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

Transcriptional profiling clarifies a program of enzalutamide extreme non-response in lethal prostate cancer.

转录组分析揭示了致命性前列腺癌中恩扎卢胺极度无反应的机制

Kumaraswamy Anbarasu, Hu Ya-Mei, Yates Joel A, Zhang Chao, Rodansky Eva, Khokhani Dhruv, Flores Diana, Duan Zhi, Zhang Yi, Tabatabaei Shaadi, Slottke Rachel, Ye Shangyuan, Lara Primo, Foye Adam, Ryan Charles J, Quigley David A, Huang Jiaoti, Aggarwal Rahul, Reiter Robert E, Wicha Max S, Beer Tomasz M, Rettig Matthew, Gleave Martin, Evans Christopher P, Witte Owen N, Stuart Joshua M, Thomas George V, Feng Felix Y, Small Eric J, Xia Zheng, Alumkal Joshi J

Role of Central Sensitization Syndrome in Patients With Autonomic Symptoms

中枢敏化综合征在自主神经症状患者中的作用

Novak, Peter; Marciano, Sadie P; Witte, Aleandra

Erratum: Role of Central Sensitization Syndrome in Patients With Autonomic Symptoms

勘误:中枢敏化综合征在自主神经症状患者中的作用

Novak, Peter; Marciano, Sadie P; Witte, Alexandra

Hypermobile Ehlers-Danlos Syndrome: Cerebrovascular, Autonomic and Neuropathic Features

高活动性埃勒斯-当洛斯综合征:脑血管、自主神经和神经病变特征

Novak, Peter; Systrom, David M; Marciano, Sadie P; Witte, Alexandra; Warren, Arabella; Felsenstein, Donna; Giannetti, Matthew P; Hamilton, Matthew J; Nicoloro-SantaBarbara, Jennifer; Castells, Mariana; Farhad, Khosro; Pilgrim, David M; Mullally, William J; Fishman, Mark C; Milunsky, Jeff M; Milunsky, Aubrey; Krier, Joel

Cancer metastasis through the lymphatic versus blood vessels

癌症通过淋巴系统与血管转移的比较

Leong, Stanley P; Witte, Marlys H

Efficient in vivo base editing via single adeno-associated viruses with size-optimized genomes encoding compact adenine base editors

通过具有大小优化基因组并编码紧凑型腺嘌呤碱基编辑器的单个腺相关病毒进行有效的体内碱基编辑

Jessie R Davis, Xiao Wang, Isaac P Witte, Tony P Huang, Jonathan M Levy, Aditya Raguram, Samagya Banskota, Nabil G Seidah, Kiran Musunuru, David R Liu

Excessive IL-10 and IL-18 trigger hemophagocytic lymphohistiocytosis-like hyperinflammation and enhanced myelopoiesis

IL-10 和 IL-18 过量会引发噬血细胞性淋巴组织细胞增生症样过度炎症反应和髓系造血增强。

Yuting Tang ,Qian Xu ,Hui Luo ,Xiaomei Yan ,Gaoxiang Wang ,Liang Hu ,Jin Jin ,David P Witte ,Rebecca A Marsh ,Liang Huang ,Gang Huang ,Jianfeng Zhou

Digenic Inheritance of a FOXC2 Mutation and Two PIEZO1 Mutations Underlies Congenital Lymphedema in a Multigeneration Family

在多代家族中,FOXC2 突变和两个 PIEZO1 突变的双基因遗传是先天性淋巴水肿的根本原因。

Mustacich, Debbie J; Lai, Li-Wen; Bernas, Michael J; Jones, Jazmine A; Myles, Reginald J; Kuo, Phillip H; Williams, Walter H; Witte, Charles L; Erickson, Robert P; Witte, Marlys Hearst

Inherited DNA Repair Defects Disrupt the Structure and Function of Human Skin

遗传性 DNA 修复缺陷破坏人类皮肤的结构和功能

Sonya Ruiz-Torres, Marion G Brusadelli, David P Witte, Kathryn A Wikenheiser-Brokamp, Sharon Sauter, Adam S Nelson, Mathieu Sertorio, Timothy M Chlon, Adam Lane, Parinda A Mehta, Kasiani C Myers, Mary C Bedard, Bidisha Pal, Dorothy M Supp, Paul F Lambert, Kakajan Komurov, Melinda Butsch Kovacic, Ste

Lung shunt fraction calculation using (99m)Tc-MAA SPECT/CT imaging for (90)Y microsphere selective internal radiation therapy of liver tumors

利用 (99m)Tc-MAA SPECT/CT 成像技术计算肝肿瘤 (90)Y 微球选择性内放射治疗的肺分流率

Georgiou, Mike F; Kuker, Russ A; Studenski, Matthew T; Ahlman, Preeti P; Witte, Megan; Portelance, Lorraine