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Characterization of complement factor H-related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical hemolytic uremic syndrome

artículo científico publicado en 2009

Chronic granulomatous disease in Morocco: genetic, immunological, and clinical features of 12 patients from 10 kindreds

artículo científico publicado en 2014

Disruption of an antimycobacterial circuit between dendritic and helper T cells in human SPPL2a deficiency

scientific article published on 20 August 2018

Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome

artículo científico publicado en 2015

Inherited human IFNγ deficiency underlies mycobacterial disease

artículo científico publicado en 2020

Interferon-gamma-dependent Immunity in Bacillus Calmette-Guérin Vaccine Osteitis Survivors

artículo científico publicado en 2016

Mendelian susceptibility to mycobacterial disease: 2014-2018 update

scientific article published on 25 October 2018

Paracoccidioidomycosis Associated With a Heterozygous STAT4 Mutation and Impaired IFN-γ Immunity

artículo científico publicado en 2017

The human gene damage index as a gene-level approach to prioritizing exome variants

artículo científico publicado en 2015

The molecular and structural bases for the association of complement C3 mutations with atypical hemolytic uremic syndrome.

artículo científico publicado en 2015

The mutation significance cutoff: gene-level thresholds for variant predictions

artículo científico publicado en 2016

Tuberculosis and impaired IL-23-dependent IFN-γ immunity in humans homozygous for a common missense variant

scientific article published on 01 December 2018

Unique and shared signaling pathways cooperate to regulate the differentiation of human CD4+ T cells into distinct effector subsets.

artículo científico publicado en 2016

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