Review article inferior vena cava thrombosis: a case series of patients observed in Taiwan and literature review

por Lin, Hsuan-Yu, Lin, Ching-Yeh, Shen, Ming-Ching
Publicado 2021

Hesperetin Induces Autophagy and Delayed Apoptosis by Modulating the AMPK/Akt/mTOR Pathway in Human Leukemia Cells In Vitro

por Lin, Ching-Yeh, Chen, Ya-Hui, Huang, Ying-Chih
Publicado 2023

Hydroxychloroquine and risk of development of cancers: a nationwide population-based cohort study

por Mao, I-Chieh, Lin, Ching-Yeh, Wu, Chia-Lin, Kor, Chew-Teng, Chang, Chia-Chu
Publicado 2018

Origin and timing of de novo variants implicated in type 2 von Willebrand disease

por Chen, Ming, Shen, Ming‐Ching, Chang, Shun‐Ping, Ma, Gwo‐Chin, Huang, Ying‐Chih, Lin, Ching‐Yeh
Publicado 2022

Arctigenin Reduces Myofibroblast Activities in Oral Submucous Fibrosis by LINC00974 Inhibition

por Lin, Ching-Yeh, Hsieh, Pei-Ling, Liao, Yi-Wen, Peng, Chih-Yu, Yu, Cheng-Chia, Lu, Ming-Yi
Publicado 2019

De novo mutation and somatic mosaicism of gene mutation in type 2A, 2B and 2M VWD

por Shen, Ming-Ching, Chen, Ming, Ma, Gwo-Chin, Chang, Shun-Ping, Lin, Ching-Yeh, Lin, Bo-Do, Hsieh, Han-Ni
Publicado 2016

A large family of hereditary spherocytosis and a rare case of hereditary elliptocytosis with a novel SPTA1 mutation underdiagnosed in Taiwan: A case report and literature review

por Shih, Yu-Hung, Huang, Ying-Chih, Lin, Ching-Yeh, Lin, Hsuan-Yu, Kuo, Su-Feng, Lin, Jen-Shiou, Shen, Ming-Ching
Publicado 2023

Prevalence of non-Alcoholic Fatty Liver Disease and Associated Factors in Patients with Moderate or Severe Hemophilia: A Multicenter-Based Study

por Shen, Ming-Ching, Chiou, Shyh-Shin, Chou, Sheng-Chieh, Weng, Te-Fu, Lin, Ching-Yeh, Wang, Jiaan-Der, Lee, Shou-Wu, Peng, Ching-Tien
Publicado 2022

Congenital factor V deficiency in Taiwan: identification of a novel variant p.Tyr1813(∗) and two variants specific to East Asians

por Lin, Hsuan-Yu, Lin, Ching-Yeh, Kuo, Su-Feng, Lin, Jen-Shiou, Lin, Po-Te, Huang, Ying-Chih, Hsieh, Han-Ni, Shen, Ming-Ching
Publicado 2023

Characterization of congenital factor XII deficiency in Taiwanese patients: identification of one novel and one common mutation

por Chou, Sheng-Chieh, Lin, Ching-Yeh, Lin, Hsuan-Yu, Pai, Chen-Hsueh, Yu, Cheng-Ye, Kuo, Su-Feng, Lin, Jen-Shiou, Lin, Po-Te, Hung, Mei-Hua, Hsieh, Han-Ni, Liu, Hsiang-Chun, Shen, Ming-Ching
Publicado 2022

The evolution of multiple active site configurations in a designed enzyme

por Hong, Nan-Sook, Petrović, Dušan, Lee, Richmond, Gryn’ova, Ganna, Purg, Miha, Saunders, Jake, Bauer, Paul, Carr, Paul D., Lin, Ching-Yeh, Mabbitt, Peter D., Zhang, William, Altamore, Timothy, Easton, Chris, Coote, Michelle L., Kamerlin, Shina C. L., Jackson, Colin J.
Publicado 2018