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  • Genetic variability of immune‐related lncRNAs: polymorphisms in linc‐pint and LY86‐AS1 are associated with pemphigus foliaceus susceptibility
  • Erlotinib and Trametinib in Patients With EGFR-Mutant Lung Adenocarcinoma and Acquired Resistance to a Prior Tyrosine Kinase Inhibitor
  • Influence of CYP4F2, ApoE, and CYP2A6 gene polymorphisms on the variability of Warfarin dosage requirements and susceptibility to cardiovascular disease in Jordan
  • RET compound inheritance in Chinese patients with Hirschsprung disease: lack of penetrance from insufficient gene dysfunction
  • Association of KATP Gene Polymorphisms with Dyslipidemia and Ischemic Stroke Risks Among Hypertensive Patients in South China
  • The association of lncRNA SNPs and SNPs‐environment interactions based on GWAS with HBV‐related HCC risk and progression
  • Interplay of circadian clock and melatonin pathway gene variants in adults with autism, intellectual disability and sleep problems
  • Impact of STAT1 polymorphisms on crizotinib-induced hepatotoxicity in ALK-positive non-small cell lung cancer patients
  • De novo hepatocellular carcinoma in a non‐cirrhotic allograft 27 years after liver transplantation: A case report
  • Chinese Tuina Protects against Neonatal Hypoxia-Ischemia through Inhibiting the Neuroinflammatory Reaction
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