Fras1, a basement membrane-associated protein mutated in Fraser syndrome, mediates both the initiation of the mammalian kidney and the integrity of renal glomeruli

Por Pitera, Jolanta E., Scambler, Peter J., Woolf, Adrian S.
Publicado em 2008

Analysis of Coronary Vessels in Cleared Embryonic Hearts

Por Ivins, Sarah, Roberts, Catherine, Vernay, Bertrand, Scambler, Peter J.
Publicado no J Vis Exp (2016)

Tbx1 Regulates the BMP-Smad1 Pathway in a Transcription Independent Manner

Por Fulcoli, F. Gabriella, Huynh, Tuong, Scambler, Peter J., Baldini, Antonio
Publicado em 2009

An Ift80 mouse model of short rib polydactyly syndromes shows defects in hedgehog signalling without loss or malformation of cilia

Por Rix, Suzanne, Calmont, Amelie, Scambler, Peter J., Beales, Philip L.
Publicado em 2011

HIC2 regulates isoform switching during maturation of the cardiovascular system

Por Dykes, Iain M., van Bueren, Kelly Lammerts, Scambler, Peter J.
Publicado no J Mol Cell Cardiol (2018)

A 117-kb Microdeletion Removing HOXD9–HOXD13 and EVX2 Causes Synpolydactyly

Por Goodman, Frances R., Majewski, Frank, Collins, Amanda L., Scambler, Peter J.
Publicado em 2002

Sprouty1 Haploinsufficiency Prevents Renal Agenesis in a Model of Fraser Syndrome

Por Pitera, Jolanta E., Woolf, Adrian S., Basson, M. Albert, Scambler, Peter J.
Publicado em 2012

Histone Chaperone HIRA in Regulation of Transcription Factor RUNX1

Por Majumder, Aditi, Syed, Khaja Mohieddin, Joseph, Sunu, Scambler, Peter J., Dutta, Debasree
Publicado no J Biol Chem (2015)

Hyperdynamic Plasticity of Chromatin Proteins in Pluripotent Embryonic Stem Cells

Por Meshorer, Eran, Yellajoshula, Dhananjay, George, Eric, Scambler, Peter J., Brown, David T., Misteli, Tom
Publicado em 2006

Loss of CXCL12/CXCR4 signalling impacts several aspects of cardiovascular development but does not exacerbate Tbx1 haploinsufficiency

Por Page, Mahalia, Ridge, Liam, Gold Diaz, Diana, Tsogbayar, Tsolmon, Scambler, Peter J., Ivins, Sarah
Publicado no PLoS One (2018)

Defective Vagal Innervation in Murine Tbx1 Mutant Hearts

Por Calmont, Amélie, Anderson, Naomi, Suntharalingham, Jenifer P., Ang, Richard, Tinker, Andrew, Scambler, Peter J.
Publicado no J Cardiovasc Dev Dis (2018)

Direct Selection of Conserved cDNAs from the DiGeorge Critical Region: Isolation of a Novel CDC45-Like Gene

Por McKie, Judith M., Wadey, Roy B., Sutherland, Helen F., Taylor, Catherine L., Scambler, Peter J.
Publicado em 1998

The CXCL12/CXCR4 Axis Plays a Critical Role in Coronary Artery Development

Por Ivins, Sarah, Chappell, Joel, Vernay, Bertrand, Suntharalingham, Jenifer, Martineau, Alexandrine, Mohun, Timothy J., Scambler, Peter J.
Publicado no Dev Cell (2015)

Neural crest–derived SEMA3C activates endothelial NRP1 for cardiac outflow tract septation

Por Plein, Alice, Calmont, Amélie, Fantin, Alessandro, Denti, Laura, Anderson, Naomi A., Scambler, Peter J., Ruhrberg, Christiana
Publicado no J Clin Invest (2015)

Expression of Fraser syndrome genes in normal and polycystic murine kidneys

Por Kerecuk, Larissa, Long, David A., Ali, Zahabia, Anders, Corina, Kolatsi-Joannou, Maria, Scambler, Peter J., Woolf, Adrian S.
Publicado em 2012

CHD7 Maintains Neural Stem Cell Quiescence and Prevents Premature Stem Cell Depletion in the Adult Hippocampus

Por Jones, Kieran M., Sarić, Nemanja, Russell, John P., Andoniadou, Cynthia L., Scambler, Peter J., Basson, M. Albert
Publicado no Stem Cells (2014)

Molecular genetics of 22q11.2 deletion syndrome

Por Morrow, Bernice E., McDonald-McGinn, Donna M., Emanuel, Beverly S., Vermeesch, Joris R., Scambler, Peter J.
Publicado no Am J Med Genet A (2018)

A critical role for the chromatin remodeller CHD7 in anterior mesoderm during cardiovascular development

Por Payne, Sophie, Burney, Matthew J., McCue, Karen, Popal, Nelo, Davidson, Sean M., Anderson, Robert H., Scambler, Peter J.
Publicado no Dev Biol (2015)

HIRA directly targets the enhancers of selected cardiac transcription factors during in vitro differentiation of mouse embryonic stem cells

Por Saleh, Rasha Noureldin M., Dilg, Daniel, Abou Zeid, Abla A., Hashad, Doaa I., Scambler, Peter J., Chapgier, Ariane L. A.
Publicado no Mol Biol Rep (2018)

Hearing Loss in a Mouse Model of 22q11.2 Deletion Syndrome

Por Fuchs, Jennifer C., Zinnamon, Fhatarah A., Taylor, Ruth R., Ivins, Sarah, Scambler, Peter J., Forge, Andrew, Tucker, Abigail S., Linden, Jennifer F.
Publicado em 2013