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

A proof-of-concept study of growth hormone in children with Phelan-McDermid syndrome

一项关于生长激素治疗费兰-麦克德米德综合征患儿的概念验证研究

Sethuram, S; Levy, T; Foss-Feig, J; Halpern, D; Sandin, S; Siper, P M; Walker, H; Buxbaum, J D; Rapaport, R; Kolevzon, A

Clinical trial of insulin-like growth factor-1 in Phelan-McDermid syndrome

胰岛素样生长因子-1治疗费兰-麦克德米德综合征的临床试验

Kolevzon, A; Breen, M S; Siper, P M; Halpern, D; Frank, Y; Rieger, H; Weismann, J; Trelles, M P; Lerman, B; Rapaport, R; Buxbaum, J D

A randomized controlled trial of intranasal oxytocin in Phelan-McDermid syndrome

一项关于鼻内催产素治疗费兰-麦克德米德综合征的随机对照试验

Fastman, J; Foss-Feig, J; Frank, Y; Halpern, D; Harony-Nicolas, H; Layton, C; Sandin, S; Siper, P; Tang, L; Trelles, P; Zweifach, J; Buxbaum, J D; Kolevzon, A

A novel Alzheimer disease locus located near the gene encoding tau protein

一种位于编码tau蛋白基因附近的新型阿尔茨海默病基因位点

Jun, G; Ibrahim-Verbaas, C A; Vronskaya, M; Lambert, J-C; Chung, J; Naj, A C; Kunkle, B W; Wang, L-S; Bis, J C; Bellenguez, C; Harold, D; Lunetta, K L; Destefano, A L; Grenier-Boley, B; Sims, R; Beecham, G W; Smith, A V; Chouraki, V; Hamilton-Nelson, K L; Ikram, M A; Fievet, N; Denning, N; Martin, E R; Schmidt, H; Kamatani, Y; Dunstan, M L; Valladares, O; Laza, A R; Zelenika, D; Ramirez, A; Foroud, T M; Choi, S-H; Boland, A; Becker, T; Kukull, W A; van der Lee, S J; Pasquier, F; Cruchaga, C; Beekly, D; Fitzpatrick, A L; Hanon, O; Gill, M; Barber, R; Gudnason, V; Campion, D; Love, S; Bennett, D A; Amin, N; Berr, C; Tsolaki, Magda; Buxbaum, J D; Lopez, O L; Deramecourt, V; Fox, N C; Cantwell, L B; Tárraga, L; Dufouil, C; Hardy, J; Crane, P K; Eiriksdottir, G; Hannequin, D; Clarke, R; Evans, D; Mosley, T H Jr; Letenneur, L; Brayne, C; Maier, W; De Jager, P; Emilsson, V; Dartigues, J-F; Hampel, H; Kamboh, M I; de Bruijn, R F A G; Tzourio, C; Pastor, P; Larson, E B; Rotter, J I; O'Donovan, M C; Montine, T J; Nalls, M A; Mead, S; Reiman, E M; Jonsson, P V; Holmes, C; St George-Hyslop, P H; Boada, M; Passmore, P; Wendland, J R; Schmidt, R; Morgan, K; Winslow, A R; Powell, J F; Carasquillo, M; Younkin, S G; Jakobsdóttir, J; Kauwe, J S K; Wilhelmsen, K C; Rujescu, D; Nöthen, M M; Hofman, A; Jones, L; Haines, J L; Psaty, B M; Van Broeckhoven, C; Holmans, P; Launer, L J; Mayeux, R; Lathrop, M; Goate, A M; Escott-Price, V; Seshadri, S; Pericak-Vance, M A; Amouyel, P; Williams, J; van Duijn, C M; Schellenberg, G D; Farrer, L A

Latrepirdine improves cognition and arrests progression of neuropathology in an Alzheimer's mouse model

拉特吡啶可改善阿尔茨海默病小鼠模型的认知功能并阻止神经病理学的进展。

Steele, J W; Lachenmayer, M L; Ju, S; Stock, A; Liken, J; Kim, S H; Delgado, L M; Alfaro, I E; Bernales, S; Verdile, G; Bharadwaj, P; Gupta, V; Barr, R; Friss, A; Dolios, G; Wang, R; Ringe, D; Fraser, P; Westaway, D; St George-Hyslop, P H; Szabo, P; Relkin, N R; Buxbaum, J D; Glabe, C G; Protter, A A; Martins, R N; Ehrlich, M E; Petsko, G A; Yue, Z; Gandy, S

Rare structural variation of synapse and neurotransmission genes in autism

自闭症中突触和神经传递基因的罕见结构变异

Gai, X; Xie, H M; Perin, J C; Takahashi, N; Murphy, K; Wenocur, A S; D'arcy, M; O'Hara, R J; Goldmuntz, E; Grice, D E; Shaikh, T H; Hakonarson, H; Buxbaum, J D; Elia, J; White, P S

High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility

高密度SNP关联研究和AUTS1和AUTS5基因座拷贝数变异分析表明IMMP2L-DOCK4基因区域与自闭症易感性有关。

Maestrini, E; Pagnamenta, A T; Lamb, J A; Bacchelli, E; Sykes, N H; Sousa, I; Toma, C; Barnby, G; Butler, H; Winchester, L; Scerri, T S; Minopoli, F; Reichert, J; Cai, G; Buxbaum, J D; Korvatska, O; Schellenberg, G D; Dawson, G; de Bildt, A; Minderaa, R B; Mulder, E J; Morris, A P; Bailey, A J; Monaco, A P

Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene.

对 NRG1-ERBB4 信号传导的分子解析表明 PTPRZ1 可能是一种精神分裂症易感基因

Buxbaum J D, Georgieva L, Young J J, Plescia C, Kajiwara Y, Jiang Y, Moskvina V, Norton N, Peirce T, Williams H, Craddock N J, Carroll L, Corfas G, Davis K L, Owen M J, Harroch S, Sakurai T, O'Donovan M C

Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity

2号染色体上存在自闭症易感基因以及遗传异质性的证据

Buxbaum, J D; Silverman, J M; Smith, C J; Kilifarski, M; Reichert, J; Hollander, E; Lawlor, B A; Fitzgerald, M; Greenberg, D A; Davis, K L

The Alzheimer amyloid precursor protein (APP) and FE65, an APP-binding protein, regulate cell movement

阿尔茨海默病淀粉样前体蛋白(APP)及其结合蛋白FE65调控细胞运动。

Sabo, S L; Ikin, A F; Buxbaum, J D; Greengard, P