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vergessen Mobilisieren nichts breast cancer information core bic so viel Stange Müll

Research Projects
Research Projects

Genes | Free Full-Text | Imprecise Medicine: BRCA2 Variants of Uncertain  Significance (VUS), the Challenges and Benefits to Integrate a Functional  Assay Workflow with Clinical Decision Rules | HTML
Genes | Free Full-Text | Imprecise Medicine: BRCA2 Variants of Uncertain Significance (VUS), the Challenges and Benefits to Integrate a Functional Assay Workflow with Clinical Decision Rules | HTML

PDF) Interpreting epidemiological research: blinded comparison of methods  used to estimate the prevalence of inherited mutations in BRCA1 | Lawrence  Brody - Academia.edu
PDF) Interpreting epidemiological research: blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1 | Lawrence Brody - Academia.edu

BIC Definition: Breast Cancer Information Core | Abbreviation Finder
BIC Definition: Breast Cancer Information Core | Abbreviation Finder

Abbreviation: BIC, Breast Cancer Information Core database. a GenBank... |  Download Scientific Diagram
Abbreviation: BIC, Breast Cancer Information Core database. a GenBank... | Download Scientific Diagram

BRCA2 c.8827C>T pathogenic mutation in a consanguineous Chinese family with  hereditary breast cancer - Wang - 2020 - Molecular Genetics & Genomic  Medicine - Wiley Online Library
BRCA2 c.8827C>T pathogenic mutation in a consanguineous Chinese family with hereditary breast cancer - Wang - 2020 - Molecular Genetics & Genomic Medicine - Wiley Online Library

Table 1 from BRCA1 and BRCA2 germline mutations in Korean ovarian cancer  patients | Semantic Scholar
Table 1 from BRCA1 and BRCA2 germline mutations in Korean ovarian cancer patients | Semantic Scholar

Identification of recurrent BRCA1 mutation and its clinical relevance in  Chinese Triple-negative breast cancer cohort – topic of research paper in  Clinical medicine. Download scholarly article PDF and read for free on
Identification of recurrent BRCA1 mutation and its clinical relevance in Chinese Triple-negative breast cancer cohort – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on

Prevalence and characterization of BRCA1 and BRCA2 germline mutations in  Chinese women with familial breast cancer - Document - Gale OneFile: Health  and Medicine
Prevalence and characterization of BRCA1 and BRCA2 germline mutations in Chinese women with familial breast cancer - Document - Gale OneFile: Health and Medicine

BIC - Breast Cancer Information Core
BIC - Breast Cancer Information Core

Frameshift mutations detected in BRCA genes | Download Table
Frameshift mutations detected in BRCA genes | Download Table

BRCA germline mutations in an unselected nationwide cohort of Chinese  patients with ovarian cancer and healthy controls - Gynecologic Oncology
BRCA germline mutations in an unselected nationwide cohort of Chinese patients with ovarian cancer and healthy controls - Gynecologic Oncology

Cancers | Free Full-Text | The Genetic Analyses of French Canadians of  Quebec Facilitate the Characterization of New Cancer Predisposing Genes  Implicated in Hereditary Breast and/or Ovarian Cancer Syndrome Families |  HTML
Cancers | Free Full-Text | The Genetic Analyses of French Canadians of Quebec Facilitate the Characterization of New Cancer Predisposing Genes Implicated in Hereditary Breast and/or Ovarian Cancer Syndrome Families | HTML

BRCA1/2 testing: therapeutic implications for breast cancer management |  British Journal of Cancer
BRCA1/2 testing: therapeutic implications for breast cancer management | British Journal of Cancer

Comparative oncogenomics identifies combinations of driver genes and drug  targets in BRCA1-mutated breast cancer | Nature Communications
Comparative oncogenomics identifies combinations of driver genes and drug targets in BRCA1-mutated breast cancer | Nature Communications

BRCA1 And BRCA2 analysis of Argentinean breast/ovarian cancer patients  selected for age and family history highlights a role for novel mutations  of putative south-American origin – topic of research paper in Biological
BRCA1 And BRCA2 analysis of Argentinean breast/ovarian cancer patients selected for age and family history highlights a role for novel mutations of putative south-American origin – topic of research paper in Biological

Concordance of Genomic Variants in Matched Primary Breast Cancer,  Metastatic Tumor, and Circulating Tumor DNA: The MIRROR Study | JCO  Precision Oncology
Concordance of Genomic Variants in Matched Primary Breast Cancer, Metastatic Tumor, and Circulating Tumor DNA: The MIRROR Study | JCO Precision Oncology

Prevalence and characterization of BRCA1 and BRCA2 germline mutations in  Chinese women with familial breast cancer - Document - Gale OneFile: Health  and Medicine
Prevalence and characterization of BRCA1 and BRCA2 germline mutations in Chinese women with familial breast cancer - Document - Gale OneFile: Health and Medicine

BRCA1 and BRCA2 genes mutations among high risk breast cancer patients in  Jordan | Scientific Reports
BRCA1 and BRCA2 genes mutations among high risk breast cancer patients in Jordan | Scientific Reports

Family specific genetic predisposition to breast cancer: results from  Tunisian whole exome sequenced breast cancer cases | Journal of  Translational Medicine | Full Text
Family specific genetic predisposition to breast cancer: results from Tunisian whole exome sequenced breast cancer cases | Journal of Translational Medicine | Full Text

Spectrum and prevalence of BRCA1/2 germline mutations in Pakistani breast  cancer patients: results from a large comprehensive study | Hereditary  Cancer in Clinical Practice | Full Text
Spectrum and prevalence of BRCA1/2 germline mutations in Pakistani breast cancer patients: results from a large comprehensive study | Hereditary Cancer in Clinical Practice | Full Text

PDF] Identification and evaluation of 55 genetic variations in the BRCA1  and the BRCA2 genes of patients from 50 Japanese breast cancer families |  Semantic Scholar
PDF] Identification and evaluation of 55 genetic variations in the BRCA1 and the BRCA2 genes of patients from 50 Japanese breast cancer families | Semantic Scholar

PDF) The Breast Cancer Information Core: Database design, structure, and  scope
PDF) The Breast Cancer Information Core: Database design, structure, and scope

PDF) The Breast Cancer Information Core: Database design, structure, and  scope
PDF) The Breast Cancer Information Core: Database design, structure, and scope

Opportunities and hurdles in the treatment of BRCA1-related breast cancer |  Oncogene
Opportunities and hurdles in the treatment of BRCA1-related breast cancer | Oncogene

Genes | Free Full-Text | BRCA1/2 Mutations in Vietnamese Patients with  Hereditary Breast and Ovarian Cancer Syndrome | HTML
Genes | Free Full-Text | BRCA1/2 Mutations in Vietnamese Patients with Hereditary Breast and Ovarian Cancer Syndrome | HTML

Targeted sequencing of BRCA1 and BRCA2 across a large unselected breast  cancer cohort suggests that one-third of mutations are somatic - Annals of  Oncology
Targeted sequencing of BRCA1 and BRCA2 across a large unselected breast cancer cohort suggests that one-third of mutations are somatic - Annals of Oncology