1. Angiopoietin-Like 3 Induces Podocyte F-Actin Rearrangement through Integrin αVβ3/FAK/PI3K Pathway-Mediated Rac1 Activation. (5th November 2013) Authors: Lin, Yi; Rao, Jia; Zha, Xi-liang; Xu, Hong Other Names: Hochwald Steven N. Academic Editor. Journal: BioMed research international Issue: Volume 2013(2013) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. BH3 mimetic ABT‐737 induces apoptosis in CD34+ acute myeloid leukemia cells and shows synergistic effect with conventional chemotherapeutic drugs. Issue 2 (9th November 2015) Authors: Rao, Jia; Li, Fei; Zhang, Rong‐yan; Zhou, Huan‐huan; Chen, Guo‐an Journal: Asia-Pacific journal of clinical oncology Issue: Volume 13:Issue 2(2017) Page Start: e144 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. COQ8B nephropathy: Early detection and optimal treatment. Issue 8 (16th June 2020) Authors: Song, Xiaoxiang; Fang, Xiaoyan; Tang, Xiaoshan; Cao, Qi; Zhai, Yihui; Chen, Jing; Liu, Jialu; Zhang, Zhiqing; Xiang, Tianchao; Qian, Yanyan; Wu, Bingbing; Wang, Huijun; Zhou, Wenhao; Liu, Cuihua; Shen, Qian; Xu, Hong; Rao, Jia Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 8(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Cover. Issue 8 (18th August 2020) Authors: Song, Xiaoxiang; Fang, Xiaoyan; Tang, Xiaoshan; Cao, Qi; Zhai, Yihui; Chen, Jing; Liu, Jialu; Zhang, Zhiqing; Xiang, Tianchao; Qian, Yanyan; Wu, Bingbing; Wang, Huijun; Zhou, Wenhao; Liu, Cuihua; Shen, Qian; Xu, Hong; Rao, Jia Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 8(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Genetic and pathological findings in a boy with psoriasis and C3 glomerulonephritis: A case report and literature review. Issue 10 (28th July 2020) Authors: Wei, Lei; Fang, Ye; Cao, Guanghai; Zhang, Shufeng; Tian, Ming; Shen, Qian; Xu, Hong; Liu, Cuihua; Rao, Jia Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 10(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration system. Issue 5 (25th July 2019) Authors: Rao, Jia; Liu, Xiaorong; Mao, Jianhua; Tang, Xiaoshan; Shen, Qian; Li, Guomin; Sun, Li; Bi, Yunli; Wang, Xiang; Qian, Yanyan; Wu, Bingbing; Wang, Huijun; Zhou, Wenhao; Ma, Duan; Zheng, Bixia; Shen, Ying; Chen, Zhi; Luan, Jiangwei; Wang, Xiaowen; Wang, Mo Journal: Clinical genetics Issue: Volume 96:Issue 5(2019) Page Start: 402 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome. Issue 3 (9th March 2018) Authors: Braun, Daniela A; Warejko, Jillian K; Ashraf, Shazia; Tan, Weizhen; Daga, Ankana; Schneider, Ronen; Hermle, Tobias; Jobst-Schwan, Tilman; Widmeier, Eugen; Majmundar, Amar J; Nakayama, Makiko; Schapiro, David; Rao, Jia; Schmidt, Johanna Magdalena; Hoogstraten, Charlotte A; Hugo, Hannah; Bakkaloglu... Journal: Nephrology dialysis transplantation Issue: Volume 34:Issue 3(2019) Page Start: 485 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Multicenter study of the clinical features and mutation gene spectrum of Chinese children with Dent disease. Issue 3 (13th January 2020) Authors: Ye, Qing; Shen, Qian; Rao, Jia; Zhang, Aihua; Zheng, Bixia; Liu, Xiaorong; Shen, Ying; Chen, Zhi; Wu, Yubing; Hou, Ling; Jian, Shan; Wei, Min; Ma, Mingsheng; Sun, Shuzhen; Li, Qian; Dang, Xiqiang; Wang, Ying; Xu, Hong; Mao, Jianhua Journal: Clinical genetics Issue: Volume 97:Issue 3(2020) Page Start: 407 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Mutations in WDR4 as a new cause of Galloway–Mowat syndrome. Issue 11 (6th August 2018) Authors: Braun, Daniela A.; Shril, Shirlee; Sinha, Aditi; Schneider, Ronen; Tan, Weizhen; Ashraf, Shazia; Hermle, Tobias; Jobst‐Schwan, Tilman; Widmeier, Eugen; Majmundar, Amar J.; Daga, Ankana; Warejko, Jillian K.; Nakayama, Makiko; Schapiro, David; Chen, Jing; Airik, Merlin; Rao, Jia; Schmidt, Johanna M... Journal: American journal of medical genetics Issue: Volume 176:Issue 11(2018) Page Start: 2460 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Panel sequencing distinguishes monogenic forms of nephritis from nephrosis in children. Issue 3 (21st March 2018) Authors: Schapiro, David; Daga, Ankana; Lawson, Jennifer A; Majmundar, Amar J; Lovric, Svjetlana; Tan, Weizhen; Warejko, Jillian K; Fessi, Inés; Rao, Jia; Airik, Merlin; Gee, Heon Yung; Schneider, Ronen; Widmeier, Eugen; Hermle, Tobias; Ashraf, Shazia; Jobst-Schwan, Tilman; van der Ven, Amelie T; Nakayama... Journal: Nephrology dialysis transplantation Issue: Volume 34:Issue 3(2019) Page Start: 474 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