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Journal of Biological Chemistry, ISSN 0021-9258, 05/2015, Volume 290, Issue 22, pp. 13875 - 13887
Journal Article
Journal of Investigative Dermatology, ISSN 0022-202X, 05/2004, Volume 122, Issue 5, pp. 1235 - 1244
Corneodesmosin (CDSN), desmoglein 1 (DSG1), and desmocollin 1 (DSC1) are adhesive proteins of the extracellular part of the corneodesmosomes, the junctional... 
kallikreins | stratum corneum | cadherin | desmosomes | proteinases | epidermis | Desmosomes | Epidermis | Stratum corneum | Cadherin | Proteinases | Kallikreins | THIOL PROTEASE | CYSTEINE PROTEASE | HUMAN STRATUM-CORNEUM | CORNEUM CHYMOTRYPTIC ENZYME | HUMAN-EPIDERMIS | DERMATOLOGY | ENDOGENOUS PROTEOLYSIS | TERMINAL DIFFERENTIATION | PIG EPIDERMIS | NETHERTON-SYNDROME | INTERMEDIATE-FILAMENTS | Antibody Specificity | Cadherins - metabolism | Membrane Glycoproteins - metabolism | Humans | Glycoproteins - metabolism | Desmosomes - enzymology | Oligosaccharides - pharmacology | Cadherins - immunology | Serine Endopeptidases - genetics | Desmoglein 1 | Membrane Glycoproteins - immunology | Recombinant Proteins - metabolism | Epidermis - metabolism | Gene Expression | Cells, Cultured | Kallikreins - genetics | Glycosylation | Kidney - cytology | Recombinant Proteins - genetics | Desmocollins | Oligosaccharides - metabolism | Glycoproteins - immunology | Serine Endopeptidases - metabolism | Kallikreins - metabolism | Hydrogen-Ion Concentration | Index Medicus | Cells; Cultured | Cadherins/immunology/metabolism | Glycoproteins/immunology/metabolism | Serine Endopeptidases/genetics/metabolism | Desmosomes/enzymology | Oligosaccharides/metabolism/pharmacology | Epidermis/metabolism | Kidney/cytology | Kallikreins/genetics/metabolism | Recombinant Proteins/genetics/metabolism | Membrane Glycoproteins/immunology/metabolism
Journal Article
Molecular Carcinogenesis, ISSN 0899-1987, 02/2014, Volume 53, Issue 2, pp. 85 - 97
As a link between inflammation and cancer has been reported in many studies, we established an in vitro model of prostatic inflammation to investigate the loss... 
androgen | loss of p53 | inflammation | DNA damage | ROS | prostate | NFkB | Loss of p53 | Androgen | Inflammation | Prostate | SURVIVAL | OXIDATIVE STRESS | CANCER CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | GLUTATHIONE-PEROXIDASE | CARCINOGENESIS | ONCOLOGY | NKX3.1 | CARCINOMAS | LINK | HOMEOBOX GENE | EXPRESSION | Proto-Oncogene Proteins c-mdm2 - genetics | Reactive Oxygen Species - metabolism | Apoptosis - drug effects | Antioxidants - metabolism | Homeodomain Proteins - metabolism | Humans | Transcriptional Activation - drug effects | Tumor Necrosis Factor-alpha - genetics | Apoptosis - genetics | Male | NF-kappa B - metabolism | Interleukin-1beta - genetics | Prostatitis - metabolism | Inflammation - metabolism | Matrix Metalloproteinase 9 - metabolism | Phosphorylation - genetics | Acetylcysteine - analogs & derivatives | Interleukin-1beta - metabolism | Matrix Metalloproteinase 9 - genetics | U937 Cells | Prostate-Specific Antigen - metabolism | Phosphorylation - drug effects | Interleukin-6 - metabolism | Prostate-Specific Antigen - genetics | Glutathione Peroxidase - metabolism | Lysine - analogs & derivatives | Interleukin-6 - genetics | Down-Regulation - genetics | Glutathione Peroxidase - genetics | Prostatitis - drug therapy | Androgens - genetics | Macrophages - metabolism | Receptors, Androgen - genetics | Signal Transduction - drug effects | Cell Line, Tumor | Androgens - metabolism | Tumor Necrosis Factor-alpha - metabolism | Prostatic Neoplasms - metabolism | Receptors, Androgen - metabolism | I-kappa B Proteins - metabolism | I-kappa B Proteins - genetics | Prostatitis - pathology | Tumor Suppressor Protein p53 - genetics | Cell Differentiation - genetics | Prostatic Neoplasms - genetics | Inflammation Mediators - metabolism | Proto-Oncogene Proteins c-mdm2 - metabolism | Prostatic Neoplasms - pathology | Kallikreins - genetics | Tumor Suppressor Protein p53 - metabolism | Antioxidants - pharmacology | Transcription Factors - genetics | Down-Regulation - drug effects | Homeodomain Proteins - genetics | Transcription Factors - metabolism | Up-Regulation - drug effects | Lysine - pharmacology | NF-kappa B - genetics | Cell Differentiation - drug effects | Acetylcysteine - pharmacology | Inflammation - genetics | Macrophages - drug effects | Kallikreins - metabolism | Ubiquitin | Analysis | Kallikrein | Hormones, Sex | Tumor proteins | Mitogens | Androgens | Cytokines | Molecular biology | Gene expression | Prostate cancer | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2016, Volume 11, Issue 8, pp. e0161465 - e0161465
Harlequin Ichthyosis is a severe skin disease caused by mutations in the human gene encoding ABCA12. Here, we characterize a novel mutation in intron 29 of the... 
