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Gene-editing technique CRISPR identifies dangerous breast cancer mutations

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Gene-editing technique CRISPR identifies dangerous breast cancer mutations

Mutations in BRCA genes are linked to the early onset of breast and ovarian cancers. But the effect of most mutations is unclear. Now new research can distinguish harmless from dangerous mutations.

Genes, Free Full-Text

Genes, Free Full-Text

Gene-editing technique CRISPR identifies dangerous breast cancer mutations

Gene-editing technique CRISPR identifies dangerous breast cancer mutations

Early-onset cancer – News, Research and Analysis – The Conversation – page 1

Early-onset cancer – News, Research and Analysis – The Conversation – page 1

CRISPR – News, Research and Analysis – The Conversation – page 4

CRISPR – News, Research and Analysis – The Conversation – page 4

BRCA1 – News, Research and Analysis – The Conversation – page 1

BRCA1 – News, Research and Analysis – The Conversation – page 1

Strategies to overcome the main challenges of the use of CRISPR/Cas9 as a  replacement for cancer therapy, Molecular Cancer

Strategies to overcome the main challenges of the use of CRISPR/Cas9 as a replacement for cancer therapy, Molecular Cancer

Genes, Free Full-Text

Genes, Free Full-Text

New breast cancer gene tests will mean hard choices for many women

New breast cancer gene tests will mean hard choices for many women

BRCA1 – News, Research and Analysis – The Conversation – page 1

BRCA1 – News, Research and Analysis – The Conversation – page 1

Home – Articles, Analysis, Opinion – The Conversation – page 488

Home – Articles, Analysis, Opinion – The Conversation – page 488

Ovarian cancer – News, Research and Analysis – The Conversation – page 1

Ovarian cancer – News, Research and Analysis – The Conversation – page 1

Genome editing and cancer: How far has research moved forward on CRISPR/Cas9?  - ScienceDirect

Genome editing and cancer: How far has research moved forward on CRISPR/Cas9? - ScienceDirect

Breakthrough gene-editing therapy transforms lives of patients with a  hereditary disorder

Breakthrough gene-editing therapy transforms lives of patients with a hereditary disorder