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Jiannis Ragoussis

Researcher at King's College London

Publications -  8
Citations -  436

Jiannis Ragoussis is an academic researcher from King's College London. The author has contributed to research in topics: Gene & Intron. The author has an hindex of 7, co-authored 8 publications receiving 426 citations.

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Subchromosomal Positioning of the Epidermal Differentiation Complex (EDC) in Keratinocyte and Lymphoblast Interphase Nuclei

TL;DR: This study of the epidermal differentiation complex at 1q21 provides a further example of a gene-dense complex capable of assuming extraterritorial positioning in relation to cell type/transcription status.
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Comparison of human chromosome 6p25 with mouse chromosome 13 reveals a greatly expanded ov-serpin gene repertoire in the mouse.

TL;DR: Compared with human, this larger mouse serpin repertoire probably reflects the need to regulate a larger proteinase repertoire arising from differing evolutionary pressures on the reproductive and immune systems.
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Fine mapping of the human MHC class II region within chromosome band 6p21 and evaluation of probe ordering using interphase fluorescence in situ hybridization.

TL;DR: Eight previously well-characterized and mapped probes derived from the human major histocompatibility complex (MHC) class II region were used to investigate the advantages and limitations of fluorescence in situ hybridization (FISH) techniques for fine mapping.
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Human ovalbumin serpin evolution: phylogenic analysis, gene organization, and identification of new PI8-related genes suggest that two interchromosomal and several intrachromosomal duplications generated the gene clusters at 18q21-q23 and 6p25

TL;DR: A new gene (PI8L1) at 6p25 is identified that is 72% identical to the 18q21 gene PI8, and it is proposed that the ov-serpin gene clusters arose via interchromosomal duplication of PI5 (or a precursor to 6p 25, followed by duplication at 6 p25, and a more recent interchromOSomal duplication from 7p25 to 18q to yield PI8.
Journal Article

Antihuman epidermal growth factor receptor 2 antibody herceptin inhibits autocrine motility factor (AMF) expression and potentiates antitumor effects of AMF inhibitors.

TL;DR: Results presented here suggest that HCT can effectively block both ligand-induced and constitutive expression of AMF associated with high HER2 overexpression, implying a role of the AMF pathway in the action of HCT.