SPHINGOLIPID METABOLISM | TRANSPORTER ABCA12 | GENE | MULTIDISCIPLINARY SCIENCES | GOLGI-APPARATUS | LAMELLAR GRANULES | EPIDERMAL-KERATINOCYTES | MICE | TERMINAL DIFFERENTIATION | MUTATIONS | PERMEABILITY BARRIER | Exons | Skin - metabolism | Ichthyosis, Lamellar - therapy | ATP-Binding Cassette Transporters - genetics | Base Sequence | Skin Transplantation | Skin - pathology | Disease Models, Animal | Desmosomes - metabolism | Epidermis - metabolism | Epidermis - pathology | Ceramides - metabolism | Chromosome Mapping | Permeability | Genes, Recessive | Sequence Analysis, DNA | Phenotype | Animals | Epidermis - ultrastructure | Ichthyosis, Lamellar - genetics | Keratinocytes - metabolism | Models, Biological | Alleles | Skin - ultrastructure | Mice | Mutation | Glucosylceramides - metabolism | Kallikreins - metabolism | Ichthyosis, Lamellar - pathology | Gene mutations | Physiological aspects | Genetic aspects | Skin | Research | Risk factors | Ichthyosis | Neonates | Animal models | Calcium | Transcription | Veterans | Lamellae | Lipids | Defects | Ceramide glucosyltransferase | Metabolites | Proteolysis | Ceramide | Skin diseases | Enzymes | Congenital diseases | Stratum corneum | Dermatology | Intracellular levels | Secretion | Proteolytic enzymes | Kallikrein | Keratinocytes | Cell division | Epidermis | Metabolism | Ribonucleic acid--RNA | Mutants | Medicine | Pathology | Hypotheses | Index Medicus | RNA | Ribonucleic acid
Journal Article
Aging Cell, ISSN 1474-9718, 08/2017, Volume 16, Issue 4, pp. 837 - 846
Kallistatin, an endogenous protein, protects against vascular injury by inhibiting oxidative stress and inflammation in hypertensive rats and enhancing the... 
