Detection of chromosomal imbalances in retinoblastoma by matrix-based comparative genomic hybridization.
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RetinoblastomaKIAA1797/FOCAD encodes a novel focal adhesion protein with tumour suppressor function in gliomasDiffuse anterior retinoblastoma: current conceptsGenomic differences between retinoma and retinoblastoma.Jacobsen syndrome and Beckwith-Wiedemann syndrome caused by a parental pericentric inversion inv(11)(p15q24).Analysis of array-CGH data using the R and Bioconductor software suite.Low physiologic oxygen tensions reduce proliferation and differentiation of human multipotent mesenchymal stromal cells.MYC high level gene amplification is a distinctive feature of angiosarcomas after irradiation or chronic lymphedemaCdh11 acts as a tumor suppressor in a murine retinoblastoma model by facilitating tumor cell death.Delineation of two clinically and molecularly distinct subgroups of posterior fossa ependymoma.Binding of pro-prion to filamin A: by design or an unfortunate blunderEstablishment of a patient-derived orthotopic osteosarcoma mouse modelMurine bilateral retinoblastoma exhibiting rapid-onset, metastatic progression and N-myc gene amplificationRetinoblastoma: Recent trends A mini review based on published literature.Chromosome 6p amplification and cancer progression.Array-based profiling of reference-independent methylation status (aPRIMES) identifies frequent promoter methylation and consecutive downregulation of ZIC2 in pediatric medulloblastoma.Loss of photoreceptorness and gain of genomic alterations in retinoblastoma reveal tumor progression.A Meta-Analysis of Retinoblastoma Copy Numbers Refines the List of Possible Driver Genes Involved in Tumor Progression.Recent advances in array comparative genomic hybridization technologies and their applications in human genetics.BRAF gene duplication constitutes a mechanism of MAPK pathway activation in low-grade astrocytomas.Somatic genomic alterations in retinoblastoma beyond RB1 are rare and limited to copy number changes.KIF14 and E2F3 mRNA expression in human retinoblastoma and its phenotype association.Insights from mouse models into human retinoblastomaConstitutional trisomy 8p11.21-q11.21 mosaicism: a germline alteration predisposing to myeloid leukaemia.The genomic landscape of retinoblastoma: a review.Genome-wide analysis for micro-aberrations in familial exstrophy of the bladder using array-based comparative genomic hybridization.Molecular classification of diffuse cerebral WHO grade II/III gliomas using genome- and transcriptome-wide profiling improves stratification of prognostically distinct patient groups.Screening for large rearrangements of the RB1 gene in Iranian patients with retinoblastoma using multiplex ligation-dependent probe amplification.Phosphorylation of pRb: mechanism for RB pathway inactivation in MYCN-amplified retinoblastoma.Oncogenic FAM131B-BRAF fusion resulting from 7q34 deletion comprises an alternative mechanism of MAPK pathway activation in pilocytic astrocytoma.Genotyping of Polymorphic Microsatellite Markers Linked to RB1 Locus in Iranian Population.Dissecting the genotype in syndromic intellectual disability using whole exome sequencing in addition to genome-wide copy number analysis.Frequent loss of chromosome 9, homozygous CDKN2A/p14(ARF)/CDKN2B deletion and low TSC1 mRNA expression in pleomorphic xanthoastrocytomas.Genomic profiling to assess the clonal relationship between histologically distinct intracranial tumours.Mapping candidate regions and genes for congenital anomalies of the kidneys and urinary tract (CAKUT) by array-based comparative genomic hybridization.Loss at chromosome arm 16q in retinoblastoma: confirmation of the association with diffuse vitreous seeding and refinement of the recurrently deleted region.Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation.Uniparental disomy at chromosome 11p15.5 followed by HRAS mutations in embryonal rhabdomyosarcoma: lessons from Costello syndrome.Genomic profiling reveals distinctive molecular relapse patterns in IDH1/2 wild-type glioblastoma.Molecular characterization of long-term survivors of glioblastoma using genome- and transcriptome-wide profiling.
P2860
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P2860
Detection of chromosomal imbalances in retinoblastoma by matrix-based comparative genomic hybridization.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh
2005年學術文章
@zh-hant
name
Detection of chromosomal imbal ...... arative genomic hybridization.
@en
type
label
Detection of chromosomal imbal ...... arative genomic hybridization.
@en
prefLabel
Detection of chromosomal imbal ...... arative genomic hybridization.
@en
P2093
P50
P356
P1476
Detection of chromosomal imbal ...... arative genomic hybridization.
@en
P2093
Boris Zielinski
Dietmar R Lohmann
Frank Mendrzyk
Grischa Toedt
Sandrine Gratias
P304
P356
10.1002/GCC.20186
P577
2005-07-01T00:00:00Z