Search Results - (Author, Cooperation:A. J. Gonzalez)
-
1Latest Papers from Table of Contents or Articles in PressN. D. Young ; F. Debelle ; G. E. Oldroyd ; R. Geurts ; S. B. Cannon ; M. K. Udvardi ; V. A. Benedito ; K. F. Mayer ; J. Gouzy ; H. Schoof ; Y. Van de Peer ; S. Proost ; D. R. Cook ; B. C. Meyers ; M. Spannagl ; F. Cheung ; S. De Mita ; V. Krishnakumar ; H. Gundlach ; S. Zhou ; J. Mudge ; A. K. Bharti ; J. D. Murray ; M. A. Naoumkina ; B. Rosen ; K. A. Silverstein ; H. Tang ; S. Rombauts ; P. X. Zhao ; P. Zhou ; V. Barbe ; P. Bardou ; M. Bechner ; A. Bellec ; A. Berger ; H. Berges ; S. Bidwell ; T. Bisseling ; N. Choisne ; A. Couloux ; R. Denny ; S. Deshpande ; X. Dai ; J. J. Doyle ; A. M. Dudez ; A. D. Farmer ; S. Fouteau ; C. Franken ; C. Gibelin ; J. Gish ; S. Goldstein ; A. J. Gonzalez ; P. J. Green ; A. Hallab ; M. Hartog ; A. Hua ; S. J. Humphray ; D. H. Jeong ; Y. Jing ; A. Jocker ; S. M. Kenton ; D. J. Kim ; K. Klee ; H. Lai ; C. Lang ; S. Lin ; S. L. Macmil ; G. Magdelenat ; L. Matthews ; J. McCorrison ; E. L. Monaghan ; J. H. Mun ; F. Z. Najar ; C. Nicholson ; C. Noirot ; M. O'Bleness ; C. R. Paule ; J. Poulain ; F. Prion ; B. Qin ; C. Qu ; E. F. Retzel ; C. Riddle ; E. Sallet ; S. Samain ; N. Samson ; I. Sanders ; O. Saurat ; C. Scarpelli ; T. Schiex ; B. Segurens ; A. J. Severin ; D. J. Sherrier ; R. Shi ; S. Sims ; S. R. Singer ; S. Sinharoy ; L. Sterck ; A. Viollet ; B. B. Wang ; K. Wang ; M. Wang ; X. Wang ; J. Warfsmann ; J. Weissenbach ; D. D. White ; J. D. White ; G. B. Wiley ; P. Wincker ; Y. Xing ; L. Yang ; Z. Yao ; F. Ying ; J. Zhai ; L. Zhou ; A. Zuber ; J. Denarie ; R. A. Dixon ; G. D. May ; D. C. Schwartz ; J. Rogers ; F. Quetier ; C. D. Town ; B. A. Roe
Nature Publishing Group (NPG)
Published 2011Staff ViewPublication Date: 2011-11-18Publisher: Nature Publishing Group (NPG)Print ISSN: 0028-0836Electronic ISSN: 1476-4687Topics: BiologyChemistry and PharmacologyMedicineNatural Sciences in GeneralPhysicsKeywords: *Biological Evolution ; *Genome, Plant ; Medicago truncatula/*genetics/*microbiology ; Molecular Sequence Data ; Nitrogen Fixation/genetics ; Rhizobium/*physiology ; Soybeans/genetics ; *Symbiosis ; Synteny ; Vitis/geneticsPublished by: -
2Latest Papers from Table of Contents or Articles in PressStaff View
Publication Date: 2018-03-06Publisher: American Physical Society (APS)Print ISSN: 0556-2821Electronic ISSN: 1089-4918Topics: PhysicsKeywords: Astrophysics and astroparticle physicsPublished by: -
3Latest Papers from Table of Contents or Articles in PressE. O. Gracheva ; J. F. Cordero-Morales ; J. A. Gonzalez-Carcacia ; N. T. Ingolia ; C. Manno ; C. I. Aranguren ; J. S. Weissman ; D. Julius
Nature Publishing Group (NPG)
Published 2011Staff ViewPublication Date: 2011-08-05Publisher: Nature Publishing Group (NPG)Print ISSN: 0028-0836Electronic ISSN: 1476-4687Topics: BiologyChemistry and PharmacologyMedicineNatural Sciences in GeneralPhysicsKeywords: Alternative Splicing/*genetics ; Amino Acid Sequence ; Animals ; Cattle ; Chiroptera/anatomy & histology/classification/*genetics/*physiology ; Face/anatomy & histology/innervation ; Feeding Behavior/physiology ; HEK293 Cells ; Hot Temperature ; Humans ; *Infrared Rays ; Molecular Sequence Data ; Organ Specificity/genetics ; Phylogeny ; Predatory Behavior/physiology ; Protein Isoforms/chemistry/genetics/metabolism ; Protein Structure, Tertiary ; Sensation/*physiology ; TRPV Cation Channels/chemistry/*genetics/metabolism ; Trigeminal Ganglion/*metabolismPublished by: -
4Articles: DFG German National LicensesDíaz, A. Navas ; Sánchez, F. García ; García, J. A. GonzáLez