34a | sirtuin 1 | RNA | micro | kallistatin | vascular senescence | aging | oxidative stress | microRNA-34a | NECROSIS-FACTOR-ALPHA | TISSUE KALLIKREIN INHIBITOR | BINDING PROTEIN | CELL BIOLOGY | GERIATRICS & GERONTOLOGY | ORGAN INJURY | CAENORHABDITIS-ELEGANS | PROTECTIVE ROLE | PROGENITOR-CELL SENESCENCE | ENDOTHELIAL-CELLS | RENAL INJURY | Sirtuin 1 - metabolism | Diabetes Mellitus, Experimental - drug therapy | Endothelial Progenitor Cells - cytology | MicroRNAs - antagonists & inhibitors | Streptozocin | Humans | Diabetes Mellitus, Experimental - genetics | NADPH Oxidases - metabolism | Caenorhabditis elegans Proteins - metabolism | Cellular Senescence - drug effects | Male | MicroRNAs - metabolism | Sirtuin 1 - genetics | Telomerase - genetics | Plasminogen Activator Inhibitor 1 - metabolism | Superoxides - metabolism | beta-Galactosidase - metabolism | NADPH Oxidases - genetics | Telomerase - metabolism | Diabetes Mellitus, Experimental - chemically induced | Superoxides - antagonists & inhibitors | Nitric Oxide Synthase Type III - metabolism | Plasminogen Activator Inhibitor 1 - genetics | Diabetes Mellitus, Experimental - metabolism | Sirtuins - genetics | Endothelial Progenitor Cells - metabolism | Cellular Senescence - genetics | Caenorhabditis elegans - metabolism | Caenorhabditis elegans - genetics | Catalase - genetics | Endothelial Progenitor Cells - drug effects | Cells, Cultured | Cyclin-Dependent Kinase Inhibitor p16 - genetics | Nitric Oxide Synthase Type III - genetics | Serpins - pharmacology | Catalase - metabolism | Tumor Necrosis Factor-alpha - pharmacology | Animals | Caenorhabditis elegans - drug effects | Genistein - pharmacology | Cyclin-Dependent Kinase Inhibitor p16 - metabolism | Mice | MicroRNAs - genetics | beta-Galactosidase - genetics | Caenorhabditis elegans Proteins - genetics | Sirtuins - metabolism | Tumor Necrosis Factor-alpha - antagonists & inhibitors | Gene expression | MicroRNA | Oxidative stress | Senescence | Genistein | INK4a protein | Kinases | NAD(P)H oxidase | Catalase | Rodents | Aging | Aorta | Telomerase | Protein-tyrosine kinase | Tyrosine | Enzymes | Diabetes mellitus | p16 Protein | MiRNA | Superoxide | SIRT1 protein | Life span | Tumor necrosis factor | MicroRNAs | Stem cells | Nematodes | Diabetes | Index Medicus | microRNA‐34a | Original
Journal Article
Urology, ISSN 0090-4295, 2013, Volume 81, Issue 2, pp. 293 - 300
Journal Article
Cancer Research, ISSN 0008-5472, 02/2010, Volume 70, Issue 3, pp. 968 - 978
Journal Article
International Journal of Molecular Sciences, ISSN 1661-6596, 03/2017, Volume 18, Issue 3, pp. 642 - 642
Osteosarcoma (OS) is an aggressive malignancy of bone affecting children, adolescents and young adults. Understanding vitamin D metabolism and vitamin D... 
Oxidative stress | Membrane vesicle biogenesis | Fibroblast growth factor 23 | Osteosarcoma | Calcitriol | Biomarkers | Inflammation | Microarray | Runx2 | membrane vesicle biogenesis | biomarkers | fibroblast growth factor 23 | BIOCHEMISTRY & MOLECULAR BIOLOGY | 25-HYDROXYVITAMIN D-3-1-ALPHA-HYDROXYLASE | D SYSTEM | CHEMISTRY, MULTIDISCIPLINARY | MICROARRAY ANALYSIS | BREAST-CANCER | microarray | TO-MESENCHYMAL TRANSITION | MESSENGER-RNA | calcitriol | inflammation | COLORECTAL-CANCER | 1,25-DIHYDROXYVITAMIN D-3 | CANDIDATE ONCOGENE | osteosarcoma | oxidative stress | PANCREATIC-CANCER CELLS | Matrix Metalloproteinases - genetics | Oxidative Stress | Humans | Glycoproteins - metabolism | Fibroblast Growth Factors - genetics | Gene Regulatory Networks | Phosphoproteins - metabolism | Core Binding Factor Alpha 1 Subunit - metabolism | Integrin beta4 - metabolism | Vitamins - pharmacology | Fibroblast Growth Factors - metabolism | Bone Morphogenetic Protein 1 - genetics | Bone Morphogenetic Protein 1 - metabolism | Nuclear Proteins - genetics | DNA Helicases - genetics | Extracellular Matrix Proteins - metabolism | Osteosarcoma - metabolism | Glycoproteins - genetics | Extracellular Matrix Proteins - genetics | Kallikreins - genetics | Vitamin D - pharmacology | Nuclear Proteins - metabolism | Phosphoproteins - genetics | Transcription Factors - genetics | Integrin beta4 - genetics | Transcription Factors - metabolism | DNA Helicases - metabolism | Transport Vesicles - metabolism | Transport Vesicles - genetics | Cell Line, Tumor | Inflammation - genetics | Matrix Metalloproteinases - metabolism | Core Binding Factor Alpha 1 Subunit - genetics | Kallikreins - metabolism | Index Medicus
Journal Article
European Urology, ISSN 0302-2838, 2013, Volume 64, Issue 5, pp. 753 - 761
Abstract Background Primary culture and animal and cell-line models of prostate and bladder development have limitations in describing human biology, and novel... 
