Luo JW - Search Results

1

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: luo jw. 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.

2

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. 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.

3

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

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

4

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. Among authors: luo jw. 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.

5

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. Among authors: luo jw. 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.

6

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: luo jw. 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

7

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: luo jw. 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.

8

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.

9

Mutational Analysis of a Familial Adenomatous Polyposis Pedigree with Bile Duct Polyp Phenotype.

Xie LJ, Ruan DD, Zhang JH, Li Y, Chen L, Yan ML, Yu MD, Luo JW, Zhang HZ. Xie LJ, et al. Among authors: luo jw. Can J Gastroenterol Hepatol. 2021 Apr 12;2021:6610434. doi: 10.1155/2021/6610434. eCollection 2021. Can J Gastroenterol Hepatol. 2021. PMID: 33954154 Free PMC article.

10

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: luo jw. Biomed Res Int. 2021 May 10;2021:9973161. doi: 10.1155/2021/9973161. eCollection 2021. Biomed Res Int. 2021. PMID: 34046503 Free PMC article.

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