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Blog

Apr 27
0

Promising mouse model for a devastating genetic deficiency

By NGLY1.org | Research and Science | No Comments
Researchers from the RIKEN Global Research Cluster in Japan have developed a potential mouse model for the genetic disorder known as an NGLY1 deficiency. Published in the journal PLOS Genetics,...
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Apr 12
0

Leftwich Family Adventures at the St. Louis Half-Marathon

By NGLY1.org | NGLY1 Families | No Comments

Congratulations to Gage, his brother, and his parents Greg and Jennifer Leftwich, for a great race in the St. Louis half-marathon! Jennifer, Gage’s mom, shares “We are creating a ‘Bucket…

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Apr 05
0

Mitali Tambe, Ph.D. – On a RARE Journey to Therapy

By NGLY1.org | Researchers and Clinicians | No Comments

Mitali Tambe, Ph.D., from the Hudson Freeze Lab at Sanford Burnham Prebys Research Institute presented on NGLY1 for the ASBMB’s Art of Science Communication.

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Apr 01
0

Upcoming Web Event: Aligning Incentives for Sharing Clinical Trial Data

By NGLY1.org | Events, Rare Disease, Research and Science | No Comments

NGLY1.org president and co-founder, Matt Might, PhD, will be participating in the upcoming live web event “Aligning Incentives for Sharing  Clinical Trial Data” hosted by the New England Journal of…

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Recent Posts

  • Why can’t Bertrand Might cry? Scientists offer an answer: missing water channels
  • NGLY1.org Research update: Generation of an induced pluripotent stem cell line …
  • Research Update: Suggestion that targeting NGLY1 represents a novel anti-melanoma strategy
  • Superhuman Video: The Might Family
  • NGLY1 Family Story – Marc F

Recent Comments

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  • Emile najm on NGLY1: Data as a Drug Presentation at NIH/NCATS
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