Wei W - Search Results

1

Prenatal diagnosis of Duchenne muscular dystrophy in 131 Chinese families with dystrophinopathy.

Wang H, Xu Y, Liu X, Wang L, Jiang W, Xiao B, Wei W, Chen Y, Ye W, Ji X. Wang H, et al. Among authors: wei w. Prenat Diagn. 2017 Apr;37(4):356-364. doi: 10.1002/pd.5019. Epub 2017 Mar 6. Prenat Diagn. 2017. PMID: 28181689

2

Novel noncontiguous duplications identified with a comprehensive mutation analysis in the DMD gene by DMD gene-targeted sequencing.

Xu Y, Wang H, Xiao B, Wei W, Liu Y, Ye H, Ying X, Chen Y, Liu X, Ji X, Sun Y. Xu Y, et al. Among authors: wei w. Gene. 2018 Mar 1;645:113-118. doi: 10.1016/j.gene.2017.12.037. Epub 2017 Dec 19. Gene. 2018. PMID: 29273555

3

[Diagnosis of two cases from one family with Joubert syndrome caused by novel mutations of TCTN1 gene by whole exome sequencing].

Wang H, Jiang W, Dai M, Xiao B, Xu Y, Sun Y, Liu Y, Ying X, Sun Y, Wei W, Ji X. Wang H, et al. Among authors: wei w. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jul 10;36(7):686-689. doi: 10.3760/cma.j.issn.1003-9406.2019.07.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31302911 Chinese.

4

A Recurrent Variant in MAGEL2 in Five Siblings with Severe Respiratory Disturbance after Birth.

Xiao B, Ji X, Wei W, Hui Y, Sun Y. Xiao B, et al. Among authors: wei w. Mol Syndromol. 2020 Jan;10(5):286-290. doi: 10.1159/000501376. Epub 2019 Jul 5. Mol Syndromol. 2020. PMID: 32021601 Free PMC article.

5

Marked yield of re-evaluating phenotype and exome/target sequencing data in 33 individuals with intellectual disabilities.

Xiao B, Qiu W, Ji X, Liu X, Huang Z, Liu H, Fan Y, Xu Y, Liu Y, Yie H, Wei W, Yan H, Gong Z, Shen L, Sun Y. Xiao B, et al. Among authors: wei w. Am J Med Genet A. 2018 Jan;176(1):107-115. doi: 10.1002/ajmg.a.38542. Epub 2017 Nov 21. Am J Med Genet A. 2018. PMID: 29159939

6

Biallelic UNC80 mutations caused infantile hypotonia with psychomotor retardation and characteristic facies 2 in two Chinese patients with variable phenotypes.

He Y, Ji X, Yan H, Ye X, Liu Y, Wei W, Xiao B, Sun Y. He Y, et al. Among authors: wei w. Gene. 2018 Jun 20;660:13-17. doi: 10.1016/j.gene.2018.03.063. Epub 2018 Mar 20. Gene. 2018. PMID: 29572195

7

[Genotypic and phenotypic analysis of a patient with de novo partial monosomy 18p and partial trisomy 18q].

Xiao B, Ji X, Ye H, Liu Y, Cao Y, Sun Y, Wei W, Qiu W. Xiao B, et al. Among authors: wei w. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 May 10;36(5):484-487. doi: 10.3760/cma.j.issn.1003-9406.2019.05.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31030439 Chinese.

8

A comparative study of systemic subantimicrobial and topical treatment of minocycline in experimental periodontitis of rats.

Xu Y, Wei W. Xu Y, et al. Among authors: wei w. Arch Oral Biol. 2006 Sep;51(9):794-803. doi: 10.1016/j.archoralbio.2006.03.018. Epub 2006 May 18. Arch Oral Biol. 2006. PMID: 16712777

9

EMC3 coordinates surfactant protein and lipid homeostasis required for respiration.

Tang X, Snowball JM, Xu Y, Na CL, Weaver TE, Clair G, Kyle JE, Zink EM, Ansong C, Wei W, Huang M, Lin X, Whitsett JA. Tang X, et al. Among authors: wei w. J Clin Invest. 2017 Dec 1;127(12):4314-4325. doi: 10.1172/JCI94152. Epub 2017 Oct 30. J Clin Invest. 2017. PMID: 29083321 Free PMC article.

10

Hierarchical Nanostructures and Self-Assemblies in Smectic-Nematic Liquid Crystalline Diblock Copolymers.

Wei W, Liu Y, Xiong H. Wei W, et al. ACS Macro Lett. 2014 Sep 16;3(9):892-895. doi: 10.1021/mz500460j. Epub 2014 Aug 27. ACS Macro Lett. 2014. PMID: 35596355

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