Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Aaron B. Clark"'
Autor:
Matthew H. Porteus, Shengdar Q. Tsai, Siyuan Liu, Cicera R. Lazzarotto, Suk See De Ravin, Colin L. Sweeney, Sherry Koontz, Ronald J. Meis, Uimook Choi, GaHyun Lee, Sandra Burkett, Douglas B. Kuhns, Narda Theobald, Harry L. Malech, Xiaolin Wu, Taylor Liu, Benjamin P. Kleinstiver, Gary A. Dahl, Aaron B. Clark, Linhong Li, Stephen Headey, Mara Pavel-Dinu, Julie Brault
Publikováno v:
Blood
Lentivector gene therapy for X-linked chronic granulomatous disease (X-CGD) has proven to be a viable approach, but random vector integration and subnormal protein production from exogenous promoters in transduced cells remain concerning for long-ter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14f9f171481b9948298c668cd83bed5d
https://doi.org/10.1182/blood.2020008503
https://doi.org/10.1182/blood.2020008503
Autor:
Linhong Li, Harry L. Malech, Kennichi C. Dowdell, Julie Brault, Ezekiel Bello, Sherry Koontz, Aaron B. Clark, Ronald J. Meis, Michael J. Lenardo, Colin L. Sweeney, Narda Theobald, Juan C. Ravell, Janet Lee, Gary A. Dahl, Taylor Liu, Suk See De Ravin, Cornell Allen
Publikováno v:
Cytotherapy. 23:203-210
Background aim X-linked MAGT1 deficiency with increased susceptibility to EBV-infection and N-linked glycosylation defect' (XMEN) disease is caused by mutations in the magnesium transporter 1 (MAGT1) gene. Loss of MAGT1 function results in a glycosyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::605d0c3740d24eafd0fe68f135dbbb36
https://doi.org/10.1016/j.jcyt.2020.08.013
https://doi.org/10.1016/j.jcyt.2020.08.013
Autor:
Vera Bzhilyanskaya, Julie Brault, Siyuan Liu, Andres F. Zea Vera, Nikita Kozhushko, Amanda Lawson, Uimook Choi, Aaron B. Clark, Ronald J. Meis, Michelle Ma, Cicera Lazzarotto, Shengdar Tsai, Xiaolin Wu, Gary A. Dahl, Jenna Bergerson, Alexandra F. Freeman, Benjamin Kleinstiver, Harry L Malech, Suk See De Ravin
Publikováno v:
Blood. 140:7766-7767
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::646c3b4c37dc6ae023f3048c9cf9e9de
https://doi.org/10.1182/blood-2022-170252
https://doi.org/10.1182/blood-2022-170252
Autor:
Ezekiel Bello, Marita Bosticardo, Ronald J. Meis, Sherry Koontz, Shengdar Q. Tsai, Juan C Ravell, Michael J. Lenardo, Luigi D. Notarangelo, Benjamin P. Kleinstiver, Xiaolin Wu, Cicera R. Lazzarotto, Harry L. Malech, Guillaume Vayssière, Kennichi C. Dowdell, Colin L. Sweeney, Gary A. Dahl, Taylor Q. Liu, Aaron B. Clark, Uimook Choi, Cristina Corsino, Suk See De Ravin, Siyuan Liu, Julie Brault
Publikováno v:
Blood
XMEN disease, defined as “X-linked MAGT1 deficiency with increased susceptibility to Epstein-Barr virus infection and N-linked glycosylation defect,” is a recently described primary immunodeficiency marked by defective T cells and natural killer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc4b75a7fdafd4fa4d8bff8e2be88729
https://europepmc.org/articles/PMC8718624/
https://europepmc.org/articles/PMC8718624/
Autor:
Taylor Q. Liu, David F. Stroncek, Narda Theobald, Sherry Koontz, Elizabeth M. Kang, Steven L. Highfill, Michail S. Lionakis, Julie Brault, Mark E. Metzger, Robert E. Donahue, John F. Tisdale, Hong Lei, Aaron B. Clark, Suk See De Ravin, Harry L. Malech, Linhong Li, Kamille A. West, Aylin C. Bonifacino, Gary A. Dahl, Ronald J. Meis, Cynthia E. Dunbar, Jigar V. Desai, Marissa A. Zarakas, Douglas B. Kuhns, Uimook Choi, Cristina Corsino
Publikováno v:
Blood Adv
Granulocytes from patients with chronic granulomatous disease (CGD) have dysfunctional phagocyte reduced nicotinamide adenine dinucleotide phosphate (NADPH) oxidase that fails to generate sufficient antimicrobial reactive oxidative species. CGD patie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30891cb9fa6444f4e4751824d0360377
https://pubmed.ncbi.nlm.nih.gov/33284949
https://pubmed.ncbi.nlm.nih.gov/33284949
Autor:
Taylor Liu, Ronald J. Meis, Linhong Li, Suk See De Ravin, Juan C. Ravell, Narda Theobald, Michael J. Lenardo, Janet Lee, Ezekiel Bello, Sherry Koontz, Cornell Allen, Harry L. Malech, Kennichi C. Dowdell, Julie Brault, Gary A. Dahl, Aaron B. Clark
Publikováno v:
Blood. 134:4637-4637
Introduction 'X-linked immunodeficiency with magnesium defect, Epstein-Barr virus (EBV) infection, and neoplasia' (XMEN) disease is a primary immunodeficiency disease caused by loss-of-function mutations in the MAGT1 gene encoding for the magnesium t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2880b3e0c484a12374a6d3a737838b87
https://doi.org/10.1182/blood-2019-129062
https://doi.org/10.1182/blood-2019-129062
Publikováno v:
Biomarker Insights, Vol 2016, Iss Suppl. 1, Pp 1-8 (2016)
Externí odkaz:
https://doaj.org/article/ce608da2073f4432b5492f65e7ca1f77