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

A deletion involving CD38 and BST1 results in a fusion transcript in a patient with autism and asthma

CD38 和 BST1 的缺失导致患有自闭症和哮喘的患者出现融合转录本

Fabiola Ceroni, Angela Sagar, Nuala H Simpson, Alex J T Gawthrope, Dianne F Newbury, Dalila Pinto, Sunday M Francis, Dorothy C Tessman, Edwin H Cook, Anthony P Monaco, Elena Maestrini, Alistair T Pagnamenta, Suma Jacob

Abnormal intracellular accumulation and extracellular Aβ deposition in idiopathic and Dup15q11.2-q13 autism spectrum disorders

特发性和 Dup15q11.2-q13 自闭症谱系障碍中的异常细胞内积累和细胞外 Aβ 沉积

Jerzy Wegiel, Janusz Frackowiak, Bozena Mazur-Kolecka, N Carolyn Schanen, Edwin H Cook Jr, Marian Sigman, W Ted Brown, Izabela Kuchna, Jarek Wegiel, Krzysztof Nowicki, Humi Imaki, Shuang Yong Ma, Abha Chauhan, Ved Chauhan, David L Miller, Pankaj D Mehta, Michael Flory, Ira L Cohen, Eric London, Barr

Endogenous siRNAs and noncoding RNA-derived small RNAs are expressed in adult mouse hippocampus and are up-regulated in olfactory discrimination training

内源性 siRNA 和非编码 RNA 衍生的小 RNA 在成年小鼠海马中表达,并在嗅觉辨别训练中上调

Neil R Smalheiser, Giovanni Lugli, Jyothi Thimmapuram, Edwin H Cook, John Larson

Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE

利用阵列比较基因组杂交(array CGH)技术检测自闭症家族基因组中外显子拷贝数变异,发现TMLHE基因存在一个新的缺失。

Patricia B S Celestino-Soper ,Chad A Shaw, Stephan J Sanders, Jian Li, Michael T Murtha, A Gulhan Ercan-Sencicek, Lea Davis, Susanne Thomson, Tomasz Gambin, A Craig Chinault, Zhishuo Ou, Jennifer R German, Aleksandar Milosavljevic, James S Sutcliffe, Edwin H Cook Jr, Pawel Stankiewicz, Matthew W State, Arthur L Beaudet

Population-specific GSTM1 copy number variation

人群特异性 GSTM1 拷贝数变异

R Stephanie Huang, Peixian Chen, Steve Wisel, Shiwei Duan, Wei Zhang, Edwin H Cook, Soma Das, Nancy J Cox, M Eileen Dolan