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The Journal of Clinical Investigation
|
November 25, 2010
Hepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic mice
Sara Gardenghi, Pedro Ramos, Maria Franca Marongiu, et al.
Cell Metabolism
|
September 25, 2012
Divalent metal transporter 1 regulates iron-mediated ROS and pancreatic β cell fate in response to cytokines
Jakob Bondo Hansen, Morten Fog Tonnesen, Andreas Nygaard Madsen, et al.
Science Translational Medicine
|
May 29, 2015
Research in academic medical centers: two threats to sustainable support
Arthur S Levine, Robert J Alpern, Nancy C Andrews, et al.
NPJ Genomic Medicine
|
February 27, 2025
International Precision Child Health Partnership (IPCHiP): an initiative to accelerate discovery and improve outcomes in rare pediatric disease
Katherine B Howell, Susan M White, Amy McTague, et al.
Nature Genetics
|
December 8, 2015
A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency
Haifa H Jabara, Steven E Boyden, Janet Chou, et al.
NPJ Genomic Medicine
|
December 2, 2024
Hospital-wide access to genomic data advanced pediatric rare disease research and clinical outcomes
Courtney E French, Nancy C Andrews, Alan H Beggs, et al.
Molecular Therapy. Methods & Clinical Development
|
August 11, 2021
Evidence generation and reproducibility in cell and gene therapy research: A call to action
Mohamed Abou-El-Enein, Aris Angelis, Frederick R Appelbaum, et al.
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Search research articles
Search
Showing results (91-100 of 97) with videos related to
Sort By:
Page
of 10
You have reached the last page of results.
This site can display upto 97 results.
The Journal of Clinical Investigation
|
November 25, 2010
Hepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic mice
Sara Gardenghi, Pedro Ramos, Maria Franca Marongiu, et al.
Cell Metabolism
|
September 25, 2012
Divalent metal transporter 1 regulates iron-mediated ROS and pancreatic β cell fate in response to cytokines
Jakob Bondo Hansen, Morten Fog Tonnesen, Andreas Nygaard Madsen, et al.
Science Translational Medicine
|
May 29, 2015
Research in academic medical centers: two threats to sustainable support
Arthur S Levine, Robert J Alpern, Nancy C Andrews, et al.
NPJ Genomic Medicine
|
February 27, 2025
International Precision Child Health Partnership (IPCHiP): an initiative to accelerate discovery and improve outcomes in rare pediatric disease
Katherine B Howell, Susan M White, Amy McTague, et al.
Nature Genetics
|
December 8, 2015
A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency
Haifa H Jabara, Steven E Boyden, Janet Chou, et al.
NPJ Genomic Medicine
|
December 2, 2024
Hospital-wide access to genomic data advanced pediatric rare disease research and clinical outcomes
Courtney E French, Nancy C Andrews, Alan H Beggs, et al.
Molecular Therapy. Methods & Clinical Development
|
August 11, 2021
Evidence generation and reproducibility in cell and gene therapy research: A call to action
Mohamed Abou-El-Enein, Aris Angelis, Frederick R Appelbaum, et al.
Page
of 10