Associated Papers
A systematic in-silico functional and structural analysis reveals deleterious missense nsSNPs in the human CSF1R gene.
Malhotra P et al.
Molecular Biology Research Communications, 2025
40949796 (PubMed )
Supplement: mbrc-14-291-s001.pdf
CSF1R-related disorder: State of the art, challenges, and proposition of a new terminology.
Dulski J et al.
Parkinsonism & Related Disorders, 2024
Actionable Molecular Alterations Are Revealed in Majority of Advanced Non-Small Cell Lung Cancer Patients by Genomic Tumor Profiling at Progression after First Line Treatment.
Frank MS et al.
Cancers, 2021
35008297 (PubMed )
Supplement: cancers-14-00132-s001.zip › Supplementary_Table_S1.xlsx › Overview_ver2
Phenotypic impacts of CSF1R deficiencies in humans and model organisms.
Hume DA et al.
Journal of Leukocyte Biology, 2020
Implementation of next generation sequencing into pediatric hematology-oncology practice: moving beyond actionable alterations.
Oberg JA et al.
Genome Medicine, 2016
28007021 (PubMed )
Supplement: 13073_2016_389_MOESM5_ESM.xlsx › VOUS
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