Lista de obras - Shen-Ying Zhang - Dominio Público Uruguay

A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes

artículo científico publicado en 2022

A novel kindred with inherited STAT2 deficiency and severe viral illness

artículo científico publicado en 2017

A partial form of recessive STAT1 deficiency in humans

artículo científico publicado en 2009

Addressing diagnostic challenges in primary immunodeficiencies: laboratory evaluation of Toll-like receptor- and NF-κB-mediated immune responses

artículo científico publicado en 2014

Age-dependent Mendelian predisposition to herpes simplex virus type 1 encephalitis in childhood

artículo científico publicado en 2010

Auto-antibodies against type I IFNs in patients with life-threatening COVID-19

artículo científico publicado en 2020

Autosomal Recessive Cardiomyopathy Presenting as Acute Myocarditis

artículo científico publicado en 2017

Cleaved/associated TLR3 represents the primary form of the signaling receptor

artículo científico publicado en 2012

Deciphering Human Cell-Autonomous Anti-HSV-1 Immunity in the Central Nervous System

artículo científico publicado en 2015

EVER2 deficiency is associated with mild T-cell abnormalities

artículo científico publicado en 2012

Erratum: Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation

artículo científico publicado en 2015

From infectious diseases to primary immunodeficiencies

artículo científico publicado en 2008

Genetic susceptibility to herpes simplex virus 1 encephalitis in mice and humans

artículo científico publicado en 2007

Genome-wide Innate Immune Responsiveness Profiles of Patients with Inborn Errors of Toll-like Receptor Signaling

scholarly article by Laia Alsina et al published January 2010 in Clinical Immunology

HGCS: an online tool for prioritizing disease-causing gene variants by biological distance

artículo científico publicado en 2014

Herpes simplex encephalitis in a patient with a distinctive form of inherited IFNAR1 deficiency

scientific article published on 22 September 2020

Herpes simplex encephalitis in children with autosomal recessive and dominant TRIF deficiency

artículo científico publicado en 2011

Herpes simplex virus 2 encephalitis in a patient heterozygous for a TLR3 mutation

scientific article published on 25 November 2020

Herpes simplex virus encephalitis in a patient with complete TLR3 deficiency: TLR3 is otherwise redundant in protective immunity

artículo científico publicado en 2011

Herpes simplex virus encephalitis in human UNC-93B deficiency

artículo científico publicado en 2006

Herpes simplex virus encephalitis of childhood: inborn errors of central nervous system cell-intrinsic immunity

artículo científico publicado en 2020

Heterozygous TBK1 mutations impair TLR3 immunity and underlie herpes simplex encephalitis of childhood

artículo científico publicado en 2012

Heterozygous TLR3 Mutation in Patients with Hantavirus Encephalitis

scientific article published on 16 September 2020

Host genetics of severe influenza: from mouse Mx1 to human IRF7

artículo científico publicado en 2016

Human CD14dim monocytes patrol and sense nucleic acids and viruses via TLR7 and TLR8 receptors

artículo científico publicado en 2010

Human SNORA31 variations impair cortical neuron-intrinsic immunity to HSV-1 and underlie herpes simplex encephalitis

scientific article published on 05 December 2019

Human TBK1 is required for early autophagy induction upon HSV1 infection

article

Human TBK1: A Gatekeeper of Neuroinflammation

artículo científico publicado en 2016

Human TRAF3 adaptor molecule deficiency leads to impaired Toll-like receptor 3 response and susceptibility to herpes simplex encephalitis

artículo científico publicado en 2010

Human Toll-like receptor-dependent induction of interferons in protective immunity to viruses

artículo científico publicado en 2007

Human genetic and immunological determinants of critical COVID-19 pneumonia

artículo científico publicado en 2022

Human iPSC-derived trigeminal neurons lack constitutive TLR3-dependent immunity that protects cortical neurons from HSV-1 infection

article published in the Proceedings of the National Academy of Sciences of the United States of America

Human inborn errors of immunity to herpes viruses

scientific article published on 31 January 2020

Human inborn errors of immunity to infection affecting cells other than leukocytes: from the immune system to the whole organism

scientific article published on 20 May 2019

Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation

artículo científico publicado en 2014

Human primary immunodeficiencies of type I interferons

artículo científico publicado en 2007

IRAK-4- and MyD88-dependent pathways are essential for the removal of developing autoreactive B cells in humans

artículo científico publicado en 2008

IgM+IgD+CD27+ B cells are markedly reduced in IRAK-4-, MyD88-, and TIRAP- but not UNC-93B-deficient patients

artículo científico publicado en 2012

Impaired intrinsic immunity to HSV-1 in human iPSC-derived TLR3-deficient CNS cells

artículo científico publicado en 2012

Inborn Errors of RNA Lariat Metabolism in Humans with Brainstem Viral Infection

artículo científico publicado en 2018

Inborn errors in RNA polymerase III underlie severe varicella zoster virus infections

artículo científico

Inborn errors of anti-viral interferon immunity in humans

artículo científico publicado en 2011

Inborn errors of interferon (IFN)-mediated immunity in humans: insights into the respective roles of IFN-alpha/beta, IFN-gamma, and IFN-lambda in host defense

artículo científico publicado en 2008

Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

scientific article published on 24 September 2020

Inborn errors underlying herpes simplex encephalitis: From TLR3 to IRF3.

