arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays.
about
Positional and functional mapping of a neuroblastoma differentiation gene on chromosome 11Focal DNA copy number changes in neuroblastoma target MYCN regulated genesMIMAS: an innovative tool for network-based high density oligonucleotide microarray data management and annotationFISH Oracle: a web server for flexible visualization of DNA copy number data in a genomic context.aCGHViewer: a generic visualization tool for aCGH data.ADaCGH: A parallelized web-based application and R package for the analysis of aCGH data.Interrogation of genomes by molecular copy-number counting (MCC).The Annotation, Mapping, Expression and Network (AMEN) suite of tools for molecular systems biologyCADM1 is a strong neuroblastoma candidate gene that maps within a 3.72 Mb critical region of loss on 11q23Disease-causing 7.4 kb cis-regulatory deletion disrupting conserved non-coding sequences and their interaction with the FOXL2 promotor: implications for mutation screening.Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samples.Identification of two critically deleted regions within chromosome segment 7q35-q36 in EVI1 deregulated myeloid leukemia cell linesMultiplex Amplicon Quantification (MAQ), a fast and efficient method for the simultaneous detection of copy number alterations in neuroblastomaCNV-WebStore: online CNV analysis, storage and interpretation.Early-onset primary antibody deficiency resembling common variable immunodeficiency challenges the diagnosis of Wiedeman-Steiner and Roifman syndromes.Isolation of disseminated neuroblastoma cells from bone marrow aspirates for pretreatment risk assessment by array comparative genomic hybridization.Submicroscopic interstitial deletion of chromosome 11q22.3 in a girl with mild mental retardation and facial dysmorphism: Case report.Array comparative genomic hybridization in male infertility.Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domain.CAPweb: a bioinformatics CGH array Analysis PlatformThe H3K27me3 demethylase UTX is a gender-specific tumor suppressor in T-cell acute lymphoblastic leukemiaNonsyndromic bilateral and unilateral optic nerve aplasia: first familial occurrence and potential implication of CYP26A1 and CYP26C1 genes.RNA G-quadruplexes cause eIF4A-dependent oncogene translation in cancer.Genomic aberrations of the CACNA2D1 gene in three patients with epilepsy and intellectual disabilityFocus on 16p13.3 Locus in Colon CancerA Cre-conditional MYCN-driven neuroblastoma mouse model as an improved tool for preclinical studies.Pharmacological activation of the p53 pathway by nutlin-3 exerts anti-tumoral effects in medulloblastomasCD200/BTLA deletions in pediatric precursor B-cell acute lymphoblastic leukemia treated according to the EORTC-CLG 58951 protocol.Redefining the MED13L syndromeEhlers-Danlos Syndrome, Hypermobility Type, Is Linked to Chromosome 8p22-8p21.1 in an Extended Belgian Family.Allelic imbalances in radiation-associated acute myeloid leukemia.Profiling of conserved non-coding elements upstream of SHOX and functional characterisation of the SHOX cis-regulatory landscape.Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports.Characterization of breast cancer by array comparative genomic hybridization.Report of a female patient with mental retardation and tall stature due to a chromosomal rearrangement disrupting the OPHN1 gene on Xq12Deficiency for the ER-stress transducer OASIS causes severe recessive osteogenesis imperfecta in humans.aCGH-MAS: analysis of aCGH by means of multiagent system.Low-grade chromosomal mosaicism in human somatic and embryonic stem cell populations.Identification of a novel recurrent 1q42.2-1qter deletion in high risk MYCN single copy 11q deleted neuroblastomas.Phenotype of a Belgian Family With 6p25 Deletion Syndrome.
P2860
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P2860
arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays.
description
2005 nî lūn-bûn
@nan
2005 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays
@nl
arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays.
@ast
arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays.
@en
type
label
arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays
@nl
arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays.
@ast
arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays.
@en
prefLabel
arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays
@nl
arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays.
@ast
arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays.
@en
P2093
P2860
P50
P356
P1433
P1476
arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays.
@en
P2093
Bart De Moor
Evi Michels
Joris Vermeesch
Karen Buysse
Piet Robbrecht
Stefan Vermeulen
Yves Moreau
P2860
P2888
P356
10.1186/1471-2105-6-124
P407
P50
P577
2005-05-23T00:00:00Z
P5875
P6179
1001223892