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

Recognizing familial Huntington's disease in an Asian cohort: Insights from the Philippines

在亚洲人群中识别家族性亨廷顿病:来自菲律宾的启示

Garcia, Jao Jarro B; Cabataña, Gilbert J Jr; Ditan, Iris; Separa, Karl Josef Niño J; Rocha-Tulagan, Ida Ingrid; Lin, Han-I; Lin, Chin-Hsien; Supnet-Wells, Melanie Leigh D; Diaz, Alejandro F; Ng, Arlene R; Jamora, Roland Dominic G; Saranza, Gerard

Reprogramming of a human induced pluripotent stem cell (iPSC) line (IBMSi012-A) from an early-onset Parkinson's disease patient harboring a homozygous p.D331Y mutation in the PLA2G6 gene

对来自早发性帕金森病患者的人类诱导性多能干细胞 (iPSC) 系 (IBMSi012-A) 进行重新编程,该患者携带 PLA2G6 基因纯合 p.D331Y 突变

Yu-Che Cheng, Han-I Lin, Shih-Han Syu, Huai-En Lu, Ching-Ying Huang, Chin-Hsien Lin, Patrick C H Hsieh

Generation of induced pluripotent stem cells (IBMSi011-A) from a patient with Parkinson's disease carrying LRRK2 p.I1371V mutation

从携带 LRRK2 p.I1371V 突变的帕金森病患者体内生成诱导性多能干细胞 (IBMSi011-A)

Han-I Lin, Yu-Che Cheng, Hui-Wen Ko, Cheng-Hao Wen, Huai-En Lu, Ching-Ying Huang, Patrick C H Hsieh, Chin-Hsien Lin

Generation of 2 induced pluripotent stem cell lines derived from patients with Parkinson's disease carrying LRRK2 G2385R variant

产生 2 种源自携带 LRRK2 G2385R 变异的帕金森病患者的诱导性多能干细胞系

Yu-Che Cheng, Ching-Ying Huang, Ming-Ching Ho, Yu-Hung Hsu, Shih-Han Syu, Huai-En Lu, Han-I Lin, Chin-Hsien Lin, Patrick C H Hsieh

A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: a case study and literature review

RUNX2基因突变导致的肢带型肌病表型在锁骨颅骨发育不良患者中的病例报告及文献综述

Hsueh, Sung-Ju; Lee, Ni-Chung; Yang, Shu-Hua; Lin, Han-I; Lin, Chin-Hsien