List of works - Caroline Walker

A Registry Framework Enabling Patient-Centred Care

scientific article published on January 2015

A Web-Based Registry for Familial Hypercholesterolaemia

scientific article published on 30 November 2016

A novel ADP-ribosylation like factor (ARL-6), interacts with the protein-conducting channel SEC61beta subunit

scientific article (publication date: October 1999)

Characterization of retinaldehyde dehydrogenase 3

scientific journal article

Current trends in biobanking for rare diseases: a review [Corrigendum]

scientific article published in March 2015

Functional characterization of missense mutations at codon 838 in retinal guanylate cyclase correlates with disease severity in patients with autosomal dominant cone-rod dystrophy

scientific article published on 01 December 2000

Generation of transgenic mice with mild and severe retinal neovascularisation

scientific article published on July 2005

Identification of a novel AU-Rich element in the 3' untranslated region of epidermal growth factor receptor mRNA that is the target for regulated RNA-binding proteins

scientific article

Laser photocoagulation: ocular research and therapy in diabetic retinopathy

scientific article

Long-term effect of therapeutic laser photocoagulation on gene expression in the eye.

scientific article published on 14 December 2005

Long-term global retinal microvascular changes in a transgenic vascular endothelial growth factor mouse model

scientific article published on 10 May 2006

Mutation screening and isoform prevalence of the follicle stimulating hormone receptor gene in women with premature ovarian failure, resistant ovary syndrome and polycystic ovary syndrome

scientific article published in July 1999

Optimized RNA gel-shift and UV cross-linking assays for characterization of cytoplasmic RNA-protein interactions

scientific article published in November 1999

Regulation of EGF-receptor expression by EGF and TGF alpha in epidermoid cancer cells is cell type-specific

scientific article

The collective impact of rare diseases in Western Australia: an estimate using a population-based cohort

scientific article

The destabilization of human GCAP1 by a proline to leucine mutation might cause cone-rod dystrophy

scientific article

The rare and undiagnosed diseases diagnostic service - application of massively parallel sequencing in a state-wide clinical service

scientific article published on 11 June 2016

Use of mechanical airway clearance devices in the home by people with neuromuscular disorders: effects on health service use and lifestyle benefits

scientific article published on 6 May 2015

List of works by Caroline Walker

A Registry Framework Enabling Patient-Centred Care

A Web-Based Registry for Familial Hypercholesterolaemia

A novel ADP-ribosylation like factor (ARL-6), interacts with the protein-conducting channel SEC61beta subunit

Characterization of retinaldehyde dehydrogenase 3

Current trends in biobanking for rare diseases: a review [Corrigendum]

Functional characterization of missense mutations at codon 838 in retinal guanylate cyclase correlates with disease severity in patients with autosomal dominant cone-rod dystrophy

Generation of transgenic mice with mild and severe retinal neovascularisation

Identification of a novel AU-Rich element in the 3' untranslated region of epidermal growth factor receptor mRNA that is the target for regulated RNA-binding proteins

Laser photocoagulation: ocular research and therapy in diabetic retinopathy

Long-term effect of therapeutic laser photocoagulation on gene expression in the eye.

Long-term global retinal microvascular changes in a transgenic vascular endothelial growth factor mouse model

Mutation screening and isoform prevalence of the follicle stimulating hormone receptor gene in women with premature ovarian failure, resistant ovary syndrome and polycystic ovary syndrome

Optimized RNA gel-shift and UV cross-linking assays for characterization of cytoplasmic RNA-protein interactions

Regulation of EGF-receptor expression by EGF and TGF alpha in epidermoid cancer cells is cell type-specific

The collective impact of rare diseases in Western Australia: an estimate using a population-based cohort

The destabilization of human GCAP1 by a proline to leucine mutation might cause cone-rod dystrophy

The rare and undiagnosed diseases diagnostic service - application of massively parallel sequencing in a state-wide clinical service

Use of mechanical airway clearance devices in the home by people with neuromuscular disorders: effects on health service use and lifestyle benefits