Liu Z - Search Results

1

Accurate detection and grading of pterygium through smartphone by a fusion training model.

Liu Y, Xu C, Wang S, Chen Y, Lin X, Guo S, Liu Z, Wang Y, Zhang H, Guo Y, Huang C, Wu H, Li Y, Chen Q, Hu J, Luo Z, Liu Z. Liu Y, et al. Among authors: liu z. Br J Ophthalmol. 2024 Feb 21;108(3):336-342. doi: 10.1136/bjo-2022-322552. Br J Ophthalmol. 2024. PMID: 36858799 Free PMC article.

2

Chronic Sleep Deprivation Impairs Visual Functions via Oxidative Damage in Mice.

Tang L, Zhang H, Liao Y, Zhou S, Yang Y, Zhang M, Guo Y, Xie T, Chen S, Ouyang W, Lin X, Wang S, Huang C, Zhang M, Zhuang J, Zhao J, Zhang R, Zhang C, Jin Z, Hu J, Liu Z. Tang L, et al. Among authors: liu z. Am J Pathol. 2024 Feb;194(2):307-320. doi: 10.1016/j.ajpath.2023.11.004. Am J Pathol. 2024. PMID: 38245252

3

Guidelines for the application of artificial intelligence in the diagnosis of anterior segment diseases (2023).

Shao Y, Jie Y, Liu ZG; Expert Workgroup of Guidelines for the application of artificial intelligence in the diagnosis of anterior segment diseases (2023); Ophthalmic Imaging and Intelligent Medicine Branch of Chinese Medicine Education Association; Ophthalmology Committee of International Association of Translational Medicine; Chinese Ophthalmic Imaging Study Groups. Shao Y, et al. Int J Ophthalmol. 2023 Sep 18;16(9):1373-1385. doi: 10.18240/ijo.2023.09.03. eCollection 2023. Int J Ophthalmol. 2023. PMID: 37724278 Free PMC article.

4

Fenofibrate suppresses corneal neovascularization by regulating lipid metabolism through PPARα signaling pathway.

Zhou T, Yan K, Zhang Y, Zhu L, Liao Y, Zheng X, Chen Y, Li X, Liu Z, Zhang Z. Zhou T, et al. Among authors: liu z. Front Pharmacol. 2022 Dec 16;13:1000254. doi: 10.3389/fphar.2022.1000254. eCollection 2022. Front Pharmacol. 2022. PMID: 36588740 Free PMC article.

5

Novel Biallelic DNAH1 Variations Cause Multiple Morphological Abnormalities of the Sperm Flagella.

Hu HY, Wei TY, Feng ZK, Li SJ, Zhao R, Yi XL, Hu TL, Zhao H, Li CX, Liu ZG. Hu HY, et al. DNA Cell Biol. 2021 Jun;40(6):833-840. doi: 10.1089/dna.2021.0097. Epub 2021 May 14. DNA Cell Biol. 2021. PMID: 33989052

6

Novel mutation (V505D) of the TGFBI gene found in a Chinese family with lattice corneal dystrophy, type I.

Tian X, Fujiki K, Wang W, Murakami A, Xie P, Kanai A, Liu Z. Tian X, et al. Among authors: liu z. Jpn J Ophthalmol. 2005 Mar-Apr;49(2):84-8. doi: 10.1007/s10384-004-0167-7. Jpn J Ophthalmol. 2005. PMID: 15838722

7

Mutation analysis of CHST6 gene in Chinese patients with macular corneal dystrophy.

Liu Z, Tian X, Iida N, Fujiki K, Xie P, Wang W, Ma Z, Kanai A, Murakami A. Liu Z, et al. Cornea. 2010 Aug;29(8):883-8. doi: 10.1097/ICO.0b013e3181ca2e74. Cornea. 2010. PMID: 20539220

8

Comprehensive strategy improves the genetic diagnosis of different polycystic kidney diseases.

Hu HY, Zhang J, Qiu W, Liang C, Li CX, Wei TY, Feng ZK, Guo Q, Yang K, Liu ZG. Hu HY, et al. J Cell Mol Med. 2021 May 25;25(13):6318-32. doi: 10.1111/jcmm.16608. Online ahead of print. J Cell Mol Med. 2021. PMID: 34032358 Free PMC article.

9

[Analysis of gene mutation in Chinese patients with Reis-Bücklers corneal dystrophy].

Tian X, Liu ZG, Li Q, Li B, Wang W, Xie PY, Fujiki K, Murakami A, Kanai A. Tian X, et al. Zhonghua Yan Ke Za Zhi. 2005 Mar;41(3):239-42. Zhonghua Yan Ke Za Zhi. 2005. PMID: 15840366 Chinese.

10

Compound heterozygous mutations of M1S1 gene in gelatinous droplike corneal dystrophy.

Tian X, Fujiki K, Li Q, Murakami A, Xie P, Kanai A, Wang W, Liu Z. Tian X, et al. Among authors: liu z. Am J Ophthalmol. 2004 Mar;137(3):567-9. doi: 10.1016/j.ajo.2003.08.008. Am J Ophthalmol. 2004. PMID: 15013888

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

83,008 results

Search Page