Andrew P. South

Division of Cancer Research, University of Dundee

Research Area

Biography

Andrew P. South has not added Biography.
If you are Andrew P. South and would like to personalize this page please email our Author Liaison for assistance.

JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 7	2014

Other Publications

Article	Year
Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1). Human molecular genetics\| PubMed ID: 11929856	2002
Positional cloning identifies a novel cyclophilin as a candidate amplified oncogene in 1q21. Oncogene\| PubMed ID: 11948409	2002
Strategies to identify disease genes. Drugs of today (Barcelona, Spain : 1998)\| PubMed ID: 12532192	2002
Extracellular matrix protein 1 gene (ECM1) mutations in lipoid proteinosis and genotype-phenotype correlation. The Journal of investigative dermatology\| PubMed ID: 12603844	2003
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\| PubMed ID: 12789646	2003
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\| PubMed ID: 12839569	2003
Lack of plakophilin 1 increases keratinocyte migration and reduces desmosome stability. Journal of cell science\| PubMed ID: 12840072	2003
Autoantibodies to extracellular matrix protein 1 in lichen sclerosus. Lancet\| PubMed ID: 12867112	2003
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\| PubMed ID: 14962093	2004
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\| PubMed ID: 15140235	2004
Development of antigen-specific ELISA for circulating autoantibodies to extracellular matrix protein 1 in lichen sclerosus. The Journal of clinical investigation\| PubMed ID: 15173881	2004
Rapid diagnosis of lipoid proteinosis using an anti-extracellular matrix protein 1 (ECM1) antibody. Journal of dermatological science\| PubMed ID: 15265527	2004
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\| PubMed ID: 16098887	2005
Increased keratinocyte proliferation initiated through downregulation of desmoplakin by RNA interference. Experimental cell research\| PubMed ID: 17475244	2007
Patients with recessive dystrophic epidermolysis bullosa develop squamous-cell carcinoma regardless of type VII collagen expression. The Journal of investigative dermatology\| PubMed ID: 17495952	2007
Oncostatin M receptor-beta mutations underlie familial primary localized cutaneous amyloidosis. American journal of human genetics\| PubMed ID: 18179886	2008
Increased invasive behaviour in cutaneous squamous cell carcinoma with loss of basement-membrane type VII collagen. Journal of cell science\| PubMed ID: 19435799	2009
Loss-of-function FERMT1 mutations in kindler syndrome implicate a role for fermitin family homolog-1 in integrin activation. The American journal of pathology\| PubMed ID: 19762710	2009
Understanding the pathogenesis of recessive dystrophic epidermolysis bullosa squamous cell carcinoma. Dermatologic clinics\| PubMed ID: 19945632	2010
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\| PubMed ID: 20130592	2010
The molecular skin pathology of familial primary localized cutaneous amyloidosis. Experimental dermatology\| PubMed ID: 20507362	2010
Identification and characterization of DSPIa, a novel isoform of human desmoplakin. Cell and tissue research\| PubMed ID: 20524011	2010
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\| PubMed ID: 20739945	2010
Mathematical modeling of cancer cell invasion of tissue: biological insight from mathematical analysis and computational simulation. Journal of mathematical biology\| PubMed ID: 20872264	2011
Spatial analysis of preterm birth demonstrates opportunities for targeted intervention. Maternal and child health journal\| PubMed ID: 21290172	2012
Isolation and culture of squamous cell carcinoma lines. Methods in molecular biology (Clifton, N.J.)\| PubMed ID: 21516406	2011
Feeder layers: co-culture with nonneoplastic cells. Methods in molecular biology (Clifton, N.J.)\| PubMed ID: 21516429	2011
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\| PubMed ID: 22006338	2011
RHBDF2 mutations are associated with tylosis, a familial esophageal cancer syndrome. American journal of human genetics\| PubMed ID: 22265016	2012
The double-edged sword of Notch signaling in cancer. Seminars in cell & developmental biology\| PubMed ID: 22309843	2012
Wnt5a is strongly expressed at the leading edge in non-melanoma skin cancer, forming active gradients, while canonical Wnt signalling is repressed. PloS one\| PubMed ID: 22384081	2012
The DSPII splice variant is crucial for desmosome-mediated adhesion in HaCaT keratinocytes. Journal of cell science\| PubMed ID: 22454510	2012
Fibroblast-derived dermal matrix drives development of aggressive cutaneous squamous cell carcinoma in patients with recessive dystrophic epidermolysis bullosa. Cancer research\| PubMed ID: 22564523	2012
Germline Mutation in EXPH5 Implicates the Rab27B Effector Protein Slac2-b in Inherited Skin Fragility. American journal of human genetics\| PubMed ID: 23176819	2012
Spatial analysis in support of community health intervention strategies. AMIA ... Annual Symposium proceedings / AMIA Symposium. AMIA Symposium\| PubMed ID: 23304301	2012
Metaanalysis of the prevalence of intrauterine fetal death in gastroschisis. American journal of obstetrics and gynecology\| PubMed ID: 23628262	2013
Gauging NOTCH1 Activation in Cancer Using Immunohistochemistry. PloS one\| PubMed ID: 23825651	2013
Mutations in AQP5, encoding a water-channel protein, cause autosomal-dominant diffuse nonepidermolytic palmoplantar keratoderma. American journal of human genetics\| PubMed ID: 23830519	2013
The design and optimization of RNA trans-splicing molecules for skin cancer therapy. Molecular oncology\| PubMed ID: 23998959	2013
BPAG1-e Restricts Keratinocyte Migration through Control of Adhesion Stability. The Journal of investigative dermatology\| PubMed ID: 24025550	2014
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\| PubMed ID: 24357722	2014
BPAG1-e Restricts Keratinocyte Migration through Control of Adhesion Stability. The Journal of investigative dermatology\| PubMed ID: 24552685	2014