Srinjan Lab

@srinjan.bsky.social

Lecturer @imperiallifesci.bsky.social @imperialsci.bsky.social @imperialcollegeldn.bsky.social |Unravelling DNA mysteries in stem cells by staring at little dots| #salsa dancer| he/him | https://profiles.imperial.ac.uk/srinjan.basu

Our work on the role of the proteasome in developmental tempo is out!!!! 🐭⌛️👤⏳ Six years after identifying an association between protein stability and developmental tempo, we now demonstrate a causal link between protein turnover and developmental tempo through proteasomal degradation

Developmental Cell@cp-devcell.bsky.social · 3w ago

Online now: Proteasome-dependent protein degradation shapes developmental tempo in mouse and human neural progenitors #biology #science

We wrote this introductory review on how concepts from dynamical systems can help us understand developmental biology, hope it’s useful to somebody! It was a lot of fun to put together, and great to collaborate with brilliant colleagues across theory and experiments

Pau Formosa-Jordan@pauformosa.bsky.social · last yr.

Introducing five concepts from dynamical systems to decode developmental regulatory mechanisms, have a read! @perez-carrasco.bsky.social@roederlab.bsky.social @mpipz.bsky.social This effort started in a morphogenesis meeting @kitp-ucsb.bsky.social‬ in 2023. journals.biologists.com/dev/article/...

Adapted from Fig. 1 from Kadiyala et al 2025.

📣 We are advertising for a postdoc to join our team at the University of Edinburgh! Our lab studies gene regulatory mechanisms in development, and how genetic changes may impact these processes to alter development and shape human craniofacial form and function 🧬🧪

Postdoctoral Researcher

Our research is focused on understanding how genetic changes in the non-coding genome can impact gene regulatory mechanisms, alter developmental processes and ultimately affect human craniofacial shap...

elxw.fa.em3.oraclecloud.com

New paper from our lab is out! We investigated the function of the NuRD subunit CHD3 in cranial neural crest specification. CHD3 variants are the cause of Snijder-Block-Campeau Syndrome, which manifests with craniofacial anomalies and intellectual disability 1/n

bioRxiv Developmental Biology@biorxiv-devbio.bsky.social · 2y ago

CHD3 regulates BMP signalling response during cranial neural crest cell specification https://www.biorxiv.org/content/10.1101/2025.02.14.638260v1