Associated Papers
Tumor evolution and immune microenvironment dynamics in primary and relapsed mantle cell lymphoma.
Wan H et al.
Cell Reports. Medicine, 2025
40876452 (PubMed )
Supplement: mmc2.xlsx › TableS3._Nonsilent_mutations
From CFTR to a CF signalling network: a systems biology approach to study Cystic Fibrosis.
Najm M et al.
Bmc Genomics, 2024
Update on Calcium Signaling in Cystic Fibrosis Lung Disease.
Rimessi A et al.
Frontiers in Pharmacology, 2021
Phospholipase C families: Common themes and versatility in physiology and pathology.
Katan M et al.
Progress in Lipid Research, 2020
Rare Tumor-Normal Matched Whole Exome Sequencing Identifies Novel Genomic Pathogenic Germline and Somatic Aberrations.
Sprissler R et al.
Cancers, 2020
32570879 (PubMed )
Supplement: cancers-12-01618-s001.zip › cancers-817200-Supplementary_Materials3 › Supplementary_table_S1.xlsx › TSG
Role of Cystic Fibrosis Bronchial Epithelium in Neutrophil Chemotaxis.
Cabrini G et al.
Frontiers in Immunology, 2020
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.
Justice AE et al.
Nature Genetics, 2019
30778226 (PubMed )
Supplement: NIHMS1016010-supplement-SupplementaryData16.xlsx › SD16._Locus_Lookups
PLCB3 Loss of Function Reduces Pseudomonas aeruginosa-Dependent IL-8 Release in Cystic Fibrosis.
Rimessi A et al.
American Journal of Respiratory Cell and Molecular Biology, 2018
Phospholipase C-β3 is a key modulator of IL-8 expression in cystic fibrosis bronchial epithelial cells.
Bezzerri V et al.
Journal of Immunology (baltimore, Md. : 1950), 2011
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