1. Congenital Middle Ear Malformation with Common Deafness Gene Mutation Analysis: A Review of 813 Profound Sensorineural Hearing Loss Child Patients. Issue 3 (26th December 2019) Authors: Dong, Yunpeng; He, Xiangbo; Wu, Weijing; Yang, Shu; Peng, Anquan; Xiao, Zian; Liu, Yuyuan; Gao, Shuichao; Tan, Donghui; Liu, Xue Zhong; Xie, Dinghua Journal: Anatomical record Issue: Volume 303:Issue 3(2020) Page Start: 594 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Efficient introduction of an isogenic homozygous mutation to induced pluripotent stem cells from a hereditary hearing loss family using CRISPR/Cas9 and single-stranded donor oligonucleotides. Issue 4 (April 2019) Authors: Dong, Yunpeng; Peng, Tao; Wu, Weijing; Tan, Donghui; Liu, Xuezhong; Xie, Dinghua Journal: Journal of international medical research Issue: Volume 47:Issue 4(2019) Page Start: 1717 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Encapsulation of Platinum Prodrugs into PC7A Polymeric Nanoparticles Combined with Immune Checkpoint Inhibitors for Therapeutically Enhanced Multimodal Chemotherapy and Immunotherapy by Activation of the STING Pathway. Issue 4 (11th December 2022) Authors: Gao, Xiangjie; Lei, Guanxiong; Wang, Bin; Deng, Zhong; Karges, Johannes; Xiao, Haihua; Tan, Donghui Journal: Advanced science Issue: Volume 10:Issue 4(2023) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