Search research articles
Contact Us
Filters
Showing results (151-160 of 154) with videos related to
Page
of 16
Sort By:
You have reached the last page of results.
This site can display upto 154 results.
Science (New York, N.Y.)
|
December 20, 2022
Inborn errors of OAS-RNase L in SARS-CoV-2-related multisystem inflammatory syndrome in children
Danyel Lee, Jérémie Le Pen, Ahmad Yatim, et al.
Science (New York, N.Y.)
|
February 29, 2024
The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants
Marie Materna, Ottavia M Delmonte, Marita Bosticardo, et al.
Nature
|
November 8, 2023
Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency
Tom Le Voyer, Audrey V Parent, Xian Liu, et al.
American Journal of Medical Genetics. Part A
|
January 22, 2015
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1
Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, et al.
Page
of 16
Search research articles
Search
Showing results (151-160 of 154) with videos related to
Sort By:
Page
of 16
You have reached the last page of results.
This site can display upto 154 results.
Science (New York, N.Y.)
|
December 20, 2022
Inborn errors of OAS-RNase L in SARS-CoV-2-related multisystem inflammatory syndrome in children
Danyel Lee, Jérémie Le Pen, Ahmad Yatim, et al.
Science (New York, N.Y.)
|
February 29, 2024
The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants
Marie Materna, Ottavia M Delmonte, Marita Bosticardo, et al.
Nature
|
November 8, 2023
Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency
Tom Le Voyer, Audrey V Parent, Xian Liu, et al.
American Journal of Medical Genetics. Part A
|
January 22, 2015
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1
Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, et al.
Page
of 16