artículo científico publicado en 2015

Induced pluripotent stem cells: a novel frontier in the study of human primary immunodeficiencies

artículo científico publicado en 2010

Infectious disease. Life-threatening influenza and impaired interferon amplification in human IRF7 deficiency

artículo científico publicado en 2015

Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections

artículo científico publicado en 2015

Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines

artículo científico publicado en 2019

Inherited MST1 deficiency underlies susceptibility to EV-HPV infections

artículo científico publicado en 2012

Lethal Influenza in Two Related Adults with Inherited GATA2 Deficiency

artículo científico publicado en 2018

Life-Threatening COVID-19: Defective Interferons Unleash Excessive Inflammation

artículo científico publicado en 2020

Life-threatening influenza pneumonitis in a child with inherited IRF9 deficiency

artículo científico publicado en 2018

Mendelian predisposition to herpes simplex encephalitis

artículo científico publicado en 2013

NEMO is a key component of NF-κB- and IRF-3-dependent TLR3-mediated immunity to herpes simplex virus.

artículo científico publicado en 2011

Negative selection on human genes underlying inborn errors depends on disease outcome and both the mode and mechanism of inheritance

artículo científico publicado en 2021

Parsing the Interferon Transcriptional Network and Its Disease Associations

artículo científico publicado en 2016

PopViz: a webserver for visualizing minor allele frequencies and damage prediction scores of human genetic variations

scholarly article by Peng Zhang et al published 15 December 2018 in Bioinformatics

Primary immunodeficiencies of protective immunity to primary infections

artículo científico publicado en 2010

Revisiting human primary immunodeficiencies

artículo científico publicado en 2008

Selective predisposition to bacterial infections in IRAK-4-deficient children: IRAK-4-dependent TLRs are otherwise redundant in protective immunity

artículo científico publicado en 2007

Severe COVID-19 in the young and healthy: monogenic inborn errors of immunity?

scientific article published on 18 June 2020

Severe influenza pneumonitis in children with inherited TLR3 deficiency

scientific article published on 19 June 2019

T-cell Responses to HSV-1 in Persons Who Have Survived Childhood Herpes Simplex Encephalitis

artículo científico publicado en 2017

TLR3 deficiency in herpes simplex encephalitis: high allelic heterogeneity and recurrence risk

artículo científico publicado en 2014

TLR3 deficiency in patients with herpes simplex encephalitis

artículo científico publicado en 2007

TLR3 immunity to infection in mice and humans

artículo científico publicado en 2013

The human gene connectome as a map of short cuts for morbid allele discovery

artículo científico publicado en 2013

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

artículo científico publicado en 2015

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

artículo científico publicado en 2016

The proteome of Toll-like receptor 3-stimulated human immortalized fibroblasts: implications for susceptibility to herpes simplex virus encephalitis

artículo científico publicado en 2013

The risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies

artículo científico publicado en 2022

Varicella-zoster virus CNS vasculitis and RNA polymerase III gene mutation in identical twins

article

WITHDRAWN: Genetic infectious susceptibility and TLR defects in human

retracted paper

Lista de obras de Shen-Ying Zhang

A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes

A novel kindred with inherited STAT2 deficiency and severe viral illness

A partial form of recessive STAT1 deficiency in humans

Addressing diagnostic challenges in primary immunodeficiencies: laboratory evaluation of Toll-like receptor- and NF-κB-mediated immune responses

Age-dependent Mendelian predisposition to herpes simplex virus type 1 encephalitis in childhood

Auto-antibodies against type I IFNs in patients with life-threatening COVID-19

Autosomal Recessive Cardiomyopathy Presenting as Acute Myocarditis

Cleaved/associated TLR3 represents the primary form of the signaling receptor

Deciphering Human Cell-Autonomous Anti-HSV-1 Immunity in the Central Nervous System

EVER2 deficiency is associated with mild T-cell abnormalities

Erratum: Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation

From infectious diseases to primary immunodeficiencies

Genetic susceptibility to herpes simplex virus 1 encephalitis in mice and humans

Genome-wide Innate Immune Responsiveness Profiles of Patients with Inborn Errors of Toll-like Receptor Signaling

HGCS: an online tool for prioritizing disease-causing gene variants by biological distance

