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-stimulating factor 1 receptor (CSF-1R), resulting in phosphorylation of the intracellular tyrosine residues, which causes cell proliferation and differentiation ( 11 ). Recently, it has been reported that IL-34 also binds to other receptors via low
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CHU Lille, Service de Biochimie Hormonologie, Métabolisme, Nutrition-Oncologie, Centre de Biologie Pathologie Génétique, Lille, France
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genes using the Illumina TruSeq Amplicon Cancer Panel ( ABL1 , AKT1 , ALK , APC , ATM , BRAF , CDH1 , CDKN2A , CSF1R , CTNNB1 , EGFR , ERBB2 , ERBB4 , FBXW7 , FGFR1 , FGFR2 , FGFR3 , FLT3 , GNA11 , GNAQ , GNAS , HNF1A , HRAS , IDH1
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ALK FGFR1 KDR PTPN11 APC FGFR2 KIT RB1 ATM FGFR3 KRAS RET BRAF FLT3 MET SMAD4 CDH1 GNA11 MLH1 SMARCB1 CDKN2A GNAQ MPL SMO CSF1R GNAS NOTCH1 SRC CTNNB1 HNF1A NPM1
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identified in ALK, ATM, CSF1R, GNAS, SMARCB1 , and NOTCH1 genes. This alteration was not previously reported in metastatic MTC. Spoziello et al . detected germline p.Arg417Gln mutation in the MET gene in siblings diagnosed with MTC and other primary