Galaxies with Background QSOs: II. An Automated Search for Multiple Galaxy Emission Lines

We have improved upon our previous search technique of systematically searching QSO spectra for narrow galactic H-alpha emission, which indicates a foreground galaxy within the Sloan Digital Sky Survey (SDSS) spectral fiber. We now search for H-alpha plus eight other galactic emission lines in the same manner. We have scanned the SDSS DR7 QSO catalog spectra searching for these emission lines. Here we present our sample which focuses on the redshift range z<0.401 where galactic H-alpha is detectable in the SDSS spectra. This has revealed 27 unique galaxies on top of QSOs (GOTOQs). We have deblended the QSOs from the respective galaxies and determined the photometric properties of these systems. We find upon deblending that most of the galaxies are primarily blue, late-type galaxies with colors in the range -0.71<(u-r)<2.07. We find a slight anti-correlation between reddening and impact parameter (E(B-V)_(g-i) vs. b). The galaxies have average star formation rates of 0.01 to 1 M_sun yr^-1, with an average of 0.6 M_sun} yr^-1. They range in z from 0 to 0.4 and in stellar luminosity from about 0.01 L* to 3.0 L*. They are foreground to QSOs of brightness 17.4 to 20.4 magnitudes (r-band) with impact parameters of 1 to 10 kpc. They represent a fair sample of typical galaxies for which it should be possible to determine accurately various quantities (e.g. abundances, dust extinction, Faraday rotation) using follow-up analysis of the background QSOs. [...]Comment: 9 pages, 8 figure

Emerg. Infect. Dis

The multidrug-resistant (MDR) Salmonella enterica serotype Newport strain that produces CMY-2 β-lactamase(Newport MDR-AmpC) was the source of sporadic cases and outbreaks in humans in France during 2000–2005. Because this strain was not detected in food animals, it was most likely introduced into France through imported food products

Letter to Carol Avery Nicholson regarding speaker expenses, Willis Whichard, May 3, 1994

A letter from Willis Whichard to Carol Avery Nicholson regarding Whichard\u27s reimbursement for speaker expenses at the SEAALL Annual meeting

The Gathering Storm: Infectious Diseases and Human Rights in Burma

Documents how decades of repressive rule, civil war, and poor governance in Burma have contributed to the spread of HIV/AIDS, tuberculosis, malaria, and other infectious diseases

Glass formation and properties in the gallia-calcia system

“The critical cooling rate for glass formation for melts containing from 37.5 to 68.0 mol % Ga2O3 varied from 310 ± 80°C/s to 855 ± 115°C/s. The crystallization temperature, microhardness, UV and visible transmission were measured. The density increased from 4.075 g/cm3 at 37.5 3 mol % Ga2O3 to 4.402 g/cm3 at 56.0 mol % Ga2O3. The refractive index, nD, increased from 1.778 at 37.5 mol % Ga2O3 to 1.802 at 62.0 mol % Ga2O3. The IR spectra indicate that both GaO4 tetrahedra and GaO6 octahedra are present in these glasses”--Abstract, page 1

Expression of CD44 molecules and CD44 ligands during human thymic fetal development: expression of CD44 isoforms is developmentally regulated

It has recently been recognized that CD44 comprises a large family of alternatively spliced forms.In the thymus, CD44 has been postulated to play an important role in immature T cell migration and maturation. In this paper, we have studied the expression of CD44 molecules and two CD44 ligands, hyaluronan (HA) and fibronectin (FN), during human thymic fetal development. We found that mAbs against all CD44 isoforms (A3D8 or A1G3) reacted with both thymic epithelial (TE) cells and thymocytes beginning at the time of initial colonization of the human thymus by hematopoietic stem cells at 8.2 weeks of fetal gestation. However, mAbs specific for splice variants of CD44 containing membrane-proximal inserts (11.24, 11.10 and 11.9) reacted only with terminally differentiated TE cells in and around Hassall's bodies beginning at 16-19 weeks of fetal gestation. Studies of differentiated versus undifferentiated TE cells in vitro confirmed the selective expression of CD44 variant isoforms on terminally differentiated TE cells. Expression of HA and FN was determined by fluorescence microscopy using either biotlnylated-HA binding protein or an anti-FN mAb. We found that whereas FN was present throughout the human fetal thymus beginning at 8.2 weeks, HA was not present until 16 weeks of gestational age. These data demonstrate the differential expression of standard versus variant CD44 isoforms during thymic ontogeny and implicate CD44 interactions with ligands other than HA as important in the earlier stages of humanthymus developmen