Valerie Wilson

Visualization of whole-mount skeletal expression patterns of LacZ reporters using a tissue clearing protocol.

Growth and early postimplantation defects in mice deficient for the bromodomain-containing protein Brd4.

Axial progenitors with extensive potency are localised to the mouse chordoneural hinge.

Role of heparan sulfate-2-O-sulfotransferase in the mouse.

Environmental risk factors for breast cancer among African-American women.

Heparan sulfate 2-O-sulfotransferase (Hs2st) and mouse development.

In vitro generation of neuromesodermal progenitors reveals distinct roles for wnt signalling in the specification of spinal cord and paraxial mesoderm identity.

Childhood IQ, social class, deprivation, and their relationships with mortality and morbidity risk in later life: prospective observational study linking the Scottish Mental Survey 1932 and the Midspan studies.

A polymorphism of the cholesteryl ester transfer protein gene predicts cardiovascular events in non-smokers in the West of Scotland Coronary Prevention Study.

Putting the action into learning: the experience of an action learning set.

Identification of Jade1, a gene encoding a PHD zinc finger protein, in a gene trap mutagenesis screen for genes involved in anteroposterior axis development.

Specific modification of heparan sulphate is required for normal cerebral cortical development.

Childhood mental ability and blood pressure at midlife: linking the Scottish Mental Survey 1932 and the Midspan studies.

Functional evidence for a single endodermal origin for the thymic epithelium.

Role of the CD40 locus in Graves' disease.

New semidominant mutations that affect mouse development.

In vivo and in vitro assays of thymic organogenesis.

No association of the codon 55 methionine to valine polymorphism in the SUMO4 gene with Graves' disease.

Understanding the workplace culture of a special care nursery.

Anonymous versus confidential HIV testing: client and provider decision making under uncertainty.

The cognitive cost of being a twin: two whole-population surveys.

Large, consistent estimates of the heritability of cognitive ability in two entire populations of 11-year-old twins from Scottish mental surveys of 1932 and 1947.

Childhood IQ and social factors on smoking behaviour, lung function and smoking-related outcomes in adulthood: linking the Scottish Mental Survey 1932 and the Midspan studies.

Critical realism as emancipatory action: the case for realistic evaluation in practice development.

The NuRD component Mbd3 is required for pluripotency of embryonic stem cells.

Genetic association studies of the FOXP3 gene in Graves' disease and autoimmune Addison's disease in the United Kingdom population.

Essential alterations of heparan sulfate during the differentiation of embryonic stem cells to Sox1-enhanced green fluorescent protein-expressing neural progenitor cells.

Cytotoxic T-lymphocyte-associated antigen-4 single nucleotide polymorphisms and haplotypes in primary biliary cirrhosis.

A novel triple fusion reporter system for use in gene trap mutagenesis.

Two distinct sources for a population of maturing axial progenitors.

The Lothian Birth Cohort 1936: a study to examine influences on cognitive ageing from age 11 to age 70 and beyond.

Experiences of parents of young people with diabetes using insulin pump therapy.

Commentary on Booth J, Tolson D, Hotchkiss R and Schofield I (2007) Using action research to construct national evidence-based nursing care guidance for gerontological nursing. Journal of Clinical Nursing 16, 945-953.

Localised axial progenitor cell populations in the avian tail bud are not committed to a posterior Hox identity.

Stem cells, signals and vertebrate body axis extension.

Expression-independent gene trap vectors for random and targeted mutagenesis in embryonic stem cells.

Redefining the progression of lineage segregations during mammalian embryogenesis by clonal analysis.

Cdx mutant axial progenitor cells are rescued by grafting to a wild type environment.

How do facilitators of practice development gain the expertise required to support vital transformation of practice and workplace cultures?

MLH1 Differential allelic expression in mutation carriers and controls.

Students' experiences of managing type 1 diabetes.

The heart beads program.

Narratives of the heart: telling the story of children with a cardiac condition through a bead program.

Non-diabetic hypoglycaemia: causes and pathophysiology.

Heart to heart: a programme for children on a cardiac ward.

Sibling involvement in childhood chronic heart disease through a bead program.

Appreciation of a Child's Journey: Implementation of a Cardiac Action Research Project.

The developmental dismantling of pluripotency is reversed by ectopic Oct4 expression.

Evaluation of the care received by older people with diabetes.

In Vivo differentiation potential of epiblast stem cells revealed by chimeric embryo formation.

Cognitive impairment in patients with diabetes.

Type 2 diabetes: an epidemic in children.

The management of type 1 diabetes in primary school: review of the literature.

Genotype/phenotype correlations in complement factor H deficiency arising from uniparental isodisomy.

The role of pluripotency gene regulatory network components in mediating transitions between pluripotent cell states.

A realist review of interventions and strategies to promote evidence-informed healthcare: a focus on change agency.

Distinct Wnt-driven primitive streak-like populations reflect in vivo lineage precursors.

Relationship between 25-hydroxyvitamin D and cognitive function in older adults: the Health, Aging and Body Composition Study.

Parental experiences with a hospital-based bead programme for children with congenital heart disease.

The management of type 1 diabetes in Australian primary schools.

A longitudinal study of aspects of a hospital's family-centred nursing: changing practice through data translation.

East meets West in reflective practice.

Factors determining penetrance in familial atypical haemolytic uraemic syndrome.

REACH: an exploration of nursing development.

Visual impairment and incident mobility limitations: the health, aging and body composition study.

Mapping interactions between complement C3 and regulators using mutations in atypical hemolytic uremic syndrome.

Distinct Wnt-driven primitive streak-like populations reflect in vivo lineage precursors.

SPG7 mutations are a common cause of undiagnosed ataxia.

<i>CYLD</i> GeneticTesting for Brooke-Spiegler Syndrome, Familial Cylindromatosis and Multiple Familial Trichoepitheliomas.

Opportunities for Nurses to Increase Parental Health Literacy: A Discussion Paper.

Assessing the bipotency of in vitro-derived neuromesodermal progenitors.

Intrinsic factors and the embryonic environment influence the formation of extragonadal teratomas during gestation.

A De Novo Deletion in the Regulators of Complement Activation Cluster Producing a Hybrid Complement Factor H/Complement Factor H-Related 3 Gene in Atypical Hemolytic Uremic Syndrome.