Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Samuel B Reynolds"'
Autor:
Po-Shun Lee, Anna S K Wilhelmson, Anton P Hubner, Samuel B Reynolds, Dana A Gallacchi, Terry T Chiou, David J Kwiatkowski
Publikováno v:
PLoS ONE, Vol 5, Iss 12, p e14399 (2010)
mTORC1 (mammalian target of rapamycin complex 1) activation has been demonstrated in response to endotoxin challenge, but the mechanism and significance are unclear. We investigated the effect of mTORC1 suppression in an animal model of endotoxemia a
Externí odkaz:
https://doaj.org/article/a9c7fa2bab1b4ab7816a3510db84f54a
Autor:
Rahul Mhaskar, Bryan Kane, Jordan Davies, Angela Davis, Maria Karagias, Matthew Molnar, Robert Postlethwaite, Brittany Quinn, Samuel B. Reynolds, Monica Stewart, Nicholas Werbeckes, Robert Barraco
BACKGROUND The information-seeking behavior of physicians to cater to the patient's information needs is not comprehensively studied. OBJECTIVE Our cross-sectional study's key goals were to understand providers' information-seeking behavior regarding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22656c17fac9019a373bfc1696acddef
https://doi.org/10.2196/preprints.48180
https://doi.org/10.2196/preprints.48180
Autor:
Samuel B. Reynolds, Kristen Pettit
Publikováno v:
Hematology Am Soc Hematol Educ Program
Myelofibrosis (MF) is a clonal hematopoietic stem cell neoplasm characterized by constitutional symptoms, splenomegaly, and risks of marrow failure or leukemic transformation and is universally driven by Jak/STAT pathway activation. Despite sharing t
Publikováno v:
Journal of Onco-Nephrology. 5:178-182
Hereditary leiomyomatosis is a genetic disorder that follows an autosomal dominant pattern of inheritance. Along with a variety of leiomyomas, affected individuals are predisposed to developing an aggressive form of type 2 papillary renal malignancy
Publikováno v:
Cancer Research. 83:4537-4537
Erdheim Chester Disease (ECD) is a rare, non-Langerhans cell histiocytic disease, characterized as a neoplastic disorder in 2016. MAP Kinase and PI3-AKT pathway somatic mutations and/or fusion genes have been shown to play a significant role in disea
Publikováno v:
Cancer Research. 83:4536-4536
Introduction: Rosai Dorfman Disease (RDD) is a non-Langerhans cell histiocytic disease whose pathologic features include sinus histiocytosis with variable emperipolesis. Traditional management consists of local therapies (resection, radiation) for li
Publikováno v:
Cureus.
Publikováno v:
Annals of Clinical Psychiatry. 33:53-55
Publikováno v:
Cureus
Ignatzschineria is a recently identified genus of bacteria that has been isolated from the digestive tract of multiple flies associated with decomposing tissue. Species within this genus are rarely implicated in human disease, and less than 10 cases