نتایج جستجو برای: تشخیص تقلب کمیسازی mtdna 12s rrna real

تعداد نتایج: 609955  

2014
Jie Qing Denise Yan Yuan Zhou Qiong Liu Weijing Wu Zian Xiao Yuyuan Liu Jia Liu Lilin Du Dinghua Xie Xue Zhong Liu Andreas R. Janecke

Inherited deafness has been shown to have high genetic heterogeneity. For many decades, linkage analysis and candidate gene approaches have been the main tools to elucidate the genetics of hearing loss. However, this associated study design is costly, time-consuming, and unsuitable for small families. This is mainly due to the inadequate numbers of available affected individuals, locus heteroge...

2012
Cristina Olivieri Luca Ermini Ermanno Rizzi Giorgio Corti Stefania Luciani Isolina Marota Gianluca De Bellis Franco Rollo

BACKGROUND Sheep (Ovis aries) were domesticated in the Fertile Crescent region about 9,000-8,000 years ago. Currently, few mitochondrial (mt) DNA studies are available on archaeological sheep. In particular, no data on archaeological European sheep are available. METHODOLOGY/PRINCIPAL FINDINGS Here we describe the first portion of mtDNA sequence of a Copper Age European sheep. DNA was extract...

Journal: :RNA 2006
Tim J M Welting Bastiaan J Kikkert Walther J van Venrooij Ger J M Pruijn

RNase MRP is a eukaryotic endoribonuclease involved in nucleolar and mitochondrial RNA processing events. RNase MRP is a ribonucleoprotein particle, which is structurally related to RNase P, an endoribonuclease involved in pre-tRNA processing. Most of the protein components of RNase MRP have been reported to be associated with RNase P as well. In this study we determined the association of thes...

Journal: :Bulletin of entomological research 2011
B A Hatteland W O C Symondson R A King M Skage C Schander T Solhøy

The invasive Iberian slug, Arion lusitanicus, is spreading through Europe and poses a major threat to horticulture and agriculture. Natural enemies, capable of killing A. lusitanicus, may be important to our understanding of its population dynamics in recently invaded regions. We used polymerase chain reaction (PCR) to study predation on A. lusitanicus by carabid beetles in the field. A first m...

Journal: :Systematic biology 2005
Tine Huyse Filip A M Volckaert

The combination of exceptionally high species diversity, high host specificity, and a complex reproduction system raises many questions about the underlying mechanisms triggering speciation in the flatworm genus Gyrodactylus. The coevolutionary history with their goby hosts was investigated using both topology- and distance-based approaches; phylogenies were constructed of the V4 region of the ...

Journal: :European journal of taxonomy 2021

Sampling of remote inland aquatic habitats in South Africa has constantly been yielding novel endemic freshwater crab species (Potamonautes MacLeay,1838). During the present study, we report on discovery and description two new baziya sp. nov., P. mariepskoppie nov.) from Afrotemperate forested mountain regions Eastern Cape Mpumalanga provinces Africa, respectively. Phylogenetic evidence derive...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تهران - دانشکده علوم 1379

dna میتوکندری انسان (mtdna) مولکولی است حلقوی و شامل 16569 جفت نوکلئوتید که کدکننده 13 پروتئین از کمپلکس های آنزیمی زنجیره تنفسی، 22 عدد trna و 2 عدد rrna می باشد. در هر سلول هزاران نسخه از mtdna وجود دارد و یک جهش می تواند در تمام (هموپلاسمی) و یا در تعدادی از مولکول های mtdna (هتروپلاسمی) اتفاق بیفتد. توارث mtdna مادری است یعنی تنها مادر، mtdna را به فرزندان خود منتقل می کند. چنانچه مادرهتروپ...

Amin Honarmand, Fatemeh Divsalar, Kouros Divsalar, Majid Mahmoodi, Mohammad Pour-Ranjbar, Navidreza Giahi, Sara Hesami,

Background: Based on the studies, variation in the mitochondrial DNA (mtDNA) copy number in peripheral blood leukocytes is associated with increased susceptibility to diseases including cancer. Opiate abusers are at high risk for diseases. In this study, we measured the mtDNA copy number in peripheral blood leukocytes in a group of opiate abusers compared with those in healthy individuals. Met...

2009
Soo-Young Choi Young-Eun Kim Dong-bin Ahn Tae-Hoon Kim Jae-Hyuk Choi Hye-Ryung Lee Sang-Joon Hwang Un-Kyung Kim Sang-Heun Lee

OBJECTIVES Hearing loss is the most common sensory disorder in humans and genetic causes are estimated to cause more than 50% of all incidents of congenital hearing loss. To develop an efficient method for a genetic diagnosis of hearing loss, we have developed and validated a genetic hearing loss DNA chip that allows the simultaneous analysis of 7 different mutations in the GJB2, SLC26A4, and t...

Journal: :Human molecular genetics 2001
M X Guan N Fischel-Ghodsian G Attardi

The pathogenetic mechanism of the human mitochondrial 12S rRNA gene mutation at position 1555, associated with non-syndromic deafness and aminoglycoside-induced deafness, has been investigated in 33 transformants obtained by transferring mitochondria from lymphoblastoid cell lines into human mitochondrial DNA (mtDNA)-less (rho *206) cells. In this nearly constant nuclear background, 15 transfor...

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