Associated Papers
Bridging pleiotropic mechanisms in leprosy type-1 reactions and neurodegenerative diseases.
Fava VM et al.
Scientific Reports, 2025
41430073 (PubMed )
Supplement: 41598_2025_30734_MOESM2_ESM.xlsx › Variants
Genetic analyses of early-onset Alzheimer's disease using next generation sequencing.
Giau VV et al.
Scientific Reports, 2019
31182772 (PubMed )
Supplement: 41598_2019_44848_MOESM1_ESM.pdf
Rare mutations of ADAM17 from TOFs induce hypertrophy in human embryonic stem cell-derived cardiomyocytes via HB-EGF signaling.
Xie Y et al.
Clinical Science (london, England : 1979), 2019
Whole-exome sequencing identifies Y1495X of SCN5A to be associated with familial conduction disease and sudden death.
Tan ZP et al.
Scientific Reports, 2014
25010007 (PubMed )
Supplement: srep05616-s2.xls › dominant_result_new
Evidence against a role for rare ADAM10 mutations in sporadic Alzheimer disease.
Cai G et al.
Neurobiology of Aging, 2012
Computational analysis and molecular dynamics simulation of high-risk single nucleotide polymorphisms of the ADAM10 gene.
Namme JN et al.
Journal of Biomolecular Structure & Dynamics, 0
36995110 (PubMed )
Supplement: supplement_1.zip › suppl_data › Supplementary_file_1_423_nsSNPs_10_tools.xlsx › Sheet1
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