Associated Papers
Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions.
Park H et al.
Acta Neuropathologica Communications, 2022
35246273 (PubMed )
Supplement: 40478_2022_1333_MOESM3_ESM.xlsx › Exome_summary
Identification of HLA class I-restricted immunogenic neoantigens in triple negative breast cancer.
Aparicio B et al.
Frontiers in Immunology, 2022
36405725 (PubMed )
Supplement: Table_1.xlsx › P85
Somatic mutation driven codon transition bias in human cancer.
Son H et al.
Scientific Reports, 2017
29079855 (PubMed )
Supplement: 41598_2017_14543_MOESM1_ESM.pdf
A novel null homozygous mutation confirms CACNA2D2 as a gene mutated in epileptic encephalopathy.
Pippucci T et al.
Plos One, 2013
24358150 (PubMed )
Supplement: pone.0082154.s002.xls › Sheet1
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