Associated Papers
Deafness DFNB128 Associated with a Recessive Variant of Human MAP3K1 Recapitulates Hearing Loss of Map3k1-Deficient Mice.
Faridi R et al.
Genes, 2024
39062623 (PubMed )
Supplement: genes-15-00845-s001.zip › genes-3045527-Table_S4.xlsx › PKDF1419_SumandMuh_121423_Genet
Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population.
Ostrowski J et al.
Scientific Reports, 2016
28008999 (PubMed )
Supplement: srep39831-s2.xls › Table_S7
Infrequent TRIB3 coding variants and coronary artery disease in type 2 diabetes.
Prudente S et al.
Atherosclerosis, 2015
The mammalian tribbles homolog TRIB3, glucose homeostasis, and cardiovascular diseases.
Prudente S et al.
Endocrine Reviews, 2012
The emerging role of TRIB3 as a gene affecting human insulin resistance and related clinical outcomes.
Prudente S et al.
Acta Diabetologica, 2009
The functional Q84R polymorphism of mammalian Tribbles homolog TRB3 is associated with insulin resistance and related cardiovascular risk in Caucasians from Italy.
Prudente S et al.
Diabetes, 2005
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