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Browsing by Author Cavanaugh, Juleen

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Showing results 4 to 22 of 22

CARD15 and Crohns Disease

Author(s)Peters, Kirsten; Cavanaugh, Juleen
TypeJournal article
Date Published2004
Date Created-

CARD15/NOD2 Risk alleles in the development of Crohn's disease in the Australian population

Author(s)Cavanaugh, Juleen; Adams, K E; Quak, E J, et al
TypeJournal article
Date Published2003
Date Created-

Characterisation of a highly sensitive troponin I assay and its application to a cardio-healthy population

Author(s)Koerbin, Gus; Tate, Jill; Potter, Julia, et al
TypeJournal article
Date Published2012
Date Created-

Deletion of Glu155 causes a deficiency of glutathione transferase Omega 1-1 but does not alter sensitivity to arsenic trioxide and other cytotoxic drugs

Author(s)Schmuck, Erica; Cappello, Jean; Coggan, Marjorie, et al
TypeJournal article
Date Published2008
Date Created-

Further Evidence for Allelic Heterogeneity in Hartnup Disorder

Author(s)Azmanov, Dimitar; Kowalczuk, Sonja; Rodgers, Helen, et al
TypeJournal article
Date Published2008
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
TypeJournal article
Date Published2004
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
TypeJournal article
Date Published2013
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
TypeJournal article
Date Published2010
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
TypeJournal article
Date Published2005
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
TypeJournal article
Date Published2004
Date Created-

Neutral amino acid transport in epithelial cells and its malfunction in Hartnup disorder

Author(s)Broer, Stefan; Cavanaugh, Juleen; Rasko, John Edward
TypeJournal article
Date Published2005
Date Created-

NOD2: Ethnic and geographic differences

Author(s)Cavanaugh, Juleen
TypeJournal article
Date Published2006
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
TypeJournal article
Date Published2007
Date Created-

Prevalence of CARD15/NOD2 mutations in Caucasian healthy people

Author(s)Hugot, Jean-Pierre; Isabelle, Zaccaria; Cavanaugh, Juleen, et al
TypeJournal article
Date Published2007
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
TypeJournal article
Date Published2006
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
TypeJournal article
Date Published2006
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
TypeJournal article
Date Published2005
Date Created-

The molecular basis of neutral aminoacidurias

Author(s)Broer, Angelika; Cavanaugh, Juleen; Rasko, John Edward, et al
TypeJournal article
Date Published2006
Date Created-

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