Tang FQ - Search Results

1

Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations.

Zhang JH, Ruan DD, Hu YN, Ruan XL, Zhu YB, Yang X, Wu JB, Lin XF, Luo JW, Tang FQ. Zhang JH, et al. Among authors: tang fq. Biomed Res Int. 2021 May 10;2021:9973161. doi: 10.1155/2021/9973161. eCollection 2021. Biomed Res Int. 2021. PMID: 34046503 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: tang fq. 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

Analysis of mutations in six Chinese families with autosomal dominant polycystic kidney disease.

Wang H, Dai S, Zhang J, Li Y, Gan Y, Lu T, Zhu Y, Wu J, Lin N, Tang F, Luo J. Wang H, et al. Am J Transl Res. 2020 Dec 15;12(12):8123-8136. eCollection 2020. Am J Transl Res. 2020. PMID: 33437386 Free PMC article.

4

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: tang fq. Neurol Sci. 2022 Apr;43(4):2555-2563. doi: 10.1007/s10072-021-05673-6. Epub 2021 Nov 16. Neurol Sci. 2022. PMID: 34783933

5

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

6

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: tang fq. Front Pediatr. 2022 May 6;10:878172. doi: 10.3389/fped.2022.878172. eCollection 2022. Front Pediatr. 2022. PMID: 35601416 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: tang fq. 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

Prevalence, Risk Factors, and Prognostic Factors of Primary Malignant Bone Neoplasms with Bone Metastasis at Initial Diagnosis: A Population-Based Study.

Xiao ZW, Guo HL, Chen HC, Yan LP, Liao YL, Li SL, Zhao LL, Su LB, Li JJ, Tang FQ. Xiao ZW, et al. Among authors: tang fq. J Oncol. 2022 Mar 26;2022:9935439. doi: 10.1155/2022/9935439. eCollection 2022. J Oncol. 2022. PMID: 35378768 Free PMC article.

9

Promotive Role of CircATRNL1 on Chondrogenic Differentiation of BMSCs Mediated by miR-338-3p.

Zheng J, Lin Y, Tang F, Guo H, Yan L, Hu S, Wu H. Zheng J, et al. Arch Med Res. 2021 Jul;52(5):514-522. doi: 10.1016/j.arcmed.2021.02.003. Epub 2021 Feb 18. Arch Med Res. 2021. PMID: 33610389 Free article.

10

Effect of melittin on iNOS and NF-κB expression induced by IL-1βin C518 cells.

Tang F, Wu H, Zheng J, Guo H, Yan L, Lin Y, Xu C, Hu S. Tang F, et al. Pak J Pharm Sci. 2021 Jan;34(1):95-101. Pak J Pharm Sci. 2021. PMID: 34248008

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