Shen Z - Search Results

1

Application of tandem mass spectrometry in the screening and diagnosis of mucopolysaccharidoses.

Li JW, Mao SJ, Chao YQ, Hu CX, Qian YJ, Dai YL, Huang K, Shen Z, Zou CC. Li JW, et al. Among authors: shen z. Orphanet J Rare Dis. 2024 Apr 29;19(1):179. doi: 10.1186/s13023-024-03195-w. Orphanet J Rare Dis. 2024. PMID: 38685110 Free PMC article. Review.

2

WT1 mutation as a cause of 46 XY DSD and Wilm's tumour: a case report and literature review.

Dai YL, Fu JF, Hong F, Xu S, Shen Z. Dai YL, et al. Among authors: shen z. Acta Paediatr. 2011 Jul;100(7):e39-42. doi: 10.1111/j.1651-2227.2011.02167.x. Epub 2011 Feb 14. Acta Paediatr. 2011. PMID: 21314844 Review.

3

Differences of DNA methylation patterns in the placenta of large for gestational age infant.

Shen Z, Tang Y, Song Y, Shen W, Zou C. Shen Z, et al. Among authors: shen w. Medicine (Baltimore). 2020 Sep 25;99(39):e22389. doi: 10.1097/MD.0000000000022389. Medicine (Baltimore). 2020. PMID: 32991460 Free PMC article.

4

Regulatory roles and mechanisms of alternative RNA splicing in adipogenesis and human metabolic health.

Chao Y, Jiang Y, Zhong M, Wei K, Hu C, Qin Y, Zuo Y, Yang L, Shen Z, Zou C. Chao Y, et al. Among authors: shen z. Cell Biosci. 2021 Apr 1;11(1):66. doi: 10.1186/s13578-021-00581-w. Cell Biosci. 2021. PMID: 33795017 Free PMC article. Review.

5

An unusual presentation of fucosidosis in a Chinese boy: a case report and literature review (childhood fucosidosis).

Mao SJ, Zhao J, Shen Z, Zou CC. Mao SJ, et al. Among authors: shen z. BMC Pediatr. 2022 Jul 11;22(1):403. doi: 10.1186/s12887-022-03414-y. BMC Pediatr. 2022. PMID: 35820891 Free PMC article. Review.

6

Dysregulated adipose tissue expansion and impaired adipogenesis in Prader-Willi syndrome children before obesity-onset.

Chao Y, Gao L, Wang X, Cai Y, Shu Y, Zou X, Qin Y, Hu C, Dai Y, Zhu M, Shen Z, Zou C. Chao Y, et al. Among authors: shen z. Metabolism. 2022 Nov;136:155295. doi: 10.1016/j.metabol.2022.155295. Epub 2022 Aug 22. Metabolism. 2022. PMID: 36007622 Free article.

7

Effects of early recombinant human growth hormone treatment in young Chinese children with Prader-Willi syndrome.

Gao Y, Yang LL, Dai YL, Shen Z, Zhou Q, Zou CC. Gao Y, et al. Among authors: shen z. Orphanet J Rare Dis. 2023 Feb 7;18(1):25. doi: 10.1186/s13023-023-02615-7. Orphanet J Rare Dis. 2023. PMID: 36750945 Free PMC article.

8

Using sno-lncRNAs as potential markers for Prader-Willi syndrome diagnosis.

Sun JR, Yang LZ, Dai YL, Wu H, Li S, Xu YF, Huang Y, Wu H, Shen Z, Zou C, Chen LL. Sun JR, et al. Among authors: shen z. RNA Biol. 2023 Jan;20(1):419-430. doi: 10.1080/15476286.2023.2230406. RNA Biol. 2023. PMID: 37405372 Free PMC article.

9

The influence of genotype makeup on the effectiveness of growth hormone therapy in children with Prader-Willi syndrome.

Zhou Q, Chao YQ, Dai YL, Gao Y, Shen Z, Dong GP, Zou CC. Zhou Q, et al. Among authors: shen z. BMC Pediatr. 2024 Oct 1;24(1):627. doi: 10.1186/s12887-024-05109-y. BMC Pediatr. 2024. PMID: 39354420 Free PMC article.

10

Rapid typing diagnosis and clinical analysis of subtypes A and B of human respiratory syncytial virus in children.

Shen Z, Zhang Y, Li H, Du L. Shen Z, et al. Virol J. 2022 Jan 21;19(1):15. doi: 10.1186/s12985-022-01744-y. Virol J. 2022. PMID: 35062975 Free PMC article.

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