Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Ana Domazetovska"'
Publikováno v:
Microbiology Spectrum, Vol 10, Iss 4 (2022)
ABSTRACT Currently available methods for the laboratory investigation of Legionella pneumophila outbreaks require organism culture. The ability to sequence L. pneumophila directly from clinical samples would significantly reduce delays. Here, we deve
Externí odkaz:
https://doaj.org/article/e9ebfda495d04cf8b50c51c71ef47c67
Autor:
Ana Domazetovska, Rogan Lee, Chandra Adhikari, Matthew Watts, Nicole Gilroy, Damien Stark, Shobini Sivagnanam
Publikováno v:
Tropical Medicine and Infectious Disease, Vol 3, Iss 3, p 73 (2018)
In Australia, amoebiasis is thought to occur in travellers, immigrants from endemic areas, and among men who have sex with men. Prevalence of amoebiasis in communities with immigrants from Entamoeba histolytica-endemic countries is unknown. The prese
Externí odkaz:
https://doaj.org/article/c10adfc42224409f94fb28116a9d4e12
Publikováno v:
European Journal of Clinical Microbiology & Infectious Diseases. 42:665-667
Akademický článek
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Publikováno v:
Pathology. 54:S85-S86
Autor:
Rogan Lee, Shobini Sivagnanam, Matthew R Watts, Damien Stark, Ana Domazetovska, Chandra Adhikari, Nicole Gilroy
Publikováno v:
Tropical Medicine and Infectious Disease
Tropical Medicine and Infectious Disease, Vol 3, Iss 3, p 73 (2018)
Volume 3
Issue 3
Tropical Medicine and Infectious Disease, Vol 3, Iss 3, p 73 (2018)
Volume 3
Issue 3
In Australia, amoebiasis is thought to occur in travellers, immigrants from endemic areas, and among men who have sex with men. Prevalence of amoebiasis in communities with immigrants from Entamoeba histolytica-endemic countries is unknown. The prese
Autor:
Sandra T. Cooper, Biljana Ilkovski, Sophie Clément, Kathryn N. North, Nigel G. Laing, Kristen J. Nowak, Ana Domazetovska, Adam Maxwell, Kay E. Davies
Publikováno v:
Human Molecular Genetics, Vol. 13, No 16 (2004) pp. 1727-1743
We have studied a cohort of nemaline myopathy (NM) patients with mutations in the muscle alpha-skeletal actin gene (ACTA1). Immunoblot analysis of patient muscle demonstrates increased gamma-filamin, myotilin, desmin and alpha-actinin in many NM pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::460df143422778a3e6970b2f2d12e2df
http://doc.rero.ch/record/291276/files/ddh185.pdf
http://doc.rero.ch/record/291276/files/ddh185.pdf
Autor:
Leigh B. Waddell, Nigel F. Clarke, Andrew J. Kornberg, Ana Domazetovska, Catriona McLean, Kathryn N. North
Publikováno v:
Neuromuscular Disorders. 19:348-351
Cap disease or cap myopathy is a form of congenital myopathy in which peripheral, well-demarcated 'caps' of disorganised thin filaments are seen in muscle fibres. Mutation of the TPM2 gene, that encodes beta-tropomyosin, is the first reported genetic
Autor:
Michelle Peckham, David O. Hutchinson, Valentina A. Valova, Phillip J. Robinson, Sandra T. Cooper, Ana Domazetovska, Aurelie Vandebrouck, Biljana Ilkovski, Kathryn N. North, Vikash Kumar, John C. Sparrow
Publikováno v:
Annals of Neurology. 62:597-608
Objective Mutations in the α-skeletal actin gene (ACTA1) result in a variety of inherited muscle disorders characterized by different pathologies and variable clinical phenotypes. Mutations at Val163 in ACTA1 result in pure intranuclear rod myopathy
Autor:
James R. Bamburg, Edna C. Hardeman, Ana Domazetovska, Biljana Ilkovski, Peter W. Gunning, Laurie S. Minamide, Majid Ghoddusi, Sandra T. Cooper, Kathryn N. North
Publikováno v:
Brain. 130:3275-3284
Specific mutations within the alpha-skeletal actin gene (ACTA1) result in intranuclear rod myopathy (IRM), characterized by rod-like aggregates containing actin and alpha-actinin-2 inside the nucleus of muscle cells. The mechanism leading to formatio