Zhou DZ - Search Results

1

The effect of blastomere loss during frozen embryo transfer on the transcriptome of offspring's umbilical cord blood.

Wu YT, Dong ZH, Li C, Zhou DZ, Zhang JY, Wu Y, Xu JJ, Wang Y, Ye XQ, Sheng JZ, Wang L, Huang HF. Wu YT, et al. Among authors: zhou dz. Mol Biol Rep. 2020 Nov;47(11):8407-8417. doi: 10.1007/s11033-020-05878-6. Epub 2020 Oct 17. Mol Biol Rep. 2020. PMID: 33068229

2

A genome-wide association study identifies a locus on TERT for mean telomere length in Han Chinese.

Liu Y, Cao L, Li Z, Zhou D, Liu W, Shen Q, Wu Y, Zhang D, Hu X, Wang T, Ye J, Weng X, Zhang H, Zhang D, Zhang Z, Liu F, He L, Shi Y. Liu Y, et al. PLoS One. 2014 Jan 21;9(1):e85043. doi: 10.1371/journal.pone.0085043. eCollection 2014. PLoS One. 2014. PMID: 24465473 Free PMC article.

3

Basonuclin 1 deficiency is a cause of primary ovarian insufficiency.

Zhang D, Liu Y, Zhang Z, Lv P, Liu Y, Li J, Wu Y, Zhang R, Huang Y, Xu G, Qian Y, Qian Y, Chen S, Xu C, Shen J, Zhu L, Chen K, Zhu B, Ye X, Mao Y, Bo X, Zhou C, Wang T, Chen D, Yang W, Tan Y, Song Y, Zhou D, Sheng J, Gao H, Zhu Y, Li M, Wu L, He L, Huang H. Zhang D, et al. Hum Mol Genet. 2018 Nov 1;27(21):3787-3800. doi: 10.1093/hmg/ddy261. Hum Mol Genet. 2018. PMID: 30010909

4

Recurrent human 16p11.2 microdeletions in type I Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome patients in Chinese Han population.

Su K, Liu H, Ye X, Jin H, Xie Z, Yang C, Zhou D, Huang H, Wu Y. Su K, et al. Mol Genet Genomic Med. 2024 Jan;12(1):e2280. doi: 10.1002/mgg3.2280. Epub 2023 Oct 3. Mol Genet Genomic Med. 2024. PMID: 37789575 Free PMC article.

5

Incidence, management and mortality of acute hypoxemic respiratory failure and acute respiratory distress syndrome from a prospective study of Chinese paediatric intensive care network.

Hu X, Qian S, Xu F, Huang B, Zhou D, Wang Y, Li C, Fan X, Lu Z, Sun B; Chinese Collaborative Study Group for Pediatric Respiratory Failure. Hu X, et al. Acta Paediatr. 2010 May;99(5):715-721. doi: 10.1111/j.1651-2227.2010.01685.x. Epub 2010 Jan 21. Acta Paediatr. 2010. PMID: 20096024

6

A Common variant near the melanocortin 4 receptor is associated with low-density lipoprotein cholesterol and total cholesterol in the Chinese Han population.

Tao L, Zhang Z, Chen Z, Zhou D, Li W, Kan M, Zhang D, He L, Huang G, Liu Y. Tao L, et al. Mol Biol Rep. 2012 Jun;39(6):6487-93. doi: 10.1007/s11033-012-1476-4. Epub 2012 Feb 17. Mol Biol Rep. 2012. PMID: 22350153

7

Elevated serum transaminase activities were associated with increased serum levels of iron regulatory hormone hepcidin and hyperferritinemia risk.

An P, Wang H, Wu Q, Guo X, Wu A, Zhang Z, Zhang D, Xu X, Mao Q, Shen X, Zhang L, Xiong Z, He L, Liu Y, Min J, Zhou D, Wang F. An P, et al. Sci Rep. 2015 Aug 20;5:13106. doi: 10.1038/srep13106. Sci Rep. 2015. PMID: 26290281 Free PMC article.

8

Comparative transcriptome analysis reveals that the extracellular matrix receptor interaction contributes to the venous metastases of hepatocellular carcinoma.

Zhang H, Ye J, Weng X, Liu F, He L, Zhou D, Liu Y. Zhang H, et al. Cancer Genet. 2015 Oct;208(10):482-91. doi: 10.1016/j.cancergen.2015.06.002. Epub 2015 Jun 18. Cancer Genet. 2015. PMID: 26271415

9

Epigenome-wide DNA methylation profiling of portal vein tumor thrombosis (PVTT) tissues in hepatocellular carcinoma patients.

Fan X, Li Y, Yi X, Chen G, Jin S, Dai Y, Cui B, Dai B, Lin H, Zhou D. Fan X, et al. Neoplasia. 2020 Nov;22(11):630-643. doi: 10.1016/j.neo.2020.09.007. Epub 2020 Oct 13. Neoplasia. 2020. PMID: 33059309 Free PMC article.

10

A novel heterozygous missense variant of the ARID4A gene identified in Han Chinese families with schizophrenia-diagnosed siblings that interferes with DNA-binding activity.

Ren D, Wei X, Lin L, Yuan F, Bi Y, Guo Z, Liu L, Ji L, Yang X, Han K, Yang F, Wu X, Li X, Yi Z, Xu Y, Cai C, Wang P, Li W, He L, Zhou D, Yu T, Shi Y, Lu Q, He G. Ren D, et al. Mol Psychiatry. 2022 Jun;27(6):2777-2786. doi: 10.1038/s41380-022-01530-w. Epub 2022 Apr 1. Mol Psychiatry. 2022. PMID: 35365808

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