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The Adenomatous Polyposis Coli Protein Unambiguously Localizes to Microtubule Plus Ends and Is Involved in Establishing Parallel Arrays of Microtubule Bundles in Highly Polarized Epithelial Cells

The Journal of cell biology, 2002-06, Vol.157 (6), p.1041-1048

2002

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Advanced neutral gas diagnostics for magnetic confinement devices

Journal of instrumentation, 2017-09, Vol.12 (9), p.C09008-C09008

2017

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Perceptions of Australian clients towards male radiographers working in breast imaging: Quantitative results from a pilot study

Radiography (London, England. 1995), 2017-02, Vol.23 (1), p.3-8

2017

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Genetic heterogeneity in primary hyperoxaluria type 1: impact on diagnosis

Molecular genetics and metabolism, 2004-09, Vol.83 (1), p.38-46

2004

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Does Fever Response to Acetaminophen Predict Bloodstream Infections in Febrile Neutropenia?

Curēus (Palo Alto, CA), 2023-03

2023

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Assessment of tolerance, safety and efficacy of ambulatory oesophageal ph monitoring using the catheter-free bravo system in a scottish population

Gut, 2011-04, Vol.60 (Suppl 1), p.A182-A183

2011

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Do associated proximal fibula fractures help predict the severity of tibial plateau fractures?

European journal of orthopaedic surgery & traumatology, 2023-10, Vol.33 (7), p.2959-2963

2023

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P01.03 Encouraging aboriginal gay men to test for hiv

Sexually transmitted infections, 2015-09, Vol.91 (Suppl 2), p.A80-A80

2015

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Preliminary Evidence for Ethnic Differences in Primary Hyperoxaluria Type 1 Genotype

American journal of nephrology, 2005-05, Vol.25 (3), p.264-268

Coulter-Mackie, Marion B.

2005

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Overexpression of recombinant human antiquitin in E. coli: Partial enzyme activity in selected ALDH7A1 missense mutations associated with pyridoxine-dependent epilepsy

Molecular genetics and metabolism, 2014-04, Vol.111 (4), p.462-466

2014

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SNP Variants in RET and PAX2 and Their Possible Contribution to the Primary Hyperoxaluria Type 1 Phenotype

Biochemical genetics, 2015-04, Vol.53 (1-3), p.23-28

Coulter-Mackie, Marion B.

2015

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Heart Transplant Recipients with pAMR1 (H+) and pAMR2 Rejection Have the Same Amount of Myocardial Injury by Molecular Microscope

The Journal of heart and lung transplantation, 2021-04, Vol.40 (4), p.S44-S44

2021

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Heart Transplant Recipients with pAMR1(H+) and pAMR2 Rejection Have the Same Amount of Myocardial Injury by Allosure

The Journal of heart and lung transplantation, 2021-04, Vol.40 (4), p.S48-S48

2021

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The major allele of the alanine:glyoxylate aminotransferase gene: seven novel mutations causing primary hyperoxaluria type 1

Molecular genetics and metabolism, 2004-05, Vol.82 (1), p.64-68

2004

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Partial trypsin digestion as an indicator of mis-folding of mutant alanine:glyoxylate aminotransferase and chaperone effects of specific ligands. Study of a spectrum of missense mutants

Molecular genetics and metabolism, 2008-07, Vol.94 (3), p.368-374

2008

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(104) Relation Between Individual Blood Gene Expression Profile (GEP) and Tissue GEP in Antibody-Mediated Rejection in Heart Transplant

The Journal of heart and lung transplantation, 2023-04, Vol.42 (4), p.S55-S56

2023

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(1002) Differences in Individual Blood Gene Expression Profile (GEP) Levels in T-Cell Mediated Rejection Assessed by Molecular Microscopy in Heart Transplant

The Journal of heart and lung transplantation, 2023-04, Vol.42 (4), p.S431-S432

2023

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Spectrum of mutations in the arylsulfatase A gene in a Canadian DNA collection including two novel frameshift mutations, a new missense mutation (C488R) and an MLD mutation (R84Q) in cis with a pseudodeficiency allele

Molecular genetics and metabolism, 2003-06, Vol.79 (2), p.91-98

2003

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Intensity of Continuous Renal-Replacement Therapy in Critically Ill Patients

