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List of works by David I. Wilson

ADAM33 expression in asthmatic airways and human embryonic lungs

scientific article

BRCA1 EXON 11, a CERES (composite regulatory element of splicing) element involved in splice regulation

scientific article

BRCA1 exon 11 alternative splicing, multiple functions and the association with cancer.

scientific article published on August 2012

Beta cell differentiation during early human pancreas development

scientific article

Beta-cell differentiation during human development does not rely on nestin-positive precursors: implications for stem cell-derived replacement therapy

scientific article (publication date: July 2002)

Centriolar association of ALMS1 and likely centrosomal functions of the ALMS motif-containing proteins C10orf90 and KIAA1731

scientific article

Characterization and multipotentiality of human fetal femur-derived cells: implications for skeletal tissue regeneration

scientific article published on 22 December 2005

Characterization of ciliated bronchial epithelium 1, a ciliated cell-associated gene induced during mucociliary differentiation

scientific article

Differences between human and mouse alpha-fetoprotein expression during early development

scientific article published on 01 May 2001

Ectopic SOX9 mediates extracellular matrix deposition characteristic of organ fibrosis

scientific article

Epigenetic regulation during fetal femur development: DNA methylation matters.

scientific article

Evaluating Human Embryonic Germ Cells: Concord and Conflict as Pluripotent Stem Cells

scientific article

Evidence for centriolar satellite localization of CDK1 and cyclin B2.

scientific article published on 2 May 2013

Evidence for reciliation of RPE1 cells in late G1 phase, and ciliary localisation of cyclin B1.

scientific article published on 11 August 2013

Expression and localisation of thymosin beta-4 in the developing human early fetal heart

scientific article published in PLoS ONE

Expression profiles of SF-1, DAX1, and CYP17 in the human fetal adrenal gland: potential interactions in gene regulation

scientific article

FRA2A is a CGG repeat expansion associated with silencing of AFF3

scientific article

Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes

scientific article (publication date: April 2014)

Hepatic differentiation of murine embryonic stem cells

scientific article (publication date: 2002)

Human embryo and early fetus research

scientific article published on August 2006

Human embryonic germ cells for future neuronal replacement therapy

scientific article

Human endothelial and foetal femur-derived stem cell co-cultures modulate osteogenesis and angiogenesis.

scientific article

In humans, early cortisol biosynthesis provides a mechanism to safeguard female sexual development

scientific article

In vitro expression of NGN3 identifies RAB3B as the predominant Ras-associated GTP-binding protein 3 family member in human islets

scientific article

In vitro fertilization improves childhood growth and metabolism.

scientific article published on 12 June 2007

Induction of a disintegrin and metalloprotease 33 during embryonic lung development and the influence of IL-13 or maternal allergy

scientific article

Long-range evolutionary constraints reveal cis-regulatory interactions on the human X chromosome

scientific article

MicroRNA-146a regulates human foetal femur derived skeletal stem cell differentiation by down-regulating SMAD2 and SMAD3.

scientific article

Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome

scientific article

Narrowing the critical region within 11q24-qter for hypoplastic left heart and identification of a candidate gene, JAM3, expressed during cardiogenesis

scientific article (publication date: April 2002)

Nek2 localises to the distal portion of the mother centriole/basal body and is required for timely cilium disassembly at the G2/M transition.

scientific article

Novel SOX9 expression during human pancreas development correlates to abnormalities in Campomelic dysplasia

scientific article published in August 2002

Phospholamban and sarcolipin are maintained in the endoplasmic reticulum by retrieval from the ER-Golgi intermediate compartment

scientific article published on 13 January 2007

Probing the epigenetic regulation of HIF-1α transcription in developing tissue.

scientific article

RBFOX2 protein domains and cellular activities.

scientific article

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.

scientific article published in July 2014

Rare variants in NR2F2 cause congenital heart defects in humans

scientific article published on April 2014

Regionally-derived cell populations and skeletal stem cells from human foetal femora exhibit specific osteochondral and multi-lineage differentiation capacity in vitro and ex vivo

scientific article

Science, medicine, and the future: Genetics and cardiovascular risk.

scientific article

Separation of the PROX1 gene from upstream conserved elements in a complex inversion/translocation patient with hypoplastic left heart.

scientific article published on 27 May 2009

Soluble ADAM33 initiates airway remodeling to promote susceptibility for allergic asthma in early life

scientific article

Stem cell marker TRA-1-60 is expressed in foetal and adult kidney and upregulated in tubulo-interstitial disease

scientific article published on 19 September 2010

Subcellular localization of ALMS1 supports involvement of centrosome and basal body dysfunction in the pathogenesis of obesity, insulin resistance, and type 2 diabetes

scientific article

The early human germ cell lineage does not express SOX2 during in vivo development or upon in vitro culture

scientific article published on 16 January 2008

The soluble form of a disintegrin and metalloprotease 33 promotes angiogenesis: implications for airway remodeling in asthma.

scientific article published on 14 April 2008

Transcriptional regulation of the Alström syndrome gene ALMS1 by members of the RFX family and Sp1

scientific article

Two children with subtelomeric 11q deletions: a description and interpretation of their clinical presentations and molecular genetic findings.

scientific article published in April 2009