Search Results - (Author, Cooperation:D. Travis)
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1Staff View
Publication Date: 2018-03-14Publisher: Nature Publishing Group (NPG)Electronic ISSN: 2041-1723Topics: BiologyChemistry and PharmacologyNatural Sciences in GeneralPhysicsPublished by: -
2J. George ; J. S. Lim ; S. J. Jang ; Y. Cun ; L. Ozretic ; G. Kong ; F. Leenders ; X. Lu ; L. Fernandez-Cuesta ; G. Bosco ; C. Muller ; I. Dahmen ; N. S. Jahchan ; K. S. Park ; D. Yang ; A. N. Karnezis ; D. Vaka ; A. Torres ; M. S. Wang ; J. O. Korbel ; R. Menon ; S. M. Chun ; D. Kim ; M. Wilkerson ; N. Hayes ; D. Engelmann ; B. Putzer ; M. Bos ; S. Michels ; I. Vlasic ; D. Seidel ; B. Pinther ; P. Schaub ; C. Becker ; J. Altmuller ; J. Yokota ; T. Kohno ; R. Iwakawa ; K. Tsuta ; M. Noguchi ; T. Muley ; H. Hoffmann ; P. A. Schnabel ; I. Petersen ; Y. Chen ; A. Soltermann ; V. Tischler ; C. M. Choi ; Y. H. Kim ; P. P. Massion ; Y. Zou ; D. Jovanovic ; M. Kontic ; G. M. Wright ; P. A. Russell ; B. Solomon ; I. Koch ; M. Lindner ; L. A. Muscarella ; A. la Torre ; J. K. Field ; M. Jakopovic ; J. Knezevic ; E. Castanos-Velez ; L. Roz ; U. Pastorino ; O. T. Brustugun ; M. Lund-Iversen ; E. Thunnissen ; J. Kohler ; M. Schuler ; J. Botling ; M. Sandelin ; M. Sanchez-Cespedes ; H. B. Salvesen ; V. Achter ; U. Lang ; M. Bogus ; P. M. Schneider ; T. Zander ; S. Ansen ; M. Hallek ; J. Wolf ; M. Vingron ; Y. Yatabe ; W. D. Travis ; P. Nurnberg ; C. Reinhardt ; S. Perner ; L. Heukamp ; R. Buttner ; S. A. Haas ; E. Brambilla ; M. Peifer ; J. Sage ; R. K. Thomas
Nature Publishing Group (NPG)
Published 2015Staff ViewPublication Date: 2015-07-15Publisher: Nature Publishing Group (NPG)Print ISSN: 0028-0836Electronic ISSN: 1476-4687Topics: BiologyChemistry and PharmacologyMedicineNatural Sciences in GeneralPhysicsPublished by: -
3Staff View
Publication Date: 2018-02-16Publisher: American Association for the Advancement of Science (AAAS)Print ISSN: 0036-8075Electronic ISSN: 1095-9203Topics: BiologyChemistry and PharmacologyGeosciencesComputer ScienceMedicineNatural Sciences in GeneralPhysicsKeywords: EcologyPublished by: -
4P. Sriramarao ; M. P. Murtaugh ; K. Berger ; D. Travis ; S. Kennedy ; C. J. Steer ; C. Cardona
American Association for the Advancement of Science (AAAS)
Published 2015Staff ViewPublication Date: 2015-01-17Publisher: American Association for the Advancement of Science (AAAS)Print ISSN: 0036-8075Electronic ISSN: 1095-9203Topics: BiologyChemistry and PharmacologyComputer ScienceMedicineNatural Sciences in GeneralPhysicsKeywords: Animals ; *Environment ; *Health ; Humans ; Interdisciplinary Communication ; *Public PolicyPublished by: -
5Staff View
ISSN: 0019-1035Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: PhysicsType of Medium: Electronic ResourceURL: -
6Friedman, N. ; Hawkins, J. ; Travis, D. ; Laurence, G.