New York : Wiley-Blackwell
Published 1995Staff ViewISSN: 0884-3996Keywords: Luminol ; enhanced chemiluminescence ; phenolic acid ; Chemistry ; Biochemistry and BiotechnologySource: Wiley InterScience Backfile Collection 1832-2000Topics: BiologyChemistry and PharmacologyNotes: We explored the behaviour of a series of phenolic acids used as enhancers or inhibitors of luminol chemiluminescence by three different methods to determine if behaviour was associated with phenolic acid structure and redox character. All the phenolic acids inhibited chemiluminescence when hexacyanoferrate(III) was reacted with the phenolic acids before adding luminol. The redox character of these compounds was clearly related to structure. When hexacyanoferrate(III)-luminol-O2 chemiluminescence was initiated by phenolic acid-luminol mixtures some phenolic acids behaved as enhancers of chemiluminescence, and others as inhibitors. We propose a mechanism to explain these findings. We found direct relationships between the redox character of the phenolic acids and the enhancement or inhibition of the chemiluminescence of the luminol-H2O2-peroxidase system and we propose mechanism to explain these phenomena.Additional Material: 7 Ill.Type of Medium: Electronic ResourceURL: -
5Articles: DFG German National LicensesDíaz, A. Navas ; Sanchez, F. García ; García, J. A. González ; Del Rio, V. Bracho
New York : Wiley-Blackwell
Published 1995Staff ViewISSN: 0884-3996Keywords: Cholinesterase ; luminol ; pro-enhancer ; chemiluminescence ; Chemistry ; Biochemistry and BiotechnologySource: Wiley InterScience Backfile Collection 1832-2000Topics: BiologyChemistry and PharmacologyNotes: 2-Naphthyl acetate acts as a pro-enhancer of the luminol-H2O2-horseradish peroxidase reaction. Cholinesterase hydrolyses the bound acetyl group and produces 2-naphthol, and this compound is an enhancer of the chemiluminescent reaction. We studied the kinetics of chemiluminescent emission and the influence of 2-naphthyl acetate and cholinesterase enzyme concentration. The cholinesterase concentration versus chemiluminescence intensity maximum was linear for cholinesterase between 0 and 181 μU/mL, with a detection limit of 8 μU/mL and a relative standard deviation of 9.5% (n = 3), for a sample containing 90.67 μU/mL of cholinesterase.Additional Material: 5 Ill.Type of Medium: Electronic ResourceURL: -
6Articles: DFG German National LicensesOrozco, J. A. Gonzalez ; Rego, J. M. ; Katime, Issa
New York, NY [u.a.] : Wiley-Blackwell
Published 1990Staff ViewISSN: 0021-8995Keywords: Chemistry ; Polymer and Materials ScienceSource: Wiley InterScience Backfile Collection 1832-2000Topics: Chemistry and PharmacologyMechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision MechanicsPhysicsNotes: The dynamic mechanical properties of different low-density and linear low-density polyethylenes have been measured as a function of crystallization conditions. The mechanical results have been explained accounting for molecular segregation as well as reorganization capacity of the crystallizable segments during isothermal thickening. The presence of a high amount of segregated material does not allow detection of any relationship between crystallization conditions and mechanical relaxations for three of the four samples. The average values of the resonance relaxation temperatures and the relaxation strengths are dependent on branch content and branch type.Additional Material: 5 Ill.Type of Medium: Electronic ResourceURL: -
7Articles: DFG German National LicensesRego, J. M. ; Orozco, J. A. Gonzalez ; Katime, Issa
New York, NY [u.a.] : Wiley-Blackwell
