Jiazhen Chang - Search Results

Year	Number of Results
2014	1
2015	4
2018	1
2019	1
2020	1
2021	1
2022	1
2023	5
2024	2

1

Taxifolin attenuates neuroinflammation and microglial pyroptosis via the PI3K/Akt signaling pathway after spinal cord injury.

Hu Z, Xuan L, Wu T, Jiang N, Liu X, Chang J, Wang T, Han N, Tian X. Hu Z, et al. Among authors: chang j. Int Immunopharmacol. 2023 Jan;114:109616. doi: 10.1016/j.intimp.2022.109616. Epub 2022 Dec 22. Int Immunopharmacol. 2023. PMID: 36700780

2

Expression and localization of HSD17B13 along mouse urinary tract.

Zhang H, Chang J, Dai Z, Wang Q, Qiao R, Huang Y, Ma B, Jiang J, Zhu C, Su W, Zhang X, Guan Y. Zhang H, et al. Among authors: chang j. Am J Physiol Renal Physiol. 2024 May 23. doi: 10.1152/ajprenal.00069.2024. Online ahead of print. Am J Physiol Renal Physiol. 2024. PMID: 38779753

3

Factors associated with test failure in pregnant women undergoing cell-free DNA-based testing for fetal trisomy.

Chang J, Qi Q, Zhou X, Jiang Y, Hao N, Liu J. Chang J, et al. J Med Screen. 2021 Dec;28(4):411-418. doi: 10.1177/09691413211009940. Epub 2021 Apr 22. J Med Screen. 2021. PMID: 33884933

4

High levels of circulating cell-free DNA are a biomarker of active SLE.

Xu Y, Song Y, Chang J, Zhou X, Qi Q, Tian X, Li M, Zeng X, Xu M, Zhang W, Cram DS, Liu J. Xu Y, et al. Among authors: chang j. Eur J Clin Invest. 2018 Nov;48(11):e13015. doi: 10.1111/eci.13015. Epub 2018 Aug 23. Eur J Clin Invest. 2018. PMID: 30079480

5

Detection of Mosaic Absence of Heterozygosity (AOH) Using Low-Pass Whole Genome Sequencing in Prenatal Diagnosis: A Preliminary Report.

Lü Y, Jiang Y, Zhou X, Hao N, Xu C, Guo R, Chang J, Li M, Zhang H, Zhou J, Zhang WV, Qi Q. Lü Y, et al. Among authors: chang j. Diagnostics (Basel). 2023 Sep 9;13(18):2895. doi: 10.3390/diagnostics13182895. Diagnostics (Basel). 2023. PMID: 37761262 Free PMC article.

6

Simultaneous Detection of CNVs and SNVs Improves the Diagnostic Yield of Fetuses with Ultrasound Anomalies and Normal Karyotypes.

Qi Q, Jiang Y, Zhou X, Meng H, Hao N, Chang J, Bai J, Wang C, Wang M, Guo J, Ouyang Y, Xu Z, Xiao M, Zhang VW, Liu J. Qi Q, et al. Among authors: chang j. Genes (Basel). 2020 Nov 25;11(12):1397. doi: 10.3390/genes11121397. Genes (Basel). 2020. PMID: 33255631 Free PMC article.

7

Evaluation and Analysis of Absence of Homozygosity (AOH) Using Chromosome Analysis by Medium Coverage Whole Genome Sequencing (CMA-seq) in Prenatal Diagnosis.

Lü Y, Jiang Y, Zhou X, Hao N, Lü G, Guo X, Guo R, Liu W, Xu C, Chang J, Li M, Zhang H, Zhou J, Zhang WV, Qi Q. Lü Y, et al. Among authors: chang j. Diagnostics (Basel). 2023 Feb 2;13(3):560. doi: 10.3390/diagnostics13030560. Diagnostics (Basel). 2023. PMID: 36766665 Free PMC article.

8

Novel de novo nonsense mutation of the PHEX gene (p.Lys50Ter) in a Chinese patient with hypophosphatemic rickets.

Huang Y, Mei L, Pan Q, Tan H, Quan Y, Gui B, Chang J, Ma R, Peng Y, Yang P, Liang D, Wu L. Huang Y, et al. Among authors: chang j. Gene. 2015 Jul 1;565(1):150-4. doi: 10.1016/j.gene.2015.03.066. Epub 2015 Mar 31. Gene. 2015. PMID: 25839938

9

Pachygyria, seizures, hypotonia, and growth retardation in a patient with an atypical 1.33Mb inherited microduplication at 22q11.23.

Chang J, Zhao L, Chen C, Peng Y, Xia Y, Tang G, Bai T, Zhang Y, Ma R, Guo R, Mei L, Liang D, Cao Q, Wu L. Chang J, et al. Gene. 2015 Sep 10;569(1):46-50. doi: 10.1016/j.gene.2015.04.090. Epub 2015 Jun 20. Gene. 2015. PMID: 26099517

10

[Molecular diagnosis and functional study of a pedigree affected with Lubs X-linked mental retardation syndrome].

Jiang C, Pan N, Lyu W, Peng Y, Liu J, Guo R, Chang J, Liang D, Wu L. Jiang C, et al. Among authors: chang j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Apr 10;36(4):340-343. doi: 10.3760/cma.j.issn.1003-9406.2019.04.012. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 30950021 Chinese.

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