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UNC Catalyst proslijedio/la je Tweet
At the
@ICR_London with Paul Workman, David Drewry, and Opher Gileadi to kick off the next phase of our chordoma drug discovery project with@TheMarkFdn@ChordomaFDN. This productive team is tackling a tough "undruggable" target.@thesgconline@UNCPharmacy@sommerjopic.twitter.com/CC6yKB9GFH – mjesto: Institute Of Cancer Research
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UNC Catalyst proslijedio/la je Tweet
Post: Registre international des patients ARSACS https://www.arsacs.com/fr/registre-international-des-patients-arsacs/ …pic.twitter.com/l8GMXSfeGq
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UNC Catalyst proslijedio/la je Tweet
We are proud to have
@NUFeinbergMed as a partner in our mission to cultivate awareness and education around Rare Diseases like Cystic Fibrosis.#RareRockstarshttps://bit.ly/30CpmswHvala. Twitter će to iskoristiti za poboljšanje vaše vremenske crte. PoništiPoništi -
UNC Catalyst proslijedio/la je Tweet
New! Share the official social media visuals for the
#RareDiseaseDay 2020 campaign now available to download via http://rarediseaseday.org/downloads The visuals are also available in editable files to be translated.pic.twitter.com/Nm6o7e8PRi
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UNC Catalyst proslijedio/la je Tweet
Did you know?
#RareDiseaseDay is an international campaign created with 60 national alliances of rare disease patient organisations from around the world! https://www.rarediseaseday.org/national-alliances …pic.twitter.com/KPOLziWlN8
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UNC Catalyst proslijedio/la je Tweet
Very excited that I’m part of the
#IAmNumber17 campaign - a very exciting initiative. Watch this space
#RareDiseasepic.twitter.com/42LsVNZQH1
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UNC Catalyst proslijedio/la je Tweet
Have you already checked
#CheckOrphan? Learn about#RareDiseases, their#symptoms and#treatments at http://5.102.147.165/diseasesHvala. Twitter će to iskoristiti za poboljšanje vaše vremenske crte. PoništiPoništi -
UNC Catalyst proslijedio/la je Tweet
There are currently 7,000 rare diseases affecting 25-30 million Americans today. Join us for our Rare Disease Day 2020 Symposium to raise awareness amongst the general public and decision-makers about rare diseases http://bit.ly/2thiC7m pic.twitter.com/CxldcBYLfY
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UNC Catalyst proslijedio/la je Tweet
The Chordoma Foundation Patient Navigation Service is a free & confidential resource that serves the worldwide
#chordoma community by providing personalized info & support to anyone affected by chordoma at any stage of their journey. Need help? http://chordoma.org/request-help pic.twitter.com/lT7KpRmQt8
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Excited to see this progress in rare disease research.https://twitter.com/CheckRare/status/1217428668122849280 …
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UNC Catalyst proslijedio/la je Tweet
Locus Biosciences initiates world’s first controlled clinical trial for a CRISPR enhanced bacteriophage therapy:http://www.microbiometimes.com/locus-biosciences-initiates-worlds-first-controlled-clinical-trial-for-a-crispr-enhanced-bacteriophage-therapy/ …
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UNC Catalyst proslijedio/la je Tweet
Post: ARSACS reference article in the GeneReviews updated https://www.arsacs.com/arsacs-reference-article-in-the-genereviews-updated/ …pic.twitter.com/ANfBVlAPHo
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UNC Catalyst proslijedio/la je Tweet
Out now! Download the official poster for
#RareDiseaseDay 2020 now available via http://rarediseaseday.org/downloads . Share it today to show your support for the rare disease community!pic.twitter.com/1SJigTalxs
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Another great example of research into a rare disease that sheds light on more prevalent diseases. In this case understanding tuberous sclerosis can shed light on pathways involved in autism.https://www.nature.com/articles/s41467-019-12962-4 …
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UNC Catalyst proslijedio/la je Tweet
First post of 2020! A newly-proposed treatment strategy might be effective against several forms of spinocerebellar
#ataxia and other CAG repeat-associated disorders.#RareDiseasehttps://scasource.net/2020/01/03/two-or-more-birds-with-one-stone-designing-a-single-therapeutic-strategy-to-treat-multiple-types-of-spinocerebellar-ataxia/ …Hvala. Twitter će to iskoristiti za poboljšanje vaše vremenske crte. PoništiPoništi -
Happy new year! We're so excited to see all the progress 2020 has in store for rare disease treatments!https://www.fool.com/investing/2019/12/27/4-rare-disease-drug-launches-to-watch-in-2020.aspx …
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Thanks
@MalanSyndrome for visiting our labs and discussing more about Malan Syndrome and how the Catalyst can help shed light on this disease!pic.twitter.com/KbiZhh5v5l
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Excited to meet UNC researchers working on Rare Diseases. Thanks for coming out to support and meet the members of the UNC Catalyst for Rare Diseases. We look forward to future collaborations
#ShowYourRare#RareDiseaseDay#Chordoma#ARSACS#EhlersDanlosSyndrome#UNCPharmacypic.twitter.com/DeLeviwSyD
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Searching for a diagnosis: how scientists are untangling the mystery of developmental disorders
#rarediseases@mosaicsciencehttps://mosaicscience.com/story/developmental-delay-disorders-milestones-childhood-genetic?utm_medium=mosaic-share&utm_source=twitter …Hvala. Twitter će to iskoristiti za poboljšanje vaše vremenske crte. PoništiPoništi -
This week is Mitochondrial Disease Awareness Week
#mitoaware#gmdaw@MitoCanada The Mito-Find project is empowering Next Generation Sequencing for diagnosing mitochondrial disease, find out more about the project by checking out here: http://www.magiccalgary.ca/MitoFIND.html https://twitter.com/MitoCanada/status/1042745178568761345 …Hvala. Twitter će to iskoristiti za poboljšanje vaše vremenske crte. PoništiPoništi
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