Selection of patients with germline MLH1 mutated Lynch syndrome by determination of MLH1 methylation and BRAF mutation [PDF]
Lynch syndrome is one of the most common hereditary colorectal cancer (CRC) syndrome and is caused by germline mutations of MLH1, MSH2 and more rarely MSH6, PMS2, MLH3 genes.
Benhattar, Jean +4 more
core
Mapping genetic interactions in cancer: a road to rational combination therapies. [PDF]
The discovery of synthetic lethal interactions between poly (ADP-ribose) polymerase (PARP) inhibitors and BRCA genes, which are involved in homologous recombination, led to the approval of PARP inhibition as a monotherapy for patients with BRCA1/2 ...
Krogan, Nevan J, Tutuncuoglu, Beril
core
BRIP-1 germline mutation and its role in colon cancer: presentation of two case reports and review of literature. [PDF]
BackgroundHereditary colon cancer is characterized by the inheritance of an abnormal gene mutation which predisposes to malignancy. Recent advances in genomic medicine have identified mutations in "novel" genes as conferring an increased risk of ...
Ali, Mir +2 more
core
Long term response on Regorafenib in non-V600E BRAF mutated colon cancer: a case report [PDF]
Callebout, Eduard +7 more
core +2 more sources
Clinicopathological Features of Non-Small Cell Lung Carcinoma with BRAF Mutation. [PDF]
Ambrosini-Spaltro A +12 more
europepmc +1 more source
BRAF V600E Mutation in Malignant Melanoma—A Romanian Research Experience
Background and Objectives: The most common mutation in malignant melanoma (MM) is the single-point mutation of v-raf murine sarcoma viral oncogene homolog B1 (BRAF) oncogene.
Elena-Roxana Avădănei +6 more
doaj +1 more source
Therapeutic strategies for BRAF mutation in non-small cell lung cancer: a review. [PDF]
Puri M, Gawri K, Dawar R.
europepmc +1 more source
Prevalence and Impact of BRAF mutation in patients with concomitant papillary thyroid carcinoma and Hashimoto's thyroiditis: a systematic review with meta-analysis. [PDF]
Janicki L +3 more
europepmc +1 more source

