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of 8
pro vyhledávání: '"David, Sokol"'
Autor:
Róbert, Čellár, Erik, Dorko, Kvetoslava, Rimárová, Matúš, Bereš, David, Sokol, Ahmad, Gharaibeh, Martin, Folvarský, István, Mitró, Viliam, Knap
Publikováno v:
Central European Journal of Public Health. 30:S22-S26
The objective of this study was to evaluate the effect of long-term treatment of patients with osteoporosis being actively managed by medical staff and following the therapeutic methods and principles of treatment of osteoporosis.The medical records
Autor:
David Sokol
Publikováno v:
caa.reviews.
Autor:
Visweswaran Ravikumar, Yaping Sun, David Sokol, Julia Wu, Arvind Rao, Guoqing Hou, Arul M. Chinnaiyan, Hideaki Fujiwara, Israel Henig, Stephanie Kim, Katherine Oravecz-Wilson, Daniel R. Goldstein, Molly Radosevich, Sherri C. Wood, Pavan Reddy, Cynthia Zajac, Austin Taylor, Daniel Peltier, Thomas Decoville, Sethuramasundaram Pitchiaya
Publikováno v:
Sci Transl Med
Mechanisms governing allogeneic T-cell responses after allogeneic hematopoietic stem cell (HSC) and solid organ transplantation are incompletely understood. To identify lncRNAs involved in regulation of human donor T cells after clinical HSCT, we per
This study aims to investigate the effect of laser peening with (LP) and without coating (LPwC) process on subsurface microstructural evolution, mechanical properties, and stress corrosion cracking (SCC) of laser-welded samples fabricated using 304 s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8091aba9ac4c81041c1826bee8f380f
https://aperta.ulakbim.gov.tr/record/233558
https://aperta.ulakbim.gov.tr/record/233558
Autor:
Yaping Sun, Isreal Henig, Stephanie Kim, Molly Radosevich, Pavan Reddy, Daniel Peltier, Hideaki Fujiwara, David Sokol, Cynthia Zajac, Julia Wu, Katherine Oravecz-Wilson, Guoqing Hou, Austin Taylor
Mechanisms governing allogeneic T-cell responses after allogeneic hematopoietic stem cell (HSC) and solid organ transplantation are incompletely understood. Long non-coding RNAs (lncRNA) do not code for, but control gene expression with tissue specif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27554d086a7634220d091ba32fbcc4e7
https://doi.org/10.1101/2020.04.16.045567
https://doi.org/10.1101/2020.04.16.045567
Publikováno v:
Blood. 132:5005-5005
Complement-mediated thrombotic microangiopathy (TMA), also known as atypical hemolytic uremic syndrome (aHUS) is a rare, hereditary, progressive, life-threatening disorder caused by a disruption in regulation of the alternative pathway of the complem
Autor:
David Sokol
Publikováno v:
Annals of Internal Medicine. 128:957
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