Published 1990Staff ViewISSN: 0021-8995Keywords: Chemistry ; Polymer and Materials ScienceSource: Wiley InterScience Backfile Collection 1832-2000Topics: Chemistry and PharmacologyMechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision MechanicsPhysicsNotes: This work is aimed at determining the influence of molecular weight distribution, branch content, and thermal history on the dynamic mechanical properties of four high density polyethylenes. Molecular segregation as a function of crystallization conditions has been measured by means of differential thermal analysis, whereas infrared spectroscopy allowed us to relate the structural changes introduced by the use of different crystallization conditions with both molecular segregation and dynamic mechanical properties. The α-relaxation is the most affected transition by thermal treatments. Molecular segregation plays an important role in the mechanical behavior when the amount of segregated material is big enough as to shield the effect due to the isothermally thickened crystals. The presence of a high degree of segregation brings about asymmetry in the α-relaxation peak as well as detectable changes in the reorganization factor (which defines the degree of order within the system) obtained by infrared spectroscopy. The supermolecular structure is found not to affect the dynamic mechanical properties. The β-relaxation depends on the branch content, whereas the λ-relaxation remains constant regardless of structural characteristics and thermal conditions.Additional Material: 13 Ill.Type of Medium: Electronic ResourceURL: -
8Articles: DFG German National LicensesStaff View
ISSN: 1573-7284Keywords: S. sonnei ; Plasmid typing ; Epidemic ; Plasmid relationshipSource: Springer Online Journal Archives 1860-2000Topics: MedicineNotes: Abstract We conducted a surveillance program on epidemic and/or endemic Shigella strains in Asturias (Spain), their frequency and dispersion in our community, and their R-plasmids. We analyzed initial isolates of Shigella sonnei from two epidemic outbreaks using antibiotic resistance patterns and plasmid profile analysis as epidemiological markers. We found that the 2 outbreaks were caused by different S. sonnei strains, which respectively carried one and two R-plasmids together with other plasmids. The molecular relationship among these and three other R-plasmids from two S. sonnei strains isolated during a previous outbreak, were studied by restriction enzyme analysis and DNA-DNA hybridizations. We were able to establish different levels of relationship among the six R-plasmids.Type of Medium: Electronic ResourceURL: -
9Articles: DFG German National LicensesStaff View
ISSN: 0001-1541Keywords: Chemistry ; Chemical EngineeringSource: Wiley InterScience Backfile Collection 1832-2000Topics: Chemistry and PharmacologyProcess Engineering, Biotechnology, Nutrition TechnologyNotes: A new method is presented for the determination of adsorption equilibria for pure components and mixtures both at high and low pressures. Isotherms for carbon dioxide, methane, ethane, propane, i-butane, n-butane, i-pentane, and n-pentane on activated carbon (Columbia grade NXC 8/10) and on silica gel (Mobil Sorbead H) at 75°, 125°, 200°, and 300°F. are given for pressures ranging from below atmospheric to 1,000 lb./sq. in. Also, adsorption equilibria data are presented for several multicomponent mixtures of the light hydrocarbon gases.The data collected were correlated with good accuracy by use of the two-layer kinetic model developed previously by Gonzalez.Additional Material: 5 Ill.Type of Medium: Electronic ResourceURL: