Xu Y - Search Results

1

Metabolome implies increased fatty acid utilization and histone methylation in the follicles from hyperandrogenic PCOS women.

Xu Y, Zhou Z, Zhang G, Yang Z, Shi Y, Jiang Z, Liu Y, Chen H, Huang H, Zhang Y, Pan J. Xu Y, et al. J Nutr Biochem. 2024 Mar;125:109548. doi: 10.1016/j.jnutbio.2023.109548. Epub 2023 Dec 15. J Nutr Biochem. 2024. PMID: 38104867

2

Elevated plasma pentraxin-3 in polycystic ovary syndrome is associated with hyperandrogenism: a case-control study.

Jin C, Zou K, Xu Y, Yang H, Pan J. Jin C, et al. Among authors: xu y. BMC Endocr Disord. 2021 Dec 3;21(1):240. doi: 10.1186/s12902-021-00886-4. BMC Endocr Disord. 2021. PMID: 34856980 Free PMC article.

3

Associations Between Asthma and Polycystic Ovary Syndrome: Current Perspectives.

Xu Y, Zhou ZY, Pan JX, Huang HF. Xu Y, et al. Front Endocrinol (Lausanne). 2022 Jul 5;13:936948. doi: 10.3389/fendo.2022.936948. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35865312 Free PMC article. Review.

4

Identification of Potential Genes in Pathogenesis and Diagnostic Value Analysis of Partial Androgen Insensitivity Syndrome Using Bioinformatics Analysis.

Peng Y, Zhu H, Han B, Xu Y, Liu X, Song H, Qiao J. Peng Y, et al. Among authors: xu y. Front Endocrinol (Lausanne). 2021 Nov 18;12:731107. doi: 10.3389/fendo.2021.731107. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34867780 Free PMC article.

5

Lessons from 17β-HSD3 deficiency: Clinical spectrum and complex molecular basis in Chinese patients.

Zhu H, Yao H, Liu X, Xu Y, Liu Y, Luo Q, Chen Y, Shi Y, Chen F, Zhao S, Song H, Han B, Qiao J. Zhu H, et al. Among authors: xu y. J Steroid Biochem Mol Biol. 2023 Jan;225:106191. doi: 10.1016/j.jsbmb.2022.106191. Epub 2022 Sep 22. J Steroid Biochem Mol Biol. 2023. PMID: 36154887

6

Bioinformatic Analysis Identifies Potential Key Genes in the Pathogenesis of Turner Syndrome.

Wang H, Zhu H, Zhu W, Xu Y, Wang N, Han B, Song H, Qiao J. Wang H, et al. Among authors: xu y. Front Endocrinol (Lausanne). 2020 Mar 6;11:104. doi: 10.3389/fendo.2020.00104. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 32210915 Free PMC article.

7

In-frame deletion of SMC5 related with the phenotype of primordial dwarfism, chromosomal instability and insulin resistance.

Zhu W, Shi Y, Zhang C, Peng Y, Wan Y, Xu Y, Liu X, Han B, Zhao S, Kuang Y, Song H, Qiao J. Zhu W, et al. Among authors: xu y. Clin Transl Med. 2023 Jan;13(1):e1007. doi: 10.1002/ctm2.1007. Clin Transl Med. 2023. PMID: 36627765 Free PMC article.

8

Phenotypic and biochemical characteristics and molecular basis in 36 Chinese patients with androgen receptor variants.

Zhu H, Yao H, Xu Y, Chen Y, Han B, Wang N, Wang H, Zhang Q, Zhu W, Shi Y, Sun H, Zhao S, Song H, Liu Y, Qiao J. Zhu H, et al. Among authors: xu y. Orphanet J Rare Dis. 2021 Mar 9;16(1):122. doi: 10.1186/s13023-021-01765-w. Orphanet J Rare Dis. 2021. PMID: 33750429 Free PMC article.

9

Sal003 alleviated intervertebral disc degeneration by inhibiting apoptosis and extracellular matrix degradation through suppressing endoplasmic reticulum stress pathway in rats.

Chen Y, Li B, Xu Y, Zhou T, Zhao C, Zhao J. Chen Y, et al. Among authors: xu y. Front Pharmacol. 2023 Jan 20;14:1095307. doi: 10.3389/fphar.2023.1095307. eCollection 2023. Front Pharmacol. 2023. PMID: 36744257 Free PMC article.

10

Reproductive endocrine characteristics and in vitro fertilization treatment of female patients with partial 17α-hydroxylase deficiency: Two pedigree investigations and a literature review.

Jiang S, Xu Y, Qiao J, Wang Y, Kuang Y. Jiang S, et al. Among authors: xu y. Front Endocrinol (Lausanne). 2022 Sep 14;13:970190. doi: 10.3389/fendo.2022.970190. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36187111 Free PMC article. Review.

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