Lu C - Search Results

1

Molecular analysis of inherited cardiomyopathy using next generation semiconductor sequencing technologies.

Lu C, Wu W, Liu F, Yang K, Li J, Liu Y, Wang R, Si N, Gao P, Liu Y, Zhang S, Zhang X. Lu C, et al. J Transl Med. 2018 Aug 30;16(1):241. doi: 10.1186/s12967-018-1605-5. J Transl Med. 2018. PMID: 30165862 Free PMC article.

2

Novel Phenotype-Genotype Correlations of Restrictive Cardiomyopathy With Myosin-Binding Protein C (MYBPC3) Gene Mutations Tested by Next-Generation Sequencing.

Wu W, Lu CX, Wang YN, Liu F, Chen W, Liu YT, Han YC, Cao J, Zhang SY, Zhang X. Wu W, et al. J Am Heart Assoc. 2015 Jul 10;4(7):e001879. doi: 10.1161/JAHA.115.001879. J Am Heart Assoc. 2015. PMID: 26163040 Free PMC article.

3

[Detection of pathogenic mutations in Marfan syndrome by targeted next-generation semiconductor sequencing].

Lu C, Wu W, Xiao J, Meng Y, Zhang S, Zhang X. Lu C, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Jun;30(3):301-4. doi: 10.3760/cma.j.issn.1003-9406.2013.03.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23744319 Chinese.

4

Application of next-generation sequencing to screen for pathogenic mutations in 123 unrelated Chinese patients with Marfan syndrome or a related disease.

Li J, Lu C, Wu W, Liu Y, Wang R, Si N, Meng X, Zhang S, Zhang X. Li J, et al. Among authors: lu c. Sci China Life Sci. 2019 Dec;62(12):1630-1637. doi: 10.1007/s11427-018-9491-8. Epub 2019 May 15. Sci China Life Sci. 2019. PMID: 31098894

5

Restrictive Cardiomyopathy Resulting from a Troponin I Type 3 Mutation in a Chinese Family.

Ruan YP, Lu CX, Zhao XY, Liang RJ, Lian H, Routledge M, Wu W, Zhang X, Fan ZJ. Ruan YP, et al. Chin Med Sci J. 2016 Mar 20;31(1):1-7. doi: 10.1016/s1001-9294(16)30015-3. Chin Med Sci J. 2016. PMID: 28031081

6

Next generation sequencing as a rapid molecular diagnosis for Marfan syndrome in a Chinese family with mutations in the fibrillin-1 gene.

Xiao Y, Liu Y, Yang K, Yang Y, Zhou X, Lu C, Xiao J, Liu F, Zhang X. Xiao Y, et al. Among authors: lu c. Clin Chim Acta. 2015 Jan 15;439:58-60. doi: 10.1016/j.cca.2014.09.034. Epub 2014 Oct 7. Clin Chim Acta. 2015. PMID: 25304743 No abstract available.

7

Gross deletions in FBN1 results in variable phenotypes of Marfan syndrome.

Li J, Wu W, Lu C, Liu Y, Wang R, Si N, Liu F, Zhou J, Zhang S, Zhang X. Li J, et al. Among authors: lu c. Clin Chim Acta. 2017 Nov;474:54-59. doi: 10.1016/j.cca.2017.08.023. Epub 2017 Aug 24. Clin Chim Acta. 2017. PMID: 28842177

8

Keratin 5-Cre-driven deletion of Ncstn in an acne inversa-like mouse model leads to a markedly increased IL-36a and Sprr2 expression.

Yang J, Wang L, Huang Y, Liu K, Lu C, Si N, Wang R, Liu Y, Zhang X. Yang J, et al. Among authors: lu c. Front Med. 2020 Jun;14(3):305-317. doi: 10.1007/s11684-019-0722-8. Epub 2019 Dec 28. Front Med. 2020. PMID: 31884525

9

A novel frameshift mutation of epithelial sodium channel β-subunit leads to Liddle syndrome in an isolated case.

Yang KQ, Lu CX, Xiao Y, Liu YX, Jiang XJ, Zhang X, Zhou XL. Yang KQ, et al. Clin Endocrinol (Oxf). 2015 Apr;82(4):611-4. doi: 10.1111/cen.12650. Epub 2015 Jan 6. Clin Endocrinol (Oxf). 2015. PMID: 25378078

10

A Novel Splicing Mutation Identified in a Chinese Family with X-linked Alport Syndrome Using Targeted Next-Generation Sequencing.

Chen C, Lu CX, Wang Q, Cao LH, Luo Y, Zhang X. Chen C, et al. Among authors: lu cx. Genet Test Mol Biomarkers. 2016 Apr;20(4):203-7. doi: 10.1089/gtmb.2015.0248. Epub 2016 Feb 11. Genet Test Mol Biomarkers. 2016. PMID: 26866448

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