-
公开(公告)号:EP4095265A1
公开(公告)日:2022-11-30
申请号:EP21305694.8
申请日:2021-05-26
申请人: Université Paris-Saclay , INSERM (Institut National de la Santé et de la Recherche Médicale) , Assistance Publique-Hôpitaux de Paris , Centre Hospitalier de l'Université de Montréal
IPC分类号: C12Q1/6883
摘要: The present invention proposes to detect genetic abnormalities (mutations and LOH) in the KDM1A gene of subjects, in order to diagnose a genetic predisposition to an endocrine disease and/or to an endocrine hyperplasia / or adenoma formation. Also, it proposes to treat patients with GIP-dependent PBMAH with Cushing's syndrome by restoring the expression of the KDM1A gene, by gene therapy.
-
公开(公告)号:EP4347888A1
公开(公告)日:2024-04-10
申请号:EP22730465.6
申请日:2022-05-24
申请人: Université Paris-Saclay , Institut National de la Santé et de la Recherche Médicale (INSERM) , Assistance Publique - Hôpitaux de Paris , Centre Hospitalier de l'Université de Montréal
IPC分类号: C12Q1/6883
-