and Cancer Classification.Evaluation of ATM heterozygous mutations underlying individual differences in radiosensitivity using genome editing in human cultured cells.Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds.Potentially pathogenic germline CHEK2 c.319+2T>A among multiple early-onset cancer families.Germline mutations in patients with multiple colorectal polyps in China.Identification of genetic variants for clinical management of familial colorectal tumors.Targeted next generation sequencing identifies functionally deleterious germline mutations in novel genes in early-onset/familial prostate cancer.Exploration of genetic basis underlying individual differences in radiosensitivity within human populations using genome editing technology.

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P2860

Implementation of next-generation sequencing for molecular diagnosis of hereditary breast and ovarian cancer highlights its genetic heterogeneity.

http://www.wikidata.org/entity/Q49097031

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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Implementation of next-generat ...... hts its genetic heterogeneity.

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Implementation of next-generat ...... hts its genetic heterogeneity.

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Implementation of next-generat ...... hts its genetic heterogeneity.

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Implementation of next-generat ...... hts its genetic heterogeneity.

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Implementation of next-generat ...... hts its genetic heterogeneity.

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Implementation of next-generat ...... hts its genetic heterogeneity.

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Breast Cancer Research and Treatment

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Implementation of next-generat ...... hts its genetic heterogeneity.

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Paula Paulo

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P2860

Multigene testing of moderate-risk genes: be mindful of the missense

A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1

Germline mutations in RAD51D confer susceptibility to ovarian cancer

Guidelines for splicing analysis in molecular diagnosis derived from a set of 327 combined in silico/in vitro studies on BRCA1 and BRCA2 variants

CHEK2 mutations affecting kinase activity together with mutations in TP53 indicate a functional pathway associated with resistance to epirubicin in primary breast cancer

CNV-seq, a new method to detect copy number variation using high-throughput sequencing

A general framework for estimating the relative pathogenicity of human genetic variants

Identification of the breast cancer susceptibility gene BRCA2

Understanding the limitations of next generation sequencing informatics, an approach to clinical pipeline validation using artificial data sets.

Prioritization Of Nonsynonymous Single Nucleotide Variants For Exome Sequencing Studies Via Integrative Learning On Multiple Genomic Data.

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245-256

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scholarly article

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10.1007/S10549-016-3948-Z

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2

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Manuel R. Teixeira

Manuela Pinheiro

Catarina Santos

Patrícia Rocha

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2016-08-23T00:00:00Z

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1020546012

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27553368

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