Wang YP - Search Results

1

Whole exome sequencing identified a novel compound heterozygous variation in COL7A1 gene causing dystrophic epidermolysis bullosa.

Cui LM, Jiang JY, Hu NN, Zou HE, Zhao BZ, Han CY, Yang K, Wang YP, Xing HX. Cui LM, et al. Among authors: wang yp. Mol Genet Genomic Med. 2022 May;10(5):e1907. doi: 10.1002/mgg3.1907. Epub 2022 Feb 28. Mol Genet Genomic Med. 2022. PMID: 35225434 Free PMC article.

2

Investigation of an inherited PCGF2: p.Pro65Leu mutation causing Turnpenny-Fry syndrome.

Qi KY, Shen M, Yang K, Yan YS, Wu J, Wang YP, Yin CH. Qi KY, et al. Among authors: wang yp. Am J Transl Res. 2022 Aug 15;14(8):5591-5597. eCollection 2022. Am J Transl Res. 2022. PMID: 36105049 Free PMC article.

3

Assessment of a novel variation in DHODH gene causing Miller syndrome: The first report in Chinese population.

Yang K, Fu LM, Chu XY, Zhang J, Chen WQ, Yan YS, Wang YP, Zhang DL, Yin CH, Guo Q. Yang K, et al. Among authors: wang yp. Mol Genet Genomic Med. 2023 Jul;11(7):e2186. doi: 10.1002/mgg3.2186. Epub 2023 Apr 30. Mol Genet Genomic Med. 2023. PMID: 37120754 Free PMC article.

4

NTRK1 knockdown induces mouse cognitive impairment and hippocampal neuronal damage through mitophagy suppression via inactivating the AMPK/ULK1/FUNDC1 pathway.

Yang K, Wu J, Li S, Wang S, Zhang J, Wang YP, Yan YS, Hu HY, Xiong MF, Bai CB, Sun YQ, Chen WQ, Zeng Y, Yuan JL, Yin CH. Yang K, et al. Among authors: wang s, wang yp. Cell Death Discov. 2023 Oct 31;9(1):404. doi: 10.1038/s41420-023-01685-7. Cell Death Discov. 2023. PMID: 37907480 Free PMC article.

5

Identify gestational diabetes mellitus by deep learning model from cell-free DNA at the early gestation stage.

Wang Y, Sun P, Zhao Z, Yan Y, Yue W, Yang K, Liu R, Huang H, Wang Y, Chen Y, Li N, Feng H, Li J, Liu Y, Chen Y, Shen B, Zhao L, Yin C. Wang Y, et al. Brief Bioinform. 2023 Nov 22;25(1):bbad492. doi: 10.1093/bib/bbad492. Brief Bioinform. 2023. PMID: 38168840 Free PMC article.

6

SGMS1 facilitates osteogenic differentiation of MSCs and strengthens osteogenesis-angiogenesis coupling by modulating Cer/PP2A/Akt pathway.

Yang K, Luan YY, Wang S, Yan YS, Wang YP, Wu J, Sun YQ, Zhang J, Chen WQ, Xiang YL, Li ZL, Zhang DL, Yin CH. Yang K, et al. Among authors: wang s, wang yp. iScience. 2024 Mar 5;27(4):109358. doi: 10.1016/j.isci.2024.109358. eCollection 2024 Apr 19. iScience. 2024. PMID: 38544565 Free PMC article.

7

[Analysis of the efficacy of non-invasive prenatal testing in the system of prenatal screening and diagnosis].

Wang Y, Li S, Wang W, Wang X, Li L, Yin C. Wang Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Apr 10;38(4):309-312. doi: 10.3760/cma.j.cn511374-20200401-00230. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 33834453 Chinese.

8

[Exploration of the process of prenatal screening and diagnosis for women with advanced maternal age based on results of 351 cases of fetal chromosomal abnormalities].

Dong Y, Zhang M, Wang Y, Li S, Guan X, Lyu W. Dong Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jun 10;36(6):538-542. doi: 10.3760/cma.j.issn.1003-9406.2019.06.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31055800 Chinese.

9

Cell-free DNA screening for sex chromosome aneuploidies by non-invasive prenatal testing in maternal plasma.

Wang Y, Li S, Wang W, Dong Y, Zhang M, Wang X, Yin C. Wang Y, et al. Mol Cytogenet. 2020 Mar 12;13:10. doi: 10.1186/s13039-020-0478-5. eCollection 2020. Mol Cytogenet. 2020. PMID: 32190123 Free PMC article.

10

[Progress of research on clinical use of non-invasive prenatal screening for special groups of pregnant women].

Yan Y, Wang Y, Liu Y, Yin C. Yan Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Jul 10;38(7):694-698. doi: 10.3760/cma.j.cn511374-20201103-00772. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34247381 Chinese.

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