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

Modeling Adeno-Associated Viral Vector 6-mediated In Vivo Gene Delivery to Expanded Non-Mobilized Haemopoietic Stem Cells from Transfusion-dependent Thalassemia Patients in a Humanized Mouse

在人源化小鼠中模拟腺相关病毒载体6介导的体内基因递送至输血依赖型地中海贫血患者扩增的非动员造血干细胞

Ramesh, Janani; Kandasamy, Karthikeyan; Yusof, Nur Nazneen; Sujuandy, Ihsan; Keng, Choong Tat; Chen, Liwei; Chia, Bing Shao; Liu, Min; Her, Zhisheng; Kukumberg, Marek; Sia, Kian Chuan; Mohd Rodhi, Siti Humairah; Fu, Zhen Ying; Rufaihah, A J; Franco-Obregón, Alfredo; Choolani, Mahesh; Sesurajan, Binny Priya; Lai, Poh-San; Lee, Shir Ying; Koh, Pei Lin; Chen, Qingfeng; Gan, Shu-Uin; Chew, Wei Leong; Mattar, Citra Nz

A clinical approach to diagnosis and management of mitochondrial myopathies

线粒体肌病诊断和治疗的临床方法

Chin, Hui-Lin; Lai, Poh San; Tay, Stacey Kiat Hong

Embryo and fetal gene editing: Technical challenges and progress toward clinical applications

胚胎和胎儿基因编辑:技术挑战及临床应用进展

Mattar, Citra N Z; Chew, Wei Leong; Lai, Poh San

Exploring RNF213 in Ischemic Stroke and Moyamoya Disease: From Cellular Models to Clinical Insights

探索RNF213在缺血性卒中和烟雾病中的作用:从细胞模型到临床见解

Tan, Benjamin Y Q; Kok, Charlene H P; Ng, Megan B J; Loong, Shaun; Jou, Eric; Yeo, Leonard L L; Han, Weiping; Anderson, Christopher D; Khor, Chiea Chuen; Lai, Poh San

Clinical and Genetic Profiles of 5q- and Non-5q-Spinal Muscular Atrophy Diseases in Pediatric Patients

儿童脊髓性肌萎缩症(5q-和非5q-)的临床和遗传特征

Nishio, Hisahide; Niba, Emma Tabe Eko; Saito, Toshio; Okamoto, Kentaro; Lee, Tomoko; Takeshima, Yasuhiro; Awano, Hiroyuki; Lai, Poh-San

Genetics in Ischemic Stroke: Current Perspectives and Future Directions

缺血性卒中的遗传学:现状与未来方向

Zhang, Ka; Loong, Shaun S E; Yuen, Linus Z H; Venketasubramanian, Narayanaswamy; Chin, Hui-Lin; Lai, Poh San; Tan, Benjamin Y Q

Loss of FOCAD, operating via the SKI messenger RNA surveillance pathway, causes a pediatric syndrome with liver cirrhosis

FOCAD 的缺失(通过 SKI 信使 RNA 监视通路发挥作用)会导致一种伴有肝硬化的儿童综合征。

Ricardo Moreno Traspas,Tze Shin Teoh,Pui-Mun Wong,Michael Maier,Crystal Y Chia,Kenneth Lay,Nur Ain Ali,Austin Larson,Fuad Al Mutairi,Nouriya Abbas Al-Sannaa,Eissa Ali Faqeih,Majid Alfadhel,Huma Arshad Cheema,Juliette Dupont,Stéphane Bézieau,Bertrand Isidor,Dorrain Yanwen Low,Yulan Wang,Grace Tan,Poh San Lai,Hugues Piloquet,Madeleine Joubert,Hulya Kayserili,Kimberly A Kripps,Shareef A Nahas,Eric P Wartchow,Mikako Warren,Gandham SriLakshmi Bhavani,Majed Dasouki,Renata Sandoval,Elisa Carvalho,Luiza Ramos,Gilda Porta,Bin Wu,Harsha Prasada Lashkari,Badr AlSaleem,Raeda M BaAbbad,Anabela Natália Abreu Ferrão,Vasiliki Karageorgou,Natalia Ordonez-Herrera,Suliman Khan,Peter Bauer,Benjamin Cogne,Aida M Bertoli-Avella,Marie Vincent,Katta Mohan Girisha,Bruno Reversade

Novel Autoantibodies in Idiopathic Small Fiber Neuropathy

特发性小纤维神经病变中的新型自身抗体

Amanda C Y Chan, Hiu Yi Wong, Yao Feng Chong, Poh San Lai, Hock Luen Teoh, Alison Y Y Ng, Jennifer H M Hung, Yee Cheun Chan, Kay W P Ng, Joy Vijayan, Jonathan J Y Ong, Bharatendu Chandra, Chi Hsien Tan, Nurul H Rutt, Ti Myen Tan, Nur Hafiza Ismail, Einar Wilder-Smith, Herbert Schwarz, Hyungwon Choi,

J'Accuse….. Or The Plight of pro-bono Volunteer Scientists in Academic Publishing

我控诉……或者说,学术出版业中义务志愿科学家的困境

Reichardt, Juergen K V; Patrinos, George P; Lai, Poh San; Novelli, Giuseppe

Autosomal dominant Emery-Dreifuss muscular dystrophy caused by a mutation in the lamin A/C gene identified by exome sequencing: a case report

通过外显子组测序鉴定出由层粘蛋白A/C基因突变引起的常染色体显性遗传性埃默里-德雷福斯肌营养不良症:病例报告

Iskandar, Kristy; Sunartini; Astari, Farida Niken; Gumilang, Rizki Amalia; Ilma, Nissya; Shartyanie, Ni Putu; Adistyawan, Guritno; Tan, Grace; Gunadi; Lai, Poh San