Search results for "genetics [Transcriptome]"

showing 10 items of 3033 documents

Aminoguanidinium(2+) aminoguanidinium(1+) hexachloroantimonate(III) at 295 and 92 K

2001

The crystal and molecular structure of the title compound, (CH(7)N(4))(CH(8)N(4))[SbCl(6)], has been determined at 295 and 92 K. It is composed of isolated [SbCl(6)](3-) octahedra and aminoguanidinium mono- and dications. One of four of the crystallographically inequivalent aminoguanidinium cations is disordered at both temperatures. Two crystallographically inequivalent [SbCl(6)](3-) octahedra were found to possess three significantly longer Sb-Cl bonds than three other octahedra. The shorter bonds are in the range 2.456 (2)-2.577 (2) A, whereas the longer ones are between 2.705 (2) and 2.931 (2) A. Each short Sb-Cl bond is located trans to a long bond. It is argued that this deformation i…

CrystalCrystallographyOctahedronChemistryStereochemistryHydrogen bondMoleculeGeneral MedicineCrystal structureGeneral Biochemistry Genetics and Molecular BiologyActa Crystallographica Section C Crystal Structure Communications
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An improved goniometer head for high-temperature single-crystal X-ray diffraction

1999

A reliable and inexpensive goniometer head has been designed. Its stability, resulting from its compact construction, makes it very suitable for accurate measurements. Moreover, its space-saving design facilitates its application in X-ray data collection using charge-coupled device (CCD) detectors. This head has been improved for high-temperature measurements and has been tested by comparison of accurate K0.88Rb0.12TiOPO4data collected both at room temperature and at 973 K on the same crystal. The excellent structure results obtained at 973 K during the 360 h of measurements prove the stability of the goniometer head.

CrystalCrystallographyOpticsbusiness.industryChemistryGoniometerDetectorX-ray crystallographyHead (vessel)businessSingle crystalGeneral Biochemistry Genetics and Molecular BiologyJournal of Applied Crystallography
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1,2-Bis(methylsulfanyl)-1,2-dicarba-closo-dodecaborane(12)

2004

3 pages, 1 figure, 2 tables

Crystal-structures010405 organic chemistryStereochemistryHETEROBORANESBoranesGeneral MedicineCrystal structureBoraneDihedral angle010402 general chemistry01 natural sciencesGeneral Biochemistry Genetics and Molecular Biology3. Good health0104 chemical scienceschemistry.chemical_compoundCAGESchemistryCarboraneMoleculeCageMOLECULAR-STRUCTURECarborane
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Die Kooperativität bei der CO2-Hb-Bindung: Messungen mit Hilfe der 13C-NMR-Spektrometrie / The Cooperativity of the CO2 Hb Binding: Measurement by 13…

1979

The detailed structure of the CO2 Hb binding curve is of considerable physiological interest, because the carbamino derivates, which are formed by the reaction of CO2 with Hb, are respon­sible for the well known Haldane effect. Under physiological conditions CO2 binds to the four terminal NH2-groups of the protein chains of Hb and it is generally assumed, that there exists no cooperativity between these groups. To examine whether this assumption is correct or not, we have measured the CO2Hb binding curve over a wide PCO2-range (from 0 kPa to about 70 kPa) by using 13C-NMR spectrometry. Morrow and coworkers (1976) have shown that carbamino-Hb causes a specific NMR signal. The quantitative an…

CrystallographyChemistryCooperativityCarbon-13 NMRMass spectrometryGeneral Biochemistry Genetics and Molecular BiologyZeitschrift für Naturforschung C
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Cs[Ag4Zn2(SCN)9].

2002

Caesium tetrasilver dizinc nona­thio­cyanate, Cs[Ag4Zn2(SCN)9], forms a continuous structure, where the Ag atoms and the S atoms of the thio­cyanate groups form chains which run along [101]. These chains are bonded together through the Cs and Zn atoms. It is not possible to distinguish between space groups P1 and P\overline 1, but, if the latter space group is correct, the structure contains a thio­cyanate group disordered across a centre of inversion. The structure is described in space group P\overline 1, in which the Cs atom also lies on a centre of inversion.

CrystallographyChemistryGroup (periodic table)CaesiumAtomchemistry.chemical_elementSpace groupMoleculeGeneral MedicineCrystal structureSpace (mathematics)Inversion (discrete mathematics)General Biochemistry Genetics and Molecular BiologyActa crystallographica. Section C, Crystal structure communications
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X-ray investigation and discussion of the magnetostriction of Gd3T(T= Ni, Rh, Irx) single crystals

2000

The variations of the lattice parameters of Gd3T(T= Ni, Rh, Irx) single crystals with temperature were measured in the range 10–300 K. The compounds with Ni and Rh crystallize in the orthorhombic space groupPnma, but the compound with Ir crystallizes as Gd5Ir2in the monoclinic space groupA2/a. The three compounds exhibit an anomalous anisotropic spontaneous magnetostriction below the magnetic ordering temperature.

