Development of Unlabeled Probe Based High-Resolution Melting Analysis for Detection of Filaggrin Gene Mutation c.3321delA.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Works by Wei-Long Zhong
Results: 8
1
2
Dyskeratosis congenita with DKC1 mutation: A case report.
- Published in:
- 2020
- By:
- Publication type:
- Case Study
3
Novel mutations in SASH1 associated with dyschromatosis universalis hereditaria.
- Published in:
- Indian Journal of Dermatology, Venereology & Leprology, 2019, v. 85, n. 4, p. 438, doi. 10.4103/ijdvl.IJDVL_360_17
- By:
- Publication type:
- Article
4
Novel mutations in associated with dyschromatosis universalis hereditaria.
- Published in:
- 2019
- By:
- Publication type:
- Letter
5
Derepression of co-silenced tumor suppressor genes by nanoparticle-loaded circular ssDNA reduces tumor malignancy.
- Published in:
- Science Translational Medicine, 2018, v. 10, n. 442, p. 1, doi. 10.1126/scitranslmed.aao6321
- By:
- Publication type:
- Article
6
Alterations in the composition of the gut microbiota affect absorption of cholecalciferol in severe osteoporosis.
- Published in:
- Journal of Bone & Mineral Metabolism, 2022, v. 40, n. 3, p. 478, doi. 10.1007/s00774-021-01303-5
- By:
- Publication type:
- Article
7
Cronkhite–Canada syndrome: An investigation in clinical features and pathogenesis.
- Published in:
- Journal of Digestive Diseases, 2021, v. 22, n. 11, p. 663, doi. 10.1111/1751-2980.13062
- By:
- Publication type:
- Article
8
Protease-activated receptor-1 (PAR1) promotes epithelial-endothelial transition through Twist1 in hepatocellular carcinoma.
- Published in:
- Journal of Experimental & Clinical Cancer Research (17569966), 2018, v. 37, n. 1, p. N.PAG, doi. 10.1186/s13046-018-0858-4
- By:
- Publication type:
- Article