Yin Yao Dong lab
@CMS_CDG_Oxford
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Welcome to the Yin Yao Dong lab @UniofOxford @MRC_WIMM @NDCNOxford, home of N-glycosylation research with a focus on its importance to neuromuscular junctions.
Oxford, Oxfordshire
Joined February 2021
RT @CDGCAREorg: New Documentary Spotlight 🎥. Could the tiny fruit fly help unlock treatments for rare diseases? 🪰🔬. We're excited to share….
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RT @CDGCAREorg: Hope in Action: The ALG13-CDG Research Project Begins! . CDG CARE is proud to announce the kickoff of a groundbreaking new….
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RT @myawareUK: Whether it’s miles, muffins or multiple choice – you can help raise funds this June!. 👉MyMiles: 👉MyC….
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RT @CDGCAREorg: 🚨URGENT ACTION NEEDED .The NIH issued a special NOFO a few weeks ago that was framed to open the door for the FCDGC to REAP….
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RT @RareRevolutionM: Because glycosylation is so critical, CDGs can lead to complex, multi-system symptoms like: .⚡ Developmental delays .🧠….
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RT @RareRevolutionM: Thank you to @RareRevolution for today's powerful #CDGTakeover! 💚.Here’s how to keep the #WorldCDGDay momentum going:….
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Here is the latest paper from our group on cryo-EM structures of the human adult muscle nicotinic acetylcholine receptor in resting-like and desensitized states. This work was spearheaded by @Anna_Liiiiiiii in collaboration with @DavidBSauer.
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RT @MRC_WIMM: For International Women's Day tomorrow, we asked some of our women scientists, including @MiraKassouf & @DrSarahGooding, to r….
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I am excited to share our latest manuscript, published by @braincomms, carried out by @CossinsJudith and Imre Kozma in collaboration with Amplo Biotechnology.
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RT @rarediseasesnet: New research from @FrontierCDG:. ✅ Exploring the Role of #NGLY1Deficiency in Patients with NGLY1-#CongenitalDisorderOf….
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RT @bioprotocol: 🚨 The Curetopia Auction is LIVE!. 10,000 rare diseases ignored by Big Pharma.It's time to leave the system behind. The fir….
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RT @MyastheniaGNews: Do you find that people have preconceived ideas about what it means to live with MG? If so, what do you most want to c….
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RT @myawareUK: #MoreThanAMedicine.This is Sarah, she has myasthenia & needs treatment to manage tasks & daily life. Please share our brave….
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RT @GenovevaUzunov1: #RareDiseases are not so rare at all! However, we still don't know how to #treat them and in some instances, what cau….
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RT @myawareUK: #MoreThanAMedicine Amber is 27. Myasthenia does not discriminate & can affect anyone, any time. Amber uses art as a form of….
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RT @NDCNOxford: Myasthenia gravis is a rare autoimmune condition that causes muscle weakness and muscle fatigue. A new project, MyArchive,….
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RT @damato_v: Excited to share our work on.NMOSD and RTX, the foundation for my PhD. Thanks to team.@ANG_Oxford and the co-authors.for maki….
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RT @MRC_WIMM: Next in our Rare Disease Day series, we spoke with Yin Dong (@CMS_CDG_Oxford), whose work focuses on Congenital Myasthenia an….
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