Gan Y - Search Results

1

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. Among authors: gan y. Am J Transl Res. 2020 Dec 15;12(12):8123-8136. eCollection 2020. Am J Transl Res. 2020. PMID: 33437386 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. 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

Differences in gut microbiota structure in patients with stages 4-5 chronic kidney disease.

Wu R, Ruan XL, Ruan DD, Zhang JH, Wang HL, Zeng QZ, Lu T, Gan YM, Luo JW, Wu JB. Wu R, et al. Am J Transl Res. 2021 Sep 15;13(9):10056-10074. eCollection 2021. Am J Transl Res. 2021. PMID: 34650681 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: gan ym. 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. 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. 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. 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

Difference in oral microbiota composition between patients with stage 5 chronic kidney disease on hemodialysis and healthy controls.

Gan Y, Ruan D, Zeng Q, Zhu Y, Hu Y, Wu R, Lin X, Wu J, Meng X, Luo J, Gao M, Chen X. Gan Y, et al. Am J Transl Res. 2023 May 15;15(5):3342-3354. eCollection 2023. Am J Transl Res. 2023. PMID: 37303656 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. J Med Genet. 2023 Nov 27;60(12):1210-1214. doi: 10.1136/jmg-2023-109328. J Med Genet. 2023. PMID: 37468236

10

Triglyceride-glucose index as a mediator of body mass index and cardiovascular disease in middle-aged and older Chinese adults: a nationally representative longitudinal cohort study.

Gan YY, Zhai L, Liao Q, Huo RR. Gan YY, et al. Front Endocrinol (Lausanne). 2024 Dec 23;15:1431087. doi: 10.3389/fendo.2024.1431087. eCollection 2024. Front Endocrinol (Lausanne). 2024. PMID: 39764243 Free PMC article.

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