Yu X - Search Results

1

Identification of novel deep intronic PAH gene variants in patients diagnosed with phenylketonuria.

Jin X, Yan Y, Zhang C, Tai Y, An L, Yu X, Zhang L, Hao S, Cao X, Yin C, Ma X. Jin X, et al. Among authors: yu x. Hum Mutat. 2022 Jan;43(1):56-66. doi: 10.1002/humu.24292. Epub 2021 Nov 16. Hum Mutat. 2022. PMID: 34747549

2

Mutation Characteristics of Phenylalanine Hydroxylase Gene in Children with Phenylketonuria in Yinchuan City.

Yu X, Liu F, Wei B, Li M, Lu R, Pan L. Yu X, et al. Discov Med. 2023 Aug;35(177):533-538. doi: 10.24976/Discov.Med.202335177.54. Discov Med. 2023. PMID: 37553307

3

[Gene variant analysis of a fetus with autosomal recessive polycystic kidney disease].

Yu X, Li S, Liu F, Liu L, Zhang H. Yu X, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Oct 10;37(10):1143-1145. doi: 10.3760/cma.j.cn511374-20191027-00544. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32924121 Chinese.

4

Clinical features and genetic analysis of developmental and epileptic encephalopathy caused by biallelic variants of CACNA1B.

Yu XY, Sun QM, Lu RP, Wei B, Wang XY, Pan LH. Yu XY, et al. Heliyon. 2024 Jun 7;10(12):e32693. doi: 10.1016/j.heliyon.2024.e32693. eCollection 2024 Jun 30. Heliyon. 2024. PMID: 39005920 Free PMC article.

5

Diagnostic Value and High-Risk Factors of Two-Dimensional Ultrasonography Combined with Four-Dimensional Ultrasonography in Prenatal Ultrasound Screening of Fetal Congenital Malformations.

Yu X, Liu F, Gao W, Shi X, Lu R, Pan L. Yu X, et al. Comput Math Methods Med. 2022 Jul 12;2022:7082832. doi: 10.1155/2022/7082832. eCollection 2022. Comput Math Methods Med. 2022. PMID: 35866037 Free PMC article.

6

Clinical efficacy and adverse effects of LMWH combined with ASA in the treatment of RSA: A meta-analysis and systematic review.

Liu F, Shi D, Jin R, Yu X. Liu F, et al. Among authors: yu x. Medicine (Baltimore). 2024 Sep 13;103(37):e39603. doi: 10.1097/MD.0000000000039603. Medicine (Baltimore). 2024. PMID: 39287269 Free PMC article.

7

[Prenatal diagnosis and genetic counseling of 20 fetuses with 15q11.2 BP1-BP2 microdeletion syndrome].

Li M, Yu X, Yang L, Wang X, Wei B. Li M, et al. Among authors: yu x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2025 Jan 10;42(1):64-68. doi: 10.3760/cma.j.cn511374-20240808-00429. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2025. PMID: 39779338 Chinese.

8

[Clinical and genetic features of ring chromosome 13 syndrome: an analysis of one case].

Fan MR, Wang GJ, Yu XY. Fan MR, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2018 Jun;20(6):485-489. doi: 10.7499/j.issn.1008-8830.2018.06.011. Zhongguo Dang Dai Er Ke Za Zhi. 2018. PMID: 29972124 Free PMC article. Chinese.

9

Engineering transgenic Populus with enhanced biomass, wood quality and pest resistance through dual gene expression.

Wang D, Liu F, Zhao M, Yu X, Feng J, Wang W, Lu M, Li W, Tang X, Wang C, Zhou G. Wang D, et al. Among authors: yu x. Plant Biotechnol J. 2025 Jan 24. doi: 10.1111/pbi.14590. Online ahead of print. Plant Biotechnol J. 2025. PMID: 39854210 No abstract available.

10

Galectin-1-Induced Tumor Associated Macrophages Repress Antitumor Immunity in Hepatocellular Carcinoma Through Recruitment of Tregs.

Yu X, Qian J, Ding L, Pan C, Liu X, Wu Q, Wang S, Liu J, Shang M, Su R, Guo D, Xie H, Yin S, Zhou L, Zheng S. Yu X, et al. Adv Sci (Weinh). 2025 Jan 24:e2408788. doi: 10.1002/advs.202408788. Online ahead of print. Adv Sci (Weinh). 2025. PMID: 39853961

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