Research Topics
| M R NovelliSummaryAffiliation: University College London Country: UK Publications
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Detail Information
Publications
Unusual presentation of Lynch SyndromeVeronica Pcc Yu
Cancer Genetics Unit, Royal Marsden NHS Foundation Trust, Fulham Road, London, SW3 6JJ, UK
Hered Cancer Clin Pract 7:12. 2009..We describe a family of Lynch Syndrome with an hMLH1 mutation, that harbours an unusual tumour spectrum and its diagnostic and management challenges...
Haematopoietic development and immunological function in the absence of cathepsin DCalogero Tulone
Division of Infection and Immunity, UCL, London, UK
BMC Immunol 8:22. 2007..This study examines the reconstitution and function of the immune system in the absence of cathepsin D, using bone marrow radiation chimaeras in which all haematopoietic cells are derived from cathepsin D deficient mice...
Tumor burden and clonality in multiple intestinal neoplasia mouse/normal mouse aggregation chimerasM R Novelli
Department of Histopathology, University College London, London WC1E 6JJ, United Kingdom
Proc Natl Acad Sci U S A 96:12553-8. 1999....
X-inactivation patch size in human female tissue confounds the assessment of tumor clonalityMarco Novelli
Department of Histopathology, Rockefeller Building, University Street, University College London Hospitals, London WC1E 6JJ, United Kingdom
Proc Natl Acad Sci U S A 100:3311-4. 2003..Results show that the patch size is relatively large in both the human colon and breast, confounding assessment of tumor clonality with traditional X-inactivation studies...
DOG1 and CD117 are the antibodies of choice in the diagnosis of gastrointestinal stromal tumoursMarco Novelli
Department of Pathology, University College London NHS Trust, University Street, London, UK
Histopathology 57:259-70. 2010..The aim of this study was to examine the staining quality, sensitivity, specificity and utility of antibodies used commonly in GIST diagnosis...
Radiofrequency ablation is effective for the treatment of high-grade dysplasia in Barrett's esophagus after failed photodynamic therapyJ M Dunn
National Medical Laser Centre, Department of Surgery, University College London, London, UK
Endoscopy 43:627-30. 2011..The rate of strictures was 7?% (1/14) and there was a low rate of buried glands (0.5?% follow-up biopsies). These data suggest RFA is both safe and effective for eradication of high-grade dysplasia in patients in whom PDT has failed...
Gastrointestinal Kaposi's sarcoma: CD117 expression and the potential for misdiagnosis as gastrointestinal stromal tumourJ R Parfitt
Department of Pathology, London Health Sciences, London, Ontario, Canada
Histopathology 52:816-23. 2008..The aim was to evaluate the clinicopathological features of GI KS, including the expression of CD117 with and without antigen retrieval...
Comparison of nuclear texture analysis and image cytometric DNA analysis for the assessment of dysplasia in Barrett's oesophagusJ M Dunn
Department of Surgery, National Medical Laser Centre, University College London, London, UK
Br J Cancer 105:1218-23. 2011..We aimed to evaluate NT as a marker of dysplasia in BO and compare with image cytometric DNA analysis (ICM)...
Image cytometry accurately detects DNA ploidy abnormalities and predicts late relapse to high-grade dysplasia and adenocarcinoma in Barrett's oesophagus following photodynamic therapyJ M Dunn
Department of Surgery, National Medical Laser Centre, University College London, 67 73 Riding House Street, London W1W 7EJ, UK
Br J Cancer 102:1608-17. 2010..Our aim was to determine the accuracy of ICDA vs FC, and evaluate DNA ploidy as a prognostic biomarker after histologically successful treatment with photodynamic therapy (PDT)...
Individual crypt genetic heterogeneity and the origin of metaplastic glandular epithelium in human Barrett's oesophagusS J Leedham
Histopathology Unit, Cancer Research UK, London, UK
Gut 57:1041-8. 2008..The histogenesis of Barrett's metaplasia and neo-squamous islands has never been demonstrated. We investigated the oesophageal gland squamous ducts as the source of both epithelial sub-types...
Investigation of pathogenic mechanisms in multiple colorectal adenoma patients without germline APC or MYH/MUTYH mutationsC Thirlwell
Molecular and Population Genetics Laboratory, London Research Institute, Cancer Research UK, 44, Lincoln s Inn Fields, London WC2A 3PX, UK
Br J Cancer 96:1729-34. 2007..We suggest that, at least in some cases, the MCRA phenotype results from germline variation that acts subsequent to tumour initiation, perhaps by causing more rapid or more likely progression from microadenoma to macroadenoma...
