Preprint highlights, selected by the biological community
preLights is supported by…
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.
Physical constraints on early blastomere packings
| Selected by | Sundar Naganathan |
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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 |