المؤلفون: Harjama, L., Karvonen, V., Kettunen, K., Elomaa, O., Einarsdottir, Elisabet, Heikkilä, H., Kivirikko, S., Ellonen, P., Saarela, J., Ranki, A., Kere, J., Hannula-Jouppi, K.

المصدر: Journal of the European Academy of Dermatology and Venereology. 35(9):1874-1880

مصطلحات موضوعية: aquaporin 5, cytokeratin 9, AAGAB protein, human, Ly antigen, serine proteinase inhibitor, SERPINB7 protein, SLURP1 protein, urokinase, vesicular transport adaptor protein, AAGAB gene, adolescent, adult, AQP5 gene, Article, child, diffuse palmoplantar keratoderma, disease classification, female, focal palmoplantar keratoderma, gene, gene mutation, genetic disorder, hereditary palmoplantar keratoderma, KRT9 gene, major clinical study, male, palmoplantar keratoderma, phenotype, punctate palmoplantar keratoderma, SERPINB7 gene, SLURP1 gene, whole exome sequencing, genetics, mutation, pedigree, Adaptor Proteins, Vesicular Transport, Antigens, Ly, Humans, Keratoderma, Palmoplantar, Diffuse, Serpins, Urokinase-Type Plasminogen Activator

وصف الملف: print

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-309625

المؤلفون: Wim Teughels, Nadine Schlueter, Maria Clotilde Carra, Iain L. C. Chapple, Nigel Pitts, David J. Manton, Marja L. Laine, Peter Lingström, Maria Grazia Cagetti, Fabio Cocco, Eduardo Montero, Philippe P. Hujoel, Andreas G. Schulte, Cor van Loveren, Fridus van der Weijden, Philippe Bouchard, Svante Twetman, Guglielmo Campus, Luigi Nibali, Alexandre R. Vieira, Hélène Rangé

المساهمون: Periodontology, Preventive Dentistry, Parodontologie (OII, ACTA), Preventieve tandheelkunde (OII, ACTA)

المصدر: Journal of Clinical Periodontology, 44(S18), S39-S51. Blackwell Munksgaard
Chapple, I L C, Bouchard, P, Cagetti, M G, Campus, G, Carra, M-C, Cocco, F, Nibali, L, Hujoel, P, Laine, M L, Lingstrom, P, Manton, D J, Montero, E, Pitts, N, Rangé, H, Schlueter, N, Teughels, W, Twetman, S, van Loveren, C, van der Weijden, F, Vieira, A R & Schulte, A G 2017, ' Interaction of lifestyle, behaviour or systemic diseases with dental caries and periodontal diseases: consensus report of group 2 of the joint EFP/ORCA workshop on the boundaries between caries and periodontal diseases ', Journal of Clinical Periodontology, vol. 44, no. S18, pp. S39-S51 . https://doi.org/10.1111/jcpe.12685

مصطلحات موضوعية: Health Behavior, Dentistry, Fc gamma receptor IIA (Fc gamma RIIA) gene, vitamin C, vitamin D, PROGRESSION, Disease, Bioinformatics, SUPPLEMENTATION, gingival bleeding, Gingivitis, 0302 clinical medicine, Risk Factors, OBSTRUCTIVE SLEEP-APNEA, Tooth loss, genetics, 030212 general & internal medicine, prognostic factor, VITAMIN-D, periodontitis, RISK, diabetes, starch, oral hygiene frequency, vitamin B12, ASSOCIATION, nutrition, risk factor, prediction factor, Periodontics, genome wide association study (GWAS), medicine.symptom, Life Sciences & Biomedicine, periodontal diseases, gingivitis, acquired risk factors, macronutrient, malnutrition, Biology, Dental Caries, smoking, DIET, 03 medical and health sciences, single nucleotide polymorphism (SNP), SDG 3 - Good Health and Well-being, Dentistry, Oral Surgery & Medicine, Vitamin D and neurology, medicine, micronutrient, Humans, Risk factor, ORAL-HEALTH, hyposalivation, Life Style, Periodontal Diseases, caries, Periodontitis, vitamin D receptor (VDR) gene, saliva, Science & Technology, candidate gene study (CGS), fluoride, ASCORBIC-ACID DEPLETION, business.industry, polyunsaturated fatty acid (PUFA), 030206 dentistry, GLOBAL BURDEN, medicine.disease, Chronic periodontitis, amelogenin (AMELX) gene, sugars, carbohydrate, aquaporin (AQP5) gene, Attributable risk, Interleukin 10 (IL10) gene, business, protein

وصف الملف: Print

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53d5f87461b9abcbb299613cd716fe39
https://doi.org/10.1111/jcpe.12685

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مصطلحات الفهرس: aquaporin 5, cytokeratin 9, AAGAB protein, human, Ly antigen, serine proteinase inhibitor, SERPINB7 protein, SLURP1 protein, urokinase, vesicular transport adaptor protein, AAGAB gene, adolescent, adult, AQP5 gene, Article, child, diffuse palmoplantar keratoderma, disease classification, female, focal palmoplantar keratoderma, gene, gene mutation, genetic disorder, hereditary palmoplantar keratoderma, KRT9 gene, major clinical study, male, palmoplantar keratoderma, phenotype, punctate palmoplantar keratoderma, SERPINB7 gene, SLURP1 gene, whole exome sequencing, genetics, mutation, pedigree, Adaptor Proteins, Vesicular Transport, Antigens, Ly, Humans, Keratoderma, Palmoplantar, Diffuse, Serpins, Urokinase-Type Plasminogen Activator, Cancer and Oncology, Cancer och onkologi, Medical Genetics, Medicinsk genetik, Article in journal, info:eu-repo/semantics/article, text

URL: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-309625
Journal of the European Academy of Dermatology and Venereology, 0926-9959, 2021, 35:9, s. 1874-1880