Preprint highlights, selected by the biological community
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I am a HFSP postdoctoral fellow with Prof. Andrew Oates at EPFL, Lausanne and I did my PhD with Prof. Stephan Grill at MPI-CBG, Dresden. My major research interest is in understanding biophysical mechanisms by which (a)symmetries are established in the three principal body axes of embryos. I have extensive experience in working with both C. elegans and zebrafish model systems and my expertise lies in performing advanced microscopy and developing custom image analysis algorithms.
Self-organised symmetry breaking in zebrafish reveals feedback from morphogenesis to pattern formation
| Selected by | Sundar Naganathan |
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Embryonic geometry underlies phenotypic variation in decanalized conditions
| Selected by | Sundar Naganathan |
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Planar differential growth rates determine the position of folds in complex epithelia
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Buckling of epithelium growing under spherical confinement
| Selected by | Sundar Naganathan |
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Force inference predicts local and tissue-scale stress patterns in epithelia
| Selected by | Sundar Naganathan |
Transcriptional initiation and mechanically driven self-propagation of a tissue contractile wave during axis elongation
| Selected by | Sundar Naganathan |
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3D Tissue elongation via ECM stiffness-cued junctional remodeling
| Selected by | Sundar Naganathan |
Excitable RhoA dynamics drive pulsed contractions in the early C. elegans embryo.
| Selected by | Sundar Naganathan |
WNT signaling memory is required for ACTIVIN to function as a morphogen in human gastruloids
| Selected by | Sundar Naganathan |