Zobrazeno 1 - 10
of 3 147
pro vyhledávání: '"T, SCHMITZ"'
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2024)
BackgroundDifferent ST-segment elevation myocardial infarction (STEMI) localizations go along with dissimilarities in the size of the affected myocardium, the causing coronary vessel occlusion, and the right ventricular participation. Therefore, this
Externí odkaz:
https://doaj.org/article/280e30d58ea14d3783caddabd83b4871
Autor:
J.-N. Hoenemann, S. Moestl, A. Diedrich, E. Mulder, T. Frett, G. Petrat, W. Pustowalow, M. Arz, M.-T. Schmitz, K. Heusser, S. M. C. Lee, J. Jordan, J. Tank, F. Hoffmann
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
Impaired cardiovascular autonomic control following space flight or immobilization may limit the ability to cope with additional hemodynamic stimuli. Head-down tilt bedrest is an established terrestrial analog for space flight and offers the opportun
Externí odkaz:
https://doaj.org/article/b6301a73b520417891f3279f0ff74828
Publikováno v:
Journal of Translational Medicine, Vol 20, Iss 1, Pp 1-12 (2022)
Abstract Background The aim of this study was to investigate the association between inflammatory markers and 28-day mortality in patients with ST-elevation myocardial infarction (STEMI). Methods In 398 STEMI patients recorded between 2009 and 2013 b
Externí odkaz:
https://doaj.org/article/1178a4ce65db44b2ac57fc8a936784f2
Autor:
Matheus V. M. B. Wilke, Eva Morava-Kozicz, Matthew J. Koster, Christopher T. Schmitz, Shannon Kaye Foster, Mrinal Patnaik, Kenneth J. Warrington, Eric W. Klee, Filippo Pinto e Vairo
Publikováno v:
BMC Rheumatology, Vol 6, Iss 1, Pp 1-6 (2022)
Abstract Background VEXAS syndrome (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic syndrome) is a recently described syndrome caused by a somatic missense variant at the methionine-41 (p.(Met41)) position in the ubiquitin-like modifier acti
Externí odkaz:
https://doaj.org/article/de72d152939d4a2881d62c2b419acd4d
Publikováno v:
Quantum, Vol 7, p 1111 (2023)
Challenging combinatorial optimization problems are ubiquitous in science and engineering. Several quantum methods for optimization have recently been developed, in different settings including both exact and approximate solvers. Addressing this fiel
Externí odkaz:
https://doaj.org/article/57ea6b03c093420b93c49da77c82c579
Autor:
Erica L. Macke, Joel A. Morales‐Rosado, Sarah K. Macklin‐Mantia, Christopher T. Schmitz, Björn Oskarsson, Eric W. Klee, Klaas J. Wierenga
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 7, Pp n/a-n/a (2022)
Abstract Background Achalasia‐addisonianism‐alacrima syndrome, frequently referred to as Allgrove syndrome or Triple A syndrome, is a multisystem disorder resulting from homozygous or compound heterozygous pathogenic variants in the gene encoding
Externí odkaz:
https://doaj.org/article/df4c2837aabc49f0ad116b97a6d2a9ba
Autor:
Filippo Pinto e Vairo, Pavel N. Pichurin, Fernando C. Fervenza, Samih H. Nasr, Kevin Mills, Christopher T. Schmitz, Eric W. Klee, Sandra M. Herrmann
Publikováno v:
BMC Nephrology, Vol 21, Iss 1, Pp 1-5 (2020)
Abstract Background Genetic changes in the LIM homeobox transcription factor 1 beta (LMX1B) have been associated with focal segmental glomerulosclerosis (FSGS) without the extra-renal or ultrastructural manifestations of Nail-patella syndrome (NPS) k
Externí odkaz:
https://doaj.org/article/5adc8386c8d1429f839e2fa730c80d99
Autor:
Jared Brown, Christopher Barry, Matthew T Schmitz, Cara Argus, Jennifer M Bolin, Michael P Schwartz, Amy Van Aartsen, John Steill, Scott Swanson, Ron Stewart, James A Thomson, Christina Kendziorski
Publikováno v:
PLoS Computational Biology, Vol 17, Iss 3, p e1008778 (2021)
Human pluripotent stem cells hold significant promise for regenerative medicine. However, long differentiation protocols and immature characteristics of stem cell-derived cell types remain challenges to the development of many therapeutic application
Externí odkaz:
https://doaj.org/article/c8c89b8e35e94610b7bc51983a0d7e5e
Autor:
Laura Schultz‐Rogers, Ikuo Masuho, Filippo Pinto e Vairo, Christopher T. Schmitz, Tanya L. Schwab, Karl J. Clark, Lauren Gunderson, Pavel N. Pichurin, Klaas Wierenga, Kirill A. Martemyanov, Eric W. Klee
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 11, Pp n/a-n/a (2020)
Abstract Background GNB1 encodes a subunit of a heterotrimeric G‐protein complex that transduces intracellular signaling cascades. Disruptions to the gene have previously been shown to be embryonic lethal in knockout mice and to cause complex neuro
Externí odkaz:
https://doaj.org/article/fe7e66d8dd3c450096d3d2ed8e80544c
Autor:
Laura Schultz-Rogers, Francis P. Lach, Kimberly A. Rickman, Alejandro Ferrer, Abhishek A. Mangaonkar, Tanya L. Schwab, Christopher T. Schmitz, Karl J. Clark, Nikita R. Dsouza, Michael T. Zimmermann, Mark Litzow, Nicole Jacobi, Eric W. Klee, Agata Smogorzewska, Mrinal M. Patnaik
Publikováno v:
Haematologica, Vol 106, Iss 4 (2020)
Externí odkaz:
https://doaj.org/article/beb550a59f7b428c94671a0f636897b2