Abstract: A jet type condenser comprises a shell (8). A plurality of multilayered inner water chambers (3,4) is arranged in the shell, multilayered outer water chambers (9,10) being correspondingly in communication with the inner water chambers (3,4) are arranged outside the shell (8), each of the outer water chambers (9,10) is in communication with a water source, the lower portion of the inner water chamber (4) in a bottom layer is an air-cooling area (6), and a water guiding tube (16) in communication with the air-cooling area (6) is arranged at the bottom of the inner water chamber (4) of the bottom layer.

Abstract: A muroid nasal device for intranasal delivery of compounds to the olfactory region.

Abstract: A jet type condenser comprises a shell (8). A plurality of multilayered inner water chambers (3,4) is arranged in the shell, multilayered outer water chambers (9,10) being correspondingly in communication with the inner water chambers (3,4) are arranged outside the shell (8), each of the outer water chambers (9,10) is in communication with a water source, the lower portion of the inner water chamber (4) in a bottom layer is an air-cooling area (6), and a water guiding tube (16) in communication with the air-cooling area (6) is arranged at the bottom of the inner water chamber (4) of the bottom layer.

Abstract: A DNA microarray device having probes immobilized to the microarray surface, in which targets to be detected using the microarray are exposed to the probes to hybridize therewith. There are provided on the microarray a quantity of a group of perfect match probes for a target of interest such that the molar ratio of each such probe to the target fragment is at least about 20:1.

Abstract: 7-oxabicyclo[2.2.1]heptadiene derivatives of formula (I) in which R1 and R2, independently of one another, represent hydrogen or methyl and R3 represents a group selected from —OR4; —SR5 and —NH—R6, wherein R4, R5 and R6 independently of one another, represent hydrogen, alkyl, optionally substituted aryl, optionally substituted aralkyl, optionally substituted heterocyclyl or optionally substituted heterocyclylalkyl, are very suitable for controlling undesired microorganisms and animal pests. New 7-oxabicyclo[2.2.1]heptadiene derivatives of formula (I) in which R3 represents a group selected from —SR5 and —NH—R6.

Abstract: 7-oxabicyclo[2.2.1]heptane derivatives of formula (I) in which X, R1, R2, R3 and R4 have the meanings set forth in the specification, are very suitable for controlling undesired microorganisms and animal pests. New 7-oxabicyclo[2.2.1]heptane derivatives of formula (Ia) in which X, R1, R2, R3 and R14 have the meanings set forth in the specification, and a process for the preparation of the new compounds.