Genetics and cardiovascular risk

Por Day, Ian N M, Wilson, David I
Publicado em 2001

Evidence for centriolar satellite localization of CDK1 and cyclin B2

Por Spalluto, Cosma, Wilson, David I., Hearn, Tom
Publicado em 2013

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

Por Spalluto, Cosma, Wilson, David I., Hearn, Tom
Publicado em 2013

BRCA1 Exon 11, a CERES (Composite Regulatory Element of Splicing) Element Involved in Splice Regulation

Por Tammaro, Claudia, Raponi, Michela, Wilson, David I., Baralle, Diana
Publicado em 2014

Updating of action–outcome associations is prevented by inactivation of the posterior pedunculopontine tegmental nucleus

Por MacLaren, Duncan A.A., Wilson, David I.G., Winn, Philip
Publicado em 2013

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

Por JONES, ELIZABETH A., CLEMENT-JONES, MARK, JAMES, OLIVER F. W., WILSON, DAVID I.
Publicado em 2001

Evolutionary Constraint Helps Unmask a Splicing Regulatory Region in BRCA1 Exon 11

Por Raponi, Michela, Douglas, Andrew G. L., Tammaro, Claudia, Wilson, David I., Baralle, Diana
Publicado em 2012

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

Por Gothard, David, Cheung, Kelvin, Kanczler, Janos M., Wilson, David I., Oreffo, Richard O. C.
Publicado no Stem Cell Res Ther (2015)

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

Por Inglis, Stefanie, Christensen, David, Wilson, David I., Kanczler, Janos M., Oreffo, Richard O. C.
Publicado no Stem Cell Res Ther (2016)

MicroRNA-146a Regulates Human Foetal Femur Derived Skeletal Stem Cell Differentiation by Down-Regulating SMAD2 and SMAD3

Por Cheung, Kelvin S. C., Sposito, Nunzia, Stumpf, Patrick S., Wilson, David I., Sanchez-Elsner, Tilman, Oreffo, Richard O. C.
Publicado em 2014

Epigenetic Regulation during Fetal Femur Development: DNA Methylation Matters

Por de Andrés, María C., Kingham, Emmajayne, Imagawa, Kei, Gonzalez, Antonio, Roach, Helmtrud I., Wilson, David I., Oreffo, Richard O. C.
Publicado em 2013

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

Por Purvis, Tracey L., Hearn, Tom, Spalluto, Cosma, Knorz, Victoria J., Hanley, Karen Piper, Sanchez-Elsner, Tilman, Hanley, Neil A., Wilson, David I.
Publicado em 2010

Centriolar Association of ALMS1 and Likely Centrosomal Functions of the ALMS Motif–containing Proteins C10orf90 and KIAA1731

Por Knorz, Victoria J., Spalluto, Cosma, Lessard, Mark, Purvis, Tracey L., Adigun, Fiona F., Collin, Gayle B., Hanley, Neil A., Wilson, David I., Hearn, Thomas
Publicado em 2010

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

Por Davies, Elizabeth R., Kelly, Joanne F.C., Howarth, Peter H., Wilson, David I., Holgate, Stephen T., Davies, Donna E., Whitsett, Jeffrey A., Haitchi, Hans Michael
Publicado no JCI Insight (2016)

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

Por Goto, Masahiro, Piper Hanley, Karen, Marcos, Josep, Wood, Peter J., Wright, Sarah, Postle, Anthony D., Cameron, Iain T., Mason, J. Ian, Wilson, David I., Hanley, Neil A.
Publicado em 2006

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

Por Piper Hanley, Karen, Hearn, Tom, Berry, Andrew, Carvell, Melanie J, Patch, Ann-Marie, Williams, Louise J, Sugden, Sarah A, Wilson, David I, Ellard, Sian, Hanley, Neil A
Publicado em 2010

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

Por Docherty, Louise E, Rezwan, Faisal I, Poole, Rebecca L, Jagoe, Hannah, Lake, Hannah, Lockett, Gabrielle A, Arshad, Hasan, Wilson, David I, Holloway, John W, Temple, I Karen, Mackay, Deborah J G
Publicado em 2014

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

Por Gill, Harinder K, Parsons, Sian R, Spalluto, Cosma, Davies, Angela F, Knorz, Victoria J, Burlinson, Clare EG, Ng, Bee Ling, Carter, Nigel P, Ogilvie, Caroline Mackie, Wilson, David I, Roberts, Roland G
Publicado em 2009

FRA2A Is a CGG Repeat Expansion Associated with Silencing of AFF3

Por Metsu, Sofie, Rooms, Liesbeth, Rainger, Jacqueline, Taylor, Martin S., Bengani, Hemant, Wilson, David I., Chilamakuri, Chandra Sekhar Reddy, Morrison, Harris, Vandeweyer, Geert, Reyniers, Edwin, Douglas, Evelyn, Thompson, Geoffrey, Haan, Eric, Gecz, Jozef, FitzPatrick, David R., Kooy, R. Frank
Publicado em 2014

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

Por Naville, Magali, Ishibashi, Minaka, Ferg, Marco, Bengani, Hemant, Rinkwitz, Silke, Krecsmarik, Monika, Hawkins, Thomas A., Wilson, Stephen W., Manning, Elizabeth, Chilamakuri, Chandra S. R., Wilson, David I., Louis, Alexandra, Lucy Raymond, F., Rastegar, Sepand, Strähle, Uwe, Lenhard, Boris, Bally-Cuif, Laure, van Heyningen, Veronica, FitzPatrick, David R., Becker, Thomas S., Roest Crollius, Hugues
Publicado no Nat Commun (2015)