Epigenetic mechanisms in cartilage and osteoarthritis: DNA methylation, histone modifications and microRNAs MJ Barter, C Bui, DA Young Osteoarthritis and cartilage 20 (5), 339-349, 2012 | 212 | 2012 |
Expression of the osteoarthritis-associated gene GDF5 is modulated epigenetically by DNA methylation LN Reynard, C Bui, EG Canty-Laird, DA Young, J Loughlin Human molecular genetics 20 (17), 3450-3460, 2011 | 136 | 2011 |
cAMP response element‐binding (CREB) recruitment following a specific CpG demethylation leads to the elevated expression of the matrix metalloproteinase 13 in human articular … C Bui, MJ Barter, JL Scott, Y Xu, M Galler, LN Reynard, AD Rowan, ... The FASEB Journal 26 (7), 3000-3011, 2012 | 125 | 2012 |
CpG methylation regulates allelic expression of GDF5 by modulating binding of SP1 and SP3 repressor proteins to the osteoarthritis susceptibility SNP rs143383 LN Reynard, C Bui, CM Syddall, J Loughlin Human genetics 133, 1059-1073, 2014 | 116 | 2014 |
XYLT1 mutations in Desbuquois dysplasia type 2 C Bui, C Huber, B Tuysuz, Y Alanay, C Bole-Feysot, JG Leroy, G Mortier, ... The American Journal of Human Genetics 94 (3), 405-414, 2014 | 116 | 2014 |
Epigenetics: methylation‐associated repression of heparan sulfate 3‐O‐sulfotransferase gene expression contributes to the invasive phenotype of H‐EMC‐SS chondrosarcoma cells C Bui, M Ouzzine, I Talhaoui, S Sharp, K Prydz, MWH Coughtrie, ... FASEB journal 24 (2), 436-450, 2010 | 80 | 2010 |
The heparan sulfate sulfotransferase 3-OST3A (HS3ST3A) is a novel tumor regulator and a prognostic marker in breast cancer X Mao, C Gauche, MWH Coughtrie, C Bui, S Gulberti, F Merhi-Soussi, ... Oncogene 35 (38), 5043-5055, 2016 | 31 | 2016 |
Molecular characterization of β1, 4-galactosyltransferase 7 genetic mutations linked to the progeroid form of Ehlers–Danlos syndrome (EDS) C Bui, I Talhaoui, M Chabel, G Mulliert, MWH Coughtrie, M Ouzzine, ... FEBS letters 584 (18), 3962-3968, 2010 | 31 | 2010 |
DNA hypomethylation during MSC chondrogenesis occurs predominantly at enhancer regions MJ Barter, C Bui, K Cheung, J Falk, R Gómez, AJ Skelton, HR Elliott, ... Scientific Reports 10 (1), 1169, 2020 | 25 | 2020 |
Identification of key functional residues in the active site of human β1, 4-galactosyltransferase 7: a major enzyme in the glycosaminoglycan synthesis pathway I Talhaoui, C Bui, R Oriol, G Mulliert, S Gulberti, P Netter, MWH Coughtrie, ... Journal of biological chemistry 285 (48), 37342-37358, 2010 | 24 | 2010 |
The role of heparan sulfate maturation in cancer: A focus on the 3O-sulfation and the enigmatic 3O-sulfotransferases (HS3STs) S Gulberti, X Mao, C Bui, S Fournel-Gigleux Seminars in Cancer Biology 62, 68-85, 2020 | 16 | 2020 |
Understanding CpG methylation in the context of osteoarthritis DA Young, C Bui, MJ Barter Epigenomics 4 (6), 593-595, 2012 | 11 | 2012 |
Alterations in glycosaminoglycan biosynthesis associated with the Ehlers-Danlos syndromes D Syx, S Delbaere, C Bui, A De Clercq, G Larson, S Mizumoto, T Kosho, ... American Journal of Physiology-Cell Physiology 323 (6), C1843-C1859, 2022 | 9 | 2022 |
Tissue-specific collagen hydroxylation at GEP/GDP triplets mediated by P4HA2 D Wilhelm, A Wurtz, H Abouelfarah, G Sanchez, C Bui, JB Vincourt Matrix Biology 119, 141-153, 2023 | 3 | 2023 |
Low-frequency coding variants associated with body mass index affect the success of bariatric surgery D Antoine, RM Guéant-Rodriguez, JC Chèvre, S Hergalant, T Sharma, ... The Journal of Clinical Endocrinology & Metabolism 107 (3), e1074-e1084, 2022 | 2 | 2022 |
Impact of β1, 3-galactosyltransferase 6 deficiency in a rare connective tissue genetic disorder R Diana, A Robert, JB Vincourt, C Bui, S Fournel-Gigleux 8th FEBS Advanced Lecture Course" Matrix pathobiology, signaling and …, 2022 | | 2022 |
A versatile strategy to synthesize N-methyl-anthranilic acid-labelled glycoprobes for fluorescence-based screening assays I Bertin-Jung, A Robert, N Ramalanjaona, S Gulberti, C Bui, JB Vincourt, ... Chemical Communications 56 (73), 10746-10749, 2020 | | 2020 |
A new perspective on the pathogeny of glycosaminoglycan synthesis genetic defects: towards «omic» approaches S Fournel-Gigleux, C Bui, X Pang, T van Damme, M Fransiska, S Gulberti FEBS Advanced Lecture Course, FEBS ECM 2018, 2018 | | 2018 |
Understanding the Pathogenesis of Ehlers-Danlos Syndrome, a Rare Connective Tissue Disorder Caused by B3GALT6 Mutations: What if'Omics' Could Help? C Bui Proteoglycans Gordon Research Conference, Proteoglycans in Homeostasis and …, 2018 | | 2018 |
Monogenic Forms of Childhood Obesity C Bui, M Pigeyre, D Meyre Obésité 12, 277-290, 2017 | | 2017 |