Urology | MYC (formerly cMYC) | Tissue engineering | Bladder | POU5F1 (formerly OCT4) | KLF4 | SOX2 | Stem cells | Androgen receptor | Pluripotent | NANOG | Ureter | Differentiation | Prostate | Urothelium | INDUCTION | IN-VITRO | DIRECTED DIFFERENTIATION | MESENCHYMAL-EPITHELIAL INTERACTIONS | CULTURE | FIBROBLASTS | UROLOGY & NEPHROLOGY | UROTHELIAL CELLS | EXPRESSION | LINEAGE | HUMAN CANCER | Humans | Middle Aged | Receptors, Androgen - metabolism | Male | Ureter - cytology | Prostate - metabolism | Cellular Reprogramming | SOXB1 Transcription Factors - metabolism | Octamer Transcription Factor-3 - genetics | Cell Differentiation - genetics | Transfection | SOXB1 Transcription Factors - genetics | Time Factors | Gene Expression Regulation, Developmental | Kruppel-Like Transcription Factors - metabolism | Regeneration - genetics | Ureter - physiology | Female | Urinary Bladder - cytology | Prostate-Specific Antigen - metabolism | Prostate - physiology | Ureter - metabolism | Cell Lineage - genetics | Induced Pluripotent Stem Cells - metabolism | Biomarkers - metabolism | Tissue Engineering - methods | Induced Pluripotent Stem Cells - physiology | Urinary Bladder - metabolism | Cell Separation | Cells, Cultured | Uroplakins - metabolism | Proto-Oncogene Proteins c-myc - metabolism | Octamer Transcription Factor-3 - metabolism | Prostate - cytology | Aged | Proto-Oncogene Proteins c-myc - genetics | Kruppel-Like Transcription Factors - genetics | Kallikreins - metabolism | Urinary Bladder - physiology | Embryonic stem cells | Analysis | Index Medicus | Platinum Priority – Prostatic Disease
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2017, Volume 12, Issue 1, pp. e0170427 - e0170427
Our previous studies had reported that Human Tissue Kallikrein 1 (hKLK1) preserved erectile function in aged transgenic rats, while the detailed mechanism of... 
THERAPY | COUNTRIES | ENDOTHELIAL DYSFUNCTION | CORPUS CAVERNOSUM | GENE | NITRIC-OXIDE SYNTHASE | MULTIDISCIPLINARY SCIENCES | ASYMMETRIC DIMETHYLARGININE | TRANSGENIC RATS | EXPRESSION | EPIDEMIOLOGY | Erectile Dysfunction - physiopathology | Humans | Cytochrome P-450 Enzyme System - metabolism | Male | Tissue Kallikreins - genetics | RNA, Messenger - metabolism | Arginine - analogs & derivatives | Aging - genetics | Cyclooxygenase 2 - genetics | Erectile Dysfunction - genetics | Nitric Oxide Synthase Type III - metabolism | Intramolecular Oxidoreductases - metabolism | Cyclic AMP - metabolism | Amidohydrolases - metabolism | Recombinant Proteins - metabolism | Rats, Transgenic | Signal Transduction | RNA, Messenger - genetics | Rats | Recombinant Proteins - genetics | Nitric Oxide Synthase Type III - genetics | Rats, Sprague-Dawley | Erectile Dysfunction - metabolism | Animals | Tissue Kallikreins - physiology | Aging - physiology | Cyclic GMP - metabolism | Intramolecular Oxidoreductases - genetics | Penis - metabolism | Nitric Oxide Synthase Type I - metabolism | Cyclooxygenase 2 - metabolism | Cytochrome P-450 Enzyme System - genetics | Nitric Oxide Synthase Type I - genetics | Penile Erection - physiology | Arginine - metabolism | Penile Erection - genetics | Genetically modified mice | Usage | Impotence | Kallikrein | Genetic aspects | Genetic engineering | Cyclic adenylic acid | Research | Health aspects | Immunohistochemistry | Transgenic | Science | Smooth muscle | Urology | Signal transduction | Tissue kallikrein | Pathways | Rodents | Cyclic GMP | Blood pressure | Age | Construction | Cyclic AMP | Nitric-oxide synthase | Polymerase chain reaction | Signaling | Androgens | Hospitals | Nitric oxide | Diabetes | Cyclooxygenase-2 | Laboratory animals | Index Medicus
Journal Article