基本介紹
- 中文名：呂樂春
- 國籍：中國
- 民族：漢族
- 出生地：山東
- 職業：教師/科研人員
- 畢業院校：昆明醫科大學
- 專業方向：瘢痕發生機制、生物信息學及治療
- Name：Lechun Lu; Lechun Lyu
人物介紹,研究方向,科研情況,個人作品,
人物介紹
呂樂春，男，副教授，昆明醫科大學教師。
研究方向
1）瘢痕流行病學、發生機制研究，瘢痕治療方案探索；
2）生物信息學分析。
科研情況
主持國家、省及廳級基金8項，包括國家自然科學基金1項（NO. 81560502）。
個人作品
作為通訊作者/第一作者發表SCI論文15餘篇：
1. Deng Z, He Y, Yang X, Shi H, Shi A, Lu L, He L. MicroRNA-29: A Crucial Player inFibrotic Disease. Molecular diagnosis & therapy. 2017; PubMed [journal] PMID:28130757
2. He Y, Deng Z, Alghamdi M, Lu L, Fear MW, He L. From genetics to epigenetics: newinsights into keloid scarring. Cell proliferation. 2017; PubMed [journal] PMID:28054407
3. Deng Z, Hao J, Lei D, He Y, Lu L, He L. Pivotal MicroRNAs in Melanoma: AMini-Review. Molecular diagnosis & therapy. 2016; 20(5):449-55. PubMed [journal]PMID: 27351922
4. Yao S, Shi A, Li J, Ma J, Lu L. Angiotensin-converting enzyme gene polymorphismsmight be associated with childhood asthma in East Asia. The Journal of asthma :official journal of the Association for the Care of Asthma. 2016; :1-3. PubMed[journal] PMID: 27645324
5. Lu L, He L. Gut-brain axis dysfunction may be associated with psoriaticarthritis: comment on the article by Scher et al. Arthritis & rheumatology(Hoboken, N.J.). 2015; 67(8):2280. PubMed [journal] PMID: 25919422
6. Liu J, Chen P, Guo M, Lu L, Li L. Association of COMT Val158Met polymorphism withwearing-off susceptibility in Parkinson's disease. Neurological sciences :official journal of the Italian Neurological Society and of the Italian Societyof Clinical Neurophysiology. 2015; 36(4):621-3. PubMed [journal] PMID: 25367407
7. Lu L, Lei D, Nong X, Guo M, Ma J, He L. The null polymorphism of the GSTM1/T1gene is not associated with susceptibility to systemic lupus erythematosus: ameta-analysis. Molecular diagnosis & therapy. 2015; 19(1):65-9. PubMed [journal]PMID: 25628002
8. Chuan L, Gao J, Lei Y, Wang R, Lu L, Zhang X. Val158Met polymorphism of COMT geneand Parkinson's disease risk in Asians. Neurological sciences : official journalof the Italian Neurological Society and of the Italian Society of ClinicalNeurophysiology. 2015; 36(1):109-15. PubMed [journal] PMID: 25060648
9. Guo M, Ma J, Han Y, Lu L. Angiotensin-converting enzyme gene insertion/deletionpolymorphisms and the susceptibility to allergic rhinitis. Allergologia etimmunopathologia. 2014; 42(6):568-72. PubMed [journal] PMID: 24637107
10. Lu L, Liu L, Ji Y, Jin H, He L. Association of the 389 C/T polymorphism of thecatalase gene with susceptibility to vitiligo: a meta-analysis. Clinical andexperimental dermatology. 2014; 39(4):454-60. PubMed [journal] PMID: 24825136
11. Lu L, Tu Y, Liu L, Qi J, He L. MicroRNA-499 rs3746444 polymorphism and autoimmunediseases risk: a meta-analysis. Molecular diagnosis & therapy. 2014;18(2):237-42. PubMed [journal] PMID: 24327058
12. Lu L, Wu W, Tu Y, Yang Z, He L, Guo M. Association of glutathione S-transferaseM1/T1 polymorphisms with susceptibility to vitiligo. Gene. 2014; 535(1):12-6.PubMed [journal] PMID: 24295891
13. Liu T, Han Y, Lu L. Angiotensin-converting enzyme gene polymorphisms and the riskof psoriasis: a meta-analysis. Clinical and experimental dermatology. 2013;38(4):352-8; quiz 359. PubMed [journal] PMID: 23621089
14. Han Y, Liu T, Lu L. Apolipoprotein E gene polymorphism in psoriasis: ameta-analysis. Archives of medical research. 2013; 44(1):46-53. PubMed [journal]PMID: 23142524
15. Lechun L, Yu S, Pengling H, Changqi H. The COMT Val158Met polymorphism as anassociated risk factor for Parkinson's disease in Asian rather than Caucasianpopulations. Neurology India. 2013; 61(1):12-6. PubMed [journal] PMID: 23466833
