A pedigree analysis of deep venous thrombosis caused by rare compound heterozygous PROC mutations combined with a heterozygous THBD mutation
Midkine and TNFSF10 as downstream molecules of type I interferon are involved in the treatment of myelofibrosis
TMAO regulates OTUB1-mediated SLC7A11 stability to promote NAFLD progression
The potential role of serum and urine galectin-3 values in the diagnosis and staging of Parkinson’s disease
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