Delei Li - Search Results

Year	Number of Results
2016	1
2018	2
2019	6
2020	1
2022	1

1

F8 IVS9+5G>A mutation causes moderate haemophilia A.

Li D, Chang W, Tang N, Shen N, Lu Y, Wang X, Hu Q. Li D, et al. Haemophilia. 2019 Mar;25(2):e132-e135. doi: 10.1111/hae.13702. Epub 2019 Feb 12. Haemophilia. 2019. PMID: 30748051 No abstract available.

2

The Preparation of C-Reactive Protein Immunosensor Based on Nano-Mimetic Enzyme Co₃O₄.

Ma Y, Lu M, Deng Y, Bai R, Zhang X, Li D, Zhang K, Hu R, Yang Y. Ma Y, et al. Among authors: li d. J Biomed Nanotechnol. 2018 Jun 1;14(6):1169-1177. doi: 10.1166/jbn.2018.2566. J Biomed Nanotechnol. 2018. PMID: 29843881

3

An Enzyme-Linked Immunosorbent Assay for C-Reactive Protein Based on Gold Nanoparticles@Metal Porphyrin Porous Compound.

Wang M, Meng S, Gu M, Chi K, Ma Y, Deng Y, Zhang X, Li D, Hu R, Yang Y. Wang M, et al. Among authors: li d. J Biomed Nanotechnol. 2019 Oct 1;15(10):2100-2107. doi: 10.1166/jbn.2019.2836. J Biomed Nanotechnol. 2019. PMID: 31462374

4

Clinical evaluation of arthrodesis with Ilizarov external fixator for the treatment of end-stage ankle osteoarthritis: A retrospective study.

Ma N, Li Z, Li D, Hu Y, Sun N. Ma N, et al. Among authors: li d. Medicine (Baltimore). 2020 Dec 24;99(52):e23921. doi: 10.1097/MD.0000000000023921. Medicine (Baltimore). 2020. PMID: 33350796 Free PMC article.

5

2D-porphrinic covalent organic framework-based aptasensor with enhanced photoelectrochemical response for the detection of C-reactive protein.

Zhang X, Chi KN, Li DL, Deng Y, Ma YC, Xu QQ, Hu R, Yang YH. Zhang X, et al. Biosens Bioelectron. 2019 Mar 15;129:64-71. doi: 10.1016/j.bios.2019.01.009. Epub 2019 Jan 15. Biosens Bioelectron. 2019. PMID: 30684856

6

Hypermethylation of the SEPT9 Gene Suggests Significantly Poor Prognosis in Cancer Patients: A Systematic Review and Meta-Analysis.

Shen N, Wang T, Li D, Zhu Y, Xie H, Lu Y. Shen N, et al. Among authors: li d. Front Genet. 2019 Sep 19;10:887. doi: 10.3389/fgene.2019.00887. eCollection 2019. Front Genet. 2019. PMID: 31608117 Free PMC article.

7

Early genetic testing of STK11 is important for management and genetic counseling for Peutz-Jeghers syndrome.

Shen N, Li D, Zhu Y, Xie H, Lu Y. Shen N, et al. Among authors: li d. Dig Liver Dis. 2019 Sep;51(9):1353-1355. doi: 10.1016/j.dld.2019.06.003. Epub 2019 Jun 28. Dig Liver Dis. 2019. PMID: 31257171 No abstract available.

8

Storm surge variation along the coast of the Bohai Sea.

Feng J, Li D, Li Y, Liu Q, Wang A. Feng J, et al. Among authors: li d. Sci Rep. 2018 Jul 27;8(1):11309. doi: 10.1038/s41598-018-29712-z. Sci Rep. 2018. PMID: 30054548 Free PMC article.

9

Whole-exome sequencing identifies a novel missense variant within LOXHD1 causing rare hearing loss in a Chinese family.

Shen N, Wang T, Li D, Liu A, Lu Y. Shen N, et al. Among authors: li d. BMC Med Genet. 2019 Feb 13;20(1):30. doi: 10.1186/s12881-019-0758-2. BMC Med Genet. 2019. PMID: 30760222 Free PMC article.

10

Metal-Organic Framework Nanomaterials as Novel Signal Probes for Electron Transfer Mediated Ultrasensitive Electrochemical Immunoassay.

Liu TZ, Hu R, Zhang X, Zhang KL, Liu Y, Zhang XB, Bai RY, Li D, Yang YH. Liu TZ, et al. Among authors: li d. Anal Chem. 2016 Dec 20;88(24):12516-12523. doi: 10.1021/acs.analchem.6b04191. Epub 2016 Dec 1. Anal Chem. 2016. PMID: 28193012

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