[S.l.] : American Institute of Physics (AIP)
Published 1996Staff ViewISSN: 1089-7623Source: AIP Digital ArchiveTopics: PhysicsElectrical Engineering, Measurement and Control TechnologyNotes: The front-end Equipment Protection System (FE-EPS) at the Advanced Photon Source (APS) is a high reliability, fail-safe single-chain interlock and control system. It consists of an Allen-Bradley PLC-5/30 processor, local and remote I/O racks, monitoring and control panels, serial communication links, and field devices. Each front end is equipped with a dedicated EPS. The system monitors a variety of sensors (e.g., vacuum, cooling water, temperature, pneumatic pressure), and controls front-end (FE) photon shutters and UHV valves. The main functions of the FE-EPS are to guard the integrity of the storage ring vacuum against vacuum excursions in the FE and beam transport line, as well as to protect the front-end and beamline components from being damaged by synchrotron radiation. The FE-EPS interfaces to six other APS interlock and control systems. Information about FE interlocks and devices is displayed on UNIX machines using the EPICS software tool kit. The system design is presented. © 1996 American Institute of Physics.Type of Medium: Electronic ResourceURL: -
7Staff View
ISSN: 1533-1598Source: Blackwell Publishing Journal Backfiles 1879-2005Topics: MusicologyType of Medium: Electronic ResourceURL: -
8Fridgen, Travis D. ; Parnis, J. Mark
College Park, Md. : American Institute of Physics (AIP)
Published 1998Staff ViewISSN: 1089-7690Source: AIP Digital ArchiveTopics: PhysicsChemistry and PharmacologyNotes: Matrices formed by subjecting methanol vapor diluted in argon/krypton mixtures to electron bombardment and subsequent matrix isolation (EBMI) reveal a new feature at 885.3 cm−1 which is assigned to the v3 fundamental of the triatomic cation (ArHKr)+. In samples containing about 5% krypton, the v3 fundamental of Kr2H+ is also observed in a predominantly solid argon environment. These assignments are supported by annealing experiments and by density functional theory calculations reported in a separate paper. Similar experiments with xenon diluted in argon yield infrared spectra showing the v3 and v3+v1 bands of (ArHXe)+, and v3 of Xe2H+ in predominantly argon environments. EBMI of methanol diluted in krypton in the presence of xenon gives rise to infrared bands assigned to the v3 and v3+v1 fundamentals and combination bands of both (KrHXe)+ and Xe2H+ isolated in predominantly krypton environments. The energetics and plausible mechanisms to the formation of these homogenous and mixed proton-bound rare-gas dimers are considered. © 1998 American Institute of Physics.Type of Medium: Electronic ResourceURL: -
9Fridgen, Travis D. ; Parnis, J. Mark
College Park, Md. : American Institute of Physics (AIP)
Published 1998Staff ViewISSN: 1089-7690Source: AIP Digital ArchiveTopics: PhysicsChemistry and PharmacologyNotes: Density functional theory calculations have been performed on the various proton-bound rare-gas dimers Rg2H+ and (RgHRg′)+ (Rg=Ar, Kr, or Xe, and Rg≠Rg′) employing the BP86 method coupled with either a Gaussian split valence basis set (DZVP) or a numerical split valence basis set (DN**). The calculations with the DN** basis represent the first calculations in which correct qualitative agreement is obtained with respect to the trend in experimental data for the antisymmetric stretching wavenumbers of the three Rg2H+ cations. Good qualitative agreement is also obtained for the antisymmetric stretching wavenumber of the mixed-rare-gas species (ArHKr)+. For the xenon-containing mixed-rare-gas cations, the agreement with experimental wavenumbers is not good as is the case for the DZVP basis set with any of the aforementioned cations. This is believed to be due to the inability of these basis sets to predict some physical and chemical properties for these species. Quantitative agreement between theory and experiment with respect to the antisymmetric stretch of the Rg2H+ cations is improved when four radial argon atoms are placed at a fixed distance from the central H, intended to mimic the matrix environment. Based on these calculations, an inverse hydrogen-isotope dependence for the dissociation energy of these species is predicted. No center atom isotope dependence is predicted for the symmetric stretching vibration. Employing a polyatomic model, we have reanalyzed previously published combination band data for Xe2H+ and Xe2D+, and concluded that there is no evidence for an inverse isotope dependence for the symmetric stretching vibrations of these species. © 1998 American Institute of Physics.Type of Medium: Electronic ResourceURL: -
10Trippel, Edward A. ; Holy, Norman L. ; Palka, Debra L. ; Shepherd, Travis D. ; Melvin, Gary D. ; Terhune, John M.
