Andrew P. South

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 Are Associated with Tylosis, a Familial Esophageal Cancer Syndrome
  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
• Loss-of-function Mutations in Notch Receptors in Cutaneous and Lung Squamous Cell Carcinoma
  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
• No Evidence That Human Papillomavirus is Responsible for the Aggressive Nature of Recessive Dystrophic Epidermolysis Bullosa-associated Squamous Cell Carcinoma
  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