Associated Papers
Evolutionary history of adenomas to colorectal cancer in FAP families.
Yang C et al.
Frontiers in Genetics, 2024
39021676 (PubMed )
Supplement: DataSheet1.ZIP › Somatic › 18R12365.xls › SNVIndel
A Common Genetic Variation in Langerin (CD207) Compromises Cellular Uptake of Staphylococcus aureus.
van Dalen R et al.
Journal of Innate Immunity, 2020
Gene Polymorphisms of CD207 (Langerin) Are Associated With End-Stage Renal Disease.
Kim BW et al.
Transplantation Proceedings, 2016
Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes.
Prescott NJ et al.
Plos Genetics, 2015
25671699 (PubMed )
Supplement: pgen.1004955.s006.xlsx › SNVs
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
25352556 (PubMed )
Supplement: supp_gku1005_nar-01266-met-n-2014-File012.xlsx › TCGA-A2-A04Y-01A.domain
Genetic characterisation of Langerin gene in human immunodeficiency virus-1-infected women from Bahia, Brazil.
Costa GC et al.
Memorias Do Instituto Oswaldo Cruz, 2014
An evolutionary analysis of antigen processing and presentation across different timescales reveals pervasive selection.
Forni D et al.
Plos Genetics, 2014
Common polymorphisms in human langerin change specificity for glycan ligands.
Feinberg H et al.
The Journal of Biological Chemistry, 2013
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