Browsing by Author Cavanaugh, Juleen
Showing results 9 to 24 of 24
Further Evidence for Allelic Heterogeneity in Hartnup Disorder
Author(s) | Azmanov, Dimitar; Kowalczuk, Sonja; Rodgers, Helen, et al |
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Type | Journal article |
Date Published | 2008 |
Date Created | - |
Harmonising Reference Intervals for Three Calculated Parameters used in Clinical Chemistry
Author(s) | Hughes, David G.; Koerbin, G.; Potter, Julia, et al |
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Type | Journal article |
Date Published | 2016 |
Date Created | - |
Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19
Author(s) | Seow, Heng; Broer, Stefan; Broer, Angelika, et al |
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Type | Journal article |
Date Published | 2004 |
Date Created | - |
High-resolution SNP microarray investigation of copy number variations on chromosome 18 in a control cohort
Author(s) | Chia, Nicole; Bryce, Michaela; Hickman, Peter, et al |
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Type | Journal article |
Date Published | 2013 |
Date Created | - |
KCNN4 gene variant is associated with Ileal Crohn's disease in the Australian and New Zealand population
Author(s) | Simms, Lisa A; Doecke, James; Roberts, Rebecca L, et al |
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Type | Journal article |
Date Published | 2010 |
Date Created | - |
Lack of association of the CD14 promoter polymorphism--159C/T with Caucasian inflammatory bowel disease
Author(s) | Peters, Kirsten; O'Callaghan, N.; Cavanaugh, Juleen |
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Type | Journal article |
Date Published | 2005 |
Date Created | - |
Molecular Cloning of Mouse Amino Acid Transport System B 0 , a Neutral Amino Acid Transporter Related to Hartnup Disorder
Author(s) | Broer, Angelika; Klingel, Karen; Kowalczuk, Sonja, et al |
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Type | Journal article |
Date Published | 2004 |
Date Created | - |
Neutral amino acid transport in epithelial cells and its malfunction in Hartnup disorder
Author(s) | Broer, Stefan; Cavanaugh, Juleen; Rasko, John Edward |
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Type | Journal article |
Date Published | 2005 |
Date Created | - |
NOD2: Ethnic and geographic differences
Author(s) | Cavanaugh, Juleen |
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Type | Journal article |
Date Published | 2006 |
Date Created | - |
Persistence of the Common Hartnup disease D173N Allele in populations of European origin
Author(s) | Azmanov, Dimitar; Rodgers, Helen; Auray-Blais, Christiane, et al |
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Type | Journal article |
Date Published | 2007 |
Date Created | - |
Prevalence of CARD15/NOD2 mutations in Caucasian healthy people
Author(s) | Hugot, Jean-Pierre; Isabelle, Zaccaria; Cavanaugh, Juleen, et al |
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Type | Journal article |
Date Published | 2007 |
Date Created | - |
Screening for hemochromatosis in asymptomatic subjects with or without a family history
Author(s) | Powell, L W; Dixon, J L; Ramm , G A, et al |
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Type | Journal article |
Date Published | 2006 |
Date Created | - |
The clinical relevance of compound heterozygosity for the C282Y and H63D substitutions in hemochromatosis
Author(s) | Walsh, Alisha; Dixon, J L; Lincoln, D J, et al |
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Type | Journal article |
Date Published | 2006 |
Date Created | - |
The IBD international genetics consortium provides further evidence for linkage to IBD4 and shows gene-environment interaction
Author(s) | Pierik, Marie; Yang, Huiying; Barmada, Michael M, et al |
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Type | Journal article |
Date Published | 2005 |
Date Created | - |
The molecular basis of neutral aminoacidurias
Author(s) | Broer, Angelika; Cavanaugh, Juleen; Rasko, John Edward, et al |
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Type | Journal article |
Date Published | 2006 |
Date Created | - |
Using a thyroid disease-free population to define the reference interval for TSH and free T4 on the Abbott Architect analyser
Author(s) | Hickman, Peter; Koerbin, G.; Simpson, Aaron J., et al |
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Type | Journal article |
Date Published | 2017 |
Date Created | - |
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