Lu Z - Search Results

1

Clinical and Genetic Features in 31 Serial Chinese Children With Gitelman Syndrome.

Zhang L, Huang K, Wang S, Fu H, Wang J, Shen H, Lu Z, Chen J, Bao Y, Feng C, Dong G, Mao J. Zhang L, et al. Among authors: lu z. Front Pediatr. 2021 Apr 29;9:544925. doi: 10.3389/fped.2021.544925. eCollection 2021. Front Pediatr. 2021. PMID: 33996672 Free PMC article.

2

Evaluation of Mycophenolate Mofetil and Low-Dose Steroid Combined Therapy in Moderately Severe Henoch-Schönlein Purpura Nephritis.

Lu Z, Song J, Mao J, Xia Y, Wang C. Lu Z, et al. Med Sci Monit. 2017 May 18;23:2333-2339. doi: 10.12659/msm.904206. Med Sci Monit. 2017. PMID: 28515415 Free PMC article.

3

Clinical features and genetic findings in Chinese children with distal renal tubular acidosis.

Zhou F, Mao J, Ye Q, Zhu X, Zhang Y, Ye Y, Fu H, Shen H, Lu Z, Xia Y, Liu A, Shu Q, Du L. Zhou F, et al. Among authors: lu z. Int J Clin Exp Pathol. 2018 Jul 1;11(7):3523-3532. eCollection 2018. Int J Clin Exp Pathol. 2018. PMID: 31949730 Free PMC article.

4

PP2A protects podocytes against Adriamycin-induced injury and epithelial-to-mesenchymal transition via suppressing JIP4/p38-MAPK pathway.

Lu Z, Zhu X, Ye Y, Fu H, Mao J. Lu Z, et al. Cytotechnology. 2021 Oct;73(5):697-713. doi: 10.1007/s10616-021-00484-1. Epub 2021 Aug 13. Cytotechnology. 2021. PMID: 34629746 Free PMC article.

5

Growth Retardation in the Course of Fanconi Syndrome Caused by the 4977-bp Mitochondrial DNA Deletion: A Case Report.

Li T, Lu Z, Wang J, Chen J, Fu H, Mao J. Li T, et al. Among authors: lu z. Children (Basel). 2021 Oct 4;8(10):887. doi: 10.3390/children8100887. Children (Basel). 2021. PMID: 34682152 Free PMC article.

6

The important roles and molecular mechanisms of annexin A₂ autoantibody in children with nephrotic syndrome.

Ye Q, Zhang Y, Zhuang J, Bi Y, Xu H, Shen Q, Liu J, Fu H, Wang J, Feng C, Tang X, Liu F, Gu W, Zhao F, Zhang J, Qin Y, Shang S, Shen H, Chen X, Shen H, Liu A, Xia Y, Lu Z, Shu Q, Mao J. Ye Q, et al. Among authors: lu z. Ann Transl Med. 2021 Sep;9(18):1452. doi: 10.21037/atm-21-3988. Ann Transl Med. 2021. PMID: 34734004 Free PMC article.

7

Mosaic PKHD1 in Polycystic Kidneys Caused Aberrant Protein Expression in the Mitochondria and Lysosomes.

Xu C, Yang C, Ye Q, Xu J, Tong L, Zhang Y, Shen H, Lu Z, Wang J, Lai E, Mao J, Jiang P. Xu C, et al. Among authors: lu z. Front Med (Lausanne). 2021 Dec 16;8:743150. doi: 10.3389/fmed.2021.743150. eCollection 2021. Front Med (Lausanne). 2021. PMID: 34977057 Free PMC article.

8

Heteroplasmic and homoplasmic m.616T>C in mitochondria tRNAPhe promote isolated chronic kidney disease and hyperuricemia.

Xu C, Tong L, Rao J, Ye Q, Chen Y, Zhang Y, Xu J, Mao X, Meng F, Shen H, Lu Z, Cang X, Fu H, Wang S, Gu W, Lai EY, Guan MX, Jiang P, Mao J. Xu C, et al. Among authors: lu z. JCI Insight. 2022 Jun 8;7(11):e157418. doi: 10.1172/jci.insight.157418. JCI Insight. 2022. PMID: 35472031 Free PMC article.

9

Glomerular IgA Deposition and Serum Antineutrophil Cytoplasmic Antibody Positivity in a Child With Dystrophic Epidermolysis Bullosa: Case Report and Literature Review.

Yu L, Huang G, Lu Z, Wang J, Gu W, Li J, Mao J. Yu L, et al. Among authors: lu z. Front Pediatr. 2022 Jul 11;10:939069. doi: 10.3389/fped.2022.939069. eCollection 2022. Front Pediatr. 2022. PMID: 35899130 Free PMC article.

10

Genotype-Phenotype Correlation Reanalysis in 83 Chinese Cases with OCRL Mutations.

Zhang L, Wang S, Mao R, Fu H, Wang J, Shen H, Lu Z, Chen J, Bao Y, Feng C, Lai EY, Ye Q, Mao J. Zhang L, et al. Among authors: lu z. Genet Res (Camb). 2022 Jul 19;2022:1473260. doi: 10.1155/2022/1473260. eCollection 2022. Genet Res (Camb). 2022. PMID: 35919034 Free PMC article.

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