Tang C - Search Results

1

De Novo ring chromosome 11 and non-reciprocal translocation of 11p15.3-pter to 21qter in a patient with congenital heart disease.

Peng Y, Ma R, Zhou Y, Xia Y, Wen J, Zhang Y, Guo R, Li H, Pan Q, Zhang R, Tang C, Liang D, Wu L. Peng Y, et al. Among authors: tang c. Mol Cytogenet. 2015 Nov 9;8:88. doi: 10.1186/s13039-015-0191-y. eCollection 2015. Mol Cytogenet. 2015. PMID: 26557157 Free PMC article.

2

Pathogenic connexin-31 forms constitutively active hemichannels to promote necrotic cell death.

Chi J, Li L, Liu M, Tan J, Tang C, Pan Q, Wang D, Zhang Z. Chi J, et al. Among authors: tang c. PLoS One. 2012;7(2):e32531. doi: 10.1371/journal.pone.0032531. Epub 2012 Feb 29. PLoS One. 2012. PMID: 22393412 Free PMC article.

3

Pathogenic Cx31 is un/misfolded to cause skin abnormality via a Fos/JunB-mediated mechanism.

Tang C, Chen X, Chi J, Yang D, Liu S, Liu M, Pan Q, Fan J, Wang D, Zhang Z. Tang C, et al. Hum Mol Genet. 2015 Nov 1;24(21):6054-65. doi: 10.1093/hmg/ddv317. Epub 2015 Aug 6. Hum Mol Genet. 2015. PMID: 26251042

4

Clinical and molecular characterization of 12 prenatal cases of Cri-du-chat syndrome.

Peng Y, Pang J, Hu J, Jia Z, Xi H, Ma N, Yang S, Liu J, Huang X, Tang C, Wang H. Peng Y, et al. Among authors: tang c. Mol Genet Genomic Med. 2020 Aug;8(8):e1312. doi: 10.1002/mgg3.1312. Epub 2020 Jun 4. Mol Genet Genomic Med. 2020. PMID: 32500674 Free PMC article.

5

Whole genome sequencing reveals translocation breakpoints disrupting TP63 gene underlying split hand/foot malformation in a Chinese family.

Peng Y, Yang S, Xi H, Hu J, Jia Z, Pang J, Liu J, Yu W, Tang C, Wang H. Peng Y, et al. Among authors: tang c. Mol Genet Genomic Med. 2021 Mar;9(3):e1604. doi: 10.1002/mgg3.1604. Epub 2021 Jan 20. Mol Genet Genomic Med. 2021. PMID: 33471964 Free PMC article.

6

Case Report: Novel NIPBL Variants Cause Cornelia de Lange Syndrome in Chinese Patients.

Peng Y, Liang C, Xi H, Yang S, Hu J, Pang J, Liu J, Luo Y, Tang C, Xie W, Wang H. Peng Y, et al. Among authors: tang c. Front Genet. 2021 Jul 30;12:699894. doi: 10.3389/fgene.2021.699894. eCollection 2021. Front Genet. 2021. PMID: 34394191 Free PMC article.

7

Whole Exome Sequencing Analysis in Fetal Skeletal Dysplasia Detected by Ultrasonography: An Analysis of 38 Cases.

Peng Y, Yang S, Huang X, Pang J, Liu J, Hu J, Shen X, Tang C, Wang H. Peng Y, et al. Among authors: tang c. Front Genet. 2021 Sep 10;12:728544. doi: 10.3389/fgene.2021.728544. eCollection 2021. Front Genet. 2021. PMID: 34567078 Free PMC article.

8

Nicotinamide reduces renal interstitial fibrosis by suppressing tubular injury and inflammation.

Zheng M, Cai J, Liu Z, Shu S, Wang Y, Tang C, Dong Z. Zheng M, et al. Among authors: tang c. J Cell Mol Med. 2019 Jun;23(6):3995-4004. doi: 10.1111/jcmm.14285. Epub 2019 Apr 16. J Cell Mol Med. 2019. PMID: 30993884 Free PMC article.

9

Hypoxia, HIF, and Associated Signaling Networks in Chronic Kidney Disease.

Liu J, Wei Q, Guo C, Dong G, Liu Y, Tang C, Dong Z. Liu J, et al. Among authors: tang c. Int J Mol Sci. 2017 Apr 30;18(5):950. doi: 10.3390/ijms18050950. Int J Mol Sci. 2017. PMID: 28468297 Free PMC article. Review.

10

PKCδ promotes high glucose induced renal tubular oxidative damage via regulating activation and translocation of p66Shc.

Song P, Yang S, Xiao L, Xu X, Tang C, Yang Y, Ma M, Zhu J, Liu F, Sun L. Song P, et al. Among authors: tang c. Oxid Med Cell Longev. 2014;2014:746531. doi: 10.1155/2014/746531. Epub 2014 Oct 13. Oxid Med Cell Longev. 2014. Retraction in: Oxid Med Cell Longev. 2022 Feb 23;2022:9826078. doi: 10.1155/2022/9826078 PMID: 25371776 Free PMC article. Retracted.

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