Zhu 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: zhu 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

Association of Tongue Bacterial Flora and Subtypes of Liver-Fire Hyperactivity Syndrome in Hypertensive Patients.

Luo JW, Lin CH, Zhu YB, Zheng XY, Wu YX, Chen WW, Yang X. Luo JW, et al. Evid Based Complement Alternat Med. 2018 Jan 10;2018:9536924. doi: 10.1155/2018/9536924. eCollection 2018. Evid Based Complement Alternat Med. 2018. PMID: 29541146 Free PMC article.

3

Genetic analysis of sick sinus syndrome in a family harboring compound CACNA1C and TTN mutations.

Zhu YB, Luo JW, Jiang F, Liu G. Zhu YB, et al. Mol Med Rep. 2018 May;17(5):7073-7080. doi: 10.3892/mmr.2018.8773. Epub 2018 Mar 16. Mol Med Rep. 2018. PMID: 29568937 Free PMC article.

4

Genetic analysis of a congenital split‑hand/split‑foot malformation 4 pedigree.

Yang X, Lin X, Zhu Y, Luo J, Lin G. Yang X, et al. Among authors: zhu y. Mol Med Rep. 2018 Jun;17(6):7553-7558. doi: 10.3892/mmr.2018.8838. Epub 2018 Mar 29. Mol Med Rep. 2018. PMID: 29620206 Free PMC article.

5

Genetic analysis of three families with X-linked dominant hypophosphatemic rickets.

Lin X, Zhu Y, Luo J, Huang J. Lin X, et al. Among authors: zhu y. J Pediatr Endocrinol Metab. 2018 Jul 26;31(7):789-797. doi: 10.1515/jpem-2017-0451. J Pediatr Endocrinol Metab. 2018. PMID: 29858904

6

Genetic mutation of familial dilated cardiomyopathy based on next‑generation semiconductor sequencing.

Lin XF, Luo JW, Liu G, Zhu YB, Jin Z, Lin X. Lin XF, et al. Mol Med Rep. 2018 Nov;18(5):4271-4280. doi: 10.3892/mmr.2018.9455. Epub 2018 Sep 5. Mol Med Rep. 2018. PMID: 30221713 Free PMC article.

7

Astragaloside-IV protects H9C2(2-1) cardiomyocytes from high glucose-induced injury via miR-34a-mediated autophagy pathway.

Zhu Y, Qian X, Li J, Lin X, Luo J, Huang J, Jin Z. Zhu Y, et al. Artif Cells Nanomed Biotechnol. 2019 Dec;47(1):4172-4181. doi: 10.1080/21691401.2019.1687492. Artif Cells Nanomed Biotechnol. 2019. PMID: 31713440 Free article.

8

Screening and function discussion of a hereditary renal tubular acidosis family pathogenic gene.

Chen L, Wang HL, Zhu YB, Jin Z, Huang JB, Lin XF, Luo JW, Fang ZT. Chen L, et al. Cell Death Dis. 2020 Mar 2;11(3):159. doi: 10.1038/s41419-020-2354-y. Cell Death Dis. 2020. PMID: 32123165 Free PMC article.

9

Effect of superselective prostatic artery embolization on benign prostatic hyperplasia.

Tang Y, Zhang JH, Zhu YB, Wu SJ, Cai SL, Zhou YF, Qian X, Luo JW, Fang ZT. Tang Y, et al. Among authors: zhu yb. Abdom Radiol (NY). 2021 Apr;46(4):1726-1736. doi: 10.1007/s00261-020-02782-2. Epub 2020 Oct 6. Abdom Radiol (NY). 2021. PMID: 33025152

10

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.

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