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

Allele-Specific Regulation of the Candidate Autism Liability Gene RAI1 by the Enhancer Variant rs4925102 (C/G)

增强子变异 rs4925102 (C/G) 对候选自闭症易感基因 RAI1 的等位基因特异性调控

Yuan, Xi; Chen, Li; Saffen, David

RNA binding motif protein 10 suppresses lung cancer progression by controlling alternative splicing of eukaryotic translation initiation factor 4H

RNA 结合基序蛋白 10 通过控制真核翻译起始因子 4H 的可变剪接来抑制肺癌进展

Sirui Zhang, Yufang Bao, Xianfeng Shen, Yunjian Pan, Yue Sun, Man Xiao, Kexuan Chen, Huanhuan Wei, Ji Zuo, David Saffen, Wei-Xing Zong, Yihua Sun, Zefeng Wang, Yongbo Wang

Autoregulation of RBM10 and cross-regulation of RBM10/RBM5 via alternative splicing-coupled nonsense-mediated decay

通过选择性剪接偶联无义介导衰变进行 RBM10 的自身调节和 RBM10/RBM5 的交叉调节

Yue Sun, Yufang Bao, Wenjian Han, Fan Song, Xianfeng Shen, Jiawei Zhao, Ji Zuo, David Saffen, Wei Chen, Zefeng Wang, Xintian You, Yongbo Wang

Functional analysis reveals that RBM10 mutations contribute to lung adenocarcinoma pathogenesis by deregulating splicing

功能分析表明,RBM10 突变通过解除剪接调控导致肺腺癌发病机制

Jiawei Zhao, Yue Sun, Yin Huang, Fan Song, Zengshu Huang, Yufang Bao, Ji Zuo, David Saffen, Zhen Shao, Wen Liu, Yongbo Wang

Functional analysis of novel DEAF1 variants identified through clinical exome sequencing expands DEAF1-associated neurodevelopmental disorder (DAND) phenotype

通过临床外显子组测序鉴定出的新型DEAF1变异的功能分析扩展了DEAF1相关神经发育障碍(DAND)的表型

Chen, Li; Jensik, Philip J; Alaimo, Joseph T; Walkiewicz, Magdalena; Berger, Seth; Roeder, Elizabeth; Faqeih, Eissa A; Bernstein, Jonathan A; Smith, Ann C M; Mullegama, Sureni V; Saffen, David W; Elsea, Sarah H

Psychiatric genetics in China: achievements and challenges

中国精神病遗传学:成就与挑战

Liu, Chunyu; Saffen, David; Schulze, Thomas G; Burmeister, Margit; Sham, Pak Chung; Yao, Yong-Gang; Kuo, Po-Hsiu; Chen, Chao; An, Yu; Dai, Jiapei; Yue, Weihua; Li, Miao Xin; Xue, Hong; Su, Bing; Chen, Li; Shi, Yongyong; Qiao, Mingqi; Liu, Tiebang; Xia, Kun; Chan, Raymond C K

Evidence for genetic regulation of mRNA expression of the dosage-sensitive gene retinoic acid induced-1 (RAI1) in human brain

人类大脑中剂量敏感基因视黄酸诱导-1 (RAI1) mRNA 表达的遗传调控证据

Li Chen, Yu Tao, Fan Song, Xi Yuan, Jian Wang, David Saffen

The schizophrenia/bipolar disorder candidate gene GNB1L is regulated in human temporal cortex by a cis-acting element located within the 3'-region

精神分裂症/双相情感障碍候选基因GNB1L在人类颞叶皮层中受位于3'区内的顺式作用元件调控。

Sun, Yue; Tao, Yu; Wang, Jian; Saffen, David

Alzheimer’s disease candidate gene PION is differentially expressed in human prefrontal cortex

阿尔茨海默病候选基因PION在人类前额叶皮层中差异表达

Piton, A; Gauthier, J; Hamdan, F F; Lafrenière, R G; Yang, Y; Henrion, E; Laurent, S; Noreau, A; Thibodeau, P; Karemera, L; Spiegelman, D; Kuku, F; Duguay, J; Destroismaisons, L; Jolivet, P; Côté, M; Lachapelle, K; Diallo, O; Raymond, A; Marineau, C; Champagne, N; Xiong, L; Gaspar, C; Rivière, J-B; Tarabeux, J; Cossette, P; Krebs, M-O; Rapoport, J L; Addington, A; Delisi, L E; Mottron, L; Joober, R; Fombonne, E; Drapeau, P; Rouleau, G A; Wang, Jian; Saffen, David; Zhu, Min; Saffen, David

Evidence for population variation in TSC1 and TSC2 gene expression

TSC1和TSC2基因表达存在群体差异的证据

Jentarra, Garilyn M; Rice, Stephen G; Olfers, Shannon; Saffen, David; Narayanan, Vinodh