Nucleotide sequence analysis of a cDNA clone encoding the 34K movement protein gene of odontoglossum ringspot virus, ORSV-Cy, the Korean isolate

1994 ◽  
Vol 26 (3) ◽  
pp. 995-999 ◽  
Author(s):  
Ki Hyun Ryu ◽  
Won Mok Park
Keyword(s):  
Sequence Analysis ◽  
Nucleotide Sequence ◽  
Cdna Clone ◽  
Protein Gene ◽  
Movement Protein ◽  
Ringspot Virus ◽  
Nucleotide Sequence Analysis ◽  
Korean Isolate ◽  
Odontoglossum Ringspot Virus ◽  
Movement Protein Gene

scholarly journals Nucleotide sequence of cell-to-cell transport protein gene of odontoglossum ringspot virus

1990 ◽  
Vol 18 (24) ◽  
pp. 7448-7448 ◽  
Author(s):  
Y. Isomura ◽  
Y. Matumoto ◽  
A. Murayama ◽  
M. Chatani ◽  
N. Inouye ◽  
...  
Keyword(s):  
Nucleotide Sequence ◽  
Protein Gene ◽  
Transport Protein ◽  
Ringspot Virus ◽  
Cell Transport ◽  
Odontoglossum Ringspot Virus

Poxvirus infection in Hungarian great tits ( Parus major ): Case report

2008 ◽  
Vol 56 (4) ◽  
pp. 539-546 ◽  
Author(s):  
Elena Palade ◽  
Nóra Biró ◽  
Mihály Dobos-Kovács ◽  
Zoltán Demeter ◽  
Míra Mándoki ◽  
...  
Keyword(s):  
Sequence Analysis ◽  
Nucleotide Sequence ◽  
Protein Gene ◽  
Core Protein ◽  
Parus Major ◽  
Great Tit ◽  
Nucleotide Sequence Analysis ◽  
Chain Reaction ◽  
Base Pairs ◽  
Polymerase Chain

From a total of 1819 great tits ( Parus major ) ringed in 2007 in Pilis Mountains, Hungary, 15 birds presented nodular proliferative lesions on different areas of the head and eyelids, suggesting a poxvirus infection. Three birds were submitted for analysis. The presence of avipoxvirus infection was confirmed by histopathology, electron microscopy (EM) and a polymerase chain reaction (PCR) based technique. Nucleotide sequence analysis of a 428 base pairs (bp) fragment of the viral 4b core protein gene revealed 100% identity between two of the Hungarian isolates (PM9 HUN, PM33 HUN) and two great tit poxvirus strains isolated in Norway in 1973 (GTV A256, GTV A311). The third Hungarian isolate (PM34 HUN) was more closely related to a different Norwegian isolate (GTVA310) than to the Hungarian isolates. The nucleotide sequence analysis of a shorter fragment of the viral 4b core protein (227 bp) gene revealed 100% identity between the Hungarian isolates, the same Norwegian isolates and a great tit poxvirus strain detected in Austria in 2007.

Nucleotide sequence analysis of nucleocapsid protein gene of canine distemper virus isolates in Thailand

2005 ◽  
Vol 105 (2) ◽  
pp. 137-142 ◽  
Author(s):  
J. Keawcharoen ◽  
A. Theamboonlers ◽  
P. Jantaradsamee ◽  
A. Rungsipipat ◽  
Y. Poovorawan ◽  
...  
Keyword(s):  
Sequence Analysis ◽  
Nucleotide Sequence ◽  
Nucleocapsid Protein ◽  
Canine Distemper Virus ◽  
Protein Gene ◽  
Nucleotide Sequence Analysis ◽  
Canine Distemper ◽  
Nucleocapsid Protein Gene ◽  
Virus Isolates

Prediction of human rotavirus serotype by nucleotide sequence analysis of the VP7 protein gene.

1988 ◽  
Vol 62 (5) ◽  
pp. 1819-1823 ◽  
Author(s):  
K Y Green ◽  
J F Sears ◽  
K Taniguchi ◽  
K Midthun ◽  
Y Hoshino ◽  
...  
Keyword(s):  
Sequence Analysis ◽  
Nucleotide Sequence ◽  
Protein Gene ◽  
Nucleotide Sequence Analysis ◽  
Human Rotavirus ◽  
Vp7 Protein

Cloning of metallothionein cDNA from neonatal rat liver

1982 ◽  
Vol 2 (10) ◽  
pp. 761-768 ◽  
Author(s):  
J. F. B. Mercer ◽  
P. Hudson
Keyword(s):  
Sequence Analysis ◽  
Nucleotide Sequence ◽  
Rat Liver ◽  
Cdna Clone ◽  
Untranslated Region ◽  
Neonatal Rat ◽  
Nucleotide Sequence Analysis ◽  
Coding Sequence ◽  
Rat Livers ◽  
I Gene

A metallothionein cDNA clone was isolated from a cDNA bank prepared from neonatal rat liver poly(A)-containing RNA by a colony screening procedure using [32P]cDNA probes prepared from mRNA of either metal-induced or uninduced rat livers. Nucleotide sequence analysis of this clone showed that it contained the entire 3′ untranslated region and 30% of the coding sequence for a rat metallothionein. The sequence is remarkably homologous with the mouse metallothionein-I gene.

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