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. Cancer metabolism control by natural products: Pyruvate kinase M2 targeting therapeutics. (6th July 2022) Authors: El‐Far, Ali H.; Al Jaouni, Soad K.; Li, Xiaotao; Fu, Junjiang Journal: Phytotherapy research Issue: Volume 36:Number 8(2022) Page Start: 3181 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Cordycepin Inhibits Drug-resistance Non-small Cell Lung Cancer Progression by Activating AMPK Signaling Pathway. (June 2019) Authors: Wei, Chunli; Yao, Xiaojun; Jiang, Zebo; Wang, Yuwei; Zhang, Dianzheng; Chen, Xi; Fan, Xingxing; Xie, Chun; Cheng, Jingliang; Fu, Junjiang; Leung, Elaine Lai-Han Journal: Pharmacological research Issue: Volume 144(2019) Page Start: 79 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. 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) ↗
7. Effects of flexibility and aspect ratio on the aerodynamic performance of flapping wings. (14th March 2018) Authors: Fu, Junjiang; Liu, Xiaohui; Shyy, Wei; Qiu, Huihe Journal: Bioinspiration & biomimetics Issue: Volume 13:Number 3(2018:Sep.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Epigenetic role of thymoquinone: impact on cellular mechanism and cancer therapeutics. Issue 12 (December 2019) Authors: Khan, Md. Asaduzzaman; Tania, Mousumi; Fu, Junjiang Journal: Drug discovery today Issue: Volume 24:Issue 12(2019) Page Start: 2315 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Identification of a novel germline BRCA2 variant in a Chinese breast cancer family. Issue 2 (28th November 2019) Authors: Cheng, Jingliang; Peng, Jiangzhou; Fu, Jiewen; Khan, Md. Asaduzzaman; Tan, Pingping; Wei, Chunli; Deng, Xiyun; Chen, Hanchun; Fu, Junjiang Journal: Journal of cellular and molecular medicine Issue: Volume 24:Issue 2(2020) Page Start: 1676 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) ↗