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Identification of XylT1 mutations in Desbusquois dysplasia type 2 and functional consequences on proteoglycan synthesis

 Catherine Bui , Céline Hubert , Yasemin Alanay , Beyhan Tuysuz , Christine Bole-Feysot , et al.
LIA-FR3209 “Glycans & Proteoglycans : The Sweet & Smart Molecules of the 21st century”, Oct 2017, Vandoeuvre-les-Nancy, France
Poster de conférence hal-01707720v1

A versatile strategy to synthesize N -methyl-anthranilic acid-labelled glycoprobes for fluorescence-based screening assays

 Isabelle Bertin-Jung , Anne Robert , Nick Ramalanjaona , Sandrine Gulberti , Catherine Bui , et al.
Chemical Communications, 2020, 56 (73), pp.10746-10749. ⟨10.1039/d0cc03882b⟩
Article dans une revue hal-02945352v1

Low-frequency coding variants associated with body-mass-index impact the success of bariatric surgery

 Darlène Antoine , Rosa-Maria Guéant-Rodriguez , Jean-Claude Chèvre , Sébastien Hergalant , Tanmay Sharma , et al.
Journal of Clinical Endocrinology and Metabolism, 2021, pp.dgab774. ⟨10.1210/clinem/dgab774⟩
Article dans une revue hal-03411898v1

Tissue-specific collagen hydroxylation at GEP/GDP triplets mediated by P4HA2

 Dafné Wilhelm , Alison Wurtz , Hanane Abouelfarah , Guillaume Sanchez , Catherine Bui , et al.
Matrix Biology, 2023, 119, pp.141-153. ⟨10.1016/j.matbio.2023.03.009⟩
Article dans une revue hal-04077010v1

Impact of β1,3-galactosyltransferase 6 deficiency in a rare connective tissue genetic disorder

 Roméo Diana , Anne Robert , Jean-Baptiste Vincourt , C. Bui , Sylvie Fournel-Gigleux
8th FEBS Advanced Lecture Course "Matrix pathobiology, signaling and molecular targets", May 2022, Liménas Chersoníssou, Greece
Communication dans un congrès hal-03685837v1

A new perspective on the pathogeny of glycosaminoglycan synthesis genetic defects: towards « omic » approaches

 Sylvie Fournel-Gigleux , C. Bui , Xiaomeng Pang , Tim van Damme , Malfait Fransiska , et al.
FEBS Advanced Lecture Course, FEBS ECM 2018, Sep 2018, Patras, Greece
Communication dans un congrès hal-02945370v1

The heparan sulfate sulfotransferase 3-OST3A (HS3ST3A) is a novel tumor regulator and a prognostic marker in breast cancer

 X. Mao , C. Gauche , M. W. H. Coughtrie , C. Bui , S. Gulberti , et al.
Oncogene, 2016, 35 (38), pp.5043-5055. ⟨10.1038/onc.2016.44⟩
Article dans une revue hal-01452311v1

Identification of XylT1 mutations in Desbusquois dysplasia type 2 and functional consequences on proteoglycan synthesis

 Catherine Bui , Céline Hubert , Yasemin Alanay , Beyhan Tuysuz , Christine Bole-Feysot , et al.
7 Lakes proteoglycans conference : Proteoglycans 2017, Sep 2017, Varese, Italy
Poster de conférence hal-01708887v1

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 Disease: Cracking the PG Code., Jul 2018, Andover, United States
Communication dans un congrès hal-02945363v1
Image document

Identification of Key Functional Residues in the Active Site of Human β1,4-Galactosyltransferase 7

 Ibtissam Talhaoui , Catherine Bui , Rafael Oriol , Guillermo Mulliert , Sandrine Gulberti , et al.
Journal of Biological Chemistry, 2010, 285 (48), pp.37342 - 37358. ⟨10.1074/jbc.m110.151951⟩
Article dans une revue hal-03405867v1
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Exploration des enzymes de biosynthèse des protéoglycanes et leurs altérations lors de pathologies articulaires

 Catherine Bui
Médecine humaine et pathologie. Université Henri Poincaré - Nancy 1, 2009. Français. ⟨NNT : 2009NAN10100⟩
Thèse tel-01748292v1

Molecular characterization of β1,4-galactosyltransferase 7 genetic mutations linked to the progeroid form of Ehlers-Danlos syndrome (EDS)

 Catherine Bui , Ibtissam Talhaoui , Matthieu Chabel , Guillermo Mulliert , Michael W H Coughtrie , et al.
FEBS Letters, 2010, 584 (18), pp.3962-3968. ⟨10.1016/j.febslet.2010.08.001⟩
Article dans une revue hal-03405860v1
Image document

Epigenetics: methylation‐associated repression of heparan sulfate 3‐O‐sulfotransferase gene expression contributes to the invasive phenotype of H‐EMC‐SS chondrosarcoma cells

 Catherine Bui , Mohamed Ouzzine , Ibtissam Talhaoui , Sheila Sharp , Kristian Prydz , et al.
FASEB Journal, 2010, 24 (2), pp.436-450. ⟨10.1096/fj.09-136291⟩
Article dans une revue hal-03405886v1

DNA hypomethylation during MSC chondrogenesis occurs predominantly at enhancer regions

 Matt Barter , Catherine Bui , Kathleen Cheung , Julia Falk , Rodolfo Gómez , et al.
Scientific Reports, 2020, 10 (1), ⟨10.1038/s41598-020-58093-5⟩
Article dans une revue hal-02949383v1

XYLT1 Mutations in Desbuquois Dysplasia Type 2

 Catherine Bui , Céline Huber , Beyhan Tuysuz , Yasemin Alanay , Christine Bole-Feysot , et al.
American Journal of Human Genetics, 2014, 94 (3), pp.405 - 414. ⟨10.1016/j.ajhg.2014.01.020⟩
Article dans une revue hal-01704452v1

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 Disease: Cracking the PG Code, Jul 2018, Andover, United States
Poster de conférence hal-02946919v1

Understanding the Pathogenesis of Ehlers-Danlos Syndrome, a Rare Connective Tissue Disorder Caused by B3GALT6 Mutations: What if 'Omics' Could Help?

 C. Bui , Sandrine Gulberti , Sylvie Fournel-Gigleux
3èmes Journées scientifiques du GDR GAGoSciences, Sep 2018, Lille, France
Poster de conférence hal-02946952v1

The role of heparan sulfate maturation in cancer: A focus on the 3O-sulfation and the enigmatic 3O-sulfotransferases (HS3STs)

 Sandrine Gulberti , Xianqing Mao , Catherine Bui , Sylvie Fournel-Gigleux
Seminars in Cancer Biology, 2020, 62, pp.68-85. ⟨10.1016/j.semcancer.2019.10.009⟩
Article dans une revue hal-02886175v1
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