Andrew P. South Division of Cancer Research, Ninewells Hospital and Medical School University of Dundee Biography Publications Institution JoVE Articles Andrew P. South has not added a biography. If you are Andrew P. South and would like to personalize this page please email our Author Liaison for assistance. Publications BPAG1-e Restricts Keratinocyte Migration Through Control of Adhesion Stability The Journal of Investigative Dermatology. Feb, 2014 | Pubmed ID: 24552685 Type VII Collagen Regulates Expression of OATP1B3, Promotes Front-to-rear Polarity and Increases Structural Organisation in 3D Spheroid Cultures of RDEB Tumour Keratinocytes Journal of Cell Science. Feb, 2014 | Pubmed ID: 24357722 BPAG1-e Restricts Keratinocyte Migration Through Control of Adhesion Stability The Journal of Investigative Dermatology. Mar, 2014 | Pubmed ID: 24025550 The Design and Optimization of RNA Trans-splicing Molecules for Skin Cancer Therapy Molecular Oncology. Dec, 2013 | Pubmed ID: 23998959 Mutations in AQP5, Encoding a Water-channel Protein, Cause Autosomal-dominant Diffuse Nonepidermolytic Palmoplantar Keratoderma American Journal of Human Genetics. Aug, 2013 | Pubmed ID: 23830519 Gauging NOTCH1 Activation in Cancer Using Immunohistochemistry PloS One. 2013 | Pubmed ID: 23825651 Metaanalysis of the Prevalence of Intrauterine Fetal Death in Gastroschisis American Journal of Obstetrics and Gynecology. Aug, 2013 | Pubmed ID: 23628262 Spatial Analysis in Support of Community Health Intervention Strategies AMIA ... Annual Symposium Proceedings / AMIA Symposium. AMIA Symposium. 2012 | Pubmed ID: 23304301 Germline Mutation in EXPH5 Implicates the Rab27B Effector Protein Slac2-b in Inherited Skin Fragility American Journal of Human Genetics. Dec, 2012 | Pubmed ID: 23176819 Fibroblast-derived Dermal Matrix Drives Development of Aggressive Cutaneous Squamous Cell Carcinoma in Patients with Recessive Dystrophic Epidermolysis Bullosa Cancer Research. Jul, 2012 | Pubmed ID: 22564523 The DSPII Splice Variant is Crucial for Desmosome-mediated Adhesion in HaCaT Keratinocytes Journal of Cell Science. Jun, 2012 | Pubmed ID: 22454510 Wnt5a is Strongly Expressed at the Leading Edge in Non-melanoma Skin Cancer, Forming Active Gradients, While Canonical Wnt Signalling is Repressed PloS One. 2012 | Pubmed ID: 22384081 The Double-edged Sword of Notch Signaling in Cancer Seminars in Cell & Developmental Biology. Jun, 2012 | Pubmed ID: 22309843 RHBDF2 Mutations Sont Associées Par Thylle, Un Syndrome Genetique Cancer De L'oesophage American Journal of Human Genetics. Feb, 2012 | Pubmed ID: 22265016 Spatial Analysis of Preterm Birth Demonstrates Opportunities for Targeted Intervention Maternal and Child Health Journal. Feb, 2012 | Pubmed ID: 21290172 Mutations Perte De Fonction Des Récepteurs Notch Dans Cutanée Et Carcinome épidermoïde Du Poumon Proceedings of the National Academy of Sciences of the United States of America. Oct, 2011 | Pubmed ID: 22006338 Feeder Layers: Co-culture with Nonneoplastic Cells Methods in Molecular Biology (Clifton, N.J.). 2011 | Pubmed ID: 21516429 Isolation and Culture of Squamous Cell Carcinoma Lines Methods in Molecular Biology (Clifton, N.J.). 2011 | Pubmed ID: 21516406 Mathematical Modeling of Cancer Cell Invasion of Tissue: Biological Insight from Mathematical Analysis and Computational Simulation Journal of Mathematical Biology. Jul, 2011 | Pubmed ID: 20872264 Aucun élément De Preuve Que Le Virus Du Papillome Humain Est Responsable De La Nature Agressive De Récessif De L'épidermolyse Bulleuse Associées Aux Carcinomes épidermoïdes The Journal of Investigative Dermatology. Dec, 2010 | Pubmed ID: 20739945 Identification and Characterization of DSPIa, a Novel Isoform of Human Desmoplakin Cell and Tissue Research. Jul, 2010 | Pubmed ID: 20524011 The Molecular Skin Pathology of Familial Primary Localized Cutaneous Amyloidosis Experimental Dermatology. May, 2010 | Pubmed ID: 20507362 Homozygous Mutations in the 5' Region of the JUP Gene Result in Cutaneous Disease but Normal Heart Development in Children The