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

An Update on Single-Cell RNA Sequencing in Illuminating Disease Mechanisms of Cutaneous T-Cell Lymphoma

单细胞RNA测序在阐明皮肤T细胞淋巴瘤疾病机制中的最新进展

Suhl, Sara; Kaminsky, Alexander; Chen, Caroline; Lapolla, Brigit A; Zhou, Maggie H; Kent, Joshua; Marx, Abigail; Nebo, Ikenna David; Ramush, Geat; Luyten, Sophia; Sacknovitz, Yoni; Sung, Julie; Bear, Christina M; Schreidah, Celine M; Gru, Alejandro; Geskin, Larisa J

Methylation cytometric pretreatment blood immune profiles with tumor mutation burden as prognostic indicators for survival outcomes in head and neck cancer patients on anti-PD-1 therapy

甲基化细胞计量学预处理血液免疫谱结合肿瘤突变负荷作为头颈癌患者抗PD-1治疗生存预后的指标

Zhang, Ze; Sehgal, Kartik; Shirai, Keisuke; Butler, Rondi A; Wiencke, John K; Koestler, Devin C; Ramush, Geat; Lee, Min Kyung; Molinaro, Annette M; Stolrow, Hannah G; Birnbaum, Ariel; Salas, Lucas A; Haddad, Robert I; Kelsey, Karl T; Christensen, Brock C

Geminal-dithiol-based precursors for reactive sulfur species

基于偕二硫醇的活性硫物种前体

Xu, Shi; Ramush, Geat; Yang, Iris J; Das, Eshani; Shieh, Meg; Xian, Ming

Immunomethylomic profiles of long-term head and neck squamous cell carcinoma survivors on immune checkpoint inhibitors

接受免疫检查点抑制剂治疗的长期头颈部鳞状细胞癌幸存者的免疫甲基化组学特征

Min Kyung Lee, Ze Zhang, Kartik Sehgal, Rondi Butler, Hannah Stolrow, Geat Ramush, Keisuke Shirai, Devin C Koestler, Lucas A Salas, John K Wiencke, Robert Haddad, Karl T Kelsey, Brock C Christensen

Arterial Tortuosity Syndrome and Hypermobility of Joints - Case Presentation and a Review of Literature

动脉迂曲综合征和关节过度活动症——病例报告及文献综述

Bejiqi, Ramush; Retkoceri, Ragip; Maloku, Arlinda; Mustafa, Aferdita

Organelle-Targeted Fluorescent Probes for Sulfane Sulfur Species

靶向细胞器硫物种的荧光探针

Roy, Biswajit; Shieh, Meg; Ramush, Geat; Xian, Ming

Methods for Suppressing Hydrogen Sulfide in Biological Systems

抑制生物系统中硫化氢的方法

Wang, Yingying; Ni, Xiang; Chadha, Rahuljeet; McCartney, Caitlin; Lam, Yannie; Brummett, Brock; Ramush, Geat; Xian, Ming

A new variant of MYCN gene as a cause of Feingold syndrome

MYCN基因新变异是费恩戈尔德综合征的病因之一。

Zeka, Naim; Bejiqi, Ramush; Gerguri, Abdurrahim; Zogaj, Leonore; Jashari, Haki

Kawasaki Disease Shock Syndrome Presented with Giant Coronary Artery Dilatation - Presentation of Two Cases and a Literature Review

川崎病休克综合征伴巨大冠状动脉扩张——两例病例报告及文献综述

Bejiqi, Ramush; Pajaziti, Nafije; Agushi, Shqipe

The Diagnostic and Clinical Approach to Pediatric Myocarditis: A Review of the Current Literature

儿童心肌炎的诊断和临床方法:现有文献综述

Bejiqi, Ramush; Retkoceri, Ragip; Maloku, Arlinda; Mustafa, Aferdita; Bejiqi, Hana; Bejiqi, Rinor