Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Carolyn L. Buller"'
Autor:
Tomio Umemoto, Renee C. LeBoeuf, Tsuyoshi Chiba, Laura J. den Hartigh, Mohamed Omer, Carolyn L. Buller, E. Dale Abel, Subramaniam Pennathur, Chang Yeop Han, Ian R. Sweet, Alan Chait
Publikováno v:
Journal of Biological Chemistry. 287:10379-10393
Excess glucose and free fatty acids delivered to adipose tissue causes local inflammation, which contributes to insulin resistance. Glucose and palmitate generate reactive oxygen species (ROS) in adipocytes, leading to monocyte chemotactic factor gen
Publikováno v:
American Journal of Physiology-Renal Physiology. 301:F588-F596
Enhanced GLUT1 expression in mesangial cells plays an important role in the development of diabetic nephropathy by stimulating signaling through several pathways resulting in increased glomerular matrix accumulation. Similarly, enhanced mammalian tar
Publikováno v:
Expert Review of Endocrinology & Metabolism. 5:51-64
Diabetic nephropathy (DN) is characterized by a plethora of signaling abnormalities that together ultimately result in the clinical and pathologic hallmarks of DN, namely progressive albuminuria followed by a gradual decline in glomerular filtration
Publikováno v:
Clinical and Experimental Hypertension. 27:71-82
This study examines whether longitudinal antioxidant treatment initiated in prehypertensive spontaneously hypertensive rats (SHR) can attenuate vascular oxidant stress and prevent blood pressure elevation during development. Male SHR and age-matched
Autor:
Marc F. Hansen, Robin J. Leach, Carolyn L. Buller, Pardeep Bhatia, Dharmini Pathmanathan, Donald G. Ammerman, Teresa L. Johnson-Pais, Maggie Nellissery
Publikováno v:
International Journal of Cancer. 105:285-288
Previous analysis of tumor-specific constitutional LOH had identified a putative tumor-suppressor gene (LOH18CR) active in osteosarcoma tumorigenesis, which mapped to a subregion of chromosome 18q linked to both familial Paget's disease and FEO. Usin
Publikováno v:
Pediatric research. 70(1)
Reactive oxygen species (ROS) are hypothesized to play a key role in myocardial ischemia-reperfusion (IR) injury after cardiopulmonary bypass in children. Clinical studies in adults and several animal models suggest that myocardial IR injury involves
Autor:
Subramaniam Pennathur, Carolyn L. Buller, Jessica L. Slocum, Rodica Pop-Busui, Matthias Kretzler, David M. Lubman, Anuradha Vivekanandan-Giri, Wenjun Ju, Venkatesha Basrur
Publikováno v:
International Journal of Proteomics
Chronic kidney disease (CKD) is a significant public health problem, and progression to end-stage renal disease leads to dramatic increases in morbidity and mortality. The mechanisms underlying progression of disease are poorly defined, and current n
Autor:
Carolyn L. Buller, Frank C. Brosius, Ken Inoki, James L. Park, Ming Hui Fan, Qihong Zhu, Kun-Liang Guan, Eileen D. Vesely, Robert D. Loberg
Glucose transport is a highly regulated process and is dependent on a variety of signaling events. Glycogen synthase kinase-3 (GSK-3) has been implicated in various aspects of the regulation of glucose transport, but the mechanisms by which GSK-3 act
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbcb09991142c3846e791cdd8bf0525a
https://europepmc.org/articles/PMC2544442/
https://europepmc.org/articles/PMC2544442/
Publikováno v:
Pediatric cardiology. 28(1)
Blood pressure variability correlates with circadian rhythmicity in endothelium-derived nitric oxide (NO) production in adults. Young, hypertensive orthotopic heart transplant (OHT) patients have functional abnormalities in NO-dependent signaling pat
Autor:
Teresa L, Johnson-Pais, Maggie J, Nellissery, Donald G, Ammerman, Dharmini, Pathmanathan, Pardeep, Bhatia, Carolyn L, Buller, Robin J, Leach, Marc F, Hansen
Publikováno v:
International journal of cancer. 105(2)
Previous analysis of tumor-specific constitutional LOH had identified a putative tumor-suppressor gene (LOH18CR) active in osteosarcoma tumorigenesis, which mapped to a subregion of chromosome 18q linked to both familial Paget's disease and FEO. Usin