نتایج جستجو برای: dna mitochondrial

تعداد نتایج: 613263  

Journal: :نامه انجمن حشره شناسی ایران 0
m. m. sohani j. hajizadeh r. hosseini s. rahimi

all wasp species in the genus lysiphlebus fã¶rster are solitary endoparasitoids of aphids andconsidered a taxonomically difficult group. in this study a part of coi and its2 was used to distinguishtwo closely related species l. fabarum (marshall) and l. confusus tremblay & eady in iran. thesequencing with a similarity about 99.5% showed coi's inability to separate the species l. fabarum an...

Ali Reza Talebi Amirhossein Danafar Ghazaleh Farahmand Mehri Khatami Mohammad Mehdi Heidari, Tahere Dianat

Objective Several recent studies have shown that mitochondrial DNA mutations lead to major disabilities and premature death in carriers. More than 150 mutations in human mitochondrial DNA (mtDNA) genes have been associated with a wide spectrum of disorders. Varicocele, one of the causes of infertility in men wherein abnormal inflexion and distension of veins of the pampiniform plexus is observe...

Journal: :iranian journal of basic medical sciences 0
fatemeh khatami department of biology, yazd university, yazd, iran mohammad mehdi heidari department of biology, yazd university, yazd, iran massoud houshmand department of medical genetics, national institute for genetic engineering and biotechnology, tehran, iran

objective(s): as mitochondrial oxidative stress is probably entailed in atp production, a candidate modifier factor for the long qt syndrome (lqts) could be mitochondrial dna (mtdna). it has been notified that ion channels' activities in cardiomyocytes are sensitive to the atp level. materials and methods: the sample of the research was an iranian family with lqts for mutations by pcr-sscp...

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: :international journal of fertility and sterility 0
mohammad mehdi heidari mehri khatami amirhossein danafar tahere dianat ghazaleh farahmand ali reza talebi

objective: several recent studies have shown that mitochondrial dna mutations lead to major disabilities and premature death in carriers. more than 150 mutations in human mitochondrial dna (mtdna) genes have been associated with a wide spectrum of disorders. varicocele, one of the causes of infertility in men wherein abnormal inflexion and distension of veins of the pampiniform plexus is observ...

Journal: :progress in biological sciences 2013
sajad nazari mohammad pourkazemi majid reza khoshkholgh leila azizzade

mitochondria1 dna (mtdna) control region sequences were analyzed to evaluate the population genetic structure of persian sturgeon (acipenser persicus) in caspian sea. a total of 45 specimens were collected from the different locations of the caspian sea. mtdna control region was amplified using pcr. direct sequencing was performed according standard method. the results showed that 12 haplotypes...

Journal: :caspian journal of environmental sciences 2012
m. pourkazemi al. et

in the present study, mitochondrial dna polymerase chain reaction-restriction fragment length polymorphism (pcr-rflp) assay was used to assess the population structure and genetic relationships among six persian sturgeon, acipenser persicus populations from south caspian sea along the iranian coast. the complete nucleotide dehydrogenase subunit 5 (nadh 5) region of mtdna amplified by pcr was di...

Journal: :caspian journal of environmental sciences 2011
m. khoshkholgh m. pourkazemi s. nazari l. azizzadeh pormehr

the persian sturgeon, acipenser persicus (borodin, 1897), is an economically important species, which mainly inhabits the caspian sea. however, little is known about its population genetic structure. in this study, variation in nucleotide sequences of the mitochondrial dna (mtdna) control region of wild stock persian sturgeon was determined to assess the genetic diversity among different natura...

Objective(s): As mitochondrial oxidative stress is probably entailed in ATP production, a candidate modifier factor for the long QT syndrome (LQTS) could be mitochondrial DNA (mtDNA). It has been notified that ion channels' activities in cardiomyocytes are sensitive to the ATP level. Materials and Methods: The sample of the research was an Iranian family with LQTS for mutations by PCR-SSCP and...

Journal: :molecular biology research communications 2015
majidreza khoshkholgh sajad nazari

the genetic variation and population structure of narrow-clawed crayfish (astacus leptodactylus) was examined by means of polymerase chain reaction (pcr) restriction fragment length polymorphism (rflp) analysis of the cytochrome oxidase subunit i (coi) of mitochondrial dna. a total of 194 adult specimens were collected from seven sample sites including, two in the south caspian sea and one each...

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