List of works - Minji Byun

A major locus on chromosome 3p22 conferring predisposition to human herpesvirus 8 infection

scientific article

A mild form of SLC29A3 disorder: a frameshift deletion leads to the paradoxical translation of an otherwise noncoding mRNA splice variant

scientific article published in 2012

A novel mutation with variable expressivity in a family with unicentric and idiopathic multicentric Castleman disease

scientific article published on 01 November 2018

Autosomal Recessive Cardiomyopathy Presenting as Acute Myocarditis

scientific article published on April 2017

Cowpox virus exploits the endoplasmic reticulum retention pathway to inhibit MHC class I transport to the cell surface

scientific article published in November 2007

Crystal structure of peptidoglycan recognition protein LB from Drosophila melanogaster

scientific article

Disseminated Cutaneous Warts in X-Linked Hyper IgM Syndrome.

scientific article

Influenza virus infection causes global RNAPII termination defects

Inherited human OX40 deficiency underlying classic Kaposi sarcoma of childhood

scientific article published on 29 July 2013

Multicentric Castleman disease in an HHV8-infected child born to consanguineous parents with systematic review

scientific article published on 12 December 2011

Mycobacterial disease and impaired IFN-γ immunity in humans with inherited ISG15 deficiency

scientific article

Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia

scientific article

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

scientific article

The RNA Exosome Syncs IAV-RNAPII Transcription to Promote Viral Ribogenesis and Infectivity

scientific article published on May 2017

Topoisomerase 1 inhibition therapy protects against SARS-CoV-2-induced inflammation and death in animal models

scientific article published on 01 December 2020

Two mechanistically distinct immune evasion proteins of cowpox virus combine to avoid antiviral CD8 T cells

scientific article

Whole-Genome Sequencing Identifies STAT4 as a Putative Susceptibility Gene in Classic Kaposi Sarcoma

scientific article published on 9 December 2014

Whole-exome sequencing-based discovery of STIM1 deficiency in a child with fatal classic Kaposi sarcoma

scientific article

Whole-exome-sequencing-based discovery of human FADD deficiency

scientific article

List of works by Minji Byun

A major locus on chromosome 3p22 conferring predisposition to human herpesvirus 8 infection

A mild form of SLC29A3 disorder: a frameshift deletion leads to the paradoxical translation of an otherwise noncoding mRNA splice variant

A novel mutation with variable expressivity in a family with unicentric and idiopathic multicentric Castleman disease

Autosomal Recessive Cardiomyopathy Presenting as Acute Myocarditis

Cowpox virus exploits the endoplasmic reticulum retention pathway to inhibit MHC class I transport to the cell surface

Crystal structure of peptidoglycan recognition protein LB from Drosophila melanogaster

Disseminated Cutaneous Warts in X-Linked Hyper IgM Syndrome.

Influenza virus infection causes global RNAPII termination defects

Inherited human OX40 deficiency underlying classic Kaposi sarcoma of childhood

Multicentric Castleman disease in an HHV8-infected child born to consanguineous parents with systematic review

Mycobacterial disease and impaired IFN-γ immunity in humans with inherited ISG15 deficiency

Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia

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

The RNA Exosome Syncs IAV-RNAPII Transcription to Promote Viral Ribogenesis and Infectivity

Topoisomerase 1 inhibition therapy protects against SARS-CoV-2-induced inflammation and death in animal models

Two mechanistically distinct immune evasion proteins of cowpox virus combine to avoid antiviral CD8 T cells

Whole-Genome Sequencing Identifies STAT4 as a Putative Susceptibility Gene in Classic Kaposi Sarcoma

Whole-exome sequencing-based discovery of STIM1 deficiency in a child with fatal classic Kaposi sarcoma

Whole-exome-sequencing-based discovery of human FADD deficiency