about
A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki diseaseMapping and sequencing of structural variation from eight human genomesDNA sequence of human chromosome 17 and analysis of rearrangement in the human lineageA chromosome 8 gene-cluster polymorphism with low human beta-defensin 2 gene copy number predisposes to Crohn disease of the colonThe human genome: a multifractal analysisAntimicrobial peptides in the female reproductive tract: a critical component of the mucosal immune barrier with physiological and clinical implicationsAnalysis of the DNA sequence and duplication history of human chromosome 15Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosisPolymorphisms in human heat shock factor-1 and analysis of potential biological consequences.Rats in the genomic era.Molecular and evolutionary characteristics of the fraction of human alpha satellite DNA associated with CENP-A at the centromeres of chromosomes 1, 5, 19, and 21A novel deletion mutation in the TUSC3 gene in a consanguineous Pakistani family with autosomal recessive nonsyndromic intellectual disabilityThe centromere: chromatin foundation for the kinetochore machinery.Transmitted duplication of 8p23.1-8p23.2 associated with speech delay, autism and learning difficultiesGenomic profile of copy number variants on the short arm of human chromosome 8.Defensins couple dysbiosis to primary immunodeficiency in Crohn's disease.Tissue plasminogen activator and plasminogen activator inhibitor-1 levels in patients with acute paraquat intoxicationAn analytical workflow for accurate variant discovery in highly divergent regions.Squalene epoxidase is a bona fide oncogene by amplification with clinical relevance in breast cancer.A case report of truncus arteriosus communis and genetic counseling.Characterization of six human disease-associated inversion polymorphismsThe past, present, and future of human centromere genomics.Factor interaction analysis for chromosome 8 and DNA methylation alterations highlights innate immune response suppression and cytoskeletal changes in prostate cancer.SQLE induces epithelial-to-mesenchymal transition by regulating of miR-133b in esophageal squamous cell carcinoma.Evolution of Local Mutation Rate and Its Determinants.TUSC3: a novel tumour suppressor gene and its functional implications.Centromere evolution and CpG methylation during vertebrate speciation.Large tandem, higher order repeats and regularly dispersed repeat units contribute substantially to divergence between human and chimpanzee Y chromosomes.S-plot2: Rapid Visual and Statistical Analysis of Genomic Sequences
P2860
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P2860
description
2006 nî lūn-bûn
@nan
2006 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
DNA sequence and analysis of human chromosome 8
@ast
DNA sequence and analysis of human chromosome 8
@en
DNA sequence and analysis of human chromosome 8
@nl
type
label
DNA sequence and analysis of human chromosome 8
@ast
DNA sequence and analysis of human chromosome 8
@en
DNA sequence and analysis of human chromosome 8
@nl
prefLabel
DNA sequence and analysis of human chromosome 8
@ast
DNA sequence and analysis of human chromosome 8
@en
DNA sequence and analysis of human chromosome 8
@nl
P2093
P2860
P50
P3181
P356
P1433
P1476
DNA sequence and analysis of human chromosome 8
@en
P2093
Andre Rosenthal
Andreas Polley
Andrew R Zimmer
April Cook
Atanas H Mihalev
Atsushi Shimizu
Benjamin Corum
Bruce W Birren
Charles A Whittaker
Charles D Matthews
P2860
P2888
P3181
P356
10.1038/NATURE04406
P407
P50
P577
2006-01-19T00:00:00Z
P5875
P6179
1031486451