Luo J - Search Results

1

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. Among authors: luo j. Am J Transl Res. 2023 May 15;15(5):3342-3354. eCollection 2023. Am J Transl Res. 2023. PMID: 37303656 Free PMC article.

2

Analysis of mutations of two Gitelman syndrome family SLC12A3 genes and proposed treatments using Chinese medicine.

Luo JW, Meng XR, Yang X, Liang JX, Hong FY, Zheng XY, Li WH. Luo JW, et al. Chin J Integr Med. 2017 Jun;23(6):461-468. doi: 10.1007/s11655-016-2461-x. Epub 2016 Jan 29. Chin J Integr Med. 2017. PMID: 26825084

3

Splicing mutation of a gene within the Duchenne muscular dystrophy family.

Zhu YB, Gan JH, Luo JW, Zheng XY, Wei SC, Hu D. Zhu YB, et al. Among authors: luo jw. Genet Mol Res. 2016 Jul 14;15(2). doi: 10.4238/gmr.15028258. Genet Mol Res. 2016. PMID: 27421007 Free article.

4

The Construction of Unsmooth Pulse Images in Traditional Chinese Medicine Based on Wave Intensity Technology.

Luo JW, Guo SW, Cao SS, Lin N, Ye ZS, Wei SC, Zheng XY, Guo MM, Meng XR, Huang FM. Luo JW, et al. Evid Based Complement Alternat Med. 2016;2016:2468254. doi: 10.1155/2016/2468254. Epub 2016 Nov 24. Evid Based Complement Alternat Med. 2016. PMID: 27999604 Free PMC article.

5

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.

6

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.

7

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: luo j. 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.

8

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: luo j. J Pediatr Endocrinol Metab. 2018 Jul 26;31(7):789-797. doi: 10.1515/jpem-2017-0451. J Pediatr Endocrinol Metab. 2018. PMID: 29858904

9

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.

10

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. Among authors: luo j. 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.

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