Herpes simplex encephalitis in a patient with a distinctive form of inherited IFNAR1 deficiency

Herpes simplex encephalitis in children with autosomal recessive and dominant TRIF deficiency

Herpes simplex virus 2 encephalitis in a patient heterozygous for a TLR3 mutation

Herpes simplex virus encephalitis in a patient with complete TLR3 deficiency: TLR3 is otherwise redundant in protective immunity

Herpes simplex virus encephalitis in human UNC-93B deficiency

Herpes simplex virus encephalitis of childhood: inborn errors of central nervous system cell-intrinsic immunity

Heterozygous TBK1 mutations impair TLR3 immunity and underlie herpes simplex encephalitis of childhood

Heterozygous TLR3 Mutation in Patients with Hantavirus Encephalitis

Host genetics of severe influenza: from mouse Mx1 to human IRF7

Human CD14dim monocytes patrol and sense nucleic acids and viruses via TLR7 and TLR8 receptors

Human SNORA31 variations impair cortical neuron-intrinsic immunity to HSV-1 and underlie herpes simplex encephalitis

Human TBK1 is required for early autophagy induction upon HSV1 infection

Human TBK1: A Gatekeeper of Neuroinflammation

Human TRAF3 adaptor molecule deficiency leads to impaired Toll-like receptor 3 response and susceptibility to herpes simplex encephalitis

Human Toll-like receptor-dependent induction of interferons in protective immunity to viruses

Human genetic and immunological determinants of critical COVID-19 pneumonia

Human iPSC-derived trigeminal neurons lack constitutive TLR3-dependent immunity that protects cortical neurons from HSV-1 infection

Human inborn errors of immunity to herpes viruses

Human inborn errors of immunity to infection affecting cells other than leukocytes: from the immune system to the whole organism

Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation

Human primary immunodeficiencies of type I interferons

IRAK-4- and MyD88-dependent pathways are essential for the removal of developing autoreactive B cells in humans

IgM+IgD+CD27+ B cells are markedly reduced in IRAK-4-, MyD88-, and TIRAP- but not UNC-93B-deficient patients

Impaired intrinsic immunity to HSV-1 in human iPSC-derived TLR3-deficient CNS cells

Inborn Errors of RNA Lariat Metabolism in Humans with Brainstem Viral Infection

Inborn errors in RNA polymerase III underlie severe varicella zoster virus infections

Inborn errors of anti-viral interferon immunity in humans

Inborn errors of interferon (IFN)-mediated immunity in humans: insights into the respective roles of IFN-alpha/beta, IFN-gamma, and IFN-lambda in host defense

Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

Inborn errors underlying herpes simplex encephalitis: From TLR3 to IRF3.

Induced pluripotent stem cells: a novel frontier in the study of human primary immunodeficiencies

Infectious disease. Life-threatening influenza and impaired interferon amplification in human IRF7 deficiency

Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections

Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines

Inherited MST1 deficiency underlies susceptibility to EV-HPV infections

Lethal Influenza in Two Related Adults with Inherited GATA2 Deficiency

Life-Threatening COVID-19: Defective Interferons Unleash Excessive Inflammation

Life-threatening influenza pneumonitis in a child with inherited IRF9 deficiency

Mendelian predisposition to herpes simplex encephalitis

NEMO is a key component of NF-κB- and IRF-3-dependent TLR3-mediated immunity to herpes simplex virus.

Negative selection on human genes underlying inborn errors depends on disease outcome and both the mode and mechanism of inheritance

Parsing the Interferon Transcriptional Network and Its Disease Associations

PopViz: a webserver for visualizing minor allele frequencies and damage prediction scores of human genetic variations

Primary immunodeficiencies of protective immunity to primary infections

Revisiting human primary immunodeficiencies

Selective predisposition to bacterial infections in IRAK-4-deficient children: IRAK-4-dependent TLRs are otherwise redundant in protective immunity

Severe COVID-19 in the young and healthy: monogenic inborn errors of immunity?

Severe influenza pneumonitis in children with inherited TLR3 deficiency

T-cell Responses to HSV-1 in Persons Who Have Survived Childhood Herpes Simplex Encephalitis

TLR3 deficiency in herpes simplex encephalitis: high allelic heterogeneity and recurrence risk

TLR3 deficiency in patients with herpes simplex encephalitis

TLR3 immunity to infection in mice and humans

The human gene connectome as a map of short cuts for morbid allele discovery

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

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

The proteome of Toll-like receptor 3-stimulated human immortalized fibroblasts: implications for susceptibility to herpes simplex virus encephalitis

The risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies

Varicella-zoster virus CNS vasculitis and RNA polymerase III gene mutation in identical twins

WITHDRAWN: Genetic infectious susceptibility and TLR defects in human