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

An ancient enhancer rapidly evolving in the human lineage promotes neural development and cognitive flexibility.

人类谱系中快速进化的古老增强子能够促进神经发育和认知灵活性

Tan Kun, Higgins Kendall, Liu Qing, Wilkinson Miles F

Genetic variants reshape the m(6)A epitranscriptome and drive transcriptomic reprogramming in colorectal cancer

基因变异重塑m(6)A表观转录组并驱动结直肠癌的转录组重编程

Han, Seung Hun; Jang, Seongmin; Kim, Yeongwon; Tan, Kun; Wilkinson, Miles F; Jeong, Hyobin; Choe, Junho

Astrocytic RNA degradation suppresses calcium signaling to support synapse function and restrain anxiety

星形胶质细胞RNA降解抑制钙信号传导,从而支持突触功能并抑制焦虑

Lituma, Pablo J; Deveci, Aykut; Barrio-Alonso, Estibaliz; Tan, Kun; Wilkinson, Miles F; Castillo, Pablo E; Colak, Dilek

Developmental regulators moonlighting as transposons defense factors

发育调控因子兼具转座子防御因子的功能

Tan, Kun; Wilkinson, Miles F

Nonsense-mediated RNA decay: an emerging modulator of malignancy

无义介导的RNA衰变:恶性肿瘤的新兴调节因子

Tan, Kun; Stupack, Dwayne G; Wilkinson, Miles F

Concordant Androgen-Regulated Expression of Divergent Rhox5 Promoters in Sertoli Cells

在塞氏细胞中,雄激素调节的不同Rhox5启动子表达具有一致性

Bhardwaj, Anjana; Sohni, Abhishek; Lou, Chih-Hong; De Gendt, Karel; Zhang, Fanmao; Kim, Eunah; Subbarayalu, Panneerdoss; Chan, Waikin; Kerkhofs, Stefanie; Claessens, Frank; Kimmins, Sarah; Rao, Manjeet K; Meistrich, Marvin; Wilkinson, Miles F

The Rhox gene cluster suppresses germline LINE1 transposition

Rhox基因簇抑制种系LINE1转座

Tan, Kun; Kim, Matthew E; Song, Hye-Won; Skarbrevik, David; Babajanian, Eric; Bedrosian, Tracy A; Gage, Fred H; Wilkinson, Miles F

Response to: X-linked miR-506 family miRNAs promote FMRP expression in mouse spermatogonia

回复:X染色体连锁的miR-506家族miRNA促进小鼠精原细胞中FMRP的表达

Ramaiah, Madhuvanthi; Tan, Kun; Plank, Terra-Dawn M; Song, Hye-Won; Chousal, Jennifer N; Jones, Samantha; Shum, Eleen Y; Sheridan, Steven D; Peterson, Kevin J; Gromoll, Jörg; Haggarty, Stephen J; Cook-Andersen, Heidi; Wilkinson, Miles F

A single-cell view of spermatogonial stem cells

精原干细胞的单细胞视图

Tan, Kun; Wilkinson, Miles F

A synonymous UPF3B variant causing a speech disorder implicates NMD as a regulator of neurodevelopmental disorder gene networks

一种导致言语障碍的同义UPF3B变异表明NMD是神经发育障碍基因网络的调节因子。

Domingo, Deepti; Nawaz, Urwah; Corbett, Mark; Espinoza, Josh L; Tatton-Brown, Katrina; Coman, David; Wilkinson, Miles F; Gecz, Jozef; Jolly, Lachlan A