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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 @ChildrensTumor: Pig Models and NF1, The New Research Frontier: A Conversation with @DrJWeimer @SanfordResearch https://t.co/Re5kDkeFh… -
@StanfordMed @raredisorders @SanfordCoRDS @NAF_Ataxia https://t.co/v23SzP8qdn -
RT @SanfordCoRDS: CoRDS is the advocacy group for all #raredisease #patients & those without a support group, because rare is common for 30… -
@ataxiaandme @johnnyjots @NAF_Ataxia @SanfordCoRDS @MVEG001 @RyanDaviesLibby @johnvevans @OrphanConf… https://t.co/3iigdN5e6a -
RT @SanfordBenF: @SanfordResearch works to develop new therapies for rare diseases every day! Our @SanfordCoRDS registry ties patients to r… -
RT @hnisimasu: Single-molecule movie of DNA search and cleavage by CRISPR-Cas9. https://t.co/3NQxmbvzJF -
RT @SanfordBenF: @SanfordResearch works to develop new therapies for rare diseases every day! Our @SanfordCoRDS registry ties patients to r… -
@SanfordResearch works to develop new therapies for rare diseases every day! Our @SanfordCoRDS registry ties patien… https://t.co/qUiUl3Eu8g -
RT @Rose_of_Sharon8: @DickDurbin @SenDuckworth 36 patient orgs oppose 2 Senate's proposed weakening of #OrphanDrug Tax Credit. We urge Cong… -
RT @Rose_of_Sharon8: @RepKinzinger 35 patient orgs in opposition to Senate's proposed weakening of the #OrphanDrug Tax Credit. We urge Cong… -
RT @ataxiaandme: ICYMI yesterday @johnnyjots @NAF_Ataxia @SanfordCoRDS @MVEG001 @RyanDaviesLibby @johnvevans We launched our new #ata… -
@DickDurbin @SenDuckworth 36 patient orgs oppose 2 Senate's proposed weakening of #OrphanDrug Tax Credit. We urge C… https://t.co/nvNh0ikqrt -
@RepKinzinger 35 patient orgs in opposition to Senate's proposed weakening of the #OrphanDrug Tax Credit. We urge C… https://t.co/bvwai5fOJ6 -
RT @teaminspire: US scientists try 1st gene editing in the body https://t.co/f7pEPUZQb4 via @AP -
RT @Rose_of_Sharon8: NEW! Klippel-Feil syndrome Patient Registry. PATIENTS, provide your DATA! KFS Survey > https://t.co/9UAAMgqfkU Pls. R…