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

Combining Copper and Zinc into a Biosensor for Anti-Chemoresistance and Achieving Osteosarcoma Therapeutic Efficacy

将铜和锌结合到生物传感器中,用于抗化疗耐药性和提高骨肉瘤治疗效果

Lim, Yan Yik; Zaidi, Ahmad Mujahid Ahmad; Miskon, Azizi

Numerical Simulation Study on Relationship between the Fracture Mechanisms and Residual Membrane Stresses of Metallic Material

金属材料断裂机制与残余膜应力关系的数值模拟研究

Lim, Yan Yik; Miskon, Azizi; Zaidi, Ahmad Mujahid Ahmad; Megat Ahmad, Megat Mohamad Hamdan; Abu Bakar, Muhamad

Composing On-Program Triggers and On-Demand Stimuli into Biosensor Drug Carriers in Drug Delivery Systems for Programmable Arthritis Therapy

将程序触发和按需刺激组合到生物传感器药物载体中,用于可编程关节炎治疗的药物递送系统

Lim, Yan Yik; Zaidi, Ahmad Mujahid Ahmad; Miskon, Azizi

Structural Characterization Analyses of Low Brass Filler Biomaterial for Hard Tissue Implanted Scaffold Applications

低黄铜填充生物材料在硬组织植入支架应用中的结构表征分析

Lim, Yan Yik; Miskon, Azizi; Zaidi, Ahmad Mujahid Ahmad; Megat Ahmad, Megat Mohamad Hamdan; Abu Bakar, Muhamad

Structural Strength Analyses for Low Brass Filler Biomaterial with Anti-Trauma Effects in Articular Cartilage Scaffold Design

低黄铜填充生物材料在关节软骨支架设计中抗创伤作用的结构强度分析

Lim, Yan Yik; Miskon, Azizi; Zaidi, Ahmad Mujahid Ahmad

Antimesothelioma Immunotherapy by CTLA-4 Blockade Depends on Active PD1-Based TWIST1 Vaccination

CTLA-4 阻断抗间皮瘤免疫疗法依赖于基于 PD1 的主动 TWIST1 疫苗接种

Zhiwu Tan, Mei Sum Chiu, Chi Wing Yan, Yik Chun Wong, Haode Huang, Kwan Man, Zhiwei Chen

Induced pluripotent stem cell models of Zellweger spectrum disorder show impaired peroxisome assembly and cell type-specific lipid abnormalities

泽尔韦格谱系障碍的诱导性多能干细胞模型显示过氧化物酶体组装受损和细胞类型特异性脂质异常

Xiao-Ming Wang, Wing Yan Yik, Peilin Zhang, Wange Lu, Ning Huang, Bo Ram Kim, Darryl Shibata, Madison Zitting, Robert H Chow, Ann B Moser, Steven J Steinberg, Joseph G Hacia2

Derivation of induced pluripotent stem cells from orangutan skin fibroblasts

从猩猩皮肤成纤维细胞中衍生诱导性多能干细胞

Krishna Ramaswamy, Wing Yan Yik, Xiao-Ming Wang, Erin N Oliphant, Wange Lu, Darryl Shibata, Oliver A Ryder, Joseph G Hacia

A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population

PEX6 基因的创始突变导致法裔加拿大人群中 Zellweger 综合征的发病率增加

Sebastien Levesque, Charles Morin, Simon-Pierre Guay, Josee Villeneuve, Pascale Marquis, Wing Yan Yik, Sarn Jiralerspong, Luigi Bouchard, Steven Steinberg, Joseph G Hacia, Ken Dewar, Nancy E Braverman