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Discovery of biomarkers in rare diseases: innovative approaches by predictive and personalized medicineSerial analysis of gene expression in the hippocampus of patients with mesial temporal lobe epilepsy.Interleukin-10 gene transfer: prevention of multiple organ injury in a murine cecal ligation and puncture model of sepsis.Effect of cetiedil on erythrocyte sickling: new type of antisickling agent that may affect erythrocyte membranes.Biobanking: sample acquisition and quality assurance for 'omics' research.Statin potentiates human platelet eNOS activity without enhancing eNOS mRNA and protein levels.Bioethical challenges of the Ebola outbreak.Four novel thymidine phosphorylase gene mutations in mitochondrial neurogastrointestinal encephalomyopathy syndrome (MNGIE) patients.Neurotrophin receptor immunoreactivity in the hippocampus of patients with mesial temporal lobe epilepsy.Mutations of the CFTR gene in Turkish patients with congenital bilateral absence of the vas deferens.Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients.Novel mutations of the MLC1 gene in Turkish patients.Evidence for genetic susceptibility to thrombosis in idiopathic intracranial hypertensionDNA haplotype analysis at the phenylalanine hydroxylase locus in the Turkish populationEffect of piracetam on sickle erythrocytes and sickle hemoglobinLoss of heterozygosity in the VNTR region of intron 1 of P53 in two retinoblastoma casesMutational analysis of Turkish galactosaemia patientsStudy of 12 mutations in Turkish cystic fibrosis patientsMicrocephaly in a hyperphenylalaninemic infant leading to the diagnosis of maternal hyperphenylalaninemiaGenetic and neurological evaluation of untreated and late-treated patients with phenylketonuriaAssociation between mutations and the variable number tandem repeat alleles in a sample of Turkish phenylketonuria patientsFrequencies of TAP1 and TAP2 gene polymorphisms in the Anatolian populationAutosomal recessive spastic ataxia of Charlevoix-Saguenay in two unrelated Turkish familiesMitochondrial deletion in a boy with growth hormone deficiency mimicking cerebral palsymtDNA nt3243 mutation, external ophthalmoplegia, and hypogonadism in an adolescent girlExpression of matrix metalloproteinases in vasculitic neuropathyThe role of TAP1 and TAP2 gene polymorphism in idiopathic bronchiectasis in childrenLiposome-mediated intraperitoneal interleukin 10 gene transfer increases survival in cecal litigation and puncture model of sepsisAndrogen receptor immunostaining and androgen receptor messenger ribonucleic acid expression are increased in cremaster muscles associated with undescended testisTAP1 and TAP2 gene polymorphisms in childhood cystic echinococcosisChanges in the expression of selenoproteins in mesial temporal lobe epilepsy patients
P50
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P50
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M Ozgüç
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M Ozgüç
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M Ozgüç
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M Ozgüç
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M Ozgüç
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M Ozgüç
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M Ozgüç
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M Ozgüç
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M Ozgüç
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P106
P31
P496
0000-0003-4577-8759