1. A novel missense variant c.G644A (p.G215E) of the RPGR gene in a Chinese family causes X-linked retinitis pigmentosa. Issue 10 (18th October 2019) Authors: Fu, Jiewen; Cheng, Jingliang; Zhou, Qi; Wei, Chunli; Chen, Hanchun; Lv, Hongbin; Fu, Junjiang Journal: Bioscience reports Issue: Volume 39:Issue 10(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree. Issue 5 (20th March 2019) Authors: Cheng, Jingliang; Fu, Jiewen; Zhou, Qi; Xiang, Xiaohong; Wei, Chunli; Yang, Lisha; Fu, Shangyi; Khan, Md. Asaduzzaman; Lv, Hongbin; Fu, Junjiang Journal: Journal of cellular and molecular medicine Issue: Volume 23:Issue 5(2019) Page Start: 3776 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A novel, homozygous nonsense variant of the CDHR1 gene in a Chinese family causes autosomal recessive retinal dystrophy by NGS‐based genetic diagnosis. Issue 11 (30th August 2018) Authors: Fu, Jiewen; Ma, Lu; Cheng, Jingliang; Yang, Lisha; Wei, Chunli; Fu, Shangyi; Lv, Hongbin; Chen, Rui; Fu, Junjiang Journal: Journal of cellular and molecular medicine Issue: Volume 22:Issue 11(2018) Page Start: 5662 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. ChemInform Abstract: Copper‐Catalyzed Hydrodefluorination of Fluoroarenes by Copper Hydride Intermediates. Issue 30 (4th July 2013) Authors: Lv, Hongbin; Cai, Yuan‐Bo; Zhang, Jun‐Long Journal: ChemInform Issue: Volume 44:Issue 30(2013) Page Start: no Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Copper‐Catalyzed Hydrodefluorination of Fluoroarenes by Copper Hydride Intermediates1. (10th February 2013) Authors: Lv, Hongbin; Cai, Yuan‐Bo; Zhang, Jun‐Long Journal: Angewandte Chemie Issue: Volume 125:Number 11(2013) Page Start: 3285 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Copper‐Catalyzed Hydrodefluorination of Fluoroarenes by Copper Hydride Intermediates1. Issue 11 (10th February 2013) Authors: Lv, Hongbin; Cai, Yuan‐Bo; Zhang, Jun‐Long Journal: Angewandte Chemie international edition Issue: Volume 52:Issue 11(2013) Page Start: 3203 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Diagnostic value of a combination of next-generation sequencing, chorioretinal imaging and metabolic analysis: lessons from a consanguineous Chinese family with gyrate atrophy of the choroid and retina stemming from a novel OAT variant. Issue 3 (26th October 2018) Authors: Huang, Junting; Fu, Jiewen; Fu, Shangyi; Yang, Lisha; Nie, Kailai; Duan, Chengxia; Cheng, Jingliang; Li, Yumei; Lv, Hongbin; Chen, Rui; Liu, Longqian; Fu, Junjiang Journal: British journal of ophthalmology Issue: Volume 103:Issue 3(2019) Page Start: 428 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Effects of Combined Magnetic Fields Treatment and Nano-Hydroxyapatite Coating on Porous Biphasic Calcium Phosphate Bone Graft in Rabbit Spinal Fusion Model. Issue 11 (1st June 2018) Authors: Zhuo, Xianglong; Li, Chentian; Li, Bing; Li, Zhaoyang; Lv, Hongbin; Huang, Jianjun; Xu, Daqi; Hu, Jianzhong Journal: Spine Issue: Volume 43:Issue 11(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Extracellular vesicles derived from human umbilical cord mesenchymal stem cells relieves diabetic retinopathy through a microRNA-30c-5p-dependent mechanism. (August 2022) Authors: He, Yue; Zhang, Zhiru; Yao, Tianyu; Huang, Li; Gan, Jinhua; Lv, Hongbin; Chen, Jie Journal: Diabetes research and clinical practice Issue: Volume 190(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Identification of a Novel Heterozygous Missense Mutation in the CACNA1F Gene in a Chinese Family with Retinitis Pigmentosa by Next Generation Sequencing. (17th May 2015) Authors: Zhou, Qi; Cheng, Jingliang; Yang, Weichan; Tania, Mousumi; Wang, Hui; Khan, Md. Asaduzzaman; Duan, Chengxia; Zhu, Li; Chen, Rui; Lv, Hongbin; Fu, Junjiang Other Names: Deng Hao Academic Editor. Journal: BioMed research international Issue: Volume 2015(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