Rapid detection of VHL exon deletions using real-time quantitative PCR. - Wikidata - awgldk - TriplyDB

Rapid detection of VHL exon deletions using real-time quantitative PCR.

Rapid detection of VHL exon deletions using real-time quantitative PCR.

http://www.wikidata.org/entity/Q49125755

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Prolonged duration local anesthesia with minimal toxicity Real-Time PCR: Revolutionizing Detection and Expression Analysis of Genes RTPrimerDB: the real-time PCR primer and probe database, major update 2006.Validation of kinetics similarity in qPCR The von Hippel-Lindau tumor suppressor gene expression level has prognostic value in neuroblastoma qBase relative quantification framework and software for management and automated analysis of real-time quantitative PCR data A SAGE-based screen for genes expressed in sub-populations of neurons in the mouse dorsal root ganglion.Chromosome 15q11-q13 copy number gain detected by array-CGH in two cases with a maternal methylation pattern.Wilms tumor genetics: mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumors.Small deletion at the 7q21.2 locus in a CCM family detected by real-time quantitative PCR Regulation of the Na,K-ATPase gamma-subunit FXYD2 by Runx1 and Ret signaling in normal and injured non-peptidergic nociceptive sensory neurons.Clinical and genetic spectrum of Birt-Hogg-Dube syndrome patients in whom pneumothorax and/or multiple lung cysts are the presenting feature Low VHL mRNA expression is associated with more aggressive tumor features of papillary thyroid carcinoma.Identification of intragenic deletions and duplication in the FLCN gene in Birt-Hogg-Dubé syndrome.Von Hippel-Lindau gene product directs cytokinesis: a new tumor suppressor function.CaMKK-CaMK1a, a new post-traumatic signalling pathway induced in mouse somatosensory neurons Identification of genomic aberrations in hemangioblastoma by droplet digital PCR and SNP microarray highlights novel candidate genes and pathways for pathogenesis.Recurrent Rare Genomic Copy Number Variants and Bicuspid Aortic Valve Are Enriched in Early Onset Thoracic Aortic Aneurysms and Dissections Redefining the MED13L syndrome Genetic counseling in renal masses.Copy-number variation of MCL1 predicts overall survival of non-small-cell lung cancer in a Southern Chinese population.Associations among genotype, clinical phenotype, and intracellular localization of trafficking proteins in ARC syndrome.Intron 22 homologous regions are implicated in exons 1-22 duplications of the F8 gene.Haploinsufficiency of the platelet P2Y12 gene in a family with congenital bleeding diathesis Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency.Fxyd2 regulates Aδ- and C-fiber mechanosensitivity and is required for the maintenance of neuropathic pain.Role of VHL, HIF1A and SDH on the expression of miR-210: Implications for tumoral pseudo-hypoxic fate.Detection of large deletions in the VHL gene using a Real-Time PCR with SYBR Green.Molecular Characterization of a Novel Germline VHL Mutation by Extensive In Silico Analysis in an Indian Family with Von Hippel-Lindau Disease.Diagnosis of Pediatric Acute Adenovirus Infections: Is a Positive PCR Sufficient?Expression of three distinct families of calcium-activated chloride channel genes in the mouse dorsal root ganglion.High-throughput PCR assay design for targeted resequencing using primerXL.Impairment of IGF2 gene expression in prostate cancer is triggered by epigenetic dysregulation of IGF2-DMR0 and its interaction with KLF4.A Case of MECP2 Duplication Syndrome with Gonadotropin-Dependent Precocious Puberty.Clinical and molecular characterization of Brazilian families with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlation.Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified families.Fibroblast growth factor homologous factor 1 (FHF1) is expressed in a subpopulation of calcitonin gene-related peptide-positive nociceptive neurons in the murine dorsal root ganglia.A novel de novo 2.5 Mb microdeletion of 7q22.1 harbours candidate gene for neurobehavioural disorders and mental retardation.The contribution of 7q33 copy number variations for intellectual disability.Inhibition of neuronal FLT3 receptor tyrosine kinase alleviates peripheral neuropathic pain in mice.

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P2860

Rapid detection of VHL exon deletions using real-time quantitative PCR.

http://www.wikidata.org/entity/Q49125755

description

2005 nî lūn-bûn

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2005年の論文

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年學術文章

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2005年學術文章

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name

Rapid detection of VHL exon deletions using real-time quantitative PCR.

@en

Rapid detection of VHL exon deletions using real-time quantitative PCR.

@nl

type

label

Rapid detection of VHL exon deletions using real-time quantitative PCR.

@en

Rapid detection of VHL exon deletions using real-time quantitative PCR.

@nl

prefLabel

Rapid detection of VHL exon deletions using real-time quantitative PCR.

@en

Rapid detection of VHL exon deletions using real-time quantitative PCR.

@nl

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Laboratory Investigation

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Rapid detection of VHL exon deletions using real-time quantitative PCR.

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P2093

Anne De Paepe

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Bruce Poppe

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Els De Smet

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Gert-Jan de Jong

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Jasmien Hoebeeck

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Nurten Yigit

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Richard Zewald

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P2860

Mfold web server for nucleic acid folding and hybridization prediction

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

Measurement of locus copy number by hybridisation with amplifiable probes

MLPA and MAPH: new techniques for detection of gene deletions.

Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinoma.

RTPrimerDB: the real-time PCR primer and probe database

Physical mapping of chromosome 3p25-p26 by fluorescence in situ hybridisation (FISH).

Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations.

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labinvest.3700209

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10.1038/LABINVEST.3700209

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1

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Jo Vandesompele

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8120780

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