0000000000646608

AUTHOR

Ian O. Ellis

0000-0001-5292-8474

showing 2 related works from this author

Determination ofHER2amplification in primary breast cancer using dual-colour chromogenicin situhybridization is comparable to fluorescencein situhybr…

2010

García-Caballero T, Grabau D, Green A R, Gregory J, Schad A, Kohlwes E, Ellis I O, Watts S & Mollerup J (2010) Histopathology56, 472–480 Determination of HER2 amplification in primary breast cancer using dual-colour chromogenic in situ hybridization is comparable to fluorescence in situ hybridization: a European multicentre study involving 168 specimens Aims: Fluorescence in situ hybridization (FISH) can be used to reveal several genomic imbalances relevant to proper cancer diagnosis and to the correct treatment regime. However, FISH requires expensive and advanced fluorescence microscopes in addition to expertise in fluorescence microscopy. To determine whether a newly developed dual-colou…

In situHistologyCentromereColorChromogenic in situ hybridizationBreast NeoplasmsIn situ hybridizationBiologyPathology and Forensic Medicinebreast cancerBreast cancerFISHHER2NeoplasmsmedicineHumansCISHIn Situ Hybridization FluorescenceMicroscopyHER2 amplificationmedicine.diagnostic_testGene AmplificationCancerOriginal ArticlesGeneral MedicineGenes erbB-2CEN-17medicine.diseaseMolecular biologyEuropeMicroscopy FluorescenceCISHHybridization GeneticFemalein situ hybridizationBreast diseaseFluorescence in situ hybridizationHistopathology
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PORCNmutations in focal dermal hypoplasia: coping with lethality

2009

The X-linked dominant trait focal dermal hypoplasia (FDH, Goltz syndrome) is a developmental defect with focal distribution of affected tissues due to a block of Wnt signal transmission from cells carrying a detrimental PORCN mutation on an active X-chromosome. Molecular characterization of 24 unrelated patients from different ethnic backgrounds revealed 23 different mutations of the PORCN gene in Xp11.23. Three were microdeletions eliminating PORCN and encompassing neighboring genes such as EBP, the gene associated with Conradi-Hunermann-Happle syndrome (CDPX2). 12/24 patients carried nonsense mutations resulting in loss of function. In one case a canonical splice acceptor site was mutated…

GeneticsMutationGenetic counselingNonsense mutationBiologymedicine.disease_causemedicine.diseaseFocal dermal hypoplasiaPORCNGeneticsmedicineMissense mutationSkewed X-inactivationGenetics (clinical)Loss functionHuman Mutation
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