Sun K - Search Results

1

LARP7 Protects Against Heart Failure by Enhancing Mitochondrial Biogenesis.

Yu H, Zhang F, Yan P, Zhang S, Lou Y, Geng Z, Li Z, Zhang Y, Xu Y, Lu Y, Chen C, Wang D, Zhu W, Hu X, Wang J, Zhuang T, Zhang Y, Wu G, Liu J, Zeng C, Pu WT, Sun K, Zhang B. Yu H, et al. Among authors: sun k. Circulation. 2021 May 18;143(20):2007-2022. doi: 10.1161/CIRCULATIONAHA.120.050812. Epub 2021 Mar 5. Circulation. 2021. PMID: 33663221

2

[Frequency of 22q11 deletions in children with isolated conotruncal defects].

Shen L, Xu YJ, Zhao PJ, Sun K. Shen L, et al. Among authors: sun k. Zhongguo Dang Dai Er Ke Za Zhi. 2009 Jan;11(1):25-8. Zhongguo Dang Dai Er Ke Za Zhi. 2009. PMID: 19149917 Chinese.

3

A potential relationship among beta-defensins haplotype, SOX7 duplication and cardiac defects.

Long F, Wang X, Fang S, Xu Y, Sun K, Chen S, Xu R. Long F, et al. Among authors: sun k. PLoS One. 2013 Aug 29;8(8):e72515. doi: 10.1371/journal.pone.0072515. eCollection 2013. PLoS One. 2013. PMID: 24009689 Free PMC article.

4

Exome sequencing identifies a novel MYH7 p.G407C mutation responsible for familial hypertrophic cardiomyopathy.

Guo Q, Xu Y, Wang X, Guo Y, Xu R, Sun K, Chen S. Guo Q, et al. Among authors: sun k. DNA Cell Biol. 2014 Oct;33(10):699-704. doi: 10.1089/dna.2014.2483. Epub 2014 Jun 25. DNA Cell Biol. 2014. PMID: 24963656 Free PMC article.

5

Novel TBX1 loss-of-function mutation causes isolated conotruncal heart defects in Chinese patients without 22q11.2 deletion.

Xu YJ, Chen S, Zhang J, Fang SH, Guo QQ, Wang J, Fu QH, Li F, Xu R, Sun K. Xu YJ, et al. Among authors: sun k. BMC Med Genet. 2014 Jul 6;15:78. doi: 10.1186/1471-2350-15-78. BMC Med Genet. 2014. PMID: 24998776 Free PMC article.

6

Duplication and deletion of CFC1 associated with heterotaxy syndrome.

Cao R, Long F, Wang L, Xu Y, Guo Y, Li F, Chen S, Sun K, Xu R. Cao R, et al. Among authors: sun k. DNA Cell Biol. 2015 Feb;34(2):101-6. doi: 10.1089/dna.2014.2616. Epub 2014 Nov 25. DNA Cell Biol. 2015. PMID: 25423076 Free PMC article.

7

Identification of candidate genes for congenital heart defects on proximal chromosome 8p.

Li T, Liu C, Xu Y, Guo Q, Chen S, Sun K, Xu R. Li T, et al. Among authors: sun k. Sci Rep. 2016 Nov 3;6:36133. doi: 10.1038/srep36133. Sci Rep. 2016. PMID: 27808268 Free PMC article.

8

Mutation Screening of Gata4 Gene in CTD Patients Within Chinese Han Population.

Liu Y, Li B, Xu Y, Sun K. Liu Y, et al. Among authors: sun k. Pediatr Cardiol. 2017 Mar;38(3):506-512. doi: 10.1007/s00246-016-1542-0. Epub 2017 Feb 4. Pediatr Cardiol. 2017. PMID: 28161810

9

A 3 base pair deletion in TBX1 leads to reduced protein expression and transcriptional activity.

Xu Y, Fang S, Zhang E, Pu T, Cao R, Fu Q, Li F, Chen S, Sun K, Xu R. Xu Y, et al. Among authors: sun k. Sci Rep. 2017 Mar 8;7:44165. doi: 10.1038/srep44165. Sci Rep. 2017. PMID: 28272434 Free PMC article. Clinical Trial.

10

VEGF amplifies transcription through ETS1 acetylation to enable angiogenesis.

Chen J, Fu Y, Day DS, Sun Y, Wang S, Liang X, Gu F, Zhang F, Stevens SM, Zhou P, Li K, Zhang Y, Lin RZ, Smith LEH, Zhang J, Sun K, Melero-Martin JM, Han Z, Park PJ, Zhang B, Pu WT. Chen J, et al. Among authors: sun k, sun y. Nat Commun. 2017 Aug 29;8(1):383. doi: 10.1038/s41467-017-00405-x. Nat Commun. 2017. PMID: 28851877 Free PMC article.

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