Copp&Greene labs
@ntds_research
ID: 1886326417
20-09-2013 11:51:38
300 Tweet
365 Followers
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Come and join our MRC NMGN Congenital Anomalies for this hybrid meeting on the 23rd and 24th of November. The Congenital Anomalies Cardiovascular Geneboree aims to create a framework for accurately modelling & #phenotyping #human #heartdefects nmgn.mrc.ukri.org/news/congenita… The Mill Lab Prof Karen J Liu
Delighted that this manuscript has now been published. Hope it helps reinvigorate the conversation about closed neural tube defects. journals.biologists.com/dev/article/do… Eirini Maniou Copp&Greene labs Developmental Biology & Cancer
#EDBC2023 is over but managed to bring together scientists from across Europe. We had an amazing party night at the museum🦖, and Dr Chloe Santos (twitterless) won runner up poster🌟! British Society for Developmental Biology Copp&Greene labs Developmental Biology & Cancer
Many congratulations to lab alumnus Dr Noraishah Mydin Abd Aziz on her appointment to the Board of Directors of Universiti Putra Malaysia and National Institutes of Biotechnology Malaysia
We kick off our MRC NMGN Congenital Anomalies #CHDGeneboree at Mary Lyon Centre at MRC Harwell bringing together cardiologists, geneticists & developmental biologists to discuss challenges & opportunities for improving diagnosis & prognosis of human congenital heart disease! With organiser Deb Henderson opening…
**ALERT** Fully funded 4-year PhD Project in Gene Editing & Developmental Biology The Roslin Institute The University of Edinburgh findaphd.com/phds/project/r… Please retweet!!
Congratulations to UCL's Dr Jonathan Fisher, Dr Hossein Heidari, Dr Christina Anderson, Dr Dr Emily Kostas and Dr Lucy van Dorp for being awarded UK Research and Innovation Future Leaders Fellowships in recognition of their groundbreaking research ucl.ac.uk/news/2023/dec/…
🚨Fully-funded PhD studentships available in Child Health Research includes collaboration with University of Toronto. Explore diverse projects, get mentorship from experts, & shape the future of paediatric healthcare. Apply now! ucl.ac.uk/child-health/s… #ChildHealthResearch #PhDStudentships
For day 2, one of our group leaders and MRC NMGN Congenital Anomalies Co-Lead Steve Twigg (Steve Twigg) has joined Lisa and Isaac in York’s National STEM Learning Centre to give a talk on using mouse models for rare disease 🐭
Nice overview of MRC National Mouse Genetics Network and the aims of its constituent clusters in Cell Genomics sciencedirect.com/science/articl…
Calling all rare disease researchers and clinicians who have a variant of uncertain significance... 🧬 The MRC National Mouse Genetics Network & MRC NMGN Congenital Anomalies (co-led by our PI Steve Twigg) are currently looking for VUSs to model in mice! 🐭 (1/2)
Another example of rare disease research supported by our GEMM call is the generation of a mouse model of non-ketotic hyperglycinemia, a rare, life-limiting inherited metabolic disease, that was produced for Copp&Greene labs #RareDiseaseDay har.mrc.ac.uk/case-studies/g…
Researchers and funders unite to launch centre to tackle kidney disease | UCL Great Ormond Street Institute of Child Health - UCL – University College London ucl.ac.uk/child-health/n… Developmental Biology & Cancer
