about
DNA examination of ancient dental pulp incriminates typhoid fever as a probable cause of the Plague of Athens.Association of leptin -2548G/A and leptin receptor Q223R polymorphisms with increased risk for oral cancer.Association of angiotensin-converting enzyme gene insertion/deletion polymorphism with decreased risk for basal cell carcinoma.Linkage disequilibrium between the expanded (CAG)n repeat and an allele of the adjacent (CCG)n repeat in Huntington's disease patients of Greek origin.Huntington Disease: Genetics, Prevention, and Therapy Approaches.Predictive DNA-testing for Huntington's disease and reproductive decision making: a European collaborative study.A simple and effective approach for detecting maternal cell contamination in molecular prenatal diagnosis.Prenatal testing for Huntington's disease: a European collaborative study.Immunological and molecular detection of human immunodeficiency virus in saliva, and comparison with blood testing.Increased risk of oral cancer in diabetic animals is not associated with c-jun activation pathway.Overcoming Potential Threats to Scientific Advancements: Conflict of Interest, Ulterior Motives, False Innuendos and Harassment.Mutation Screening of Her-2, N-ras and Nf1 Genes in Brain Tumor Biopsies.An unusual phenocopy of the HANAC syndrome without genetic involvement of COL4A1/COL4A2.Effect of Olmesartan on the Level of Oral Cancer Risk Factor PAI1.Expression of ets-1 is not affected by N-ras or H-ras during oral oncogenesis.Cell proliferation and apoptosis culminate in early stages of oral oncogenesis.Gene polymorphisms related to angiogenesis, inflammation and thrombosis that influence risk for oral cancer.Diabetes enhances cell proliferation but not Bax/Bcl-2-mediated apoptosis during oral oncogenesis.Plasminogen activator inhibitor-1 polymorphism is associated with increased risk for oral cancer.Thyroid gland neurofibroma in a NF1 patient.The 1040C/T polymorphism influencing thermal stability and activity of thrombin activatable fibrinolysis inhibitor is associated with risk for oral cancer.The interleukin-8 (-251A/T) polymorphism is associated with increased risk for oral squamous cell carcinoma.Neurofibromatosis-Noonan Syndrome: A Possible Paradigm of the Combination of Genetic and Epigenetic Factors.Gene expression polymorphisms of interleukins-1β, -4, -6, -8, -10, and tumor necrosis factors-α, -β: regression analysis of their effect upon oral squamous cell carcinomaAssociation of angiotensin-converting enzyme gene insertion/deletion polymorphism with increased risk for oral cancerDiabetes may increase risk for oral cancer through the insulin receptor substrate-1 and focal adhesion kinase pathwayStrong association of interleukin-4 (−590 C/T) polymorphism with increased risk for oral squamous cell carcinoma in EuropeansThe low VEGF production allele of the +936C/T polymorphism is strongly associated with increased risk for oral cancerAssociation of platelet glycoprotein Ia polymorphism with minor increase of risk for oral cancerScreening for Familial Mediterranean Fever M694V and V726A Mutations in the Greek PopulationHereditary neuropathy with liability to pressure palsies: the same molecular defect can result in diverse clinical presentationGene Variant Causing High Blood Pressure May Be Associated With Medication-related Jaw OsteonecrosisPrenatal diagnosis of X-linked spinal and bulbar muscular atrophy in a Greek familyStrong association of interleukin-6 -174 G>C promoter polymorphism with increased risk of oral cancerReal-time PCR analysis of trinucleotide repeat allele expansions in the androgen receptor geneHomocysteinemia-associated anetoderma, in a young woman with anorexia nervosa historyBisphosphonate-induced avascular osteonecrosis of the mandible associated with a common thrombophilic mutation in the prothrombin geneHigh frequency of TTTY2-like gene-related deletions in patients with idiopathic oligozoospermia and azoospermiaRecognition of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) in Two Oligosymptomatic Sisters with Low CADASIL Scale Scores and a Venous Dysplasia: Report of a Novel Greek FamilyCerebral Thrombosis: A Neurogenetic Approach
P50
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P50
description
researcher
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wetenschapper
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name
C Yapijakis
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C Yapijakis
@nl
type
label
C Yapijakis
@en
C Yapijakis
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prefLabel
C Yapijakis
@en
C Yapijakis
@nl
P106
P31
P496
0000-0001-6695-186X