🧬 NR6A1 gene: Cracking the code of a rare syndrome! Zebrafish models reveal how mutations can impact eyes, kidneys & spine. Genomic detective work at its finest! 🔬 #RareDiseaseResearch #Genomics #MedicalBreakthrough https://emmecola.github.io/genomics-daily

🧬 Gene editing miracle! Personalized therapy saves newborn with rare disease, proving precision medicine can rewrite genetic destiny 🚀 #GenomicBreakthrough #PersonalizedMedicine #RareDiseaseResearch https://emmecola.github.io/genomics-daily

🧬 Machine learning meets genomics! Watershed-SV uncovers hidden rare disease variants by linking DNA changes to gene expression. Revolutionizing diagnostics one sequence at a time! 🔬 #GenomicInnovation #RareDiseaseResearch #PrecisionMedicine https://emmecola.github.io/genomics-daily

🧬🦟 Tiny flies, big insights! Drosophila model reveals how gene mutations disrupt neural function in rare disorder. Neurological mysteries unfolding! 🧠 #Genomics #NeuralScience #RareDiseaseResearch https://emmecola.github.io/genomics-daily

We’re trying to cure babies who have
Pyruvate Dehydrogenase Deficiency.
Right now their only treatment is a ketogenic diet (hence the butter)
So we’re trying to raise money for a cure.
DONATE
https://www.hopeforpdcd.org
#givingtuesday
#hopeforpdcd #pdcd
#pyruvatedehydrogenasedeficiency
#rarediseaseresearch #ketosis #ketogenicdiet