Research groups
Claudio Cortes Rodriguez
Postdoctoral Research Fellow
I am a Postdoctoral Research Fellow in Professor Paul Riley's group, interested in the cellular behaviours and mechanisms of heart development.
I goy my BSc from the University of Chile and then moved to Australia, where I obtained my PhD in Molecular Genetics and Development, studying rare genetic diseases (ciliopathies) as part of bench-to-bedside approaches. I then focused on heart development and moved to France for a postdoctoral position, where I specialised in developing new live imaging approaches to heart development in mice. I also focused on epithelial biology, Epithelial-to-mesenchymal transitions and how adhesion (cell-cell and the ECM) shapes development. As a side project, I also studied the role of Retinoic acid signaling in cardiac and skeletal muscle development.
I have now joined the Riley group to study human cardiac development as part of the Wellcome Trust Human Developmental Biology Initiative, imaging and mapping the cells that make up the human heart. I'm focusing on lineage-tracing and cell behaviour during compartmentalization of the heart. We have a growing number of collaborators for this, including the Srinivas group (DPAG) and the Rawlins group (Cambridge).
Recent publications
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Retinoic acid signalling regulates branchiomeric neck muscle development at the head/trunk interface
Journal article
Dumas CE. et al, (2024), Development, 151
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Protocols for Investigating the Epithelial Properties of Cardiac Progenitor Cells in the Mouse Embryo.
Chapter
Cortes C. et al, (2022), 2438, 231 - 250
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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
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Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport.
Journal article
Schmidts M. et al, (2016), Nat Commun, 7
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TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport.
Journal article
Schmidts M. et al, (2015), Nat Commun, 6