Liao LS - Search Results

1

A pedigree analysis of Rotor hyperbilirubinemia combined with hepatitis B virus infection in a SLCO1B1 and SLCO1B3 gene mutations patient.

Lin LZ, Wu QY, Zhang JH, Li SJ, Wu WZ, Ruan DD, Wu M, Chen Q, Liao LS, Fang ZT, Luo JW, Li ZA, Li Z, Li H. Lin LZ, et al. Among authors: liao ls. Heliyon. 2024 Jun 28;10(13):e33864. doi: 10.1016/j.heliyon.2024.e33864. eCollection 2024 Jul 15. Heliyon. 2024. PMID: 39071607 Free PMC article.

2

Genetic diagnosis history and osteoarticular phenotype of a non-transfusion secondary hemochromatosis.

Ruan DD, Gan YM, Lu T, Yang X, Zhu YB, Yu QH, Liao LS, Lin N, Qian X, Luo JW, Tang FQ. Ruan DD, et al. Among authors: liao ls. World J Clin Cases. 2020 Dec 6;8(23):5962-5975. doi: 10.12998/wjcc.v8.i23.5962. World J Clin Cases. 2020. PMID: 33344595 Free PMC article.

3

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: liao ls. J Gene Med. 2022 Feb;24(2):e3398. doi: 10.1002/jgm.3398. Epub 2021 Dec 30. J Gene Med. 2022. PMID: 34786791

4

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: liao ls. 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.

5

Genetic Analysis and Functional Study of a Pedigree With Bruck Syndrome Caused by PLOD2 Variant.

Wang RL, Ruan DD, Hu YN, Gan YM, Lin XF, Fang ZT, Liao LS, Tang FQ, He WB, Luo JW. Wang RL, et al. Among authors: liao ls. Front Pediatr. 2022 May 6;10:878172. doi: 10.3389/fped.2022.878172. eCollection 2022. Front Pediatr. 2022. PMID: 35601416 Free PMC article.

6

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: liao ls. 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.

7

Case report and analysis: Behçet's disease with lower extremity vein thrombosis and pseudoaneurysm.

Wang HL, Zhang JH, Wu YC, Lin JL, Tang Y, Liao LS, Luo JW, Yu QH, Fang ZT. Wang HL, et al. Among authors: liao ls. Front Immunol. 2022 Aug 29;13:949356. doi: 10.3389/fimmu.2022.949356. eCollection 2022. Front Immunol. 2022. PMID: 36105822 Free PMC article.

8

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: liao ls. Thromb J. 2023 Jan 9;21(1):3. doi: 10.1186/s12959-022-00443-6. Thromb J. 2023. PMID: 36624481 Free PMC article.

9

Clinical phenotype and genetic function analysis of a rare family with hereditary leiomyomatosis and renal cell carcinoma complicated with Birt-Hogg-Dubé syndrome.

Pan HH, Ruan DD, Wu M, Chen T, Lu T, Gan YM, Wang C, Liao LS, Lin XF, Chen X, Zhu YB, Fang ZT, Yu QH, Yang GK, Ye LF, Luo JW. Pan HH, et al. Among authors: liao ls. J Med Genet. 2023 Nov 27;60(12):1210-1214. doi: 10.1136/jmg-2023-109328. J Med Genet. 2023. PMID: 37468236

10

Potential regulatory role of the Nrf2/HMGB1/TLR4/NF-κB signaling pathway in lupus nephritis.

Li SJ, Ruan DD, Wu WZ, Wu M, Wu QY, Wang HL, Ji YY, Zhang YP, Lin XF, Fang ZT, Liao LS, Luo JW, Gao MZ, Wu JB. Li SJ, et al. Among authors: liao ls. Pediatr Rheumatol Online J. 2023 Oct 23;21(1):130. doi: 10.1186/s12969-023-00909-5. Pediatr Rheumatol Online J. 2023. PMID: 37872565 Free PMC article.

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