Journal of Investigative Dermatology. Jun, 2010 | Pubmed ID: 20130592 Understanding the Pathogenesis of Recessive Dystrophic Epidermolysis Bullosa Squamous Cell Carcinoma Dermatologic Clinics. Jan, 2010 | Pubmed ID: 19945632 Loss-of-function FERMT1 Mutations in Kindler Syndrome Implicate a Role for Fermitin Family Homolog-1 in Integrin Activation The American Journal of Pathology. Oct, 2009 | Pubmed ID: 19762710 Increased Invasive Behaviour in Cutaneous Squamous Cell Carcinoma with Loss of Basement-membrane Type VII Collagen Journal of Cell Science. Jun, 2009 | Pubmed ID: 19435799 Oncostatin M Receptor-beta Mutations Underlie Familial Primary Localized Cutaneous Amyloidosis American Journal of Human Genetics. Jan, 2008 | Pubmed ID: 18179886 Patients with Recessive Dystrophic Epidermolysis Bullosa Develop Squamous-cell Carcinoma Regardless of Type VII Collagen Expression The Journal of Investigative Dermatology. Oct, 2007 | Pubmed ID: 17495952 Increased Keratinocyte Proliferation Initiated Through Downregulation of Desmoplakin by RNA Interference Experimental Cell Research. Jul, 2007 | Pubmed ID: 17475244 The Use of Non-nutritive Sucking to Decrease the Physiologic Pain Response During Neonatal Circumcision: a Randomized Controlled Trial American Journal of Obstetrics and Gynecology. Aug, 2005 | Pubmed ID: 16098887 Rapid Diagnosis of Lipoid Proteinosis Using an Anti-extracellular Matrix Protein 1 (ECM1) Antibody Journal of Dermatological Science. Aug, 2004 | Pubmed ID: 15265527 Development of Antigen-specific ELISA for Circulating Autoantibodies to Extracellular Matrix Protein 1 in Lichen Sclerosus The Journal of Clinical Investigation. Jun, 2004 | Pubmed ID: 15173881 Reduced Expression of Insulin-like Growth Factor-binding Protein-3 (IGFBP-3) in Squamous Cell Carcinoma Complicating Recessive Dystrophic Epidermolysis Bullosa The Journal of Investigative Dermatology. May, 2004 | Pubmed ID: 15140235 Recurrent Mutations in Kindlin-1, a Novel Keratinocyte Focal Contact Protein, in the Autosomal Recessive Skin Fragility and Photosensitivity Disorder, Kindler Syndrome The Journal of Investigative Dermatology. Jan, 2004 | Pubmed ID: 14962093 Autoantibodies to Extracellular Matrix Protein 1 in Lichen Sclerosus Lancet. Jul, 2003 | Pubmed ID: 12867112 Lack of Plakophilin 1 Increases Keratinocyte Migration and Reduces Desmosome Stability Journal of Cell Science. Aug, 2003 | Pubmed ID: 12840072 Alterations in Desmosome Size and Number Coincide with the Loss of Keratinocyte Cohesion in Skin with Homozygous and Heterozygous Defects in the Desmosomal Protein Plakophilin 1 The Journal of Investigative Dermatology. Jul, 2003 | Pubmed ID: 12839569 Loss of Kindlin-1, a Human Homolog of the Caenorhabditis Elegans Actin-extracellular-matrix Linker Protein UNC-112, Causes Kindler Syndrome American Journal of Human Genetics. Jul, 2003 | Pubmed ID: 12789646 Extracellular Matrix Protein 1 Gene (ECM1) Mutations in Lipoid Proteinosis and Genotype-phenotype Correlation The Journal of Investigative Dermatology. Mar, 2003 | Pubmed ID: 12603844 Strategies to Identify Disease Genes Drugs of Today (Barcelona, Spain : 1998). Apr, 2002 | Pubmed ID: 12532192 Positional Cloning Identifies a Novel Cyclophilin As a Candidate Amplified Oncogene in 1q21 Oncogene. Mar, 2002 | Pubmed ID: 11948409 Lipoid Proteinosis Maps to 1q21 and is Caused by Mutations in the Extracellular Matrix Protein 1 Gene (ECM1) Human Molecular Genetics. Apr, 2002 | Pubmed ID: 11929856 Ingénierie tissulaire de la tumeur stromale Microenvironnement avec application de Cancer Cell Invasion Yi-Zhen Ng1,2, Andrew P. South1 1Division of Cancer Research, Ninewells Hospital and Medical School, University of Dundee, 2Institute of Medical Biology, A*Star, Singapore JoVE 51321 Bioengineering
Ingénierie tissulaire de la tumeur stromale Microenvironnement avec application de Cancer Cell Invasion Yi-Zhen Ng1,2, Andrew P. South1 1Division of Cancer Research, Ninewells Hospital and Medical School, University of Dundee, 2Institute of Medical Biology, A*Star, Singapore JoVE 51321 Bioengineering