Sun S - Search Results

1

Ubiquitin-specific peptidase 10 promotes renal interstitial fibrosis progression through deubiquitinating and stabilizing P53 protein.

Liu S, Yang Y, Li Q, Yu L, Zong Z, Zang R, Ji W, Sun S. Liu S, et al. Among authors: sun s. Biochim Biophys Acta Mol Basis Dis. 2025 Jan 7;1871(3):167660. doi: 10.1016/j.bbadis.2025.167660. Online ahead of print. Biochim Biophys Acta Mol Basis Dis. 2025. PMID: 39788218 Free article.

2

Umbelliferone attenuates cisplatin-induced acute kidney injury by inhibiting oxidative stress and inflammation via NRF2.

Yang Z, Ning R, Liu Q, Zang R, Liu S, Sun S. Yang Z, et al. Among authors: sun s. Physiol Rep. 2023 Dec;11(23):e15879. doi: 10.14814/phy2.15879. Physiol Rep. 2023. PMID: 38030388 Free PMC article.

3

oxLDL promotes podocyte migration by regulating CXCL16, ADAM10 and ACTN4.

Chen Y, Wang Z, Li Q, Yu L, Zhu Y, Wang J, Sun S. Chen Y, et al. Among authors: sun s. Mol Med Rep. 2020 Sep;22(3):1976-1984. doi: 10.3892/mmr.2020.11292. Epub 2020 Jun 30. Mol Med Rep. 2020. PMID: 32705248 Free PMC article.

4

CXCL16/ERK1/2 pathway regulates human podocytes growth, migration, apoptosis and epithelial mesenchymal transition.

Chen Y, Wang Z, Li Q, Tian M, Zhu Y, Yu L, Wang J, Sun S. Chen Y, et al. Among authors: sun s. Mol Med Rep. 2022 Jun;25(6):212. doi: 10.3892/mmr.2022.12728. Epub 2022 May 6. Mol Med Rep. 2022. PMID: 35514316 Free PMC article.

5

Low molecular weight proteinuria, congenital myopia and hearing loss in a 10-year-old boy: Questions.

Li Q, Yang Z, Wang C, Yu L, Sun S. Li Q, et al. Among authors: sun s. Pediatr Nephrol. 2023 Aug;38(8):2585. doi: 10.1007/s00467-023-05880-7. Epub 2023 Jan 23. Pediatr Nephrol. 2023. PMID: 36688941 No abstract available.

6

Low molecular weight proteinuria, congenital myopia and hearing loss in a 10-year-old boy: Answers.

Li Q, Yang Z, Wang C, Yu L, Sun S. Li Q, et al. Among authors: sun s. Pediatr Nephrol. 2023 Aug;38(8):2587-2590. doi: 10.1007/s00467-023-05883-4. Epub 2023 Jan 23. Pediatr Nephrol. 2023. PMID: 36688942 No abstract available.

7

A novel mutation of the RPGRIP1L gene in a Chinese boy with Joubert syndrome with oculorenal involvement.

Li Q, Liu Q, Liu S, Yu L, Yang Z, Wang C, Wang J, Sun S. Li Q, et al. Among authors: sun s. BMC Pediatr. 2023 Nov 23;23(1):590. doi: 10.1186/s12887-023-04415-1. BMC Pediatr. 2023. PMID: 37993833 Free PMC article.

8

Systemic lupus erythematosus combined with Wilson's disease: a case report and literature review.

Yang Z, Li Q, Liu S, Zong Z, Yu L, Sun S. Yang Z, et al. Among authors: sun s. BMC Pediatr. 2024 Apr 15;24(1):253. doi: 10.1186/s12887-024-04713-2. BMC Pediatr. 2024. PMID: 38622515 Free PMC article. Review.

9

Congenital chloride diarrhoea in a Chinese infant with a compound heterozygous SLC26A3 mutation.

Li Q, Wang J, Zang R, Yu L, Yang Z, Sun S. Li Q, et al. Among authors: sun s. BMC Pediatr. 2024 May 4;24(1):305. doi: 10.1186/s12887-024-04788-x. BMC Pediatr. 2024. PMID: 38704545 Free PMC article.

10

Clinical features and genetic analysis of 15 Chinese children with dent disease.

Li Q, Yang Z, Zang R, Liu S, Yu L, Wang J, Wang C, Wang X, Sun S. Li Q, et al. Among authors: sun s. Ren Fail. 2024 Dec;46(1):2349133. doi: 10.1080/0886022X.2024.2349133. Epub 2024 May 10. Ren Fail. 2024. PMID: 38726999 Free PMC article.

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