CrystallographyChemistryX-rayMagnetostrictionOrthorhombic crystal systemCrystal structureAnisotropyNéel temperatureGeneral Biochemistry Genetics and Molecular BiologyThermal expansionMonoclinic crystal systemJournal of Applied Crystallography
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Ab-initio crystal structure analysis and refinement approaches of oligo p-benzamides based on electron diffraction data.

2012

Ab-initio crystal structure analysis of organic materials from electron diffraction data is presented. The data were collected using the automated electron diffraction tomography (ADT) technique. The structure solution and refinement route is first validated on the basis of the known crystal structure of tri-p-benzamide. The same procedure is then applied to solve the previously unknown crystal structure of tetra-p-benzamide. In the crystal structure of tetra-p-benzamide, an unusual hydrogen-bonding scheme is realised; the hydrogen-bonding scheme is, however, in perfect agreement with solid-state NMR data.

CrystallographyElectron diffractionBasis (linear algebra)ChemistryAb initioGeneral MedicineCrystal structureNmr dataGeneral Biochemistry Genetics and Molecular BiologyElectron backscatter diffractionActa crystallographica. Section B, Structural science
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Microstructural evolution of mullites produced from single-phase gels

2007

The crystalline microstructure of mullites obtained by heating monophasic gels has been investigated. Gels with alumina to silica molar ratio of 3:2 (as in secondary mullite) and 2:1 (as in primary mullite) were prepared by gelling mixtures of aluminium nitrate and tetraethylorthosilicate. Phase transformations were induced by heating the gel precursors, with different final treatment temperatures between 1173 and 1873 K. The mullites formed as a result of thermal treatment were studied by means of X-ray diffraction, scanning electron microscopy and transmission electron microscopy. The crystalline structure (unit-cell parameters) and microstructure were determined from X-ray diffraction pa…

CrystallographyMaterials scienceChemical engineeringTransmission electron microscopyScanning electron microscopePhase (matter)NucleationMulliteThermal treatmentCrystalliteMicrostructureGeneral Biochemistry Genetics and Molecular BiologyJournal of Applied Crystallography
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Structural phase transition to disorder low-temperature phase in [Fe(ptz)6](BF4)2 spin-crossover compounds.

2012

In the spin-crossover compound [Fe(ptz)6](BF4)2 (where ptz=1-n-propyltetrazole) six different phases are observed. When a single crystal is slowly cooled from high temperatures to those below 125 K, the reflections broaden into diffuse maxima and split into two maxima along the c* direction [Kusz, Gütlich & Spiering (2004). Top. Curr. Chem. 234, 129–153]. As both maxima are broad along the c* direction, the short-range order exists only along the c direction and in the ab plane the structure remains long-range ordered. In this disordered phase additional satellite reflections appear. Upon heating above 135 K, the diffuse maxima return to their previous shape and this process is complete…

CrystallographyPhase transitionPolyhedronCondensed matter physicsSpin crossoverChemistryLattice (order)General MedicineMaximaCrystal twinningSingle crystalGeneral Biochemistry Genetics and Molecular BiologyIonActa crystallographica. Section B, Structural science
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Phase transition in bis(ethyldimethylammonium) pentachloroantimonate(III)

1999

The crystal structure of a new member of the alkylammonium chloroantimonate family, namely bis-(ethyldimethylammonium) pentachloroantimonate(III), [C 2 H 5 NH(CH 3 ) 2 ] 2 [SbCl 5 ], was determined at room temperature. The anionic sublattice consists of isolated distorted square-pyramidal [SbCl 5 ] 2- units and two crystallographically inequivalent disordered ethyldimethylammonium cations connected to anions by NH...Cl hydrogen bonds. The disorder is realised by the presence of two positions for all C, N and H atoms, and is explained as being a result of the overall reorientation of cations along the long axis of the molecule. One second-order phase transition was found at ca 160 K and resu…

CrystallographyPhase transitionPolymorphism (materials science)StereochemistryChemistryHydrogen bondMoleculeOrthorhombic crystal systemGeneral MedicineCrystal structureTriclinic crystal systemGeneral Biochemistry Genetics and Molecular BiologyMonoclinic crystal systemActa Crystallographica Section C-Crystal Structure Communications
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