نتایج جستجو برای: its1 58s its2

تعداد نتایج: 2517  

حضرتی تپه, خسرو , قلی‌زاده, صابر , گلوانی , حسین ,

 Background & Aims: Fascioliasis caused by Fasciola hepatica and Fasciola gigantica has medical and economic importance in the world. Traditional approaches are not accurate and reliable in identification of agent parasites. Thus the present study was designed to identify the Fasciola sppby molecular methods in West Azerbaijan province.Materials & Methods: In current study Fasciola isolates wer...

Journal: :The Chinese journal of dental research : the official journal of the Scientific Section of the Chinese Stomatological Association 2012
Wei Yu Gong Yan Mei Dong Xiao Feng Chen Bekir Karabucak

OBJECTIVE To observe the effects of ionic dissolution products on nano-sized 58S bioactive glass (nano-58S) on proliferation and specific osteogenic genes expression in MG-63 cells. METHODS Ionic dissolution products were prepared by incubating nano-58S or sol-gel bioactive glass 58S (58S) particulates in Dulbecco's modified Eagle's medium (DMEM) at 1% w/v for 24 hr and filtrated through 0.22...

2007
Jae-Gu Han Hyeon-Dong Shin

Some Xylaria materials growing on the fruits of Liquidambar spp. were collected. They were identified as X. persicaria on the basis of morphological characteristics and sequence analysis of the complete ITS region (ITS1-5.8S-ITS2) of rDNA. This is the first record of this species from Korea.

2013
Uma Rao Amita Sharma Nidhi Tyagi Prakash Banakar Mukesh Kumar

The cereal cyst nematodes belonging to Heterodera avenae group is a complex species consisting of 12 valid species and overlapping morphological characters make them difficult to be distinguished from one another. The non coding internal transcribed spacer sequences, ITS1 and ITS2 including 5.8S region of ribosomal DNA (rDNA) has been very useful for the accurate identification of the species a...

2013
Annette W. Coleman

Nuclear rDNA Internal Transcribed Spacers, ITS1 and ITS2, are widely used for eukaryote phylogenetic studies from the ordinal level to the species level, and there is even a database for ITS2 sequences. However, ITS regions have been ignored in mammalian phylogenetic studies, and only a few rodent and ape sequences are represented in GenBank. The reasons for this dearth, and the remedies, are d...

2014
B Babouee Flury M Weisser S Savič Prince L Bubendorf M Battegay R Frei D Goldenberger

BACKGROUND Detection of fungal DNA from formalin-fixed, paraffin-embedded (FFPE) tissue is challenging due to degradation of DNA and presence of PCR inhibitors in these samples. We analyzed FFPE samples of 26 patients by panfungal PCR and compared the results to the composite diagnosis according to the European Organization for Research and Treatment of Cancer (EORTC) criteria. Additionally we ...

Journal: :Journal of economic entomology 2006
Paul F Rugman-Jones Mark S Hoddle Laurence A Mound Richard Stouthamer

Effective plant quarantine and biological control initiatives require rapid and accurate identification of exotic and potentially invasive taxa that may cause high economic losses or environmental damage. The genus Scirtothrips Shull includes several species that are serious agricultural pests, and, because of their minute size and cryptic behavior, prone to undetected transport through interna...

2014
Xu Zheng Qiao-Cheng Chang Yan Zhang Si-Qin Tian Yan Lou Hong Duan Dong-Hui Guo Chun-Ren Wang Xing-Quan Zhu

Sequences of the complete nuclear ribosomal DNA (rDNA) gene from five individual Paramphistomum cervi were determined for the first time. The five complete rDNA sequences, which included the 18S rDNA, the internal transcribed spacer 1 (ITS1), the 5.8S rDNA, the internal transcribed spacer 2 (ITS2), the 28S rDNA, and the intergenic spacer (IGS) regions, had a length range of 8,493-10,221 bp. The...

Journal: :Journal of clinical microbiology 2003
Flavia Hebeler-Barbosa Flavia V Morais Mario R Montenegro Eiko E Kuramae Beatriz Montes Juan G McEwen Eduardo Bagagli Rosana Puccia

Paracoccidioides brasiliensis isolates from 10 nine-banded armadillos (Dasypus novemcinctus) were comparable with 19 clinical isolates by sequence analysis of the PbGP43 gene and ribosomal internal transcribed spacer 1 (ITS1) and ITS2 and by random amplified polymorphic DNA. In this original ITS study, eight isolates differed by one or three sites among five total substitution sites.

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