Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Shannon Nortman"'
Autor:
Maisam Abu-El-Haija, Balázs Németh, Tyler Thompson, Shannon Nortman, Péter Hegyi, Wenying Zhang, Anna Orekhova
Publikováno v:
Gut
We read the publication written by Lin et al 1 with great interest. The authors suggest that the majority of functionally defective carboxypeptidase A1 ( CPA1) mutations can elicit reduced expression due to nonsense-mediated decay (NMD) and therefore
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01dc19b439518fd9361d8af63d720a79
https://europepmc.org/articles/PMC8596457/
https://europepmc.org/articles/PMC8596457/
Autor:
Parinda A. Mehta, Ashley Teusink, Kejian Zhang, Sarah Dell, Tsuyoshi Fukuda, Shannon Nortman, Adam Lane, Diane Kissell, Stella M. Davies, Alexander A. Vinks, Alexandra H. Filipovich
Publikováno v:
Biology of Blood and Marrow Transplantation. 22:482-486
Invasive fungal infections are a significant cause of morbidity and mortality in recipients of hematopoietic stem cell transplantation (HSCT), warranting antifungal prophylaxis as a standard of care in these patients. Voriconazole is commonly used in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d22f950c6ec1957c8d68a66e162289e
https://doi.org/10.1016/j.bbmt.2015.11.011
https://doi.org/10.1016/j.bbmt.2015.11.011
Autor:
Morgan L. McLemore, Theodosia A. Kalfa, Shannon Nortman, Kejian Zhang, Silvia T. Bunting, Satheesh Chonat
Publikováno v:
British journal of haematology. 182(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26f90b441147fc3d3d4ba8c2ebd24531
https://pubmed.ncbi.nlm.nih.gov/29676459
https://pubmed.ncbi.nlm.nih.gov/29676459
Autor:
Lisa R. Young, Chrysi Kanellopoulou, Kejian Zhang, Shannon Nortman, Hilary Haines, Jill M. Fritz, Jason D. Hughes, Susan Price, Michael J. Lenardo, Wei Lu, Yu Zhang, Diane Kissell, Helen C. Su, Rebecca A. Marsh, Vijaya Chaturvedi, Michael B. Jordan, Jack J. Bleesing, Zhiduo Liu, Michael C. Stephens, Joshua J McElwee, Peter Mustillo, Lixin Zheng, Elif Karakoc-Aydiner, Helen F. Matthews, Jun Mo, V. Koneti Rao, Bernice Lo, Alexandra H. Filipovich, Kasper Hoebe, Cesar M. Rueda, Ammar Husami, Claire A. Chougnet, Qian Zhang
Publikováno v:
Science. 349:436-440
Trafficking from bedside to bench Typically in translational research, a discovery in cell or molecular biology is later exploited to improve patient care. Occasionally, information flows in the opposite direction. Lo et al. found that patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68a164d731b5c4eba5dcc14b3d2978cd
https://doi.org/10.1126/science.aaa1663
https://doi.org/10.1126/science.aaa1663
Autor:
Shannon Nortman, Haripriya Sakthivel, Katie Giger Seu, Omar Niss, Lionel Blanc, Carolyn Lutzko, Theodosia A. Kalfa, Clarissa E. Johnson, Jessica Meznarich, Wenying Zhang, Sana Emberesh, Hunter R. Underhill, Robert B. Lorsbach, Lisa Trump
Publikováno v:
Blood. 134:339-339
The Congenital Dyserythropoietic Anemia Registry (CDAR, ClinicalTrials.gov Identifier: NCT02964494) was created to investigate the natural history, biology, and molecular pathogenetic mechanisms of CDA. To date, there are 6 genes known to cause CDA (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::778573254f36c52bfa754edc4dd750be
https://doi.org/10.1182/blood-2019-128230
https://doi.org/10.1182/blood-2019-128230
Autor:
Bernice, Lo, Kejian, Zhang, Wei, Lu, Lixin, Zheng, Qian, Zhang, Chrysi, Kanellopoulou, Yu, Zhang, Zhiduo, Liu, Jill M, Fritz, Rebecca, Marsh, Ammar, Husami, Diane, Kissell, Shannon, Nortman, Vijaya, Chaturvedi, Hilary, Haines, Lisa R, Young, Jun, Mo, Alexandra H, Filipovich, Jack J, Bleesing, Peter, Mustillo, Michael, Stephens, Cesar M, Rueda, Claire A, Chougnet, Kasper, Hoebe, Joshua, McElwee, Jason D, Hughes, Elif, Karakoc-Aydiner, Helen F, Matthews, Susan, Price, Helen C, Su, V Koneti, Rao, Michael J, Lenardo, Michael B, Jordan
Publikováno v:
Science (New York, N.Y.). 349(6246)
Mutations in the LRBA gene (encoding the lipopolysaccharide-responsive and beige-like anchor protein) cause a syndrome of autoimmunity, lymphoproliferation, and humoral immune deficiency. The biological role of LRBA in immunologic disease is unknown.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::569c1d4f85855afc7069b127a12e02bf
https://pubmed.ncbi.nlm.nih.gov/26847262
https://pubmed.ncbi.nlm.nih.gov/26847262
Autor:
Jens Goebel, Javier El-Bietar, Stella M. Davies, Adam Lane, Michael Grimley, Sonata Jodele, Shannon Nortman, Jack J. Bleesing, Kasiani C. Myers, Kejian Zhang, Benjamin L. Laskin, Fanggeng Zou, Diane Kissell, Christopher E. Dandoy, Gregory Wallace
Publikováno v:
Biology of Blood and Marrow Transplantation. 21(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99f2ef2ec2444f0264e57edb0d051599
Autor:
Lisa Filipovich, Sarah Dell, Shannon Nortman, Stella M. Davies, Parinda A. Mehta, Lindsay Rhollans, Diane Kissell, Tsuyoshi Fukuda, Kejian Zhang, Alexander A. Vinks, Ashley Teusink
Publikováno v:
Biology of Blood and Marrow Transplantation. 19:S176-S177
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54c44572a5f399eddcf79cdd6e920015
https://doi.org/10.1016/j.bbmt.2012.11.162
https://doi.org/10.1016/j.bbmt.2012.11.162