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BRCAness revisited
by
Lord, Christopher J.
, Ashworth, Alan
in
631/208/211
/ 631/67/1059/602
/ 631/67/1059/99
/ 631/67/1244
/ 631/67/1347
/ 631/67/1517/1709
/ 631/67/1857
/ 631/67/68
/ Antineoplastic Agents - pharmacology
/ Biomarkers, Tumor - analysis
/ Biomarkers, Tumor - genetics
/ Biomedicine
/ BRCA1 protein
/ BRCA1 Protein - genetics
/ BRCA1 Protein - metabolism
/ BRCA2 protein
/ BRCA2 Protein - genetics
/ BRCA2 Protein - metabolism
/ Breast cancer
/ Cancer
/ Cancer Research
/ Cancer therapies
/ Carcinogenesis
/ Chemotherapy
/ Defects
/ Deoxyribonucleic acid
/ DNA
/ DNA damage
/ DNA repair
/ Drug Resistance, Neoplasm - drug effects
/ Drug Resistance, Neoplasm - genetics
/ Female
/ Gene mutations
/ Genetic aspects
/ Genetic Predisposition to Disease
/ Genetic research
/ Genetic susceptibility
/ Genomes
/ Genomics
/ Genotype & phenotype
/ Germ-Line Mutation
/ Health aspects
/ Humans
/ Medical research
/ Mutation
/ Neoplasms - drug therapy
/ Neoplasms - genetics
/ Oncology, Experimental
/ opinion-2
/ Ovarian cancer
/ Phthalazines - pharmacology
/ Piperazines - pharmacology
/ Poly(ADP-ribose) Polymerase Inhibitors - pharmacology
/ Proteins
/ Rad51 Recombinase - genetics
/ Rad51 Recombinase - metabolism
/ Signal transduction
/ Tumorigenesis
/ Tumors
2016
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BRCAness revisited
by
Lord, Christopher J.
, Ashworth, Alan
in
631/208/211
/ 631/67/1059/602
/ 631/67/1059/99
/ 631/67/1244
/ 631/67/1347
/ 631/67/1517/1709
/ 631/67/1857
/ 631/67/68
/ Antineoplastic Agents - pharmacology
/ Biomarkers, Tumor - analysis
/ Biomarkers, Tumor - genetics
/ Biomedicine
/ BRCA1 protein
/ BRCA1 Protein - genetics
/ BRCA1 Protein - metabolism
/ BRCA2 protein
/ BRCA2 Protein - genetics
/ BRCA2 Protein - metabolism
/ Breast cancer
/ Cancer
/ Cancer Research
/ Cancer therapies
/ Carcinogenesis
/ Chemotherapy
/ Defects
/ Deoxyribonucleic acid
/ DNA
/ DNA damage
/ DNA repair
/ Drug Resistance, Neoplasm - drug effects
/ Drug Resistance, Neoplasm - genetics
/ Female
/ Gene mutations
/ Genetic aspects
/ Genetic Predisposition to Disease
/ Genetic research
/ Genetic susceptibility
/ Genomes
/ Genomics
/ Genotype & phenotype
/ Germ-Line Mutation
/ Health aspects
/ Humans
/ Medical research
/ Mutation
/ Neoplasms - drug therapy
/ Neoplasms - genetics
/ Oncology, Experimental
/ opinion-2
/ Ovarian cancer
/ Phthalazines - pharmacology
/ Piperazines - pharmacology
/ Poly(ADP-ribose) Polymerase Inhibitors - pharmacology
/ Proteins
/ Rad51 Recombinase - genetics
/ Rad51 Recombinase - metabolism
/ Signal transduction
/ Tumorigenesis
/ Tumors
2016
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Do you wish to request the book?
BRCAness revisited
by
Lord, Christopher J.
, Ashworth, Alan
in
631/208/211
/ 631/67/1059/602
/ 631/67/1059/99
/ 631/67/1244
/ 631/67/1347
/ 631/67/1517/1709
/ 631/67/1857
/ 631/67/68
/ Antineoplastic Agents - pharmacology
/ Biomarkers, Tumor - analysis
/ Biomarkers, Tumor - genetics
/ Biomedicine
/ BRCA1 protein
/ BRCA1 Protein - genetics
/ BRCA1 Protein - metabolism
/ BRCA2 protein
/ BRCA2 Protein - genetics
/ BRCA2 Protein - metabolism
/ Breast cancer
/ Cancer
/ Cancer Research
/ Cancer therapies
/ Carcinogenesis
/ Chemotherapy
/ Defects
/ Deoxyribonucleic acid
/ DNA
/ DNA damage
/ DNA repair
/ Drug Resistance, Neoplasm - drug effects
/ Drug Resistance, Neoplasm - genetics
/ Female
/ Gene mutations
/ Genetic aspects
/ Genetic Predisposition to Disease
/ Genetic research
/ Genetic susceptibility
/ Genomes
/ Genomics
/ Genotype & phenotype
/ Germ-Line Mutation
/ Health aspects
/ Humans
/ Medical research
/ Mutation
/ Neoplasms - drug therapy
/ Neoplasms - genetics
/ Oncology, Experimental
/ opinion-2
/ Ovarian cancer
/ Phthalazines - pharmacology
/ Piperazines - pharmacology
/ Poly(ADP-ribose) Polymerase Inhibitors - pharmacology
/ Proteins
/ Rad51 Recombinase - genetics
/ Rad51 Recombinase - metabolism
/ Signal transduction
/ Tumorigenesis
/ Tumors
2016
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Journal Article
BRCAness revisited
2016
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Overview
The development of therapeutic approaches that target BRCA-mutant tumours has led to the possibility of expanding the range of patients who may benefit from such strategies. Tumours with 'BRCAness', a similar phenotype to germline BRCA-mutant tumours, are increasingly being identified, and this Opinion article discusses the advances and challenges in this context.
Over the past 20 years, there has been considerable progress in our understanding of the biological functions of the
BRCA1
and
BRCA2
cancer susceptibility genes. This has led to the development of new therapeutic approaches that target tumours with loss-of-function mutations in either
BRCA1
or
BRCA2
. Tumours that share molecular features of BRCA-mutant tumours — that is, those with 'BRCAness' — may also respond to similar therapeutic approaches. Several paradigm shifts require a reassessment of the concept of BRCAness, how this property is assayed and its relevance to our understanding of tumour biology and the treatment of cancer.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
/ Antineoplastic Agents - pharmacology
/ Biomarkers, Tumor - analysis
/ Biomarkers, Tumor - genetics
/ Cancer
/ Defects
/ DNA
/ Drug Resistance, Neoplasm - drug effects
/ Drug Resistance, Neoplasm - genetics
/ Female
/ Genetic Predisposition to Disease
/ Genomes
/ Genomics
/ Humans
/ Mutation
/ Poly(ADP-ribose) Polymerase Inhibitors - pharmacology
/ Proteins
/ Rad51 Recombinase - genetics
/ Rad51 Recombinase - metabolism
/ Tumors
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