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Minji Byun, Ph.D. - Publications

Affiliations: 
2009 Washington University, Saint Louis, St. Louis, MO 
Area:
Immunology, Virology Biology
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13 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2018 Zhao N, Sebastiano V, Moshkina N, Mena N, Hultquist J, Jimenez-Morales D, Ma Y, Rialdi A, Albrecht R, Fenouil R, Sánchez-Aparicio MT, Ayllon J, Ravisankar S, Haddad B, Ho JSY, ... ... Byun M, et al. Influenza virus infection causes global RNAPII termination defects. Nature Structural & Molecular Biology. PMID 30177761 DOI: 10.1038/S41594-018-0124-7  0.316
2017 Belkaya S, Kontorovich AR, Byun M, Mulero-Navarro S, Bajolle F, Cobat A, Josowitz R, Itan Y, Quint R, Lorenzo L, Boucherit S, Stoven C, Di Filippo S, Abel L, Zhang SY, et al. Autosomal Recessive Cardiomyopathy Presenting as Acute Myocarditis. Journal of the American College of Cardiology. 69: 1653-1665. PMID 28359509 DOI: 10.1016/J.Jacc.2017.01.043  0.393
2013 Byun M, Ma CS, Akçay A, Pedergnana V, Palendira U, Myoung J, Avery DT, Liu Y, Abhyankar A, Lorenzo L, Schmidt M, Lim HK, Cassar O, Migaud M, Rozenberg F, et al. Inherited human OX40 deficiency underlying classic Kaposi sarcoma of childhood. The Journal of Experimental Medicine. 210: 1743-59. PMID 23897980 DOI: 10.1084/Jem.20130592  0.398
2013 Bolze A, Mahlaoui N, Byun M, Turner B, Trede N, Ellis SR, Abhyankar A, Itan Y, Patin E, Brebner S, Sackstein P, Puel A, Picard C, Abel L, Quintana-Murci L, et al. Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia. Science (New York, N.Y.). 340: 976-8. PMID 23579497 DOI: 10.1126/Science.1234864  0.334
2012 Bogunovic D, Byun M, Durfee LA, Abhyankar A, Sanal O, Mansouri D, Salem S, Radovanovic I, Grant AV, Adimi P, Mansouri N, Okada S, Bryant VL, Kong XF, Kreins A, et al. Mycobacterial disease and impaired IFN-γ immunity in humans with inherited ISG15 deficiency. Science (New York, N.Y.). 337: 1684-8. PMID 22859821 DOI: 10.1126/Science.1224026  0.401
2012 Pedergnana V, Gessain A, Tortevoye P, Byun M, Bacq-Daian D, Boland A, Casanova JL, Abel L, Plancoulaine S. A major locus on chromosome 3p22 conferring predisposition to human herpesvirus 8 infection. European Journal of Human Genetics : Ejhg. 20: 690-5. PMID 22258534 DOI: 10.1038/Ejhg.2011.260  0.301
2012 Bolze A, Abhyankar A, Grant AV, Patel B, Yadav R, Byun M, Caillez D, Emile JF, Pastor-Anglada M, Abel L, Puel A, Govindarajan R, de Pontual L, Casanova JL. A mild form of SLC29A3 disorder: a frameshift deletion leads to the paradoxical translation of an otherwise noncoding mRNA splice variant. Plos One. 7: e29708. PMID 22238637 DOI: 10.1371/Journal.Pone.0029708  0.325
2012 Leroy S, Moshous D, Cassar O, Reguerre Y, Byun M, Pedergnana V, Canioni D, Gessain A, Oksenhendler E, Fieschi C, Mahlaoui N, Rivière JP, Herbigneaux RM, Muszlak M, Arnaud JP, et al. Multicentric Castleman disease in an HHV8-infected child born to consanguineous parents with systematic review. Pediatrics. 129: e199-203. PMID 22157133 DOI: 10.1542/Peds.2010-2739  0.321
2010 Bolze A, Byun M, McDonald D, Morgan NV, Abhyankar A, Premkumar L, Puel A, Bacon CM, Rieux-Laucat F, Pang K, Britland A, Abel L, Cant A, Maher ER, Riedl SJ, et al. Whole-exome-sequencing-based discovery of human FADD deficiency. American Journal of Human Genetics. 87: 873-81. PMID 21109225 DOI: 10.1016/J.Ajhg.2010.10.028  0.4
2010 Byun M, Abhyankar A, Lelarge V, Plancoulaine S, Palanduz A, Telhan L, Boisson B, Picard C, Dewell S, Zhao C, Jouanguy E, Feske S, Abel L, Casanova JL. Whole-exome sequencing-based discovery of STIM1 deficiency in a child with fatal classic Kaposi sarcoma. The Journal of Experimental Medicine. 207: 2307-12. PMID 20876309 DOI: 10.1084/Jem.20101597  0.408
2009 Byun M, Verweij MC, Pickup DJ, Wiertz EJ, Hansen TH, Yokoyama WM. Two mechanistically distinct immune evasion proteins of cowpox virus combine to avoid antiviral CD8 T cells. Cell Host & Microbe. 6: 422-32. PMID 19917497 DOI: 10.1016/J.Chom.2009.09.012  0.507
2007 Byun M, Wang X, Pak M, Hansen TH, Yokoyama WM. Cowpox virus exploits the endoplasmic reticulum retention pathway to inhibit MHC class I transport to the cell surface. Cell Host & Microbe. 2: 306-15. PMID 18005752 DOI: 10.1016/J.Chom.2007.09.002  0.505
2003 Kim MS, Byun M, Oh BH. Crystal structure of peptidoglycan recognition protein LB from Drosophila melanogaster Nature Immunology. 4: 787-793. PMID 12845326 DOI: 10.1038/Ni952  0.311
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