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

Epilepsy plus blindness in microdeletion of GABRA1 and GABRG2 in mouse and human

小鼠和人类 GABRA1 和 GABRG2 基因微缺失导致癫痫和失明

Zhang, Qi; Forster-Gibson, Cynthia; Bercovici, Eduard; Bernardo, Alexandra; Ding, Fei; Shen, Wangzhen; Langer, Katherine; Rex, Tonia; Kang, Jing-Qiong

Deficient histone H3 propionylation by BRPF1-KAT6 complexes in neurodevelopmental disorders and cancer

神经发育障碍和癌症中BRPF1-KAT6复合物介导的组蛋白H3丙酰化不足

Kezhi Yan ,Justine Rousseau ,Keren Machol ,Laura A Cross ,Katherine E Agre ,Cynthia Forster Gibson ,Anne Goverde ,Kendra L Engleman ,Hannah Verdin ,Elfride De Baere ,Lorraine Potocki ,Dihong Zhou ,Maxime Cadieux-Dion ,Gary A Bellus ,Monisa D Wagner ,Rebecca J Hale ,Natacha Esber ,Alan F Riley ,Benjamin D Solomon ,Megan T Cho ,Kirsty McWalter ,Roy Eyal ,Meagan K Hainlen ,Bryce A Mendelsohn ,Hillary M Porter ,Brendan C Lanpher ,Andrea M Lewis ,Juliann Savatt ,Isabelle Thiffault ,Bert Callewaert ,Philippe M Campeau ,Xiang-Jiao Yang

Germline variants and phenotypic spectrum in a Canadian cohort of individuals with diffuse gastric cancer

加拿大一组弥漫性胃癌患者的种系变异和表型谱

Aronson, M; Swallow, C; Govindarajan, A; Semotiuk, K; Cohen, Z; Kaurah, P; Velsher, L; Ambus, I; Buckley, K; Forster-Gibson, C; Meschino, W S; Blumenthal, A; Kim, R H; Brar, S

2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders

2p15-p16.1微缺失综合征:OTX1和XPO1基因的分子特征及其与自闭症谱系障碍的关联

Liu, Xudong; Malenfant, Patrick; Reesor, Chelsea; Lee, Alana; Hudson, Melissa L; Harvard, Chansonette; Qiao, Ying; Persico, Antonio M; Cohen, Ira L; Chudley, Albert E; Forster-Gibson, Cynthia; Rajcan-Separovic, Evica; Lewis, M E Suzanne; Holden, Jeanette J A

The DLX1and DLX2 genes and susceptibility to autism spectrum disorders

DLX1和DLX2基因与自闭症谱系障碍的易感性

Liu, Xudong; Novosedlik, Natalia; Wang, Ami; Hudson, Melissa L; Cohen, Ira L; Chudley, Albert E; Forster-Gibson, Cynthia J; Lewis, Suzanne M E; Holden, Jeanette J A