The New England journal of medicine, 2009-10, Vol.361 (17), p.1627-1638

2009

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Consequences of missense mutations for dimerization and turnover of alanine:glyoxylate aminotransferase: Study of a spectrum of mutations

Molecular genetics and metabolism, 2006-12, Vol.89 (4), p.349-359

2006

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The major allele of the alanine:glyoxylate aminotransferase gene: Nine novel mutations and polymorphisms associated with primary hyperoxaluria type 1

Molecular genetics and metabolism, 2005-09, Vol.86 (1), p.172-178

2005

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Overexpression of human antiquitin in E. coli: Enzymatic characterization of twelve ALDH7A1 missense mutations associated with pyridoxine-dependent epilepsy

Molecular genetics and metabolism, 2012-08, Vol.106 (4), p.478-481

2012

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Overexpression of human alanine:glyoxylate aminotransferase in Escherichia coli: renaturation from guanidine–HCl and affinity for pyridoxal phosphate co-factor

Protein expression and purification, 2005-05, Vol.41 (1), p.18-26

2005

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The PABA story

Australasian journal of dermatology, 1999-02, Vol.40 (1), p.51-53

1999

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Hepatitis C in AustraliaImpact of a Mass Media Campaign

American journal of preventive medicine, 2006-12, Vol.31 (6), p.492-498

2006

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The Adenomatous Polyposis Coli Protein Unambiguously Localizes to Microtubule Plus Ends and Is Involved in Establishing Parallel Arrays of Microtubule Bundles in Highly Polarized Epithelial Cells

Advanced neutral gas diagnostics for magnetic confinement devices

Perceptions of Australian clients towards male radiographers working in breast imaging: Quantitative results from a pilot study

Genetic heterogeneity in primary hyperoxaluria type 1: impact on diagnosis

Does Fever Response to Acetaminophen Predict Bloodstream Infections in Febrile Neutropenia?

Assessment of tolerance, safety and efficacy of ambulatory oesophageal ph monitoring using the catheter-free bravo system in a scottish population

Do associated proximal fibula fractures help predict the severity of tibial plateau fractures?

P01.03 Encouraging aboriginal gay men to test for hiv

Preliminary Evidence for Ethnic Differences in Primary Hyperoxaluria Type 1 Genotype

Overexpression of recombinant human antiquitin in E. coli: Partial enzyme activity in selected ALDH7A1 missense mutations associated with pyridoxine-dependent epilepsy

SNP Variants in RET and PAX2 and Their Possible Contribution to the Primary Hyperoxaluria Type 1 Phenotype

Heart Transplant Recipients with pAMR1 (H+) and pAMR2 Rejection Have the Same Amount of Myocardial Injury by Molecular Microscope

Heart Transplant Recipients with pAMR1(H+) and pAMR2 Rejection Have the Same Amount of Myocardial Injury by Allosure

The major allele of the alanine:glyoxylate aminotransferase gene: seven novel mutations causing primary hyperoxaluria type 1

Partial trypsin digestion as an indicator of mis-folding of mutant alanine:glyoxylate aminotransferase and chaperone effects of specific ligands. Study of a spectrum of missense mutants

(104) Relation Between Individual Blood Gene Expression Profile (GEP) and Tissue GEP in Antibody-Mediated Rejection in Heart Transplant

(1002) Differences in Individual Blood Gene Expression Profile (GEP) Levels in T-Cell Mediated Rejection Assessed by Molecular Microscopy in Heart Transplant

Spectrum of mutations in the arylsulfatase A gene in a Canadian DNA collection including two novel frameshift mutations, a new missense mutation (C488R) and an MLD mutation (R84Q) in cis with a pseudodeficiency allele

Intensity of Continuous Renal-Replacement Therapy in Critically Ill Patients

Consequences of missense mutations for dimerization and turnover of alanine:glyoxylate aminotransferase: Study of a spectrum of mutations

The major allele of the alanine:glyoxylate aminotransferase gene: Nine novel mutations and polymorphisms associated with primary hyperoxaluria type 1

Overexpression of human antiquitin in E. coli: Enzymatic characterization of twelve ALDH7A1 missense mutations associated with pyridoxine-dependent epilepsy

Overexpression of human alanine:glyoxylate aminotransferase in Escherichia coli: renaturation from guanidine–HCl and affinity for pyridoxal phosphate co-factor

The PABA story

Hepatitis C in AustraliaImpact of a Mass Media Campaign

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