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Catherine Bui
Catherine Bui
Verified email at univ-lorraine.fr
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Cited by
Year
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
2112012
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
1362011
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
1252012
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
1162014
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
1162014
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
802010
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
312016
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
312010
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
242020
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
242010
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
162020
Understanding CpG methylation in the context of osteoarthritis
DA Young, C Bui, MJ Barter
Epigenomics 4 (6), 593-595, 2012
112012
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
92022
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
32023
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
22022
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
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