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

Ventral hernia containing a term gravid uterus: A rare challenge in surgical and obstetric management

腹壁疝内含足月妊娠子宫:外科和产科治疗中的罕见挑战

Zepeda Torres, José Maria; Flores Carlos, Juan Daniel; Suárez Carreón, Luis Osvaldo; Montes Aceves, Frida Juliette; Delgado Hernández, Gonzalo; Ángel Montoya, Daniel Alejandro; Nuñez Aviña, Pedro Mauricio; Moreno Castro, Oswaldo Efraín; Cárdenas Valdéz, Julio César; García Escoto, Víctor Salvador; González López, Ramón Jafit

Identification of novel genetic biomarkers for ChAdOx1 nCoV-19 mediated immunogenicity

鉴定ChAdOx1 nCoV-19介导的免疫原性的新型遗传生物标志物

Chou, Wan-Hsuan; Chang, Che-Mai; Ting, Jafit; Lin, Min-Rou; Liao, Hsin-Ni; Chou, Yi-Chien; Wei, Chun-Yu; Chi, Hsin-Hui; Ho, Szu-Ying; Luo, Wei-Tzu; Tsai, Cheng-Lin; Chao, Ching-Hsuan; Chen, Lu-Chun; Wu, Tsung-Hsun; Liu, Wei-Chih; Nguyen, Quynh-Anh; Chang, Hui-Wen; Hung, Ching-Sheng; Hong, Shiao-Ya; Wang, Jude Chu-Chun; Hsiao, Shih-Hsin; Chang, Wei-Chiao

Identifying malaria risks amongst forest going populations in Mondulkiri province and Kampong Speu province, Cambodia: a large cross-sectional survey

柬埔寨蒙多基里省和磅士卑省森林活动人群疟疾风险识别:一项大型横断面调查

Chen, Ingrid; Doum, Dyna; McIver, David J; Keo, Vanney; Vong, Pisey; Pech, Sophak; Meth, Vanny; Bun, Sour; Pen, Kimheng; Chea, Sopagna; Ly, Kanha; Hok, Kry; Sovannaroth, Siv; Ting, Jafit; Lovin, Diane D; Cunningham, Joanne M; Vajda, Élodie A; Tatarsky, Allison; Lobo, Neil F

Identification of Genetic Variants Associated with Severe Myocardial Bridging through Whole-Exome Sequencing

通过全外显子组测序鉴定与严重心肌桥相关的遗传变异

Yang, Tsung-Lin; Ting, Jafit; Lin, Min-Rou; Chang, Wei-Chiao; Shih, Chun-Ming

Identification of Druggable Genes for Asthma by Integrated Genomic Network Analysis

利用整合基因组网络分析鉴定哮喘可成药基因

Adikusuma, Wirawan; Chou, Wan-Hsuan; Lin, Min-Rou; Ting, Jafit; Irham, Lalu Muhammad; Perwitasari, Dyah Aryani; Chang, Wei-Pin; Chang, Wei-Chiao

Application of Whole Exome Sequencing and Functional Annotations to Identify Genetic Variants Associated with Marfan Syndrome

应用全外显子组测序和功能注释来识别与马凡氏综合征相关的遗传变异

Lin, Min-Rou; Chang, Che-Mai; Ting, Jafit; Chang, Jan-Gowth; Chou, Wan-Hsuan; Huang, Kuei-Jung; Cheng, Gloria; Chang, Hsiao-Huang; Chang, Wei-Chiao

Whole-Exome Sequencing Identifies Genetic Variants for Severe Adolescent Idiopathic Scoliosis in a Taiwanese Population

全外显子组测序鉴定出台湾人群中重度青少年特发性脊柱侧弯的遗传变异

Lin, Min-Rou; Chou, Po-Hsin; Huang, Kuei-Jung; Ting, Jafit; Liu, Chia-Ying; Chou, Wan-Hsuan; Lin, Gan-Hong; Chang, Jan-Gowth; Ikegawa, Shiro; Wang, Shih-Tien; Chang, Wei-Chiao

Drug Repurposing for Atopic Dermatitis by Integration of Gene Networking and Genomic Information

通过整合基因网络和基因组信息进行特应性皮炎药物再利用

Adikusuma, Wirawan; Irham, Lalu Muhammad; Chou, Wan-Hsuan; Wong, Henry Sung-Ching; Mugiyanto, Eko; Ting, Jafit; Perwitasari, Dyah Aryani; Chang, Wei-Pin; Chang, Wei-Chiao