about
Initial sequencing and analysis of the human genomeIdentification and analysis of functional elements in 1% of the human genome by the ENCODE pilot projectA genome annotation-driven approach to cloning the human ORFeomeSystematic analysis of off-target effects in an RNAi screen reveals microRNAs affecting sensitivity to TRAIL-induced apoptosisQuantitative genetics of CTCF binding reveal local sequence effects and different modes of X-chromosome associationThe DNA sequence and analysis of human chromosome 6DNA sequence and analysis of human chromosome 9Characterization of the human synaptogyrin gene familyThe human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene familyA Gene Map of the Human GenomeDefining functional DNA elements in the human genomeAn anthropoid-specific locus of orphan C to U RNA-editing enzymes on chromosome 22RPS6KA2, a putative tumour suppressor gene at 6q27 in sporadic epithelial ovarian cancerCharacterization of a new member of the human beta-adaptin gene family from chromosome 22q12, a candidate meningioma geneThe human homologue of unc-93 maps to chromosome 6q27 - characterisation and analysis in sporadic epithelial ovarian cancer.Reevaluating human gene annotation: a second-generation analysis of chromosome 22Identification of multiple HTF-island associated genes in the human major histocompatibility complex class III regionEnsembl 2011Human major histocompatibility complex contains genes for the major heat shock protein HSP70Ensembl's 10th yearSmall regions of overlapping deletions on 6q26 in human astrocytic tumours identified using chromosome 6 tile path array-CGHThe landscape of histone modifications across 1% of the human genome in five human cell linesThe evolution of the DLK1-DIO3 imprinted domain in mammalsThe DNA sequence of human chromosome 22Psoriasis upregulated phorbolin-1 shares structural but not functional similarity to the mRNA-editing protein apobec-1beta-1,3-Glucuronyltransferase-1 gene implicated as a candidate for a schizophrenia-like psychosis through molecular analysis of a balanced translocationEnsembl 2012Assignment of the beta B1 crystallin gene (CRYBB1) to human chromosome 22 and mouse chromosome 5Fine-mapping, genomic organization, and transcript analysis of the human ubiquitin-conjugating enzyme gene UBE2L3Ensembl 2013hORFeome v3.1: a resource of human open reading frames representing over 10,000 human genesLinking rare and common disease: mapping clinical disease-phenotypes to ontologies in therapeutic target validationWhere Next for Genetics and Genomics?Molecular mapping of the human major histocompatibility complexGenome-wide meta-analysis identifies new susceptibility loci for migraine.Literature evidence in open targets - a target validation platformAn SNP map of human chromosome 22.High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.A random STS strategy for construction of YAC contigs spanning defined chromosomal regions.Identification of region-specific yeast artificial chromosomes using pools of Alu element-mediated polymerase chain reaction probes labeled via linear amplification.
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description
hulumtues
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researcher
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ricercatore
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wetenschapper
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հետազոտող
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name
Ian Dunham
@ast
Ian Dunham
@de
Ian Dunham
@en
Ian Dunham
@es
Ian Dunham
@fr
Ian Dunham
@nl
Ian Dunham
@sl
type
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Ian Dunham
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Ian Dunham
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Ian Dunham
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Ian Dunham
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Ian Dunham
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Ian Dunham
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Ian Dunham
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prefLabel
Ian Dunham
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Ian Dunham
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Ian Dunham
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Ian Dunham
@es
Ian Dunham
@fr
Ian Dunham
@nl
Ian Dunham
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P106
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118063327X
P2456
P3029
P31
P496
0000-0003-2525-5598
P734
P735
P7859
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