Zobrazeno 1 - 10
of 596
pro vyhledávání: '"Bishara, J"'
Autor:
Giorgia Bucciol, Leen Moens, Masato Ogishi, Darawan Rinchai, Daniela Matuozzo, Mana Momenilandi, Nacim Kerrouche, Catherine M. Cale, Elsa R. Treffeisen, Mohammad Al Salamah, Bandar K. Al-Saud, Alain Lachaux, Remi Duclaux-Loras, Marie Meignien, Aziz Bousfiha, Ibtihal Benhsaien, Anna Shcherbina, Anna Roppelt, COVID Human Genetic Effort, Florian Gothe, Nadhira Houhou-Fidouh, Scott J. Hackett, Lisa M. Bartnikas, Michelle C. Maciag, Mohammed F. Alosaimi, Janet Chou, Reem W. Mohammed, Bishara J. Freij, Emmanuelle Jouanguy, Shen-Ying Zhang, Stephanie Boisson-Dupuis, Vivien Béziat, Qian Zhang, Christopher J.A. Duncan, Sophie Hambleton, Jean-Laurent Casanova, Isabelle Meyts
Publikováno v:
The Journal of Clinical Investigation, Vol 133, Iss 12 (2023)
STAT2 is a transcription factor activated by type I and III IFNs. We report 23 patients with loss-of-function variants causing autosomal recessive (AR) complete STAT2 deficiency. Both cells transfected with mutant STAT2 alleles and the patients’ ce
Externí odkaz:
https://doaj.org/article/93721eaae57f4e8c9405aeeff959098f
Autor:
Bishara J. Freij, Bassam M. Gebara, Rabail Tariq, Ay-Ming Wang, John Gibson, Nidal El-Wiher, Graham Krasan, Paul M. Patek, Kelly A. Levasseur, Mitual Amin, Joseph M. Fullmer
Publikováno v:
BMC Pediatrics, Vol 20, Iss 1, Pp 1-7 (2020)
Abstract Background Central and peripheral nervous system symptoms and complications are being increasingly recognized among individuals with pandemic SARS-CoV-2 infections, but actual detection of the virus or its RNA in the central nervous system h
Externí odkaz:
https://doaj.org/article/a0caef7316f548208a911c7efb71952b
Autor:
Freij, Bishara J1,2 (AUTHOR) Bishara.Freij@beaumont.org, Aldrich, Aileen M3,4,5 (AUTHOR), Ogrin, Sara L3 (AUTHOR), Olivero, Rosemary M3,4 (AUTHOR)
Publikováno v:
Journal of the Pediatric Infectious Diseases Society. Jan2023, Vol. 12 Issue 1, p43-48. 6p.
Autor:
Yeshurun, M., Vaxman, I., Shargian, L., Yahav, D., Bishara, J., Pasvolsky, O., Wolach, O., Lahav, M., Gurion, R., Magen, H., Vidal, L., Herscovici, C., Peck, A., Moshe, M., Sela-Navon, M., Naparstek, E., Raanani, P., Rozovski, U.
Publikováno v:
In Clinical Microbiology and Infection July 2018 24(7):749-754
Publikováno v:
Frontiers in Immunology, Vol 11 (2021)
STAT2 is a transcription factor that plays an essential role in antiviral immunity by mediating the activity of type I and III interferons (IFN-I and IFN-III). It also has a recently established function in the negative regulation of IFN-I signaling.
Externí odkaz:
https://doaj.org/article/a4adf8ca780948a0a4f0e984a53c286d
Autor:
Anuja R. Shikhare MBBS, Rimsha M. Iqbal MD, Rabail Tariq MBBS, Daniel R. Turner MD, Bassam M. Gebara MD, Bishara J. Freij MD
Publikováno v:
Global Pediatric Health, Vol 8 (2021)
COVID-19 is generally a benign or asymptomatic infection in children, but can occasionally be severe or fatal. Delayed presentation of COVID-19 with hyperinflammation and multi-organ involvement was recently recognized, designated the Multisystem Inf
Externí odkaz:
https://doaj.org/article/0671798a2d404b23b7687bfc3be0a73e
Publikováno v:
The Application of Clinical Genetics, Vol Volume 11, Pp 135-144 (2018)
John Bishara,1 Thomas G Keens,1,2 Iris A Perez1,2 1Division of Pediatric Pulmonology and Sleep Medicine, Children’s Hospital Los Angeles, Los Angeles, CA, USA; 2Department of Pediatrics, Keck School of Medicine of USC, Los Angeles, CA, USA Abstract
Externí odkaz:
https://doaj.org/article/9836ab6c1bf0428e9aaa7ec1a0ca223c
Autor:
Tissot-Dupont, H., Casalta, J.P., Gouriet, F., Hubert, S., Salaun, E., Habib, G., Fernandez-Gerlinger, M.P., Mainardi, J.L., Tattevin, P., Revest, M., Lucht, F., Botelho-Nevers, E., Gagneux-Brunon, A., Snygg-Martin, U., Chan, K.L., Bishara, J., Vilacosta, I., Olmos, C., San Román, J.A., López, J., Tornos, P., Fernández-Hidalgo, N., Durante-Mangoni, E., Utili, R., Paul, M., Baddour, L.M., DeSimone, D.C., Sohail, M.R., Steckelberg, J.M., Wilson, W.R., Raoult, D.
Publikováno v:
In Clinical Microbiology and Infection October 2017 23(10):736-739
Autor:
Bucciol, Giorgia, Moens, Leen, Ogishi, Masato, Rinchai, Darawan, Matuozzo, Daniela, Momenilandi, Mana, Kerrouche, Nacim, Cale, Catherine M, Treffeisen, Elsa R, Al Salamah, Mohammad, Al-Saud, Bandar K, Lachaux, Alain, Duclaux-Loras, Remi, Meignien, Marie, Bousfiha, Aziz, Benhsaien, Ibtihal, Shcherbina, Anna, Roppelt, Anna, COVID Human Genetic Effort, Gothe, Florian, Houhou-Fidouh, Nadhira, Hackett, Scott J, Bartnikas, Lisa M, Maciag, Michelle C, Alosaimi, Mohammed F, Chou, Janet, Mohammed, Reem W, Freij, Bishara J, Jouanguy, Emmanuelle, Zhang, Shen-Ying, Boisson-Dupuis, Stephanie, Béziat, Vivien, Zhang, Qian, Duncan, Christopher Ja, Hambleton, Sophie, Casanova, Jean-Laurent, Meyts, Isabelle
Publikováno v:
Journal of Clinical Investigation.
STAT2 is a transcription factor activated by type I and III IFNs. We report 23 patients with loss-of-function variants causing autosomal recessive (AR) complete STAT2 deficiency. Both cells transfected with mutant STAT2 alleles and the patients' cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea498a7d264d01cd381c23afc2f98a56
https://doi.org/10.1172/jci168321
https://doi.org/10.1172/jci168321
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