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Open Access#12019

Mutations in the RAS-BRAF-MAPK-ERK pathway define a specific subgroup of patients with adverse clinical features and provide new therapeutic options in chronic lymphocytic leukemia

BASE

Open Access#22013

Estimation of Copy Number Alterations from Exome Sequencing Data

BASE

Open Access#32018

Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are infrequent in familial colorectal cancer and polyposis

BASE

Open Access#42013

The Degradome database: mammalian proteases and diseases of proteolysis

BASE

Open Access#52018

Tumor xenograft modeling identifies an association between TCF4 loss and breast cancer chemoresistance

BASE

Open Access#62015

Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair

BASE

Open Access#82021

Sex differences in oncogenic mutational processes

BASE

Open Access#92021

Circulating tumour DNA from the cerebrospinal fluid allows the characterisation and monitoring of medulloblastoma

BASE

Open Access#102013

Exome Sequencing and Functional Analysis Identifies BANF1 Mutation as the Cause of a Hereditary Progeroid Syndrome

BASE

Open Access#112019

Insight into genetic predisposition to chronic lymphocytic leukemia from integrative epigenomics

BASE