Lista de obras - Sebastian Fuchs - Dominio Público Uruguay

A human inferred germline antibody binds to an immunodominant epitope and neutralizes Zika virus

artículo científico publicado en 2017

A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis.

artículo científico publicado en 2016

Antiviral and regulatory T cell immunity in a patient with stromal interaction molecule 1 deficiency

artículo científico publicado en 2011

Clinical and immunological overlap between autoimmune lymphoproliferative syndrome and common variable immunodeficiency.

artículo científico publicado en 2010

Common variable immunodeficiency, impaired neurological development and reduced numbers of T regulatory cells in a 10-year-old boy with a STAT1 gain-of-function mutation.

artículo científico publicado en 2016

Deficiency of innate and acquired immunity caused by an IKBKB mutation.

artículo científico publicado en 2013

Dengue Virus Evades AAV-Mediated Neutralizing Antibody Prophylaxis in Rhesus Monkeys

artículo científico publicado en 2017

Early-onset Evans syndrome, immunodeficiency, and premature immunosenescence associated with tripeptidyl-peptidase II deficiency

artículo científico publicado en 2014

Hemophagocytic lymphohistiocytosis as presenting manifestation of profound combined immunodeficiency due to an ORAI1 mutation

artículo científico publicado en 2017

High-dimensional single-cell proteomics analysis identifies immune checkpoint signatures and therapeutic targets in ulcerative colitis

scientific article published on 09 January 2019

Insulin modulates the inflammatory granulocyte response to streptococci via phosphatidylinositol 3-kinase.

artículo científico publicado en 2012

Missense mutation in immunodeficient patients shows the multifunctional roles of coiled-coil domain 3 (CC3) in STIM1 activation

artículo científico publicado en 2015

Omenn syndrome associated with a functional reversion due to a somatic second-site mutation in CARD11 deficiency

artículo científico publicado en 2015

Oncogenic JAK2V617F causes PD-L1 expression, mediating immune escape in myeloproliferative neoplasms.

artículo científico publicado en 2018

Potent Plasmablast-Derived Antibodies Elicited by the National Institutes of Health Dengue Vaccine

artículo científico publicado en 2017

SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signaling

artículo científico publicado en 2015

The Extended Clinical Phenotype of 26 Patients with Chronic Mucocutaneous Candidiasis due to Gain-of-Function Mutations in STAT1

artículo científico publicado en 2015

Lista de obras de Sebastian Fuchs

A human inferred germline antibody binds to an immunodominant epitope and neutralizes Zika virus

A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis.

Antiviral and regulatory T cell immunity in a patient with stromal interaction molecule 1 deficiency

Clinical and immunological overlap between autoimmune lymphoproliferative syndrome and common variable immunodeficiency.

Common variable immunodeficiency, impaired neurological development and reduced numbers of T regulatory cells in a 10-year-old boy with a STAT1 gain-of-function mutation.

Deficiency of innate and acquired immunity caused by an IKBKB mutation.

Dengue Virus Evades AAV-Mediated Neutralizing Antibody Prophylaxis in Rhesus Monkeys

Early-onset Evans syndrome, immunodeficiency, and premature immunosenescence associated with tripeptidyl-peptidase II deficiency

Hemophagocytic lymphohistiocytosis as presenting manifestation of profound combined immunodeficiency due to an ORAI1 mutation

High-dimensional single-cell proteomics analysis identifies immune checkpoint signatures and therapeutic targets in ulcerative colitis

Insulin modulates the inflammatory granulocyte response to streptococci via phosphatidylinositol 3-kinase.

Missense mutation in immunodeficient patients shows the multifunctional roles of coiled-coil domain 3 (CC3) in STIM1 activation

Omenn syndrome associated with a functional reversion due to a somatic second-site mutation in CARD11 deficiency

Oncogenic JAK2V617F causes PD-L1 expression, mediating immune escape in myeloproliferative neoplasms.

Potent Plasmablast-Derived Antibodies Elicited by the National Institutes of Health Dengue Vaccine

SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signaling

The Extended Clinical Phenotype of 26 Patients with Chronic Mucocutaneous Candidiasis due to Gain-of-Function Mutations in STAT1