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Osteology of hand and foot of Osornophryne simpsoni sp. n. in ventral view; adult male, QCAZ 45899. The molecular structure of the title compound. Displacement ellipsoids are drawn at the 30% probability level. [Symmetry code: (A) -x+1, y, -z+1/2.] The molecular structure of (I), with atom labels and 30% probability displacement ellipsoids for non-H atoms. The packing of (I), viewed along the c axis. Dashed lines indicate hydrogen bonds. H atoms not involved in hydrogen bonding have been omitted. The molecular structure of the title compound, drawn with 30% probability ellipsoids.
Schematic diagram showing the effect of coengagement of FcεRI with FcγRIIB. Coaggregation of FcεRI with FcγRIIB inhibits degranulation but not the induction of Bim and A1. MALDI-TOF spectra of pyrene-g-(TMPBA)n. Inset is extended from 500 to 700 amu A section of the structure of the title compound, showing the atomic numbering scheme with 30% probability displacement ellipsoids. [Symmetry codes: (i) 1-x, 1-y, 1-z. (ii)y, x-1, z. (iii) 2-x, 1-y,2-z.] A view of the molecule of (I) showing the atom-labelling scheme with displacement ellipsoids drawn at the 30% probability. The molecular structure of (I) showing the atom-labelling scheme. Displacement ellipsoids are drawn at the 30% probability level. Hydrogen atoms have been omitted for clarity.
The molecular structure of the title molecule, with the atom-numbering scheme. Displacement ellipsoids are drawn at the 30% probability level. The structure of the title compound showing 50% probability displacement ellipsoids. Schematic depiction of the procyclin loci in AnTat 1.1 and lineage of the knockouts [15].GPEET2 is a variant that has 5 rather than 6 copies of the pentapeptide repeat. Deletion constructs containing antibiotic-resistance genes were designed to delete tandemly linked procyclin genes by homologous recombination (see Materials and Methods). In the addback Δproc/EP2+, the neomycin-resistance gene was replaced by EP2 procyclin and the blasticidin resistance gene. The truncated 3′ UTR (ΔLII) downstream of EP2 ensures high levels of expression in procyclic forms [36], [40]. B: bloodstream form; P: procyclic form. Arrowhead: transmitted through tsetse and mice. The molecular structure of the title compound, showing displacement ellipsoids drawn at the 30% probability level. H atoms have been omitted for clarity. Schematic of the experimental setup for the excitations of enhanced evanescent fields in the microcavity and for successively changing the air-gap distance between two metals.
Overlap of expression profiles. Numbers within the 3 circles represent the genes that were differentially expressed according to our filters after 24 h treatment of MCF-7 cells with Cimicifuga racemosa (black cohosh) extract (CR), 17β-estradiol (E2) or tamoxifen (TAM). Numbers within the intersections represent genes regulated with both of the respective treatments or – in the middle – all 3 different treatments. For every intersection genes regulated in the same direction up or down (correlated) are marked with (+). Genes regulated in opposite directions (anti-correlated) are marked with (-). Molecular structure of the title compound. Displacement ellipsoids are drawn at the 30% probability level. H atoms have been omitted for clarity. The molecular structure of the title compound. Displacement ellipsoids are drawn at the 30% probability level. A view of the structure of (I), showing the atomic numbering scheme and 30% probability displacement ellipsoids. The molecular structure drawing for (I) showing 50% probability of displacement ellipsoids.
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