Publications by authors named "Florence A Arts"

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Epilepsy phenotype and developmental outcome in girls with mosaicism in X-linked neurodevelopmental disorders.
Evelina Carapancea, Donya Eizadkhah, Roberto Santalucia, Damien Lederer, Florence A Arts

Epileptic Disord· October 2025

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Penttinen syndrome-associated PDGFRB Val665Ala variant causes aberrant constitutive STAT1 signalling.
Audrey Nédélec, Emilie M Guérit, Guillaume Dachy, Sandrine Lenglez, Lok San Wong, Florence A Arts

J Cell Mol Med· July 2022

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Association of PDGFRB Mutations With Pediatric Myofibroma and Myofibromatosis.
Guillaume Dachy, Ronald R de Krijger, Sylvie Fraitag, Ivan Théate, Bénédicte Brichard, Florence A Arts

JAMA Dermatol· August 2019

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A patient with germ-line gain-of-function PDGFRB p.N666H mutation and marked clinical response to imatinib.
Dinel Pond, Florence A Arts, Nancy J Mendelsohn, Jean-Baptiste Demoulin, Gunter Scharer

Genet Med· January 2018

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miR-223 potentially targets SWI/SNF complex protein SMARCD1 in atypical proliferative serous tumor and high-grade ovarian serous carcinoma.
Florence A Arts, Lisa Keogh, Paul Smyth, Sharon O'Toole, Robert Ta

Hum Pathol· December 2017

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PDGFRB gain-of-function mutations in sporadic infantile myofibromatosis.
Florence A Arts, Raf Sciot, Bénédicte Brichard, Marleen Renard, Audrey de Rocca Serra

Hum Mol Genet· May 2017

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Unwanted acquired mutations in Ba/F3 transformation assays.
Jean-Baptiste Demoulin, Guillaume Dachy, Florence A Arts

Oncotarget· March 2017

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Idiopathic basal ganglia calcification-associated PDGFRB mutations impair the receptor signalling.
Florence A Arts, Amélie I Velghe, Monique Stevens, Jean-Christophe Renauld, Ahmed Essaghir

J Cell Mol Med· January 2015

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The tyrosine phosphatase SHP2 is required for cell transformation by the receptor tyrosine kinase mutants FIP1L1-PDGFRα and PDGFRα D842V.
Laura A Noël, Florence A Arts, Carmen P Montano-Almendras, Luk Cox, Olga Gielen

Mol Oncol· May 2014

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