Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Patricia B. Eisenhauer"'
Autor:
Kelly J. Conn, Isabel Carreras, Ana M. George, Ann C. McKee, Wenwu Gao, Richard E. Fine, John M. Wells, John A. Lynch, Patricia B. Eisenhauer, M. David Ullman
Publikováno v:
Journal of Neuroscience Research. 83:1262-1270
Insulin degrading enzyme (IDE) is expressed in the brain and may play an important role there in the degradation of the amyloid beta peptide (Abeta). Our results show that cultured human cerebrovascular endothelial cells (HCECs), a primary component
Autor:
Rosemary Garrett-Young, Kelly J. Conn, John M. Wells, Richard E. Fine, Isabel Carreras, Patricia B. Eisenhauer, M. David Ullman
Publikováno v:
Journal of Neuroscience Research. 79:495-502
Clusterin (apolipoprotein J) is a highly conserved, multifunctional, vertebrate glycoprotein. Several isoforms of clusterin have been described including the predominant secreted isoform (sCLU) and several nuclear isoforms (nCLU) associated with cell
Autor:
Hamant S. Thatte, Patricia B. Eisenhauer, M. David Ullman, Kelly J. Conn, John A. Lynch, John M. Wells, Ann C. McKee, Richard E. Fine, Wenwu Gao
Publikováno v:
Neuroscience Letters. 371:6-11
Insulin degrading enzyme (IDE) is found in the cytosol, peroxisomes and plasma membrane of many cells. Although it preferentially cleaves insulin it can also cleave many other small proteins with diverse sequences including the monomeric form of the
Autor:
John M. Wells, Kelly J. Conn, Richard E. Fine, Patricia B Eisenhauer, David S. Newburg, Mary S Jacewicz, Omanand Koul
Publikováno v:
Microbial Pathogenesis. 36:189-196
Infection with Shiga toxin (Stx)-producing Escherichia coli can lead to development of hemolytic uremic syndrome (HUS). Patients with severe HUS often exhibit central nervous system (CNS) pathology, which is thought to involve damage to brain endothe
Autor:
Patricia B. Eisenhauer, M. David Ullman, Kelly J. Conn, John M. Wells, Richard E. Fine, Michelle J. Larned
Publikováno v:
Neurochemical Research. 28:1873-1881
cDNA microarray analysis of 1-methyl-4-phenyl-pyridinium (MPP+) toxicity (1 mM, 72 h) in undifferentiated SH-SY5Y cells identified 48 genes that displayed a signal intensity greater than the mean of all differentially expressed genes and a two-fold o
Autor:
Patricia B. Eisenhauer, Richard E. Fine, M. David Ullman, Catherine McKeon-O'Malley, Wenwu Gao, John M. Wells, Kelly J. Conn
Publikováno v:
Journal of Neuroscience Research. 68:755-760
Growth arrest DNA damage-inducible 153 (GADD153) expression was increased in 1-methyl-4-phenyl-pyridinium (MPP(+))-treated human SH-SY5Y neuroblastoma cells as determined by gene microarray analysis. GADD153 expression increased after 24 hr of MPP(+)
Autor:
Barbara A. Gilchrest, Richard E. Fine, Sen Zhai, Mina Yaar, Bennett L. Arble, Patricia B. Eisenhauer, Kenneth B. Stewart
Publikováno v:
Journal of Biological Chemistry. 277:7720-7725
p75(NTR), a nerve growth factor co-receptor that has been implicated in apoptosis of neurons, is structurally related to Fas and the receptors for tumor necrosis factor-alpha that display ligand independent assembly into trimers. Using embryonic day
Publikováno v:
Journal of Neuroscience Research. 60:804-810
The amyloid beta peptide (A beta) is the major component of the neuritic and cerebrovascular amyloid plaques that are one of the characteristic features of Alzheimer's disease (AD). This peptide has been shown to be toxic to several relevant cell typ
Autor:
John Henry Wells, Heather Tibbles, Andrea M. Billingslea, Richard E. Fine, Theresa A. Davies, Derek C.L. Marshall, Patricia B. Eisenhauer, David H. Cribbs, Carmela R. Abraham, Kim Otto, Heidi J. Long, Elizabeth R. Simons
Publikováno v:
Amyloid. 5:153-162
Proteolytic cleavage of the amyloid precursor protein (A beta PP) results in the generation of the amyloidogenic fragment known as amyloid beta peptide (A beta). Deposition of A beta in the brain parenchyma and cerebrovasculature is a feature of Alzh
Autor:
Barbara A. Gilchrest, Richard E. Fine, Paul F. Pilch, Mina Yaar, Sineaid M. Doyle, S Zhai, Patricia B. Eisenhauer
Publikováno v:
Journal of Clinical Investigation. 100:2333-2340
Alzheimer's disease is a neurodegenerative disorder characterized by the extracellular deposition in the brain of aggregated beta-amyloid peptide, presumed to play a pathogenic role, and by preferential loss of neurons that express the 75-kD neurotro