Associated Papers
Accelerated drug-resistant variant discovery with an enhanced, scalable mutagenic base editor platform.
Dorighi KM et al.
Cell Reports, 2024
Custom multi‑tumor next‑generation sequencing panel for routine molecular diagnosis of solid tumors: Validation and results from three‑year clinical use.
Chevrier S et al.
International Journal of Molecular Medicine, 2022
35244186 (PubMed )
Supplement: Supplementary_Data2.xlsx › Feuil1
Simultaneous Detection of NF1, SPRED1, LZTR1, and NF2 Gene Mutations by Targeted NGS in an Italian Cohort of Suspected NF1 Patients.
Bianchessi D et al.
Genes, 2020
Integrative annotation and knowledge discovery of kinase post-translational modifications and cancer-associated mutations through federated protein ontologies and resources.
Huang LC et al.
Scientific Reports, 2018
29695735 (PubMed )
Supplement: 41598_2018_24457_MOESM1_ESM.pdf
Aberrations and clinical significance of BRAF in malignant melanoma: A series of 60 cases in Chinese Uyghur.
Kang X et al.
Medicine, 2018
Phospho-proteomic analyses of B-Raf protein complexes reveal new regulatory principles.
Eisenhardt AE et al.
Oncotarget, 2016
27034005 (PubMed )
Supplement: oncotarget-07-26628-s007.pdf
Clinical characteristics and outcome of patients with lung cancer harboring BRAF mutations.
Tissot C et al.
Lung Cancer (amsterdam, Netherlands), 2016
Rapid identification of somatic mutations in colorectal and breast cancer tissues using mismatch repair detection (MRD).
Bentivegna S et al.
Human Mutation, 2008
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