about
EGASP: the human ENCODE Genome Annotation Assessment ProjectThe DNA sequence of the human X chromosomeSequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolutionFinishing the euchromatic sequence of the human genomeQuality assessment of the human genome sequenceComputational tools and algorithms for designing customized synthetic genesStructural Insights for MPP8 Chromodomain Interaction with Histone H3 Lysine 9: Potential Effect of Phosphorylation on Methyl-Lysine BindingIdentification and characterization of abeta1,3-glucosyltransferase that synthesizes the Glc-beta1,3-Fuc disaccharide on thrombospondin type 1 repeatsMurlet: a practical multiple alignment tool for structural RNA sequencesIndependent centromere formation in a capricious, gene-free domain of chromosome 13q21 in Old World monkeys and pigsComplete Sequence Construction of the Highly Repetitive Ribosomal RNA Gene Repeats in Eukaryotes Using Whole Genome Sequence Data.Heterotachy in mammalian promoter evolution.Rats in the genomic era.Uniparental disomy determined by whole-exome sequencing in a spectrum of rare motoneuron diseases and ataxias.Altered chromosomal positioning, compaction, and gene expression with a lamin A/C gene mutation.De novo LINE-1 retrotransposition in HepG2 cells preferentially targets gene poor regions of chromosome 13Assemblathon 1: a competitive assessment of de novo short read assembly methods.Further evidence for the association between G72/G30 genes and schizophrenia in two ethnically distinct populations.FAM70B as a Novel Prognostic Marker for Cancer Progression and Cancer-Specific Death in Muscle-Invasive Bladder Cancer.Evolutionary change--patterns and processes.Schizophrenia: an integrative approach to modelling a complex disorder.Genetic variation in the DAOA gene complex: impact on susceptibility for schizophrenia and on cognitive performanceDe novo 13q13.3-21.31 deletion involving RB1 gene in a patient with hemangioendothelioma of the liver.EGPred: prediction of eukaryotic genes using ab initio methods after combining with sequence similarity approachesCommon genetic changes in leiomyosarcoma and gastrointestinal stromal tumour: implication for ataxia telangiectasia mutated involvement.Researchers decode gene sequences for chromosomes 13 and 19.Megabase deletions of gene deserts result in viable mice.Delimiting Coalescence Genes (C-Genes) in Phylogenomic Data Sets.Overexpressing TPTE2 (TPIP), a homolog of the human tumor suppressor gene PTEN, rescues the abnormal phenotype of the PTEN-/- mutant.Application of ROMA (representational oligonucleotide microarray analysis) to patients with cytogenetic rearrangements
P2860
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description
2004 nî lūn-bûn
@nan
2004 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
The DNA sequence and analysis of human chromosome 13
@ast
The DNA sequence and analysis of human chromosome 13
@en
The DNA sequence and analysis of human chromosome 13
@nl
type
label
The DNA sequence and analysis of human chromosome 13
@ast
The DNA sequence and analysis of human chromosome 13
@en
The DNA sequence and analysis of human chromosome 13
@nl
prefLabel
The DNA sequence and analysis of human chromosome 13
@ast
The DNA sequence and analysis of human chromosome 13
@en
The DNA sequence and analysis of human chromosome 13
@nl
P2093
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P50
P356
P1433
P1476
The DNA sequence and analysis of human chromosome 13
@en
P2093
Ainscough R
Almeida JP
Ambrose KD
Andrews DT
Ashcroft KJ
Ashurst JL
Ashwell RI
Babbage AK
Bagguley CL
P2860
P2888
P304
P356
10.1038/NATURE02379
P407
P50
P577
2004-04-01T00:00:00Z
P5875
P6179
1043347347