| Title : EPHX1 mutations cause a lipoatrophic diabetes syndrome due to impaired epoxide hydrolysis and increased cellular senescence - Gautheron_2021_Elife_10_ |
| Author(s) : Gautheron J , Morisseau C , Chung WK , Zammouri J , Auclair M , Baujat G , Capel E , Moulin C , Wang Y , Yang J , Hammock BD , Cerame B , Phan F , Feve B , Vigouroux C , Andreelli F , Jeru I |
| Ref : Elife , 10 : , 2021 |
| Abstract : |
| PubMedSearch : Gautheron_2021_Elife_10_ |
| PubMedID: 34342583 |
| Gene_locus related to this paper: human-EPHX1 |
| Title : LIPE-related lipodystrophic syndrome: clinical characteristics and disease modelling using adipose stem cells - Sollier_2020_Eur.J.Endocrinol_184_155 |
| Author(s) : Sollier C , Capel E , Aguilhon C , Smirnov V , Auclair M , Douillard C , Ladsous M , Defoort-Dhellemmes S , Gorwood J , Braud L , Motterlini R , Vatier C , Lascols O , Renard E , Vigouroux C , Jeru I |
| Ref : European Journal of Endocrinology , 184 :155 , 2021 |
| Abstract : |
| PubMedSearch : Sollier_2020_Eur.J.Endocrinol_184_155 |
| PubMedID: 33112291 |
| Gene_locus related to this paper: human-LIPE |
| Title : Lipodystrophic syndromes: From diagnosis to treatment - Sollier_2020_Ann.Endocrinol.(Paris)_81_51 |
| Author(s) : Sollier C , Vatier C , Capel E , Lascols O , Auclair M , Janmaat S , Feve B , Jeru I , Vigouroux C |
| Ref : Ann Endocrinol (Paris) , 81 :51 , 2020 |
| Abstract : |
| PubMedSearch : Sollier_2020_Ann.Endocrinol.(Paris)_81_51 |
| PubMedID: 31982105 |
| Title : Diagnostic Challenge in PLIN1-Associated Familial Partial Lipodystrophy - Jeru_2019_J.Clin.Endocrinol.Metab_104_6025 |
| Author(s) : Jeru I , Vantyghem MC , Bismuth E , Cervera P , Barraud S , Auclair M , Vatier C , Lascols O , Savage DB , Vigouroux C |
| Ref : J Clinical Endocrinology Metab , 104 :6025 , 2019 |
| Abstract : |
| PubMedSearch : Jeru_2019_J.Clin.Endocrinol.Metab_104_6025 |
| PubMedID: 31504636 |