Activities

• 

  Mary Grace N. Tamio   

  on February 07 2023 at 05:21 PM Edited public

  Rare genetic disease may protect Ashkenazi Jews against TB
  
  #geneticdisease #Ashkenazi #tuberculosis
  
  More info |⬇️
  https://cn1699.com/news/rare-genetic-disease-may-protect-ashkenazi-jews-against-tb

  

  Rare genetic disease may protect Ashkenazi Jews against TB | CN1699

  Scientists may have solved the question of why Ashkenazi Jews are significantly more susceptible to a rare genetic disorder known as Gaucher...
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• 

  Mary Grace N. Tamio   

  on December 02 2022 at 06:46 PM Edited public

  Research on rare genetic disease sheds light on common head and neck cancer
  
  #geneticdisease #headcancer #neckcancer
  
  More info | ⬇️
  https://cn1699.com/news/research-rare-genetic-disease-sheds-light-common-head-and-neck-cancer

  

  Research on rare genetic disease sheds light on common head and neck cancer | CN1699

  Research led by Rockefeller physician-scientist Agata Smogorzewska explains why Fanconi anemia patients are vulnerable to this cancer, known as...
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  Mary Grace N. Tamio   

  on July 18 2021 at 11:03 AM Edited public

  Gene therapy success offers hope for reversing rare genetic diseases
  
  #genetherapy #geneticdisease
  
  For more information | ⬇️
  https://cn1699.com/news/gene-therapy-success-offers-hope-reversing-rare-genetic-diseases

  

  Gene therapy success offers hope for reversing rare genetic diseases | CN1699

  A landmark study published in the journal Nature Communications is describing the extraordinarily successful results of a Phase 1 trial testing a...
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• 

  Mary Grace N. Tamio   

  on June 29 2021 at 10:15 PM Edited public

  CRISPR used to treat rare genetic disease in promising phase 1 trial
  
  #CRISPR #geneticdisease #phase1trial
  
  For more information | ⬇️
  https://cn1699.com/news/crispr-used-treat-rare-genetic-disease-promising-phase-1-trial

  

  CRISPR used to treat rare genetic disease in promising phase 1 trial | CN1699

  The first, promising results have been released from a phase 1 clinical trial using CRISPR to treat a genetic disease.
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