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Blood
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October 4, 2017
Effective "activated PI3Kδ syndrome"-targeted therapy with the PI3Kδ inhibitor leniolisib
V Koneti Rao, Sharon Webster, Virgil A S H Dalm, et al.
Biorxiv : the Preprint Server for Biology
|
March 2, 2022
Genetically diverse mouse models of SARS-CoV-2 infection reproduce clinical variation in type I interferon and cytokine responses in COVID-19
Shelly Robertson, Olivia Bedard, Kristin McNally, et al.
Blood
|
April 27, 2016
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype
Julie Toubiana, Satoshi Okada, Julia Hiller, et al.
Human Molecular Genetics
|
January 27, 2011
Partial recessive IFN-γR1 deficiency: genetic, immunological and clinical features of 14 patients from 11 kindreds
Ithaisa Sologuren, Stéphanie Boisson-Dupuis, Jose Pestano, et al.
Frontiers in Immunology
|
October 19, 2017
Corrigendum: Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56<sup>bright</sup> NKG2A<sup>+++</sup> Cells, and Yet Display Increased Degranulation and Higher Perforin Content
Kerry Dobbs, Giovanna Tabellini, Enrica Calzoni, et al.
Frontiers in Immunology
|
August 4, 2017
Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56<sup>bright</sup> NKG2A<sup>+++</sup> Cells, and Yet Display Increased Degranulation and Higher Perforin Content
Kerry Dobbs, Giovanna Tabellini, Enrica Calzoni, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 20, 2021
Genetic regulation of <i>OAS1</i> nonsense-mediated decay underlies association with risk of severe COVID-19
A Rouf Banday, Megan L Stanifer, Oscar Florez-Vargas, et al.
Nature Genetics
|
July 14, 2022
Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries
A Rouf Banday, Megan L Stanifer, Oscar Florez-Vargas, et al.
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Showing results (21-30 of 28) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 28 results.
Blood
|
October 4, 2017
Effective "activated PI3Kδ syndrome"-targeted therapy with the PI3Kδ inhibitor leniolisib
V Koneti Rao, Sharon Webster, Virgil A S H Dalm, et al.
Biorxiv : the Preprint Server for Biology
|
March 2, 2022
Genetically diverse mouse models of SARS-CoV-2 infection reproduce clinical variation in type I interferon and cytokine responses in COVID-19
Shelly Robertson, Olivia Bedard, Kristin McNally, et al.
Blood
|
April 27, 2016
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype
Julie Toubiana, Satoshi Okada, Julia Hiller, et al.
Human Molecular Genetics
|
January 27, 2011
Partial recessive IFN-γR1 deficiency: genetic, immunological and clinical features of 14 patients from 11 kindreds
Ithaisa Sologuren, Stéphanie Boisson-Dupuis, Jose Pestano, et al.
Frontiers in Immunology
|
October 19, 2017
Corrigendum: Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56<sup>bright</sup> NKG2A<sup>+++</sup> Cells, and Yet Display Increased Degranulation and Higher Perforin Content
Kerry Dobbs, Giovanna Tabellini, Enrica Calzoni, et al.
Frontiers in Immunology
|
August 4, 2017
Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56<sup>bright</sup> NKG2A<sup>+++</sup> Cells, and Yet Display Increased Degranulation and Higher Perforin Content
Kerry Dobbs, Giovanna Tabellini, Enrica Calzoni, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 20, 2021
Genetic regulation of <i>OAS1</i> nonsense-mediated decay underlies association with risk of severe COVID-19
A Rouf Banday, Megan L Stanifer, Oscar Florez-Vargas, et al.
Nature Genetics
|
July 14, 2022
Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries
A Rouf Banday, Megan L Stanifer, Oscar Florez-Vargas, et al.
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