日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

The serotonin-N-acetylserotonin-melatonin pathway as a biomarker for autism spectrum disorders

血清素-N-乙酰血清素-褪黑素通路作为自闭症谱系障碍的生物标志物

Pagan, C; Delorme, R; Callebert, J; Goubran-Botros, H; Amsellem, F; Drouot, X; Boudebesse, C; Le Dudal, K; Ngo-Nguyen, N; Laouamri, H; Gillberg, C; Leboyer, M; Bourgeron, T; Launay, J-M

Raphe-mediated signals control the hippocampal response to SRI antidepressants via miR-16.

缝核介导的信号通过 miR-16 控制海马对 SR1 类抗抑郁药的反应

Launay J M, Mouillet-Richard S, Baudry A, Pietri M, Kellermann O

Abnormal melatonin synthesis in autism spectrum disorders

自闭症谱系障碍中褪黑激素合成异常

Melke, J; Goubran Botros, H; Chaste, P; Betancur, C; Nygren, G; Anckarsäter, H; Rastam, M; Ståhlberg, O; Gillberg, I C; Delorme, R; Chabane, N; Mouren-Simeoni, M-C; Fauchereau, F; Durand, C M; Chevalier, F; Drouot, X; Collet, C; Launay, J-M; Leboyer, M; Gillberg, C; Bourgeron, T

The serotonin 5-HT2B receptor controls bone mass via osteoblast recruitment and proliferation

血清素5-HT2B受体通过成骨细胞的募集和增殖来控制骨量。

Collet, C; Schiltz, C; Geoffroy, V; Maroteaux, L; Launay, J-M; de Vernejoul, M-C

Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder

自闭症患者的血清素转运蛋白基因多态性和高血清素血症

Betancur, C; Corbex, M; Spielewoy, C; Philippe, A; Laplanche, J L; Launay, J M; Gillberg, C; Mouren-Siméoni, M C; Hamon, M; Giros, B; Nosten-Bertrand, M; Leboyer, M

Drosophila 5-HT2 serotonin receptor: coexpression with fushi-tarazu during segmentation

果蝇 5-HT2 血清素受体:在节段形成过程中与 fushi-tarazu 共表达

Colas, J F; Launay, J M; Kellermann, O; Rosay, P; Maroteaux, L

Members elected 1993

1993年当选的成员

Laplanche, J L; Chatelain, J; Dussaucy, M; Bounneau, C; Launay, J M; Brandel, J P; Delasnerie-Laupretre, N

Melatonin biosynthesis and metabolism in peripheral blood mononuclear leucocytes

外周血单核白细胞中褪黑激素的生物合成和代谢

Finocchiaro, L M; Nahmod, V E; Launay, J M

Complete coding sequence of human tryptophan hydroxylase

人类色氨酸羟化酶的完整编码序列

Boularand, S; Darmon, M C; Ganem, Y; Launay, J M; Mallet, J

Deletion in prion protein gene in a Moroccan family

摩洛哥一个家族中朊病毒蛋白基因缺失

Laplanche, J L; Chatelain, J; Launay, J M; Gazengel, C; Vidaud, M