Registration now open for our 1st NMGN Congenital Anomalies
Cardiovascular Geneboree: From Cardiac Gene Variant to Mouse Model 🗓️ Nov 23-34, 2023🗓️ MRC Harwell Advanced Training Centre, UK (or online)! ❤️ 🧬 🐁 #RareDisease #CongenitalAnomalies #CHD #DiseaseModels #HumanGenetics Register: https://www.eventbrite.co.uk/e/congenital-anomalies-cardiovascular-geneboree-gene-variant-to-mouse-model-tickets-707821602467?aff=oddtdtcreator A workshop for #clinicians, #ClinicalGeneticists & #DevBiologists with an interest in finding new genes for #CHD & validating them in models. We are grateful to #BHF for support. Join us!

Hey #techies & #AI pros- we have a NC3Rs crack-it challenge we need help with!

CHALLENGE: Develop a non-invasive & non-toxic system for #mouse identification from birth that are amenable to automated tracking technology & home cage monitoring.

NEED: Currently we can only identify individual 🐁 mice 🐁 effectively & humanely after 2wk meaning we miss alot perinatally in human disease models #CongenitalAnomalies!

Think you can help us? Join us: https://nc3rs.org.uk/crackit/atracktive

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RT @Mill_lab
🚨POSTDOC JOB ALERT🚨
Join us- 3 year MRC-funded #PostDocFellow in #CellBio, #DevBio & #Genomics as part of our team @NMGN_CongAnom in @MRCMouseNetwork! #RareDisease #CongenitalAnomalies #Ciliopathies #GeneticTherapies 🐭🧑‍🔬🧬https://elxw.fa.em3.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1001/job/7216🧬 🗓️Closes 24/05/2023🗓️ RT😉🙏