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

Heterozygosity for neurodevelopmental disorder-associated TRIO variants yields distinct deficits in behavior, neuronal development, and synaptic transmission in mice.

携带与神经发育障碍相关的 TRIO 变异体的杂合子会导致小鼠在行为、神经元发育和突触传递方面出现明显的缺陷

Ishchenko Yevheniia, Jeng Amanda T, Feng Shufang, Nottoli Timothy, Manriquez-Rodriguez Cindy, Nguyen Khanh K, Carrizales Melissa G, Vitarelli Matthew J, Corcoran Ellen E, Greer Charles A, Myers Samuel A, Koleske Anthony J

Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease

磷脂酶D3基因中的罕见编码变异会增加患阿尔茨海默病的风险。

Cruchaga, Carlos; Karch, Celeste M; Jin, Sheng Chih; Benitez, Bruno A; Cai, Yefei; Guerreiro, Rita; Harari, Oscar; Norton, Joanne; Budde, John; Bertelsen, Sarah; Jeng, Amanda T; Cooper, Breanna; Skorupa, Tara; Carrell, David; Levitch, Denise; Hsu, Simon; Choi, Jiyoon; Ryten, Mina; Sassi, Celeste; Bras, Jose; Gibbs, Raphael J; Hernandez, Dena G; Lupton, Michelle K; Powell, John; Forabosco, Paola; Ridge, Perry G; Corcoran, Christopher D; Tschanz, JoAnn T; Norton, Maria C; Munger, Ronald G; Schmutz, Cameron; Leary, Maegan; Demirci, F Yesim; Bamne, Mikhil N; Wang, Xingbin; Lopez, Oscar L; Ganguli, Mary; Medway, Christopher; Turton, James; Lord, Jenny; Braae, Anne; Barber, Imelda; Brown, Kristelle; Pastor, Pau; Lorenzo-Betancor, Oswaldo; Brkanac, Zoran; Scott, Erick; Topol, Eric; Morgan, Kevin; Rogaeva, Ekaterina; Singleton, Andy; Hardy, John; Kamboh, M Ilyas; George-Hyslop, Peter St; Cairns, Nigel; Morris, John C; Kauwe, John S K; Goate, Alison M

Novel progranulin variants do not disrupt progranulin secretion and cleavage

新型前粒蛋白变体不会干扰前粒蛋白的分泌和裂解。

Karch, Celeste M; Jeng, Amanda T; Skorupa, Tara; Cruchaga, Carlos; Goate, Alison M