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Characterization of the human tubulin tyrosine ligase-like 1 gene (TTLL1) mapping to 22q13.1The DNA sequence of human chromosome 21Frequent DNA hypomethylation of human juxtacentromeric BAGE loci in cancerGenomic structure of a copy of the human TPTE gene which encompasses 87 kb on the short arm of chromosome 21.MLL3, a new human member of the TRX/MLL gene family, maps to 7q36, a chromosome region frequently deleted in myeloid leukaemia.Juxtacentromeric region of human chromosome 21: a boundary between centromeric heterochromatin and euchromatic chromosome arms.BAGE Hypomethylation Is an Early Event in Colon Transformation and Is Frequent in Histologically Advanced Adenomas.Clinical and molecular overview of inherited disorders resulting from epigenomic dysregulation.DNA methylation at modifier genes of lung disease severity is altered in cystic fibrosis.Molecular cloning of a human cDNA IGSF3 encoding an immunoglobulin-like membrane protein: expression and mapping to chromosome band 1p13.The HDAC inhibitor SAHA does not rescue CFTR membrane expression in Cystic Fibrosis.New BAGE (B melanoma antigen) genes mapping to the juxtacentromeric regions of human chromosomes 13 and 21 have a cancer/testis expression profile.A compositional map of the cen-q21 region of human chromosome 21Centromeres and neocentromeresBAGE hypomethylation, a new epigenetic biomarker for colon cancer detectionDNA methylation changes in cystic fibrosis: Cause or consequence?Dynamic changes of DNA methylation and lung disease in cystic fibrosis: lessons from a monogenic diseaseBlood co-expression modules identify potential modifier genes of diabetes and lung function in cystic fibrosis
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wetenschapper
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0000-0002-9997-1645