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

Autism-like behavior Increases with age and is predated by molecular changes in Arid1b haploinsufficient mice

自闭症样行为随年龄增长而增加,并且在 Arid1b 单倍体不足小鼠中,这种行为的出现先于分子变化。

Ford, Thomas James L; Jeon, Byeong Tak; Lee, Hyunkyoung; Kim, Woo-Yang

Localized brain stimulation with mild magnetic hyperthermia promotes microglia activity towards reactive and autophagic phenotypes in vivo.

局部脑刺激结合温和的磁热疗可促进体内小胶质细胞向反应性和自噬表型转变

Jeon Byeong Tak, Naveed Muhammad, Puleo Matthew, Kim Woo-Yang, Kim Min-Ho

Perineuronal nets in the developing brain: implications for neurodevelopmental disorders

发育中大脑的神经元周围网:对神经发育障碍的启示

Ackerman, Jennifer M; Ford, Thomas James L; Kattewar, Shraddha Shridhar; Kim, Woo-Yang

Memory loss and aberrant neurogenesis in mice exposed to patient anti-N-methyl-d-aspartate receptor antibodies.

小鼠暴露于患者抗N-甲基-D-天冬氨酸受体抗体后出现记忆丧失和异常神经发生。

Taraschenko Olga, Fox Howard S, Heliso Priscilla, Al-Saleem Fetweh, Dessain Scott, Kim Woo-Yang, Samuelson Mystera M, Dingledine Raymond

A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome

在不平衡易位 t(7;12)(q21.13;q23.1) 中发现的隐匿性微缺失 del(12)(p11.21p11.23) 提示存在与智力障碍和卡尔曼综合征相关的新候选基因位点。

Ben-Mahmoud, Afif; Kishikawa, Shotaro; Gupta, Vijay; Leach, Natalia T; Shen, Yiping; Moldovan, Oana; Goel, Himanshu; Hopper, Bruce; Ranguin, Kara; Gruchy, Nicolas; Maas, Saskia M; Lacassie, Yves; Kim, Soo-Hyun; Kim, Woo-Yang; Quade, Bradley J; Morton, Cynthia C; Kim, Cheol-Hee; Layman, Lawrence C; Kim, Hyung-Goo

A microdeletion del(12)(p11.21p11.23) with a cryptic unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome

微缺失del(12)(p11.21p11.23)伴隐匿性不平衡易位t(7;12)(q21.13;q23.1)提示存在与智力障碍和卡尔曼综合征相关的新候选基因位点。

Ben-Mahmoud, Afif; Kishikawa, Shotaro; Gupta, Vijay; Leach, Natalia T; Shen, Yiping; Moldovan, Oana; Goel, Himanshu; Hopper, Bruce; Ranguin, Kara; Gruchy, Nicolas; Maas, Saskia M; Lacassie, Yves; Kim, Soo-Hyun; Kim, Woo-Yang; Quade, Bradley J; Morton, Cynthia C; Kim, Cheol-Hee; Layman, Lawrence C; Kim, Hyung-Goo

Neurobiology of ARID1B haploinsufficiency related to neurodevelopmental and psychiatric disorders

ARID1B单倍体功能不全与神经发育和精神疾病相关的神经生物学

Moffat, Jeffrey J; Smith, Amanda L; Jung, Eui-Man; Ka, Minhan; Kim, Woo-Yang

WDR5-HOTTIP Histone Modifying Complex Regulates Neural Migration and Dendrite Polarity of Pyramidal Neurons via Reelin Signaling

WDR5-HOTTIP 组蛋白修饰复合物通过 Reelin 信号调节锥体神经元的神经迁移和树突极性

Minhan Ka, Hyung-Goo Kim, Woo-Yang Kim

Bisphenol-A impairs synaptic formation and function by RGS4-mediated regulation of BDNF signaling in the cerebral cortex

双酚 A 通过 RGS4 介导的大脑皮层 BDNF 信号调节来损害突触的形成和功能

Sung-Ae Hyun, Moon Yi Ko, Sumi Jang, Byoung-Seok Lee, Jaerang Rho, Kee K Kim, Woo-Yang Kim, Minhan Ka

A rigorous in silico genomic interrogation at 1p13.3 reveals 16 autosomal dominant candidate genes in syndromic neurodevelopmental disorders

对1p13.3区域进行严谨的计算机基因组分析,揭示了16个与综合征性神经发育障碍相关的常染色体显性候选基因。

Ben-Mahmoud, Afif; Jun, Kyung Ran; Gupta, Vijay; Shastri, Pinang; de la Fuente, Alberto; Park, Yongsoo; Shin, Kyung Chul; Kim, Chong Ae; da Cruz, Aparecido Divino; Pinto, Irene Plaza; Minasi, Lysa Bernardes; Silva da Cruz, Alex; Faivre, Laurence; Callier, Patrick; Racine, Caroline; Layman, Lawrence C; Kong, Il-Keun; Kim, Cheol-Hee; Kim, Woo-Yang; Kim, Hyung-Goo