Methylomic changes during conversion to psychosis

Autor: M-O Krebs, M. Kazes, Célia Mam-Lam-Fook, Emilie Magadu, L P Lemieux Perreault, Zelda Prost, Amina Barhdadi, Boris Chaumette, Fabrice Rivollier, Oussama Kebir, Marion Plaze, Sylvie Provost, Gilles Martinez, M-P Dubé, Mélanie Chayet, F Miozzo, Raphaël Gaillard, Julie Bourgin, Charlotte Alexandre, V Mezger

Publikováno v: Molecular Psychiatry
Molecular Psychiatry, Nature Publishing Group, 2017, 22 (4), pp.512-518. ⟨10.1038/mp.2016.53⟩

International audience; The onset of psychosis is the consequence of complex interactions between genetic vulnerability to psychosis and response to environmental and/or maturational changes. Epigenetics is hypothesized to mediate the interplay betwe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d45358490272f290c76816bd130aaeb0
http://europepmc.org/articles/PMC5378806

Lysosomal TFEB‐TRPML1 Axis in Astrocytes Modulates Depressive‐like Behaviors.

Autor: Mo, Jia‐Wen¹ (AUTHOR), Kong, Peng‐Li¹ (AUTHOR), Ding, Li¹ (AUTHOR), Fan, Jun¹ (AUTHOR), Ren, Jing¹ (AUTHOR), Lu, Cheng‐Lin^1,2 (AUTHOR), Guo, Fang¹ (AUTHOR), Chen, Liang‐Yu¹ (AUTHOR), Mo, Ran¹ (AUTHOR), Zhong, Qiu‐Ling¹ (AUTHOR), Wen, You‐Lu³ (AUTHOR), Gu, Ting‐Ting³ (AUTHOR), Wang, Qian‐Wen⁴ (AUTHOR), Li, Shu‐Ji¹ (AUTHOR), Guo, Ting¹ (AUTHOR), Gao, Tian‐Ming¹ (AUTHOR), Cao, Xiong^1,2,5 (AUTHOR) caoxiong@smu.edu.cn

Publikováno v: Advanced Science. 11/6/2024, Vol. 11 Issue 41, p1-17. 17p.

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A Case of Diabetes Mellitus Type MODY5 as a Feature of 17q12 Deletion Syndrome.

Autor: Köstek, Hümeyra Yaşar¹ yasarrhumeyra@hotmail.com, Çömlek, Fatma Özgüç¹, Gürkan, Hakan², Özkayın, Emine Neşe³, Kökenli, Filiz Tütüncüler¹

Publikováno v: Journal of Clinical Research in Pediatric Endocrinology. Jun2024, Vol. 16 Issue 2, p205-210. 6p.

Recurrent human 16p11.2 microdeletions in type I Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome patients in Chinese Han population.

Autor: Su, Kaizhen^1,2 (AUTHOR), Liu, Han^1,2 (AUTHOR), Ye, Xiaoqun³ (AUTHOR), Jin, Hangmei³ (AUTHOR), Xie, Zhenwei³ (AUTHOR), Yang, Chunbo³ (AUTHOR), Zhou, Daizhan⁴ (AUTHOR), Huang, Hefeng^1,5,6 (AUTHOR) huanghefg@hotmail.com, Wu, Yanting^5,6 (AUTHOR) yanting_wu@163.com

Publikováno v: Molecular Genetics & Genomic Medicine. Jan2024, Vol. 12 Issue 1, p1-10. 10p.