Very similar gig at 123 Pleasant Street in Morgantown, WV, by Mustard Plug back in 2008/9ish. Much Skanking.
Very similar gig at 123 Pleasant Street in Morgantown, WV, by Mustard Plug back in 2008/9ish. Much Skanking.
β° Deadline Approaching! β°
π
15 January 2026
Under two weeks to apply for our fully funded PhD project βEngineering an in vitro human embryo implantation platform to study pathologies arising in early pregnancyβ at @sheffielduni.bsky.social. #development #endometrium #materialsscience
I strongly encourage ECRs to apply for opportunities like the Travelling Fellowships from the ever supportive @biologists.bsky.social
They are a fantastic for learning new skills, building collaborative networks, and honing scientific writing.
doi.org/10.1242/dev....
β° Deadline in two weeks! β°
Work at the interface of biology + computation to build a virtual human embryo to predict developmental success and failure.
Happy to answer questions!
π¨ Come join us @sheffielduni.bsky.social for a PhD on the evolution and development of feathers and flight! π£π¬
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... π§ͺ
π¨ PhD Projects π¨
We are advertising two UKRI funded PhD projects at the @sheffielduni.bsky.social. #stemcells #development #embryology #reproductivephysiology #mathmaticalmodelling #quantitativebiology
Do you make shipments?! Iβd love this for the lab!
Finally, a career highlight, we made it into @cellysally.bsky.social 's #PaperThemeTune s:
bsky.app/profile/cell...
[8/8]
Also, check out the behind-the-scenes interview on my path in science, a eureka moment, and what I do when I choose to leave the lab:
ποΈ doi.org/10.1242/dev....
[7/8]
and thank you to funders:
@wellcometrust.bsky.social @biologists.bsky.social @ukri.org
[6/8]
Thanks to co-authors & host institutions:
@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
[5/8]
To test this, we built a quantitative model of fate specification in the embryo. It predicts a two-step mechanism:
1οΈβ£ Physical exclusion
2οΈβ£ FGF4-driven fate bias
And it even works at the level of individual embryos!
[4/8]
Even ESCs lacking FGF4 can push host cells into the trophectoderm, just by outcompeting them for space. But with FGF4, they also bias host cells away from contributing to the embryo.
β‘οΈ Crowding first, then signalling.
[3/8]
When injected into 8-cell embryos, ESCs displace host cells from the future embryo into extra-embryonic tissues. This happens via physical crowding and, if the donor cells produce FGF4, also via molecular signalling.
[2/8]
π¨ New paper out in Development! π¨
We show that donor embryonic stem cells (ESCs) reshape the developing mouse embryo, not just by what they signal, but where they push.
π doi.org/10.1242/dev....
[1/8]
Iβve been using my CoB insulated lunch bag for work ever since Biologist @ 100 in Liverpool! π€
10/10 Thanks to:
#MRC
@wellcometrust.bsky.social
#SΓ£oPauloResearchFoundation
#JapanSocietyforthePromotionofScience #JSPS
#UEHARAMemorialFoundation
9/10 @drn-sheffield.bsky.social @sheffielduni.bsky.social @uoe-igc.bsky.social @edinburgh-uni.bsky.social @uniofaberdeen.bsky.social @uspoficial.bsky.social βͺ@lsiexeter.bsky.social @exeter.ac.uk
8/10 Thank you to all the excellent people involved! (That I can find)
@lbates.bsky.social @tazami.bsky.social
Thanks to: @scicambridge.bsky.social @pdncambridge.bsky.social @babrahaminst.bsky.social @cambiochem.bsky.social @cam.ac.uk ...
7/10 Somatic versatility
Capacitated cultures then generate neuroectoderm, paraxial mesoderm & definitive endoderm with textbook marker profilesβready for downstream lineage studies.
6/10 Forward Progression
10-day XAV capacitation guides naΓ―ve domes β primed flatsβan in-vitro window on the pre- to post-implantation transition.
5/10 Extra-embryonic power
PD03 + A83 + Y β GATA3βΊ trophoblast cysts.
LIF + ACTIVIN + CHIR β hypoblast/ExEn. Use them for blastoids or placenta work.
4/10 Hallmark naΓ―ve identity
Lines keep the classic naΓ―ve signature, form domes in t2iLGΓΆXYaa, and map to E5/6 epiblast by bulk RNA-seq.
3/10 Mosaicism in a dish
Two triplet sets showcase natural variation:
β’ 161.2A/C share a Chr2q deletion, 161.2B does not.
β’ 255.1B/C carry Chr5 trisomy, 255.1A does not.
Study how karyotype skews lineage choiceβno embryos needed.
2/10 Multiple clones per embryo
Instead of one line per blastocyst, we expanded every dome-shaped colony. Result: single embryos now come with paired, triplet or quadruplet linesβperfect for side-by-side comparisons.
1/10π§΅ New preprint! π
We built a resource of 20 clonal human naΓ―ve pluripotent stem cell lines from 10 blastocysts. Explore embryo-to-embryo and clone-to-clone variation in one place.
πdoi.org/10.1101/2025.06.02.657331
Todayβs speaker in our DRN external seminar series is Dr Thorsten Boroviak (PDN, University of Cambridge) @pdncambridge.bsky.social , who will talk on early embryonic development in primates.
Host: Anestis Tsakiridis @tsakiridis.bsky.social
All welcome!
Thanks to Anne Wiblin and the team at abcam for the invitation to share and discuss my research today! #stemcells #development
It was fantastic to have @lbates.bsky.social visit last week! Thank you for sharing your exciting work!
Check out our new research in @royalsocietypublishing.org's Open Biology! We experimentally induce a transition from chemical to mechanical patterning in the chicken embryo π£π¬ @lanevol.bsky.social π§ͺ
royalsocietypublishing.org/doi/10.1098/...