objective: depression and anxiety literature in iran is short of cultural/indigenous studies, especially with regard to azeri ethnic group. this study was carried out in order to identify depression and anxiety aspects in azeri ethnic group. methods: in a cross sectional qualitative design, 32 azeri informants (14 patients, 13 lay people, and 5 professionals) recruited in the study using purpos...

Familial Mediterranean fever (FMF), the most frequent of the periodic fever syndromes, is an auto-somal recessive disease, predominantly affecting people of Mediterranean descent, although recently it has been described in many other populations (1-3). Linkage between the gene responsible for FMF (MEFV) and the short arm of chromosome 16 was first shown in 1992. Mediterranean Fever (MEFV) gene ...

purpose: to evaluate the distribution of tnf-alpha promoter -1031t/c and -308g/a polymorphisms in an iranian population with behcet disease and ocular manifestation. method: we investigated the distribution of tnf-alpha promoter -1031t/c and -308g/a polymorphisms in 53 patients with behcet disease (bd) and 79 matched healthy controls, using the pcr-rflp technique. all subjects were from an iran...

Objective: Depression and Anxiety literature in Iran is short of cultural/indigenous studies, especially with regard to Azeri ethnic group. This study was carried out in order to identify depression and anxiety aspects in Azeri ethnic group. Methods: In a cross sectional qualitative design, 32 Azeri informants (14 patients, 13 lay people, and 5 professionals) recruited in the study using pur...

Rett syndrome is a dominant X-linked male-lethal disorder largely caused by mutations in the gene encoding methyl-CpG binding protein 2 (MECP2). Clinical manifestations include neurodevelopmental disorder characterized by early-onset intractable seizures, severe developmental delay, intellectual disability, and abnormal electroencephalograms. Afflicted females show normal development until the ...

BACKGROUND TP53 mutations are the most common genetic alterations in human cancers. There are also several polymorphisms in both exons and introns of TP53 that may influence its anti-tumor functions and increase the risk of cancer development. Associations of the TP53 intron 6 G13964C polymorphism with increased risk of development of several cancers have been investigated in numerous studies, ...

in the present study karyotype of mazani river buffalo was studied in comparison with those of azeri buffalo populations from iran. blood samples were taken from ten (5 males and 5 females) mazani buffaloes and thirty (15 males and 15 females) azeri buffaloes. the mazani buffaloes belong to mazendaran province and azeri buffaloes belong to west and east azerbaijan and ardebil provinces. blood l...

background: the variable numbers of tandem-repeat (vntr) alleles at the phenylalanine hydroxylase (pah) gene have been used in carrier detection and prenatal diagnosis in phenylketonuria families. this study was carried out to analyze vntr alleles at the pah gene in iranian azeri turkish population. methods: in this study, 200 alleles from general population were studied by pcr. results: the fr...