S. Simon

发表

Phytoestrogens and Their Human Metabolites Show Distinct Agonistic and Antagonistic Properties on Estrogen Receptor α (ERα)and ERβ in Human Cells

S. O. Mueller, S. Simon, K. Chae, 2004 .

Hsp27 (HspB1) and alphaB-crystallin (HspB5) as therapeutic targets.

S. Simon, B. Gibert, C. Diaz-latoud, 2007, FEBS letters.

Expression and functions of heat shock proteins in the normal and pathological mammalian eye.

S. Simon, A. Arrigo, 2010, Current molecular medicine.

Hsp27 (HspB1) and αB‐crystallin (HspB5) as therapeutic targets

S. Simon, B. Gibert, C. Diaz-latoud, 2007 .

Knock Down of Heat Shock Protein 27 (HspB1) Induces Degradation of Several Putative Client Proteins

S. Simon, B. Gibert, C. Diaz-latoud, 2012, PloS one.

Analysis of the Dominant Effects Mediated by Wild Type or R120G Mutant of αB-crystallin (HspB5) towards Hsp27 (HspB1)

S. Simon, P. Mehlen, B. Gibert, 2013, PloS one.

Combined pulmonary fibrosis and emphysema syndrome associated with ABCA3 mutations

S. Simon, R. Epaud, M. Louha, 2013, European Respiratory Journal.

Dynamic processes that reflect anti-apoptotic strategies set up by HspB1 (Hsp27).

S. Simon, B. Gibert, F. Manero, 2010, Experimental cell research.

NFκB is a central regulator of protein quality control in response to protein aggregation stresses via autophagy modulation

S. Simon, C. Hetz, J. Atkin, 2016, Molecular biology of the cell.

Abnormal interaction of motor neuropathy-associated mutant HspB8 (Hsp22) forms with the RNA helicase Ddx20 (gemin3)

S. Simon, M. Welsh, A. Hoppe, 2010, Cell Stress and Chaperones.

Myopathy-associated αB-crystallin Mutants

S. Simon, M. Welsh, A. Hoppe, 2007, Journal of Biological Chemistry.

Phosphorylation of the Chaperone-Like HspB5 Rescues Trafficking and Function of F508del-CFTR

S. Simon, D. Rotin, X. Decrouy, 2020, International journal of molecular sciences.

Instability of Mature ABCA3 Protein: Toward a New Classification of ABCA3 Mutations?

S. Simon, R. Epaud, B. Duriez, 2022, American journal of respiratory cell and molecular biology.

Methylprednisolone pulse treatment improves ProSP‐C trafficking in twins with SFTPC mutation: An isoform story?

S. Simon, S. Finet, R. Epaud, 2020, British journal of clinical pharmacology.

Peptide aptamers: tools to negatively or positively modulate HSPB1(27) function

S. Simon, B. Gibert, C. Diaz-latoud, 2013, Philosophical Transactions of the Royal Society B: Biological Sciences.

HSPB1(27) function Peptide aptamers: tools to negatively or positively modulate

S. Simon, B. Gibert, C. Diaz-latoud, 2013 .

N-Acetyl-L-Cysteine Prevents Stress-Induced Desmin Aggregation in Cellular Models of Desminopathy

S. Simon, S. Batonnet-Pichon, B. Segard, 2013, PloS one.

Human reporter gene assays: transcriptional activity of the androgen receptor is modulated by the cellular environment and promoter context.

S. O. Mueller, S. Simon, 2006, Toxicology.

Dual Blockade of Misfolded Alpha-Sarcoglycan Degradation by Bortezomib and Givinostat Combination

S. Simon, L. Hoch, Manon Benabides, 2022, bioRxiv.

Hsp27‐2D‐gel electrophoresis is a diagnostic tool to differentiate primary desminopathies from myofibrillar myopathies

S. Simon, K. Zerres, N. Romero, 2005, FEBS letters.

Deciphering the mechanism of Q145H SFTPC mutation unmasks a splicing defect and explains the severity of the phenotype

S. Simon, R. Epaud, X. Decrouy, 2017, European Journal of Human Genetics.

Phytoestrogens and their human metabolites show distinct agonistic and antagonistic properties on estrogen receptor alpha (ERalpha) and ERbeta in human cells.

S. O. Mueller, S. Simon, K. Chae, 2004, Toxicological sciences : an official journal of the Society of Toxicology.

Gene expression profiling in Ishikawa cells: a fingerprint for estrogen active compounds.

Stefan O Mueller, S. O. Mueller, S. Simon, 2009, Toxicology and applied pharmacology.

Deciphering an isolated lung phenotype of NKX2-1 frameshift pathogenic variant

S. Simon, R. Epaud, X. Decrouy, 2023, Frontiers in Pediatrics.

Small Hsps as Therapeutic Targets of Cystic Fibrosis Transmembrane Conductance Regulator Protein

S. Simon, A. Arrigo, A. Aissat, 2021, International journal of molecular sciences.

Assessing the mechanism and therapeutic potential of modulators of the human Mediator complex-associated protein kinases

S. Czasch, F. Rohdich, T. Dale, 2016, eLife.

Revisiting the bacterial mutagenicity assays: Report by a workgroup of the International Workshops on Genotoxicity Testing (IWGT).

E. Zeiger, K. Cross, R. Williams, 2020, Mutation research.

Abnormal small heat shock protein interactions involving neuropathy‐associated HSP22 (HSPB8) mutants

S. Simon, A. Hoppe, P. Vicart, 2006, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Unsolved severe chronic rhinosinusitis elucidated by extensive CFTR genotyping

S. Simon, I. Sermet-Gaudelus, I. Callebaut, 2019, Clinical case reports.

25 Unsolved severe chronic rhinosinusitis elucidated by extensive CFTR genotyping

S. Simon, I. Sermet-Gaudelus, I. Callebaut, 2017 .

Myopathy-associated alphaB-crystallin mutants: abnormal phosphorylation, intracellular location, and interactions with other small heat shock proteins.

S. Simon, M. Welsh, A. Hoppe, 2007, Journal of Biological Chemistry.

Myofibrillar myopathy with congenital cataract and skeletal anomalies without mutations in the desmin, αB-crystallin, myotilin, LMNA or SEPN1 genes

S. Simon, A. Ferreiro, P. Richard, 2006, Neuromuscular Disorders.

Deciphering the mechanism of Q145H SFTPC mutation unmasks a splicing defect and explains the severity of the phenotype

S. Simon, R. Epaud, X. Decrouy, 2017, European Journal of Human Genetics.