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Author Details
Full Name
Caroline E Walker
Affiliation
University of London
ORCID
Career Start Year
1998
Papers
20
H Index
16
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
28065523
A Web-Based Registry for Familial Hypercholesterolaemia.
Heart Lung Circ
2017
28468665
Initiating an undiagnosed diseases program in the Western Australian public health system.
Orphanet J Rare Dis
2017
28443272
3-Dimensional Facial Analysis-Facing Precision Public Health.
Front Public Health
2017
28344196
Design of the Familial Hypercholesterolaemia Australasia Network Registry: Creating Opportunities for Greater International Collaboration.
J Atheroscler Thromb
2017
29214566
Improved Diagnosis and Care for Rare Diseases through Implementation of Precision Public Health Framework.
Adv Exp Med Biol
2017
27657686
The collective impact of rare diseases in Western Australia: an estimate using a population-based cohort.
Genet Med
2017
27287197
The rare and undiagnosed diseases diagnostic service - application of massively parallel sequencing in a state-wide clinical service.
Orphanet J Rare Dis
2016
25943355
Use of mechanical airway clearance devices in the home by people with neuromuscular disorders: effects on health service use and lifestyle benefits.
Orphanet J Rare Dis
2015
16354724
Long-term effect of therapeutic laser photocoagulation on gene expression in the eye.
FASEB J
2006
17249575
Laser photocoagulation: ocular research and therapy in diabetic retinopathy.
Adv Exp Med Biol
2006
16752188
Long-term global retinal microvascular changes in a transgenic vascular endothelial growth factor mouse model.
Diabetologia
2006
16241904
Characterization of retinaldehyde dehydrogenase 3.
Biochem J
2006
15965177
Generation of transgenic mice with mild and severe retinal neovascularisation.
Br J Ophthalmol
2005
11136713
The destabilization of human GCAP1 by a proline to leucine mutation might cause cone-rod dystrophy.
Hum Mol Genet
2001
11238942
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.
Mol Cell Biol
2001
11115851
Functional characterization of missense mutations at codon 838 in retinal guanylate cyclase correlates with disease severity in patients with autosomal dominant cone-rod dystrophy.
Hum Mol Genet
2000
10508919
A novel ADP-ribosylation like factor (ARL-6), interacts with the protein-conducting channel SEC61beta subunit.
FEBS Lett
1999
10468971
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.
Clin Endocrinol (Oxf)
1999
10572651
Optimized RNA gel-shift and UV cross-linking assays for characterization of cytoplasmic RNA-protein interactions.
Biotechniques
1999
9839451
Regulation of EGF-receptor expression by EGF and TGF alpha in epidermoid cancer cells is cell type-specific.
Int J Biochem Cell Biol
1998
1 - 20 of 20
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