Found: 6
Select item for more details and to access through your institution.
Whole-exome sequencing analysis to identify novel potential pathogenetic NPC1 mutations in two Chinese families with Niemann-Pick disease type C.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Association between polymorphisms rs2228001 and rs2228000 in XPC and genetic susceptibility to preeclampsia: a case control study.
- Published in:
- BMC Pregnancy & Childbirth, 2021, v. 21, n. 1, p. 1, doi. 10.1186/s12884-021-04242-1
- By:
- Publication type:
- Article
Role of histidine decarboxylase gene in the pathogenesis of Tourette syndrome.
- Published in:
- Brain & Behavior, 2022, v. 12, n. 3, p. 1, doi. 10.1002/brb3.2511
- By:
- Publication type:
- Article
Unleashing the Potential of Energy Transformation in the Face of Strict Environmental Regulations, Technological Innovation, and Carbon Emissions.
- Published in:
- Polish Journal of Environmental Studies, 2024, v. 33, n. 5, p. 5703, doi. 10.15244/pjoes/183429
- By:
- Publication type:
- Article
A review of key cytokines based on gene polymorphism in the pathogenesis of pre‐eclampsia.
- Published in:
- American Journal of Reproductive Immunology, 2022, v. 87, n. 1, p. 1, doi. 10.1111/aji.13503
- By:
- Publication type:
- Article
Structural insights into the inhibition mechanism of human sterol O-acyltransferase 1 by a competitive inhibitor.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-16288-4
- By:
- Publication type:
- Article