Oxford, UK : Blackwell Publishing Ltd
Published 2003Staff ViewISSN: 1748-7692Source: Blackwell Publishing Journal Backfiles 1879-2005Topics: BiologyType of Medium: Electronic ResourceURL: -
11Staff View
ISSN: 0025-1895Topics: EconomicsURL: -
12Staff View
ISSN: 1476-4687Source: Nature Archives 1869 - 2009Topics: BiologyChemistry and PharmacologyMedicineNatural Sciences in GeneralPhysicsNotes: [Auszug] In the cases of AuBe and of AuMg, rotational structure in two band-systems has been satisfactorily resolved, and their structure indicates that the systems may be represented by B(2P), A (2Ã+) X 2Ã+, where the upper states A, B are probably in Hund's case-c. Constants are given in Tables 1 and 2. ...Type of Medium: Electronic ResourceURL: -
13Staff View
ISSN: 1476-4687Source: Nature Archives 1869 - 2009Topics: BiologyChemistry and PharmacologyMedicineNatural Sciences in GeneralPhysicsNotes: [Auszug] The occurrence of the spectrum of NCN in the flash photolysis of fulminic acid is an example of the need for caution in the assignment of observed spectra on the basis of excitation conditions or chemical considerations only. The history of spectroscopy abounds in such examples. We only need to ...Type of Medium: Electronic ResourceURL: -
14Staff View
ISSN: 1476-4687Source: Nature Archives 1869 - 2009Topics: BiologyChemistry and PharmacologyMedicineNatural Sciences in GeneralPhysicsNotes: [Auszug] This comparatively simple situation, which obtains for the lighter molecules of the group, is in strong contrast with that for the heavier molecules, particularly for SnSe, SnTe and the lead compounds. In PbO, for example, the absorption region of longer wave-length (〉 2500 Å.) shows at least ...Type of Medium: Electronic ResourceURL: -
15Staff View
ISSN: 1572-9559Source: Springer Online Journal Archives 1860-2000Topics: PhysicsNotes: Abstract An extensive study of the propyne optically pumped laser is presented. 32 new far infrared and 8 new mid infrared outputs are reported, together with pump frequency offset data. Complete assignments of some far infrared transitions and partial assignments of the mid infrared outputs are given. Very strong interactions occur between the mid and far infrared laser transitions. These interactions are of vital importance in obtaining high output energies.Type of Medium: Electronic ResourceURL: -
16Theodorou, Doros N. ; Boone, Travis D. ; Dodd, Lawrence R. ; Mansfield, Kevin F.
Basel : Wiley-Blackwell
Published 1993Staff ViewISSN: 1018-5054Keywords: Chemistry ; Polymer and Materials ScienceSource: Wiley InterScience Backfile Collection 1832-2000Topics: Chemistry and PharmacologyPhysicsNotes: The calculation of the stress tensor from molecular simulations of atomistic model polymer systems employing periodic boundary conditions is discussed. Starting from the dynamical equations governing the motion of sites, correct double summation forms of the atomic and the molecular virial equations are derived, which are valid for flexible, infinitely stiff and rigid chain models even in the presence of interactions between different images of the same parent macromolecule. A new expression for the true instantaneous stress (flux of momentum through the faces of the simulation box) is derived and shown to exhibit large fluctuations when applied in molecular dynamics simulations. A new equation for the thermodynamic stress, cast exclusively in terms of intermolecular forces on interaction sites, is also derived. Application to Monte Carlo simulations shows that the molecular virial expression exhibits the smallest fluctuations among all stress expressions discussed, and thus allows computation of the thermodynamic stress with least uncertainty. A scheme is developed for the calculation of surface tension from intermolecular forces only.Additional Material: 13 Ill.Type of Medium: Electronic ResourceURL: -
17Grieneisen, Michael L. ; Kieckbusch, Travis D. ; Mok, Amy ; Dorman, György ; Latli, Bachir ; Prestwich, Glenn D. ; Schooley, David A.
New York, NY [u.a.] : Wiley-Blackwell
Published 1995Staff ViewISSN: 0739-4462Keywords: juvenile hormone kinase ; tritiation ; HPLC ; Chemistry ; Food Science, Agricultural, Medicinal and Pharmaceutical ChemistrySource: Wiley InterScience Backfile Collection 1832-2000Topics: BiologyNotes: Juvenile hormone epoxide hydrolase (JHEH) and juvenile hormone diol phosphotransferase (JHDPT) were characterized from the Malpighian tubules of day 1 fifth instar Manduca sexta. An improved RP-HPLC assay is described for the major metabolites of (10R, 11S) juvenile hormone I: diol, acid, aciddiol, and diol-phosphate. JHEH is strictly associated with membrane fractions, while JHDPT is cytosolic. JHEH may be solubilized in active form by the nonionic detergents Thesit or MEGA-8. Separation of Malpighian tubule cytosol proteins using preparative isoelectric focusing yields two zones which contain JHDPT activity, at pl 4.8-5.1 and 6.8-8.2. The partially purified JHDPT from either zone requires both ATP and Mg2+ for activity, so this enzyme may be formally called either ATP:juvenile hormone diol phosphotransferase or juvenile hormone diol kinase (EC 2.1.7.3.). Metabolites more polar than JH I aciddiol and JH I diol-phosphate are generated in vivo from either [3H]JH I or [3H]JH I diol. © 1995 Wiley-Liss, Inc.Additional Material: 4 Ill.Type of Medium: Electronic ResourceURL: