Associated Papers
Encoding and decoding selectivity and promiscuity in the human chemokine-GPCR interaction network.
Kleist AB et al.
Cell, 2025
40273912 (PubMed )
Supplement: NIHMS2076408-supplement-MMC5.xlsx › CK_GENEATLAS
Convergent transcriptomic and genomic evidence supporting a dysregulation of CXCL16 and CCL5 in Alzheimer's disease.
Li X et al.
Alzheimer's Research & Therapy, 2023
36670424 (PubMed )
Supplement: 13195_2022_1159_MOESM2_ESM.xlsx › rare_variants
Germline recessive mutations in PI4KA are associated with perisylvian polymicrogyria, cerebellar hypoplasia and arthrogryposis.
Pagnamenta AT et al.
Human Molecular Genetics, 2015
25855803 (PubMed )
Supplement: supp_ddv117_ddv117supp_table2.xls › Table_S2
SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing.
Tariq M et al.
Genome Biology, 2011
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