Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Hannah Vuong"'
Autor:
Ivan Macciocca, Kate Dunlop, Belinda J McClaren, Fiona Haslam McKenzie, Amy Nisselle, Sylvia A Metcalfe, Clara Gaff, Hannah Vuong
Publikováno v:
Journal of Genetic Counseling. 28:367-377
We aimed to determine capacity and readiness of Australian clinical genetic healthcare professionals to provide genomic medicine. An online survey was administered to individuals with genetic counseling or clinical genetics qualifications in Australi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::295da92ba28394ddda1c71057eb2fb69
https://doi.org/10.1002/jgc4.1101
https://doi.org/10.1002/jgc4.1101
Autor:
Rawal Jaiessh, Amy Randall, Tram T. Tran, Fiona M. Adam, Daniel Siddle, Iain Gardner, Tanya Parkinson, Manos Perros, David R. Fenwick, Christopher Pickford, Juin Fok-Seang, Charles E. Mowbray, David Howard Williams, Donald Stuart Middleton, Hannah Vuong, Peter T. Stephenson, Michelle Y. Platts, Duncan Hay
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 19:5246-5249
A series of piperazine derivatives were designed and synthesised as gp120-CD4 inhibitors. SAR studies led to the discovery of potent inhibitors in a cell based anti viral assay represented by compounds 9 and 28. The rat pharmacokinetic and antiviral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da3a4d25958155d25e9e2f74217f4f79
https://doi.org/10.1016/j.bmcl.2009.06.080
https://doi.org/10.1016/j.bmcl.2009.06.080
Autor:
Gill Allan, Amy Randall, Sandra D. Newman, Romuald Corbau, Charles E. Mowbray, David Howard Williams, Manos Perros, Mike Westby, Duncan Hay, Donald Stuart Middleton, Hannah Vuong, Lyn H. Jones, Rob Webster
Publikováno v:
ChemMedChem. 3:1756-1762
A major problem associated with non-nucleoside reverse transcriptase inhibitors (NNRTIs) for the treatment of HIV is their vulnerability to mutations in the allosteric binding site of reverse transcriptase that can result in the development of a resi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d441ac28cd9f0ff20ac050167e4fa7a
https://doi.org/10.1002/cmdc.200800183
https://doi.org/10.1002/cmdc.200800183
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32869f8dd9064140d2495fb629a26fe6
https://doi.org/10.1002/chin.199434097
https://doi.org/10.1002/chin.199434097
Autor:
Jaiessh Rawal, David Howard Williams, Donald Stuart Middleton, Michelle Y. Platts, Juin Fok-Seang, Manos Perros, Frederick Calo, Duncan Hay, Christopher Pickford, David R. Fenwick, Tram T. Tran, Hannah Vuong, Fiona M. Adam, Iain Gardner, Tanya Parkinson, Peter T. Stephenson, Amy Randall
Publikováno v:
Bioorganicmedicinal chemistry letters. 19(17)
The synthesis and structure-activity relationship of a series of novel gp120-CD4 inhibitors are described. Pharmacokinetic studies and antiviral spectrum assessment of lead compounds led to the identification of compound 36, a potent gp120-CD4 inhibi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0315d777c77dc2ffe5cf5ff5806e52ce
https://pubmed.ncbi.nlm.nih.gov/19632839
https://pubmed.ncbi.nlm.nih.gov/19632839
Publikováno v:
Synlett. 1994:171-172
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ba6698631e69642b4da97057186e718
https://doi.org/10.1055/s-1994-22780
https://doi.org/10.1055/s-1994-22780