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Oncoimmunology
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February 7, 2019
A non-functional neoepitope specific CD8<sup>+</sup> T-cell response induced by tumor derived antigen exposure <i>in vivo</i>
Mathias Vormehr, Katharina Reinhard, Renata Blatnik, et al.
American Journal of Respiratory and Critical Care Medicine
|
March 13, 2010
Patient-derived granulocyte/macrophage colony-stimulating factor autoantibodies reproduce pulmonary alveolar proteinosis in nonhuman primates
Takuro Sakagami, David Beck, Kanji Uchida, et al.
Journal of Internal Medicine
|
September 23, 2025
Characterizing VEXAS syndrome in women: Findings from an international multicenter study
Rim Bourguiba, Valentin Lacombe, David Beck, et al.
Science Translational Medicine
|
October 16, 2024
Melatonin receptor 1A variants as genetic cause of idiopathic osteoporosis
Brygida Bisikirska, Rossella Labella, Alvaro Cuesta-Dominguez, et al.
Annals of the Rheumatic Diseases
|
July 22, 2022
Gain-of-function mutations in <i>ALPK1</i> cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome
Christina Torres Kozycki, Shilpa Kodati, Laryssa Huryn, et al.
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Search research articles
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Showing results (51-60 of 55) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 55 results.
Oncoimmunology
|
February 7, 2019
A non-functional neoepitope specific CD8<sup>+</sup> T-cell response induced by tumor derived antigen exposure <i>in vivo</i>
Mathias Vormehr, Katharina Reinhard, Renata Blatnik, et al.
American Journal of Respiratory and Critical Care Medicine
|
March 13, 2010
Patient-derived granulocyte/macrophage colony-stimulating factor autoantibodies reproduce pulmonary alveolar proteinosis in nonhuman primates
Takuro Sakagami, David Beck, Kanji Uchida, et al.
Journal of Internal Medicine
|
September 23, 2025
Characterizing VEXAS syndrome in women: Findings from an international multicenter study
Rim Bourguiba, Valentin Lacombe, David Beck, et al.
Science Translational Medicine
|
October 16, 2024
Melatonin receptor 1A variants as genetic cause of idiopathic osteoporosis
Brygida Bisikirska, Rossella Labella, Alvaro Cuesta-Dominguez, et al.
Annals of the Rheumatic Diseases
|
July 22, 2022
Gain-of-function mutations in <i>ALPK1</i> cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome
Christina Torres Kozycki, Shilpa Kodati, Laryssa Huryn, et al.
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