The present invention is directed to methods and compositions that are effective in the inhibition of viral replication. In particular, the methods and compositions are effective at interfering with the activity of host cell proteins required in viral replication. For example, an embodiment of the invention is directed to inhibition of flavivirus replication wherein the replication is effected by changing the normal interactions of the host cell protein TIAR or TIA-1.
Compositions And Methods For Viral Resistance Genes
Margo Brinton - Decatur GA, US Andrey Perelygin - Alpharetta GA, US
Assignee:
Georgia State University Research Foundation - Atlanta GA
International Classification:
C12Q001/70 C12Q001/68
US Classification:
435005000, 435006000
Abstract:
The present invention is directed to methods and compositions for identifying viral resistance genes and for identifying individuals having resistant or susceptible genotypes. Once identified as either resistant or susceptible, appropriate actions, such as vaccination, can be undertaken by the individuals. In particular, methods and compositions for identifying genes associated with resistance or susceptibility for flaviviruses are disclosed.
Compositions And Methods For Viral Resistance Genes
Margo Brinton - Decatur GA, US Andrey Perelygin - Alpharetta GA, US
International Classification:
C12Q 1/68
US Classification:
435006000
Abstract:
The present invention further provides a method of evaluating yellow fever virus susceptibility in a subject, which comprises obtaining a nucleic acid containing at least a portion of OAS gene from the subject, and determining whether the nucleic acid comprises SNPs relating to the susceptibility of the subject to yellow fever virus-associated condition. Also provided is a method of evaluating tick-borne encephalitis virus susceptibility in a subject, which comprises obtaining a nucleic acid containing at least a portion of OAS gene from the subject, and whether the nucleic acid comprises SNPs relating to the susceptibility of the subject to tick-borne encephalitis virus-associated condition.
Methods And Compositions For Inhibition Of Viral Replication
Margo A. Brinton - Decatur GA, US Mohamed M. Emara - Atlanta GA, US
International Classification:
A61K 31/7105 C12N 7/01 C12N 5/06 A61P 31/12
US Classification:
514 44, 4352351, 435325
Abstract:
The present invention is directed to methods and compositions that are effective in the inhibition of viral replication. In particular, the methods and compositions are effective at interfering with the activity of host cell proteins required in viral replication. For example, an embodiment of the invention is directed to methods and compositions comprising RNA sequences to which the host cell proteins TIAR and/or TIA-1 bind.
Methods And Compositions For Inhibition Of Viral Replication
The present invention is directed to methods and compositions that are effective in the inhibition of viral replication. In particular, the methods and compositions are effective at interfering with the activity of host cell proteins required in viral replication. For example, an embodiment of the invention is directed to inhibition of flavivirus replication wherein the replication is affected by changing the normal interactions of the host cell protein TIAR or TIA-1.
Dna Sequence Encoding A Cynomolgus Monkey Hepatitis A Virus Capsid Protein
Omana V. Nainan - Decatur GA Harold S. Margolis - Lilburn GA Betty H. Robertson - Chamblee GA Margo A. Brinton - Atlanta GA James W. Ebert - Lilburn GA
Assignee:
The United States of America as represented by the Department of Health and Human Services - Washington DC
International Classification:
C07H 1700 C12P 2102 C12P 1934 C12N 1500
US Classification:
536 2372
Abstract:
The present invention relates, in general, to substantially pure preparations of the cynomolgus monkey hepatitis A viral isolates CY-145 and CY-55/JM-55; cDNAs of the genomic RNAs of cynomolgus monkey hepatitis A viral isolates CY-145 and CY-55/JM-55; a method of preventing hepatitis A in an animal; and vaccines comprising the cynomolgus monkey hepatitis A viral isolates CY-145 and CY-55/JM-55.
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