127 papers found
Conservation of the H19 noncoding RNA and H19-IGF2 imprinting mechanism in therians.
Epigenetic Marking Prepares the HumanHOXACluster for Activation During Differentiation of Pluripotent Cells
Systematic evaluation of variability in ChIP-chip experiments using predefined DNA targets
A systematic library for comprehensive overexpression screens in Saccharomyces cerevisiae
Finishing the finished human chromosome 22 sequence
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
The landscape of histone modifications across 1% of the human genome in five human cell lines
Butyrate mediates decrease of histone acetylation centered on transcription start sites and down-regulation of associated genes
hORFeome v3.1: A resource of human open reading frames representing over 10,000 human genes
The evolution of imprinting: chromosomal mapping of orthologues of mammalian imprinted domains in monotreme and marsupial mammals
Sequencing and association analysis of the type 1 diabetes – linked region on chromosome 10p12-q11
Identifying gene regulatory elements by genomic microarray mapping of DNaseI hypersensitive sites
RPS6KA2, a putative tumour suppressor gene at 6q27 in sporadic epithelial ovarian cancer
The DNA sequence and biological annotation of human chromosome 1.
Evidence for Widespread Reticulate Evolution within Human Duplicons
Small regions of overlapping deletions on 6q26 in human astrocytic tumours identified using chromosome 6 tile path array CGH
Investigating chromosome organization with genomic microarrays
Replication timing of human chromosome 6.
Novel microsatellite markers and single nucleotide polymorphisms refine the tylosis with oesophageal cancer ( TOC ) minimal region on 17q25 to 42.5�kb: sequencing does not identify the causative gene
Replication timing of the human genome
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