Group Leader at University of Sheffield
Stem Cells // Development // Math(s) // ML
WV -> Ox -> Cam -> Shef
strawbridgelab.com
We built a resource of 20 clonal human naïve pluripotent stem cell lines from 10 blastocysts. Explore embryo-to-embryo and clone-to-clone variation in one place.
👉doi.org/10.1101/2025.06.02.657331
📅 15 January 2026
Under two weeks to apply for our fully funded PhD project “Engineering an in vitro human embryo implantation platform to study pathologies arising in early pregnancy” at @sheffielduni.bsky.social. #development #endometrium #materialsscience
📅 15 January 2026
Under two weeks to apply for our fully funded PhD project “Engineering an in vitro human embryo implantation platform to study pathologies arising in early pregnancy” at @sheffielduni.bsky.social. #development #endometrium #materialsscience
They are a fantastic for learning new skills, building collaborative networks, and honing scientific writing.
doi.org/10.1242/dev....
They are a fantastic for learning new skills, building collaborative networks, and honing scientific writing.
doi.org/10.1242/dev....
Work at the interface of biology + computation to build a virtual human embryo to predict developmental success and failure.
Happy to answer questions!
Work at the interface of biology + computation to build a virtual human embryo to predict developmental success and failure.
Happy to answer questions!
This project is supervised by @matt-towers.bsky.social & @alexgfletcher.bsky.social, and I'm excited to be involved as a project advisor. Please share!
www.findaphd.com/phds/project... 🧪
This project is supervised by @matt-towers.bsky.social & @alexgfletcher.bsky.social, and I'm excited to be involved as a project advisor. Please share!
www.findaphd.com/phds/project... 🧪
We are advertising two UKRI funded PhD projects at the @sheffielduni.bsky.social. #stemcells #development #embryology #reproductivephysiology #mathmaticalmodelling #quantitativebiology
We are advertising two UKRI funded PhD projects at the @sheffielduni.bsky.social. #stemcells #development #embryology #reproductivephysiology #mathmaticalmodelling #quantitativebiology
bsky.app/profile/cell...
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Do they politely converse with them via chemical signalling? Or do they just rudely push them out?
#PaperThemeTune “Push it out” by the Beta Band
#DevBio
bsky.app/profile/cell...
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🎙️ doi.org/10.1242/dev....
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🎙️ doi.org/10.1242/dev....
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@scicambridge.bsky.social @pdncambridge.bsky.social @cam.ac.uk @drn-sheffield.bsky.social @sheffielduni.bsky.social @uoe-igc.bsky.social @edinburgh-uni.bsky.social @mskcancercenter.bsky.social @uniheidelberg.bsky.social @univparissaclay.bsky.social
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1️⃣ Physical exclusion
2️⃣ FGF4-driven fate bias
And it even works at the level of individual embryos!
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1️⃣ Physical exclusion
2️⃣ FGF4-driven fate bias
And it even works at the level of individual embryos!
[4/8]
➡️ Crowding first, then signalling.
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➡️ Crowding first, then signalling.
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We show that donor embryonic stem cells (ESCs) reshape the developing mouse embryo, not just by what they signal, but where they push.
📄 doi.org/10.1242/dev....
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We show that donor embryonic stem cells (ESCs) reshape the developing mouse embryo, not just by what they signal, but where they push.
📄 doi.org/10.1242/dev....
[1/8]
#MRC
@wellcometrust.bsky.social
#SãoPauloResearchFoundation
#JapanSocietyforthePromotionofScience #JSPS
#UEHARAMemorialFoundation
@lbates.bsky.social @tazami.bsky.social
Thanks to: @scicambridge.bsky.social @pdncambridge.bsky.social @babrahaminst.bsky.social @cambiochem.bsky.social @cam.ac.uk ...
@lbates.bsky.social @tazami.bsky.social
Thanks to: @scicambridge.bsky.social @pdncambridge.bsky.social @babrahaminst.bsky.social @cambiochem.bsky.social @cam.ac.uk ...
Capacitated cultures then generate neuroectoderm, paraxial mesoderm & definitive endoderm with textbook marker profiles—ready for downstream lineage studies.
Capacitated cultures then generate neuroectoderm, paraxial mesoderm & definitive endoderm with textbook marker profiles—ready for downstream lineage studies.
10-day XAV capacitation guides naïve domes → primed flats—an in-vitro window on the pre- to post-implantation transition.
10-day XAV capacitation guides naïve domes → primed flats—an in-vitro window on the pre- to post-implantation transition.
PD03 + A83 + Y → GATA3⁺ trophoblast cysts.
LIF + ACTIVIN + CHIR → hypoblast/ExEn. Use them for blastoids or placenta work.
PD03 + A83 + Y → GATA3⁺ trophoblast cysts.
LIF + ACTIVIN + CHIR → hypoblast/ExEn. Use them for blastoids or placenta work.
Lines keep the classic naïve signature, form domes in t2iLGöXYaa, and map to E5/6 epiblast by bulk RNA-seq.
Lines keep the classic naïve signature, form domes in t2iLGöXYaa, and map to E5/6 epiblast by bulk RNA-seq.
Two triplet sets showcase natural variation:
• 161.2A/C share a Chr2q deletion, 161.2B does not.
• 255.1B/C carry Chr5 trisomy, 255.1A does not.
Study how karyotype skews lineage choice—no embryos needed.
Two triplet sets showcase natural variation:
• 161.2A/C share a Chr2q deletion, 161.2B does not.
• 255.1B/C carry Chr5 trisomy, 255.1A does not.
Study how karyotype skews lineage choice—no embryos needed.
Instead of one line per blastocyst, we expanded every dome-shaped colony. Result: single embryos now come with paired, triplet or quadruplet lines—perfect for side-by-side comparisons.
Instead of one line per blastocyst, we expanded every dome-shaped colony. Result: single embryos now come with paired, triplet or quadruplet lines—perfect for side-by-side comparisons.