نتایج جستجو برای: Mitochondrial gene

تعداد نتایج: 1242948  

Journal: :iranian biomedical journal 0
adel spotin soheila rouhani parnazsadat ghaemmaghami ali haghighi mohammad reza zolfaghari aref amirkhani

background: molecular diversity of leishmania major and its morphological changes have become a controversial issue among researchers. some aspects of polymorphic shapes of amastigotes in clinical manifestations along with molecular variation were evaluated among suspected patients of some exceptional zoonotic cutaneous leishmaniasis locations in northern khuzestan, southwestern iran. methods: ...

Journal: :iranian journal of parasitology 0
sima rostami dept. of parasitology, school of medicine, kerman university of medical sciences, kerman, iran. robin nicholas beech institute of parasitology, mcgill university, ste. anne de bellevue, quebec, canada. reza salavati institute of parasitology, mcgill university, ste. anne de bellevue, quebec, canada. mohammad reza baneshi research center for modeling in health, institute for futures studies in health, kerman university of medical sciences, kerman, iran. hossein kamyabi dept. of parasitology, school of medicine, kerman university of medical sciences, kerman, iran. majid fasihi harandi research center of tropical and infectious diseases, kerman university of medical sciences, kerman, iran.

background: the purposes of the present study were morphometric characteri-zation of rostellar hooks of taenia multiceps and to investigate the association of hook length variation and the variability within two mitochondrial genes of sheep isolates of the parasite. methods: up to 4500 sheep brains were examined for the presence of c. cerebralis . biometric characters based on the larval rostel...

Journal: :veterinary research forum 2015
marzie babazadeh hassan sharifiyazdi mohammad moazeni sedigheh gorjipour mahdi heidari

in this study, molecular characterization of echinococcus granulosus sample obtained from water buffalo originating from southwest of iran was performed using comparative sequence analysis of cox1 mitochondrial gene. dna was extracted from protoscoleces removed from hydatid cyst from the liver of a 2-year-old male buffalo slaughtered in khuzestan province. molecular and phylogenetic analyses we...

Journal: :iranian journal of child neurology 0
mohammad medhi heidari phd, assistant professor of molecular genetics, department of biology,sciences school,yazd university of medical sciences, yazd,iran mehri khatami phd, assistant professor of molecular genetics, department of biology,sciences school,yazd university of medical sciences, yazd,iran massoud houshmand phd, assistant professor of human molecular genetics,department of medical genetic,national institute of genetic engineering and biotechnology,tehran,iran eisa mahmoudi phd, assitant professor of mathematical statistic,department of statistics,yazd university, yazd,iran shahriar nafissi md, associate professor of neurology, neurology department, tehran university of medical sciences, tehran,iran

how to cite this article: heidari mm, khatami m, houshmand m, mahmoudi e, nafissi sh .increased prevalence 12308 a > g mutation in mitochondrialtrnaleu (cun) gene associated with earlier age of onset in friedreich ataxia. iranian journal of child neurology 2011;5(4):25-31. objective friedreich ataxia (frda) is an inherited recessive disorder. mitochondrial dna is a candidate modifying factor fo...

Journal: :iranian journal of ichthyology 0
arash jouladeh-roudbar department fisheries, sari university of agriculture sciences and natural resources, mazandran, iran. soheil eagderi department of fisheries, faculty of natural resources, university of tehran, karaj, iran. saber vatandoust department of fisheries, babol branch, islamic azad university, babol, iran.

paraschistura alta , formerly reported from the eastern part of sistan basin in afghanistan, is reported for the first time from the zahak river in iranian part of this basin and its morphological characteristics, coi barcode and its phylogenetic relationship within other members of the genus paraschistura from iran are provided. all the measured meristic and morphometric characters of seven co...

Journal: :مجله علوم اعصاب شفای خاتم 0
leila alizadeh shefa neuroscience research center, khatam alanbia hospital, tehran, iran.

mitochondria are membrane-enclosed organelle found in most eukaryotic cells, which known as power house in cells. this organelle transforms energy into forms that are usable by the cell. the most common psychiatric disorders such as depression and anxiety can be linked to mitochondrial disorders. furthermore, mutations of mitochondrial or nuclear dna (mtdna and ndna, respectively) have been lin...

Mitochondria are membrane-enclosed organelle found in most eukaryotic cells, which known as power house in cells. This organelle transforms energy into forms that are usable by the cell. The most common psychiatric disorders such as depression and anxiety can be linked to mitochondrial disorders. Furthermore, mutations of mitochondrial or nuclear DNA (mtDNA and nDNA, respectively) have been lin...

اقبالی ابراهیم آبادی, منیره, خاتمی, مهری,

Background and purpose: Long QT syndrome is a heart arrhythmia identified by prolongation of the QT interval which is a cause of sudden cardiac death in young individuals. In most cases, abnormalities in heart repolarization are reasons of prolongation of action potential and arrhythmia. The activity of ion channels is sensitive to ATP level, therefore, mitochondrial disorders are considered...

Dianat T, Heidari MM Khatami M Moshtaghiun M

Background: Varicocele is the abnormal tortuosity and dilatation of the veins of the pampiniform plexus within the spermatic cord. Varicocele-related pathology is suspected in infertility as it leads to elevated temperatures in the scrotum and testes, which has a deleterious effect on spermatogenesis. In Varicocele patients, ROS production is enhanced and total antioxidant capacity (TAC) is red...

Journal: :genetics in the 3rd millennium 0
صدف کسرایی sadaf kasraie national institute of genetic engineering and biotechnology (nigeb), tehran, iran مسعود هوشمند masoud houshmand محمد مهدی بانویی mommad mehdi banoei سولماز اعتماد اهری soolmaz etemad ahari مهدی شفا شریعت پناهی mehdi shafa shariat panahi پوران شریعتی pouran shariati محمد علی بهار

huntington disease (hd) is a genetically dominant condition caused by expanded cag repeats which code for glutamine in the hd gene product, huntingtin. huntingtin is expressed in almost all tissues, so abnormalities outside the brain can also be expected. involvement of nuclei and mitochondria in hd pathophysiology has been suggested. in fact, mitochondrial dysfunction is reported in brains of ...

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