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SAR1a promoter polymorphisms are not associated with fetal hemoglobin in patients with sickle cell disease from Cameroon.
Scanning indels in the 5q22.1 region and identification of the TMEM232 susceptibility gene that is associated with atopic dermatitis in the Chinese Han population
Secondary biopsy of non-oncogenic-driven lung cancer may reveal a clinically sensible histologic change. A brief report of two paradigmatic cases
Segmental allotetraploidy generates extensive homeologous expression rewiring and phenotypic diversity at the population level in rice
Serum concentrations of vitamin E and carotenoids are altered in Alzheimer’s disease: A case-control study
Rare coding variants in PLCG2, ABI3, and TREM2implicate microglial-mediated innate immunity in Alzheimer’s disease
Serum high-sensitive C-reactive protein (hsCRP) level and CRP genetic polymorphisms are associated with abdominal aortic aneurysm
Rare mutations and potentially damaging missense variants in genes encoding fibrillar collagens and proteins involved in their production are candidates for risk for preterm premature rupture of membranes
Single nucleotide polymorphisms for DNA typing in the domestic horse
Reduced dosing and liability in methadone maintenance treatment by targeting oestrogen signal for morphine addiction