Zhang YP - Search Results

1

Pharmarcomechanical thrombectomy combined with transluminal balloon angioplasty for treating transplant renal vein thrombosis.

Wu SJ, Zhang C, Wu M, Ruan DD, Zhang YP, Lin B, Tang Y, Chen X, Wang C, Pan HH, Zhu QG, Luo JW, Ye LF, Fang ZT. Wu SJ, et al. Among authors: zhang yp, zhang c. Sci Rep. 2023 Oct 12;13(1):17303. doi: 10.1038/s41598-023-44514-8. Sci Rep. 2023. PMID: 37828079 Free PMC article.

2

A thrombophilia family with protein S deficiency due to protein translation disorders caused by a Leu607Ser heterozygous mutation in PROS1.

Zhang YP, Lin B, Ji YY, Hu YN, Lin XF, Tang Y, Zhang JH, Wu SJ, Cai SL, Zhou YF, Chen T, Fang ZT, Luo JW. Zhang YP, et al. Among authors: zhang jh. Thromb J. 2021 Sep 8;19(1):64. doi: 10.1186/s12959-021-00316-4. Thromb J. 2021. PMID: 34496879 Free PMC article.

3

Different phenotypes of neurological diseases, including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism, caused by de novo ATP1A3 mutation in a family.

Wei W, Zheng XF, Ruan DD, Gan YM, Zhang YP, Chen Y, Lin XF, Tang FQ, Luo JW, Li YF. Wei W, et al. Among authors: zhang yp. Neurol Sci. 2022 Apr;43(4):2555-2563. doi: 10.1007/s10072-021-05673-6. Epub 2021 Nov 16. Neurol Sci. 2022. PMID: 34783933

4

A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiency.

Hu YN, Gan YM, Zhang YP, Ruan DD, Zhu YB, Lin XF, Fang ZT, Liao LS, Tang FQ, Luo JW. Hu YN, et al. Among authors: zhang yp. J Gene Med. 2022 Feb;24(2):e3398. doi: 10.1002/jgm.3398. Epub 2021 Dec 30. J Gene Med. 2022. PMID: 34786791

5

Retrospective Analysis of the Effect of Lidocaine Combined with Methylprednisolone on Pain Control After Uterine Artery Embolization.

Tang Y, Lin B, Zhang YP, Hu YN, Zhang JH, Wu SJ, Zhou YF, Cai SL, Luo JW, Chi W, Fang ZT. Tang Y, et al. Among authors: zhang yp, zhang jh. Front Surg. 2022 Apr 19;9:875484. doi: 10.3389/fsurg.2022.875484. eCollection 2022. Front Surg. 2022. PMID: 35521428 Free PMC article.

6

Clinical and Genetic Analysis of a Family With Sitosterolemia Caused by a Novel ATP-Binding Cassette Subfamily G Member 5 Compound Heterozygous Mutation.

Shen MF, Hu YN, Chen WX, Liao LS, Wu M, Wu QY, Zhang JH, Zhang YP, Luo JW, Lin XF. Shen MF, et al. Among authors: zhang yp, zhang jh. Front Cardiovasc Med. 2022 Apr 26;9:887618. doi: 10.3389/fcvm.2022.887618. eCollection 2022. Front Cardiovasc Med. 2022. PMID: 35557526 Free PMC article.

7

Function of PHEX mutations p.Glu145* and p.Trp749Arg in families with X-linked hypophosphatemic rickets by the negative regulation mechanism on FGF23 promoter transcription.

Gan YM, Zhang YP, Ruan DD, Huang JB, Zhu YB, Lin XF, Xiao XP, Cheng Q, Geng ZB, Liao LS, Tang FQ, Luo JW. Gan YM, et al. Among authors: zhang yp. Cell Death Dis. 2022 Jun 2;13(6):518. doi: 10.1038/s41419-022-04969-5. Cell Death Dis. 2022. PMID: 35654784 Free PMC article.

8

Eucarbwenstols A-H, eight novel compounds from Eucalyptus robusta prevents MPC-5 injury via ROS modulation and regulation of mitochondrial membrane potential.

Chen T, Ruan DD, Zhang JH, Wang HL, Wu M, Wu QY, Zhang YP, Wu JB, Ye Y, Chou GX, Luo JW. Chen T, et al. Among authors: zhang yp, zhang jh. Bioorg Chem. 2022 Dec;129:106159. doi: 10.1016/j.bioorg.2022.106159. Epub 2022 Sep 19. Bioorg Chem. 2022. PMID: 36155091

9

Comprehensive analysis of immune ferroptosis gene in renal clear cell carcinoma: prognosis and influence of tumor microenvironment.

Yang LH, Xu LZ, Huang ZJ, Pan HH, Wu M, Wu QY, Lu T, Zhang YP, Zhu YB, Wu JB, Luo JW, Yang GK, Ye LF. Yang LH, et al. Among authors: zhang yp. Am J Transl Res. 2022 Sep 15;14(9):5982-6010. eCollection 2022. Am J Transl Res. 2022. PMID: 36247256 Free PMC article.

10

Identification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiency.

Wang HL, Ruan DD, Wu M, Ji YY, Hu XX, Wu QY, Zhang YP, Lin B, Hu YN, Wang H, Tang Y, Fang ZT, Luo JW, Liao LS, Gao MZ. Wang HL, et al. Among authors: zhang yp. Thromb J. 2023 Jan 9;21(1):3. doi: 10.1186/s12959-022-00443-6. Thromb J. 2023. PMID: 36624481 Free PMC article.

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