11. Homozygous mutations in REC114 cause female infertility characterised by multiple pronuclei formation and early embryonic arrest. Issue 3 (8th November 2019) Authors: Wang, Wenjing; Dong, Jie; Chen, Biaobang; Du, Jing; Kuang, Yanping; Sun, Xiaoxi; Fu, Jing; Li, Bin; Mu, Jian; Zhang, Zhihua; Zhou, Zhou; Lin, Zhao; Wu, Ling; Yan, Zheng; Mao, Xiaoyan; Li, Qiaoli; He, Lin; Wang, Lei; Sang, Qing Journal: Journal of medical genetics Issue: Volume 57:Issue 3(2020) Page Start: 187 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
12. Identification of a novel homozygous mutation in MYO3A in a Chinese family with DFNB30 non-syndromic hearing impairment. (May 2016) Authors: Qu, Ronggui; Sang, Qing; Xu, Yao; Feng, Ruizhi; Jin, Li; He, Lin; Wang, Lei Journal: International journal of pediatric otorhinolaryngology Issue: Volume 84(2016:May) Page Start: 43 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
13. Improving genetic diagnosis of Mendelian disease with RNA sequencing: a narrative review. Issue 1 (19th March 2022) Authors: Zhou, Zhou; Sang, Qing; Wang, Lei Journal: Journal of bio-X research Issue: Volume 5:Issue 1(2022) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
14. IQUB deficiency causes male infertility by affecting the activity of p-ERK1/2/RSPH3. Issue 1 (10th November 2022) Authors: Zhang, Zhihua; Zhou, Hongbin; Deng, Xujing; Zhang, Ruixiu; Qu, Ronggui; Mu, Jian; Liu, Ruyi; Zeng, Yang; Chen, Biaobang; Wang, Lei; Sang, Qing; Bao, Shihua Journal: Human reproduction Issue: Volume 38:Issue 1(2023) Page Start: 168 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
15. Meiotic defects in human oocytes: Potential causes and clinical implications. (7th October 2022) Authors: Wu, Tianyu; Gu, Hao; Luo, Yuxi; Wang, Lei; Sang, Qing Journal: BioEssays Issue: Volume 44:Number 12(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
16. MicroRNA172 controls inflorescence meristem size through regulation of APETALA2 in Arabidopsis. Issue 1 (12th April 2022) Authors: Sang, Qing; Vayssières, Alice; Ó'Maoiléidigh, Diarmuid S.; Yang, Xia; Vincent, Coral; Bertran Garcia de Olalla, Enric; Cerise, Martina; Franzen, Rainer; Coupland, George Journal: New phytologist Issue: Volume 235:Issue 1(2022) Page Start: 356 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
17. MOS is a novel genetic marker for human early embryonic arrest and fragmentation. Issue 12 (22nd November 2021) Authors: Wang, Lei; Sang, Qing Journal: EMBO molecular medicine Issue: Volume 13:Issue 12(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
18. Mutagenesis of a Quintuple Mutant Impaired in Environmental Responses Reveals Roles for CHROMATIN REMODELING4 in the Arabidopsis Floral Transition. Issue 5 (4th March 2020) Authors: Sang, Qing; Pajoro, Alice; Sun, Hequan; Song, Baoxing; Yang, Xia; Stolze, Sara C.; Andrés, Fernando; Schneeberger, Korbinian; Nakagami, Hirofumi; Coupland, George Journal: The Plant Cell Issue: Volume 32:Issue 5(2020) Page Start: 1479 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
19. Mutations in NLRP2 and NLRP5 cause female infertility characterised by early embryonic arrest. Issue 7 (15th March 2019) Authors: Mu, Jian; Wang, Wenjing; Chen, Biaobang; Wu, Ling; Li, Bin; Mao, Xiaoyan; Zhang, Zhihua; Fu, Jing; Kuang, Yanping; Sun, Xiaoxi; Li, Qiaoli; Jin, Li; He, Lin; Sang, Qing; Wang, Lei Journal: Journal of medical genetics Issue: Volume 56:Issue 7(2019) Page Start: 471 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
20. Mutations in TUBB8 cause a multiplicity of phenotypes in human oocytes and early embryos. Issue 10 (6th June 2016) Authors: Feng, Ruizhi; Yan, Zheng; Li, Bin; Yu, Min; Sang, Qing; Tian, Guoling; Xu, Yao; Chen, Biaobang; Qu, Ronggui; Sun, Zhaogui; Sun, Xiaoxi; Jin, Li; He, Lin; Kuang, Yanping; Cowan, Nicholas J; Wang, Lei Journal: Journal of medical genetics Issue: Volume 53:Issue 10(2016) Page Start: 662 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