Wu W - Search Results

1

A novel cataract-causing mutation Ile82Met of γA crystallin trends to aggregate with unfolding intermediate.

Xu W, Xu J, Shi C, Wu J, Wang H, Wu W, Chen X, Hu L. Xu W, et al. Among authors: wu w, wu j. Int J Biol Macromol. 2022 Jun 30;211:357-367. doi: 10.1016/j.ijbiomac.2022.04.205. Epub 2022 May 2. Int J Biol Macromol. 2022. PMID: 35513103

2

Pathogenic mechanism of congenital cataract caused by the CRYBA1/A3-G91del variant and related intervention strategies.

Xu J, Wang H, Wu C, Wang A, Wu W, Xu J, Luo C, Ni S, Yao K, Chen X. Xu J, et al. Among authors: wu w, wu c. Int J Biol Macromol. 2021 Oct 31;189:44-52. doi: 10.1016/j.ijbiomac.2021.08.111. Epub 2021 Aug 19. Int J Biol Macromol. 2021. PMID: 34419537

3

Cataract-causing mutation R48C increases γA-crystallin susceptibility to oxidative stress and ultraviolet radiation.

Wu J, Xu W, Wu W, Xu J, Zheng S, Shentu X, Chen X. Wu J, et al. Among authors: wu w. Int J Biol Macromol. 2022 Jan 1;194:688-694. doi: 10.1016/j.ijbiomac.2021.11.113. Epub 2021 Nov 23. Int J Biol Macromol. 2022. PMID: 34826455

4

Cataract-Causing S93R Mutant Destabilized Structural Conformation of βB1 Crystallin Linking With Aggregates Formation and Cellular Viability.

Ren L, Hu L, Zhang Y, Liu J, Xu W, Wu W, Xu J, Chen X, Yao K, Yu Y. Ren L, et al. Among authors: wu w. Front Mol Biosci. 2022 Mar 14;9:844719. doi: 10.3389/fmolb.2022.844719. eCollection 2022. Front Mol Biosci. 2022. PMID: 35359596 Free PMC article.

5

Heterozygous variants c.781G>A and c.1066dup of serine protease 56 cause familial nanophthalmos by impairing serine-type endopeptidase activity.

Wu W, Xu J, Yin H, Fu C, Yao K, Chen X. Wu W, et al. Br J Ophthalmol. 2023 Nov;107(11):1750-1756. doi: 10.1136/bjophthalmol-2021-320909. Epub 2022 Apr 5. Br J Ophthalmol. 2023. PMID: 35383051

6

[Clinical evaluation on the coaxial 1.8 mm microincision cataract surgery].

Yao K, Wang W, Wu W, Tang XJ, Li ZC, Jin CF. Yao K, et al. Among authors: wu w. Zhonghua Yan Ke Za Zhi. 2011 Oct;47(10):903-7. Zhonghua Yan Ke Za Zhi. 2011. PMID: 22321500 Clinical Trial. Chinese.

7

A novel HNF4A mutation identified in a child with maturity onset diabetes of the young.

Zhu MQ, Dai YL, Chen XF, Lin H, Yuan JN, Huang K, Wu W, Fu JF, Dong GP. Zhu MQ, et al. Among authors: wu w. World J Pediatr. 2022 Nov;18(11):778-780. doi: 10.1007/s12519-022-00512-w. Epub 2022 Feb 3. World J Pediatr. 2022. PMID: 35118593 No abstract available.

8

tRNA methyltransferase 10 homologue A (TRMT10A) mutation in a Chinese patient with diabetes, insulin resistance, intellectual deficiency and microcephaly.

Lin H, Zhou X, Chen X, Huang K, Wu W, Fu J, Li Y, Polychronakos C, Dong GP. Lin H, et al. Among authors: wu w. BMJ Open Diabetes Res Care. 2020 Oct;8(1):e001601. doi: 10.1136/bmjdrc-2020-001601. BMJ Open Diabetes Res Care. 2020. PMID: 33067246 Free PMC article.

9

A novel missense variant in TRAPPC2 causes X-linked spondyloepiphyseal dysplasia tarda: A case report.

Zhang L, Wang J, Dong G, Wu D, Wu W. Zhang L, et al. Among authors: wu w, wu d. Medicine (Baltimore). 2021 Mar 19;100(11):e25169. doi: 10.1097/MD.0000000000025169. Medicine (Baltimore). 2021. PMID: 33726005 Free PMC article.

10

[A novel homozygous mutation in PLA2G6 gene causes infantile neuroaxonal dystrophy in a case].

Wang J, Wu W, Chen X, Zhang L, Wang X, Dong G. Wang J, et al. Among authors: wu w. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Feb;33(1):64-7. doi: 10.3760/cma.j.issn.1003-9406.2016.01.016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 26829737 Chinese.

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