Search results (14)
« Back to PublicationsCardiac conduction system regeneration prevents arrhythmias after myocardial infarction.
Journal article
Sayers JR. et al, (2025), Nat Cardiovasc Res, 4, 163 - 179
Retinoic acid signalling regulates branchiomeric neck muscle development at the head/trunk interface.
Journal article
Dumas CE. et al, (2024), Development, 151
Protocols for Investigating the Epithelial Properties of Cardiac Progenitor Cells in the Mouse Embryo.
Chapter
Cortes C. et al, (2022), 2438, 231 - 250
EPySeg: a coding-free solution for automated segmentation of epithelia using deep learning.
Journal article
Aigouy B. et al, (2020), Development, 147
Tbx1 regulates extracellular matrix-cell interactions in the second heart field.
Journal article
Alfano D. et al, (2019), Hum Mol Genet, 28, 2295 - 2308
T-box genes and retinoic acid signaling regulate the segregation of arterial and venous pole progenitor cells in the murine second heart field.
Journal article
De Bono C. et al, (2018), Hum Mol Genet, 27, 3747 - 3760
Epithelial Properties of the Second Heart Field.
Journal article
Cortes C. et al, (2018), Circ Res, 122, 142 - 154
Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 function.
Journal article
Cortés CR. et al, (2016), Sci Rep, 6
Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport.
Journal article
Schmidts M. et al, (2016), Nat Commun, 7
TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport.
Journal article
Schmidts M. et al, (2015), Nat Commun, 6
Unmasking the ciliopathies: craniofacial defects and the primary cilium.
Journal article
Cortés CR. et al, (2015), Wiley Interdiscip Rev Dev Biol, 4, 637 - 653
Mutations in the gene encoding IFT dynein complex component WDR34 cause Jeune asphyxiating thoracic dystrophy.
Journal article
Schmidts M. et al, (2013), Am J Hum Genet, 93, 932 - 944
Short-rib polydactyly and Jeune syndromes are caused by mutations in WDR60.
Journal article
McInerney-Leo AM. et al, (2013), Am J Hum Genet, 93, 515 - 523
Yeast-based assay identifies novel Shh/Gli target genes in vertebrate development.
Journal article
Milla LA. et al, (2012), BMC Genomics, 13

