Jin P - Search Results

1

Case Report: Identification of Maternal Low-Level Mosaicism in the Dystrophin Gene by Droplet Digital Polymerase Chain Reaction.

Jin P, Gao X, Wang M, Qian Y, Yang J, Yang Y, Xu Y, Xu Y, Dong M. Jin P, et al. Front Genet. 2021 Jul 1;12:686993. doi: 10.3389/fgene.2021.686993. eCollection 2021. Front Genet. 2021. PMID: 34276787 Free PMC article.

2

[Genetic analysis of a mosaic case with low proportion mutation of TSC2 gene].

Jin X, Jin P, Yan K, Qian Y, Dong M. Jin X, et al. Among authors: jin p. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2020 Oct 25;49(5):586-590. doi: 10.3785/j.issn.1008-9292.2020.10.06. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2020. PMID: 33210484 Free PMC article. Chinese.

3

Galectin-14 Promotes Trophoblast Migration and Invasion by Upregulating the Expression of MMP-9 and N-Cadherin.

Wang M, Xu Y, Wang P, Xu Y, Jin P, Wu Z, Qian Y, Bai L, Dong M. Wang M, et al. Among authors: jin p. Front Cell Dev Biol. 2021 Mar 16;9:645658. doi: 10.3389/fcell.2021.645658. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 33796532 Free PMC article.

4

Clinical Efficiency of Non-invasive Prenatal Screening for Common Trisomies in Low-Risk and Twin Pregnancies.

Xu Y, Jin P, Lei Y, Qian Y, Xu Y, Wang M, Jin J, Yin Y, Dong M. Xu Y, et al. Among authors: jin p, jin j. Front Genet. 2021 May 10;12:661884. doi: 10.3389/fgene.2021.661884. eCollection 2021. Front Genet. 2021. PMID: 34040638 Free PMC article.

5

Case Report: A Synonymous Mutation in NF1 Located at the Non-canonical Splicing Site Leading to Exon 45 Skipping.

Jin P, Yan K, Ye S, Qian Y, Wu Z, Wang M, Xu Y, Xu Y, Dong M. Jin P, et al. Front Genet. 2021 Nov 19;12:772958. doi: 10.3389/fgene.2021.772958. eCollection 2021. Front Genet. 2021. PMID: 34868260 Free PMC article.

6

Clinical Application of Noninvasive Prenatal Testing for Pregnant Women with Assisted Reproductive Pregnancy.

Jin XX, Xu YF, Ying X, Qian YQ, Jin PZ, Dong MY. Jin XX, et al. Int J Womens Health. 2021 Nov 30;13:1167-1174. doi: 10.2147/IJWH.S337249. eCollection 2021. Int J Womens Health. 2021. PMID: 34876859 Free PMC article.

7

Pro-Inflammatory Signature in Decidua of Recurrent Pregnancy Loss Regardless of Embryonic Chromosomal Abnormalities.

Wu Z, Wang M, Liang G, Jin P, Wang P, Xu Y, Qian Y, Jiang X, Qian J, Dong M. Wu Z, et al. Among authors: jin p. Front Immunol. 2021 Dec 8;12:772729. doi: 10.3389/fimmu.2021.772729. eCollection 2021. Front Immunol. 2021. PMID: 34956198 Free PMC article.

8

Prenatal diagnosis of Walker-Warburg syndrome due to compound mutations in the B3GALNT2 gene.

Wang P, Jin P, Zhu L, Chen M, Qian Y, Zeng W, Wang M, Xu Y, Xu Y, Dong M. Wang P, et al. Among authors: jin p. J Gene Med. 2022 May;24(5):e3417. doi: 10.1002/jgm.3417. Epub 2022 Apr 6. J Gene Med. 2022. PMID: 35338537 Free PMC article.

9

Case Report: Prenatal Diagnosis of Postaxial Polydactyly With Bi-Allelic Variants in Smoothened (SMO).

Fan L, Jin P, Qian Y, Shen G, Shen X, Dong M. Fan L, et al. Among authors: jin p. Front Genet. 2022 Jun 22;13:887082. doi: 10.3389/fgene.2022.887082. eCollection 2022. Front Genet. 2022. PMID: 35812756 Free PMC article.

10

Prenatal diagnosis of trisomy 8 mosaicism, initially identified by cffDNA screening.

Hu J, Yan K, Jin P, Yang Y, Sun Y, Dong M. Hu J, et al. Among authors: jin p. Mol Cytogenet. 2022 Sep 1;15(1):39. doi: 10.1186/s13039-022-00616-y. Mol Cytogenet. 2022. PMID: 36050777 Free PMC article.

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