Filip Pattyn researcher
Pattyn, Filip
VIAF ID: 314892728 (Personal)
Permalink: http://viaf.org/viaf/314892728
Preferred Forms
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100 0 _ ‡a Filip Pattyn ‡c researcher
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100 1 _ ‡a Pattyn, Filip
4xx's: Alternate Name Forms (3)
Works
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Aberrant methylation of candidate tumor suppressor genes in neuroblastoma |
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Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes |
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Analysing 454 amplicon resequencing experiments using the modular and database oriented Variant Identification Pipeline |
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arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays |
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Combined subtractive cDNA cloning and array CGH: an efficient approach for identification of overexpressed genes in DNA amplicons |
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Cost-effective and robust genotyping using double-mismatch allele-specific quantitative PCR |
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Dickkopf-3 is regulated by the MYCN-induced miR-17-92 cluster in neuroblastoma |
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Disease-causing 7.4 kb cis-regulatory deletion disrupting conserved non-coding sequences and their interaction with the FOXL2 promotor: implications for mutation screening |
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Distinct transcriptional MYCN/c-MYC activities are associated with spontaneous regression or malignant progression in neuroblastomas |
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Effective Alu repeat based RT-Qpcr normalization in cancer cell perturbation experiments |
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Efficient Synonym Search by Semantic Linking of Multiple Data Sets |
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The emerging molecular pathogenesis of neuroblastoma: implications for improved risk assessment and targeted therapy |
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External oligonucleotide standards enable cross laboratory comparison and exchange of real-time quantitative PCR data |
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Focal DNA copy number changes in neuroblastoma target MYCN regulated genes |
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High-throughput PCR assay design for targeted resequencing using primerXL. |
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Identification of a novel recurrent 1q42.2-1qter deletion in high risk MYCN single copy 11q deleted neuroblastomas |
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An integrative genomics screen uncovers ncRNA T-UCR functions in neuroblastoma tumours. |
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Mapping of 5q35 chromosomal rearrangements within a genomically unstable region. |
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Massively parallel sequencing for early molecular diagnosis in Leber congenital amaurosis |
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Meta-mining of neuroblastoma and neuroblast gene expression profiles reveals candidate therapeutic compounds |
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methBLAST and methPrimerDB: web-tools for PCR based methylation analysis |
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methGraph: a genome visualization tool for PCR-based methylation assays. |
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The microRNA body map: dissecting microRNA function through integrative genomics |
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Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platform |
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MYCN and HDAC2 cooperate to repress miR-183 signaling in neuroblastoma |
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MYCN/c-MYC-induced microRNAs repress coding gene networks associated with poor outcome in MYCN/c-MYC-activated tumors. |
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Neuroblastoma cells with overexpressed MYCN retain their capacity to undergo neuronal differentiation |
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Practical tools to implement massive parallel pyrosequencing of PCR products in next generation molecular diagnostics |
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RDML: structured language and reporting guidelines for real-time quantitative PCR data |
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RNA pre-amplification enables large-scale RT-qPCR gene-expression studies on limiting sample amounts |
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RTPrimerDB: the real-time PCR primer and probe database, major update 2006. |
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Single-nucleotide polymorphisms and other mismatches reduce performance of quantitative PCR assays. |
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Targeted expression of mutated ALK induces neuroblastoma in transgenic mice. |
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