1. 1300 nm absorption two-acceptor semiconducting polymer nanoparticles for NIR-II photoacoustic imaging system guided NIR-II photothermal therapy. Issue 64 (22nd July 2019) Authors: Zhang, Wansu; Sun, Xiaoli; Huang, Ting; Pan, Xiaoxia; Sun, Pengfei; Li, Jiewei; Zhang, Hua; Lu, Xiaomei; Fan, Quli; Huang, Wei Journal: Chemical communications Issue: Volume 55:Issue 64(2019) Page Start: 9487 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A diketopyrrolopyrrole-based conjugated polymer for efficient photodynamic and photothermal combination therapy under single 808 nm laser irradiation. (December 2021) Authors: Liu, Jiawei; Xu, Xingpeng; Wang, Jing; Sang, Ruoyu; Zhang, Zhen; Chen, Jiaqi; Lu, Xiaomei; Wang, Qi; Fan, Quli Journal: Dyes and pigments Issue: Volume 196(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A highly water-soluble triblock conjugated polymer for in vivo NIR-II imaging and photothermal therapy of cancer. Issue 22 (18th May 2018) Authors: Lu, Xiaomei; Yuan, Pengcheng; Zhang, Wansu; Wu, Qi; Wang, Xiaoxiao; Zhao, Meng; Sun, Pengfei; Huang, Wei; Fan, Quli Journal: Polymer chemistry Issue: Volume 9:Issue 22(2018) Page Start: 3118 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A macrocyclic oligoelectrolyte as a facial platform for absorbing hyaluronic acid oligomers for targeted cancer cellular imaging. Issue 29 (7th August 2015) Authors: Song, Wenli; Yin, Chao; Jiang, Rongcui; Lu, Xiaomei; Quan, Yiwu; Tian, Congcong; Li, Jie; Hu, Wenbo; Sun, Pengfei; Deng, Weixing; Fan, Quli; Huang, Wei Journal: Polymer chemistry Issue: Volume 6:Issue 29(2015) Page Start: 5295 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. A molecular‐beacon‐based asymmetric PCR assay for detecting polymorphisms related to folate metabolism. Issue 8 (15th May 2020) Authors: Peng, Qi; Liao, Shengbin; He, Yuejing; Liang, Liyun; Su, Xiaohua; Rao, Chunbao; Li, Wenrui; Li, Siping; Lu, Xiaomei Journal: Journal of clinical laboratory analysis Issue: Volume 34:Issue 8(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. A novel homozygous initiation codon variant associated with infantile alpha‐Bcrystallinopathy in a Chinese family. Issue 8 (18th June 2019) Authors: Ma, Keze; Luo, Dong; Tian, Tian; Li, Ning; He, Xiaoguang; Rao, Chunbao; Zhong, Baimao; Lu, Xiaomei Journal: Molecular genetics & genomic medicine Issue: Volume 7:Issue 8(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. A Novel IRF6 Frameshift Mutation in a Large Chinese Pedigree With Van der Woude syndrome. (April 2022) Authors: Peng, Qi; Qin, Wenyan; Li, Siping; Huang, Meihua; Rao, Chunbao; Lu, Xiaomei Journal: Cleft palate-craniofacial journal Issue: Volume 59:Number 4(2022) Page Start: 548 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. A novel missense mutation in the SLC26A4 gene causes nonsyndromic hearing loss and enlarged vestibular aqueduct. (April 2017) Authors: He, Xiaoguang; Peng, Qi; Li, Siping; Zhu, Pengyuan; Wu, Chunqiu; Rao, Chunbao; Chang, Jiang; Xie, Mingyu; Zhong, Baimao; Lu, Xiaomei Journal: International journal of pediatric otorhinolaryngology Issue: Volume 95(2017:Apr.) Page Start: 104 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. A novel mutation in the MYO7A gene is associated with Usher syndrome type 1 in a Chinese family. (August 2017) Authors: He, Xiaoguang; Peng, Qi; Li, Siping; Zhu, Pengyuan; Wu, Chunqiu; Rao, Chunbao; Lin, Jingqi; Lu, Xiaomei Journal: International journal of pediatric otorhinolaryngology Issue: Volume 99(2017:Aug.) Page Start: 40 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. A novel mutation in the SLC26A4 gene in a Chinese family with non-syndromic hearing loss and enlarged vestibular aqueduct. (April 2018) Authors: Liang, Yuan; Peng, Qi; Wang, Kangwei; Zhu, Pengyuan; Wu, Chunqiu; Rao, Chunbao; Chang, Jiang; Li, Siping; Lu, Xiaomei Journal: International journal of pediatric otorhinolaryngology Issue: Volume 107(2018:Apr.) Page Start: 97 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