Výsledky vyhledávání - "Heather Bechtel"

H-Ferritin ferroxidase induces cytoprotective pathways and inhibits microvascular stasis in transgenic sickle mice

Autor: Graham Brown, Gregory M. Vercellotti, John D. Belcher, Karl A. Nath, Heather Bechtel, Robert P. Hebbel, Fatima Khan, Carol M. Bruzzone, Chunsheng Chen, Julia Nguyen, Clifford J. Steer

Publikováno v: Frontiers in Pharmacology, Vol 5 (2014)
Frontiers in Pharmacology

Hemolysis, oxidative stress, inflammation, vaso-occlusion, and organ infarction are hallmarks of sickle cell disease (SCD). We have previously shown that increases in heme oxygenase-1 (HO-1) activity detoxify heme and inhibit vaso-occlusion in transg

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2908740262f983572f3aab5e397c0ab5
http://journal.frontiersin.org/Journal/10.3389/fphar.2014.00079/full

Zobrazit plný text záznamu

Reversible Fanconi syndrome in a pediatric patient on deferasirox

Autor: Heather Bechtel, Clifford E. Kashtan, Michelle N. Rheault, Joseph P. Neglia

Publikováno v: Pediatric Blood & Cancer. 56:674-676

Deferasirox (Exjade®, Novartis) is a widely used oral iron chelator for the treatment of patients with iron overload due to chronic transfusion therapy for diseases such as β-thalassemia and sickle cell disease. Renal side effects of deferasirox ar

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d0659fa9cfd1c4d10beb6e1f748692b4
https://doi.org/10.1002/pbc.22711

Zobrazit plný text záznamu

Reversible Fanconi syndrome in a pediatric patient on deferasirox

Autor: Michelle N, Rheault, Heather, Bechtel, Joseph P, Neglia, Clifford E, Kashtan

Publikováno v: Pediatric bloodcancer. 56(4)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::7aea28d10ecae3aa2501f14a97217452
https://pubmed.ncbi.nlm.nih.gov/21298760

Zobrazit plný text záznamu

H-Ferritin Ferroxidase Activity Induces Cytoprotective Pathways and Inhibits Microvascular Stasis in Transgenic Sickle Mice

Autor: Chunsheng Chen, John D. Belcher, Gregory M. Vercellotti, Heather Bechtel, Robert P. Hebbel, Julia Ngyuen, Carol M. Bruzzone, Clifford J. Steer

Publikováno v: Blood. 120:378-378

Abstract 378 Hemolysis, oxidative stress, inflammation, vaso-occlusion and organ infarction are hallmarks of sickle cell disease (SCD). We hypothesize that intravascular heme, liberated from hemoglobin S derived from hemolyzed sickle red blood cells,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::783cb1e17b50f8de7b93d1fbbae36299
https://doi.org/10.1182/blood.v120.21.378.378

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání