| 1381. |
- Miller, James B., et al.
(författare)
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Microstructural evolution of sol-gel derived ZnO thin films
- 2010
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Ingår i: Thin Solid Films. - : Elsevier. - 0040-6090 .- 1879-2731. ; 518:23, s. 6792-6798
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Tidskriftsartikel (refereegranskat)abstract
- Zinc oxide thin films, with thicknesses between ∼ 20 and 450 nm, were prepared by spin-coating a sol–gel precursor solution (zinc acetate dihydrate and monoethanolamine in an isopropanol solvent) onto glass substrates, followed by heat treatment at temperatures through 773 K. At 298 and 373 K, the films exhibited the structure of a lamellar ZnO precursor, Layered Basic Zinc Acetate (LBZA). At higher temperatures, LBZA released intercalated water and acetate groups and dehydroxylated to form zinc oxide nanograins with wurtzite structure, which were preferentially oriented in the c-axis direction. Both the degree of the films' c-axis orientation and the topography of their surfaces varied with heat treatment and precursor concentration. For films calcined at 773 K, a minimum of micron-scale surface wrinkles coincided with a maximum in c-axis preference at intermediate concentrations, suggesting that release of mechanical stress during densification of thicker films may have disrupted the ordering process that occurs during heat treatment.
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| 1382. |
- Miller, Jeremiah E., et al.
(författare)
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Electron tunneling in rhenium-modified Pseudomonas aeruginosa azurins
- 2004
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Ingår i: Biochimica et Biophysica Acta - Bioenergetics. - : Elsevier BV. - 0005-2728 .- 1879-2650. ; 1655:1-3, s. 59-63
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Tidskriftsartikel (refereegranskat)abstract
- Laser flash-quench methods have been used to generate tyrosine and tryptophan radicals in structurally characterized rhenium-modified Pseudomonas aeruginosa azurins. Cu(I) to “Re(II)” electron tunneling in Re(H107) azurin occurs in the microsecond range. This reaction is much faster than that studied previously for Cu(I) to Ru(III) tunneling in Ru(H107) azurin, suggesting that a multistep (“hopping”) mechanism might be involved. Although a Y108 radical can be generated by flash-quenching a Re(H107)M(II) (M=Cu, Zn) protein, the evidence suggests that it is not an active intermediate in the enhanced Cu(I) oxidation. Rather, the likely explanation is rapid conversion of Re(II)(H107) to deprotonated Re(I)(H107 radical), followed by electron tunneling from Cu(I) to the hole in the imidazole ligand.
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| 1383. |
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| 1384. |
- Miller, M. Coleman, et al.
(författare)
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AN UPPER LIMIT TO THE VELOCITY DISPERSION OF RELAXED STELLAR SYSTEMS WITHOUT MASSIVE BLACK HOLES
- 2012
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Ingår i: Astrophysical Journal. - 0004-637X. ; 755:1
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Tidskriftsartikel (refereegranskat)abstract
- Massive black holes have been discovered in all closely examined galaxies with high velocity dispersion. The case is not as clear for lower-dispersion systems such as low-mass galaxies and globular clusters. Here we suggest that above a critical velocity dispersion similar to 40 km s(-1), massive central black holes will form in relaxed stellar systems at any cosmic epoch. This is because above this dispersion primordial binaries cannot support the system against deep core collapse. If, as previous simulations show, the black holes formed in the cluster settle to produce a dense subcluster, then given the extremely high densities reached during core collapse the holes will merge with each other. For low velocity dispersions and hence low cluster escape speeds, mergers will typically kick out all or all but one of the holes due to three-body kicks or the asymmetric emission of gravitational radiation. If one hole remains, it will tidally disrupt stars at a high rate. If none remain, one is formed after runaway collisions between stars, and then it tidally disrupts stars at a high rate. The accretion rate after disruption is many orders of magnitude above Eddington. If, as several studies suggest, the hole can accept matter at that rate because the generated radiation is trapped and advected, then it will grow quickly and form a massive central black hole.
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| 1385. |
- Miller, Matt, et al.
(författare)
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STRUCTURAL EQUATION MODELING
- 2020
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Ingår i: Advanced Quantitative Research Methods for Urban Planners. - : Routledge. ; , s. 185-215
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Bokkapitel (övrigt vetenskapligt/konstnärligt)abstract
- This chapter introduces background and historical information on how structural equation modeling (SEM) came to be developed. Then, the main differences between SEM and earlier multivariate methods are explained. The chapter describes three main applications of SEM: path analysis, factor analysis, and hybrid models. Some computer programs are recommended for these applications. The step-by-step section goes over how to estimate structural models with AMOS and R. The chapter concludes with two example applications of SEM in the planning field.
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| 1386. |
- Miller-Podraza, Halina, 1948, et al.
(författare)
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Helicobacter pylori and neutrophils: sialic acid-dependent binding to various isolated glycoconjugates.
- 1999
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Ingår i: Infection and immunity. - 0019-9567. ; 67:12, s. 6309-13
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Tidskriftsartikel (refereegranskat)abstract
- Helicobacter pylori has been shown to agglutinate erythrocytes in a sialic acid-dependent manner. However, very few studies have examined relevant target cells in the human stomach. Neutrophils are required for the onset of gastritis, and the inflammatory reaction may be induced on contact between bacteria and neutrophils. In the present work, glycolipids and glycoproteins were isolated from neutrophils and were studied for binding by overlay with radiolabeled bacteria on thin-layer chromatograms and on membrane blots. There was a complex pattern of binding bands. The only practical binding activity found was sialic acid dependent, since treatment of glycoconjugates with neuraminidase or mild periodate eliminated binding. As shown before for binding to erythrocytes and other glycoconjugates, bacterial cells grown on agar bound to many glycoconjugates, while growth in broth resulted in bacteria that would bind only to polyglycosylceramides, which are highly heterogeneous and branched poly-N-acetyllactosamine-containing glycolipids. Approximately seven positive bands were found for glycoproteins, and the traditional ganglioside fraction showed a complex, slow-moving interval with very strong sialic-acid-dependent binding, probably explained by Fuc substitutions on GlcNAc.
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| 1387. |
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| 1388. |
- Miller, R. L., et al.
(författare)
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Shotgun ion mobility mass spectrometry sequencing of heparan sulfate saccharides
- 2020
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Ingår i: Nature Communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 11:1
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Tidskriftsartikel (refereegranskat)abstract
- Despite evident regulatory roles of heparan sulfate (HS) saccharides in numerous biological processes, definitive information on the bioactive sequences of these polymers is lacking, with only a handful of natural structures sequenced to date. Here, we develop a "Shotgun" Ion Mobility Mass Spectrometry Sequencing (SIMMS2) method in which intact HS saccharides are dissociated in an ion mobility mass spectrometer and collision cross section values of fragments measured. Matching of data for intact and fragment ions against known values for 36 fully defined HS saccharide structures (from di- to decasaccharides) permits unambiguous sequence determination of validated standards and unknown natural saccharides, notably including variants with 3O-sulfate groups. SIMMS2 analysis of two fibroblast growth factor-inhibiting hexasaccharides identified from a HS oligosaccharide library screen demonstrates that the approach allows elucidation of structure-activity relationships. SIMMS2 thus overcomes the bottleneck for decoding the informational content of functional HS motifs which is crucial for their future biomedical exploitation. Heparan sulfates (HS) contain functionally relevant structural motifs, but determining their monosaccharide sequence remains challenging. Here, the authors develop an ion mobility mass spectrometry-based method that allows unambiguous characterization of HS sequences and structure-activity relationships.
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| 1389. |
- Miller, Rachael, et al.
(författare)
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Socio-ecological correlates of neophobia in corvids
- 2022
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Ingår i: Current Biology. - : Elsevier BV. - 0960-9822. ; 32:1, s. 4-85
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Tidskriftsartikel (refereegranskat)abstract
- Behavioral responses to novelty, including fear and subsequent avoidance of novel stimuli, i.e., neophobia, determine how animals interact with their environment. Neophobia aids in navigating risk and impacts on adaptability and survival. There is variation within and between individuals and species; however, lack of large-scale, comparative studies critically limits investigation of the socio-ecological drivers of neophobia. In this study, we tested responses to novel objects and food (alongside familiar food) versus a baseline (familiar food alone) in 10 corvid species (241 subjects) across 10 labs worldwide. There were species differences in the latency to touch familiar food in the novel object and novel food conditions relative to the baseline. Four of seven socio-ecological factors influenced object neophobia: (1) use of urban habitat (versus not), (2) territorial pair versus family group sociality, (3) large versus small maximum flock size, and (4) moderate versus specialized caching (whereas range, hunting live animals, and genus did not), while only maximum flock size influenced food neophobia. We found that, overall, individuals were temporally and contextually repeatable (i.e., consistent) in their novelty responses in all conditions, indicating neophobia is a stable behavioral trait. With this study, we have established a network of corvid researchers, demonstrating potential for further collaboration to explore the evolution of cognition in corvids and other bird species. These novel findings enable us, for the first time in corvids, to identify the socio-ecological correlates of neophobia and grant insight into specific elements that drive higher neophobic responses in this avian family group. Video abstract: [Figure presented]
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| 1390. |
- Miller, Todd W, et al.
(författare)
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Loss of Phosphatase and Tensin Homologue Deleted on Chromosome 10 Engages ErbB3 and Insulin-Like Growth Factor-I Receptor Signaling to Promote Antiestrogen Resistance in Breast Cancer
- 2009
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Ingår i: CANCER RESEARCH. - 0008-5472. ; 69:10, s. 4192-4201
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Tidskriftsartikel (refereegranskat)abstract
- Knockdown of the tumor suppressor phosphatase Phosphatase and tensin homologue deleted on chromosome 10 (PTEN) with shRNA in three estrogen receptor (ER)-positive breast cancer cell lines resulted in increased phosphatidylinositol-3 kinase (PI3K) and AKT activities, resistance to tamoxifen and fulvestrant, and hormone-independent growth. PTEN knockdown induced the up-regulation of ER transcriptional activity in MCF-7 cells but decreased ER protein levels and transcriptional activity in T47D and MDA-361 cells. Tamoxifen and fulvestrant treatment inhibited estradiol-induced Ell transcriptional activity in all shPTEN cell lines but did not abrogate the increased cell proliferation induced by PTEN knockdown. PTEN knockdown increased basal and ligand-induced activation of the insulin-like growth factor-I (IGF-I) and ErbB3 receptor tyrosine kinases, and prolonged the association of the p85 PI3K subunit with the IGF-I receptor (IGF-IR) effector insulin receptor substrate-1 and with ErbB3, implicating VITA in the modulation of Signaling upstream of PI3K. Consistent with these data, PTEN levels inversely correlated with levels of tyrosine-phosphorylated IGF-IR in tissue lysate arrays of primary breast cancers. Inhibition of IGF-IR and/or ErbB2-mediated activation of ErbB3 with tyrosine kinase inhibitors restored hormone dependence and the growth inhibitory effect of tamoxifen and fulvestrant. oil shPTEN cells, suggesting that cotargeting both Ell and receptor tyrosine kinase pathways holds promise for the treatment of patients with ER+, PTEN-deficient breast cancers.
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