نتایج جستجو برای: mtdna cytb

تعداد نتایج: 10062  

2018
Yichi Zhang Wei Zhao Di Yang Yuan Tian Weizhe Zhang Aiqin Liu

Taenia multiceps and Taenia hydatigena are widely distributed tapeworms of canids. Due to a lack of genetic information on these two parasites in China, in this study we analyzed six coenurus cerebralis and two cysticercus tenuicollis cysts from goats or sheep in Inner Mongolia, northern China by amplifying three mitochondrial genes (cox1, nad4, and cytb). Two haplotypes were obtained at each l...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تربیت مدرس - دانشکده علوم پزشکی 1390

ناشنوایی ارثی، یک بیماری هتروژن ژنتیکی است. جهش در ژن gjb2 علت اکثریت موارد ناشنوایی اتوزومال مغلوب است. جهش 35delg اکثریت موارد جهش های gjb2 را تشکیل می دهد. 35delg، شایع ترین جهش gjb2 می باشد که 5/74 درصد کروموزوم های جهش یافته gjb2 و 8/10 درصد کروموزوم های مطالعه شده در جمعیت ناشنوای ایران را تشکیل می دهد. جهش های mtdna مسئول کمتر از 1% موارد ناشنوایی پیش از زبان باز کردن هستند. جهش های mtdn...

Journal: :Medical and veterinary entomology 2007
P Kengne C Antonio-Nkondjio H P Awono-Ambene F Simard T S Awolola D Fontenille

Distinction between members of the equatorial Africa malaria vector Anopheles moucheti (Evans) s.l. (Diptera: Culicidae) has been based mainly on doubtful morphological features. To determine the level of genetic differentiation between the three morphological forms of this complex, we investigated molecular polymorphism in the gene encoding for mitochondrial cytochrome oxidase b (CytB) and in ...

2014
Xiuqin Zhong Ning Wang Dandan Hu Jiahai Wang Tianyu Liu Xiaobin Gu Shuxian Wang Xuerong Peng Guangyou Yang

Echinococcus granulosus is the causative agent of cystic echinococcosis with medical and veterinary importance in China. Our main objective was to discuss the genotypes and genetic diversity of E. granulosus present in domestic animals and humans in western China. A total of 45 hydatid cyst samples were collected from sheep, humans, and a yak and subjected to an analysis of the sequences of mit...

Journal: :genetics in the 3rd millennium 0
سپیده صفایی sepideh safaei مسعود هوشمند masoud houshmand محمد مهدی بانویی mohammad mehdi banoei مهدی شفا شریعت پناهی mehdi shafa shariat panahi شهریار نفیسی shahriar nafisi کاظم پریور kazem parivar مریم رستمی

the spinocerebellar ataxias (sca) comprise a heterogeneous group of severe late-onset neurodegenerative diseases that are promoted by the expansion of a tandem-arrayed dna sequence that modifies the primary structure of the protein. method: genomic dna of 20 patients with scas was extracted from peripheral blood and screened for deletions in mitochondrial dna (mtdna). sequencing of trna(leu), t...

Journal: :cell journal 0

introduction: a number of maternally inherited mitochondrial diseases with distinct clinical phenotypes have been associated with point mutations in mtdna, all of which result in neurologic or neuromuscular disorders. several studies showed that mutations in the trna genes of mtdna could cause mitochondrial disease due to the decreased synthesis of mitochondrial dna coded proteins. materials an...

D.O.F. Skibinski J.A. Beardmore M. Pourkazemi

The phylogenetic relationship of five sturgeon species in the South Caspian Sea was investigated using mtDNA molecule. Sequence analysis of mtDNA D-loop region of five sturgeon species [Great sturgeon (Huso huso), Russian sturgeon (Acipenser gueldenstaedtii), Persian sturgeon (Acipenser persicus), Ship sturgeon (Acipenser nudiventris), Stellate sturgeon (Acipenser stellatus)] and DNA sequencing...

D.O.F. Skibinski, J.A. Beardmore, M. Pourkazemi,

The phylogenetic relationship of five sturgeon species in the South Caspian Sea was investigated using mtDNA molecule. Sequence analysis of mtDNA D-loop region of five sturgeon species [Great sturgeon (Huso huso), Russian sturgeon (Acipenser gueldenstaedtii), Persian sturgeon (Acipenser persicus), Ship sturgeon (Acipenser nudiventris), Stellate sturgeon (Acipenser stellatus)] and DNA sequencing...

Journal: :Molecular biology of the cell 1999
C T Moraes L Kenyon H Hao

Although the regulation of mitochondrial DNA (mtDNA) copy number is performed by nuclear-coded factors, very little is known about the mechanisms controlling this process. We attempted to introduce nonhuman ape mtDNA into human cells harboring either no mtDNA or mutated mtDNAs (partial deletion and tRNA gene point mutation). Unexpectedly, only cells containing no mtDNA could be repopulated with...

Journal: :hepatitis monthly 0
sharareh kamfar department of molecular medicine and genetics, school of medicine, hamadan university of medical sciences, hamadan, ir iran; research center for molecular medicine, hamadan university of medical sciences, hamadan, ir iran seyed moayed alavian baqiyatallah research center for gastroenterology and liver diseases (brcgl), baqiyatallah university of medical sciences, tehran, ir iran; middle east liver diseases (meld) center, tehran, ir iran massoud houshmand department of medical genetics, national institute for genetic engineering and biotechnology, tehran, ir iran reza yadegarazari shohada hospital of harsin, kermanshah university of medical sciences, kermanshah, ir iran bahram seifi zarei school of medicine, shahid beheshti hospital, hamadan university of medical sciences, hamadan, ir iran alireza khalaj obesity treatment center, department of surgery, shahed university, tehran, ir iran

results the relative expression of mtdna copy number was 3.7 fold higher in nafld patients than healthy controls (p < 0.0001). the results remained significant after adjustment for age, bmi, and gender (p = 0.02). in addition, the mtdna copy number was 4.3 (p < 0.0001) and 3.2-fold (p < 0.0001) higher in nonalcoholic fatty liver (nafl) and non-alcoholic steatohepatitis (nash) patients than heal...

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