The Mill Lab
@Mill_lab
Group at @mrc_hgu using genetics, cell biology and lots of imaging to unlock the mysteries of mammalian #cilia. Also on the otherside: @[email protected]
ID:1043195153907888129
http://www.cilialab.co.uk 21-09-2018 17:48:01
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We’re hiring! We’re looking for a Reviews Editor to work across our journals (Development, J Cell Science, Journal of Experimental Biology, DMM Journal). If you’ve got excellent communication skills and a broad interest in science, this is a job for you!
Location: Cambridge UK
biologists.com/about-us/work-…
Job Alert~! The Wallingford Lab is hiring a Lab Manager. Great opportunity for graduating seniors. Interested parties can DM me here. Official posting will go up soon. Please RT.
Society for Developmental Biology
Primary ciliary dyskinesia ( #PCD ) is a rare inherited multi-organ condition, which can lead to airway inflammation and infections. Now, scientists led by the The Mill Lab at The University of Edinburgh and the Institut Imagine at Université Paris Cité found what causes PCD. dlvr.it/T6PVp7
1/n Today in Science Magazine: ‘Risk of meningomyelocele mediated by the common 22q11.2 deletion’. science.org/doi/10.1126/sc…
Shedding a light on PCD: Part 3 targeted therapies #PatientExperienceWeek #PCD #PrimaryCiliaryDyskinesia #ReCodeTherapeutics #GeneticMedicine #PCD Foundation
Shedding a light on PCD: Part 2 Compliance and sickness
#PatientExperienceWeek #PCD #PrimaryCiliaryDyskinesia #ReCodeTherapeutics #GeneticMedicine #PCD Foundation
Acto3D: an open-source user-friendly volume rendering software for high-resolution 3D fluorescence imaging in biology
Read this Techniques and Resources Article by Naoki Takeshita, Kenta Yashiro Kenta Yashiro and colleagues:
journals.biologists.com/dev/article/15…
Exciting opportunity to work with AstraZenecaUK & NRS Renal Specialty on CKD trials in 🏴 UoD Medicine CSO(Health)Scotland Anna Dominiczak jobs.ac.uk/job/DHK987/cli…
Proud of Julia speaking to politicians/ geneticists/ advocates for rare genetic conditions about her experiences with PCD on the occasion of Undiagnosed Conditions Day at the Scottish Parliament! Rare Disease UK Genetic Alliance UK SWAN UK (syndromes without a name) PCD Support UK Institute of Genetics and Cancer
Julia spoke at the Scottish Parliament on Undiagnosed Conditions Day about her experiences of living with PCD, so proud of her! SWAN UK (syndromes without a name) Rare Disease UK Genetic Alliance UK PCD Support UK Institute of Genetics and Cancer
After countless requests, we're thrilled to introduce PK Mito Orange FX - a fixable variant of PKMO. PKMO FX allows immunolabeling and CLEM approaches.
Happy to have contributed to this project led by Zhixing Chen and Christian Jüngst.
#mitochondria
pnas.org/doi/10.1073/pn…