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Sanford Research is a non-profit research organization that is a part of Sanford Health, the largest rural, not-for-profit health care system in the nation. Transformational gifts by Denny Sanford have propelled Sanford Research in its goal of becoming a world class research institution. Sanford Research has sought to establish a core of scientists that are studying disease at a fundamental level with the expectation that these current efforts will pay off in the future by advancing disease therapy and prevention.
With a team of over 200 researchers, Sanford Research is comprised of eight groups that bridge bench, translational and clinical research including: Cancer Biology and Immunotherapies, Pediatrics and Rare Diseases, Diabetes, Cellular Therapies and Stem Cell Biology, Enabling Technology, Environmental Influences on Health and Disease, Genetics and Genomics, and Population Health. |
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Twitter Updates on Sanford Research
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RT @SanfordBenF: I'm in Philly this morning for the @GlobalGenes #Rare Patient Advocacy Symposium! Let me know if you've got questions abou… -
RT @AACR: We join with the scientific community in recognizing International Clinical Trials Day. Clinical trials are a critical component… -
@SeqComplete @ankushlab @DrDavidPearce @rarediseaseuk thank you for the insert #ATAXIA -
RT @JFCConsultants: #RareDisease #RareDiseases @teaminspire @EparentConnect @SanfordCoRDS Helping to spread the word about raising the visi… -
Key finding on a protein that helps prevent aggregation of other proteins in #neurons https://t.co/Peu3nLoRLw will… https://t.co/IBhYwfvRVc -
RT @JFCConsultants: #RareDisease #RareDiseases @teaminspire @EparentConnect @SanfordCoRDS Helping to spread the word about raising the visi… -
#RareDisease #RareDiseases @teaminspire @EparentConnect @SanfordCoRDS Helping to spread the word about raising the… https://t.co/svcGwDXItR -
RT @SanfordBenF: I'm in Philly this morning for the @GlobalGenes #Rare Patient Advocacy Symposium! Let me know if you've got questions abou… -
I'm in Philly this morning for the @GlobalGenes #Rare Patient Advocacy Symposium! Let me know if you've got questio… https://t.co/xl2sSmgWPr -
RT @NAF_Ataxia: If you are NOT at #2018AAC - check out @SanfordCoRDS online and sign up for the #Ataxia patient registry at https://t.co/gB… -
RT @rareundiagnosed: Netflix & The New York Times are filming a documentary series about people with undiagnosed medical conditions. The se… -
RT @nature: Scientific integrity needs to apply to how researchers treat people, not just to how they handle data, says @emsaurios https://… -
RT @nature: N & V: Several neurodegenerative disorders are linked to the build-up of abnormal α-synuclein protein in distinct cell types. A… -
RT @SanfordBenF: Hope to see you there! I'll be attending and can answer any questions you have about the @SanfordCoRDS registry! Excited…