Abstract: Fungicidal compounds of the general formula (I), wherein the substituents are as defined in claim 1.

Abstract: Compounds of the general Formula (1) wherein the substituents are as defined in claim 1, are useful as fungicides.

Abstract: Fungicidal compounds of the general formula (I), wherein the substituents are as defined in claim 1.

Abstract: Compounds of the general formula (I) wherein the substituents are as defined in claim 1, are useful as fungicides.

Abstract: The present invention relates to use of convertase inhibitors for the reduction of scarring during the healing of wounds and also for reducing fibrosis in the treatment of fibrotic conditions.

Abstract: Compounds of the general formula wherein the substituents are as defined in claim (1), are useful as fungicides.

Abstract: Compounds of the general formula (I); wherein the substituents are as defined in claim 1, are useful as fungicides.

Abstract: Compounds of the formula wherein the substituents are as defined in the claims, are useful as fungicides.

Abstract: A marker-tracking system includes an object, a marker illuminating device, a marker sensing device, and a computing device. The object includes a first retroreflective marker having a shape that is substantially defined by two spherical caps of different radii that are disposed substantially concentric in relation to one another. The marker illuminating device substantially illuminates the first retroreflective marker, the marker sensing device detects the illuminated first retroreflective marker and generates first data indicative of the location of the illuminated first retroreflective marker in space, and the computing device processes the first data generated by the marker sensing device to determine a position and/or orientation of the object in space.

Abstract: The invention relates to a reflector system for positioning a medical instrument or of body parts of a patient or for any determination of position, which is characterized by reflectors (3, 4, 5) that are configured as transparent retroreflective spheres and may consist of a material with a refractive index of preferably 1.9.

Abstract: The present invention relates to use of convertase inhibitors for the reduction of scarring during the healing of wounds and also for reducing fibrosis in the treatment of fibrotic conditions.

Abstract: The present invention relates to a method for quantifying the amount of active transforming growth factor beta (TGF-?) in biological samples. In particular the method comprising incubating cryosections of a tissue with cells which contain a TGF-? responsive expression vector having a structural region encoding an indicator protein and measuring the amount of said indicator protein expressed from the cells.

Abstract: The invention relates to a reflector system for positioning a medical instrument or of body parts of a patient or for any determination of position, which is characterized by reflectors (3, 4, 5) that are configured as transparent retroreflective spheres and may consist of a material with a refractive index of preferably 1.9.

Abstract: The present invention relates to a method for quantifying the amount of active transforming growth factor beta (TGF-&bgr;) in biological samples. In particular the method comprising incubating cryosections of a tissue with cells which contain a TGF-&bgr; responsive expression vector having a structural region encoding an indicator protein and measuring the amount of said indicator protein expressed from the cells.

Abstract: Compounds of the formula I in which R1 is C1-C4alkyl; R2 is cyano or NH2C(S)—; R3 is hydrogen, C1-C4alkyl, C1-C4haloalkyl, C3- or C4alkenyl, C3- or C4alkynyl, C3-C8haloalkenyl, NC—CH2—, HOC(O)—CH2— or C1-C4alkoxy-C(O)—CH2—; W is a group  and R4 to R6, R60, R61, R70, X1, X2, n1 and A1—B1 are as defined in claim 1, and the pyrazole N-oxide, agronomically acceptable salts and stereomers of these compounds of the formula I, with the exclusion of the compound of the formula  have good selective herbicidal properties when used pre- and post-emergence. The preparation of these compounds and their use as herbicidally active ingredients are described.

Abstract: Compounds of formula (I) in which A is ═N— or (a); W is a group (W1), (W2) or (W3); R11 is hydrogen, fluorine, chlorine, bromine or methyl; and R1 to R5, R13,n1 and n13 are as defined in claim 1, and the pyrazole N-oxydes, agrochemically tolerated salts and stereoisomers of these compounds of formula (I), have good pre- and post-emergent selective herbicidal properties. The preparation of these compounds and their use as herbidical active substances are described.

Abstract: Compounds of formula I ##STR1## wherein the substituents R.sub.1 and R.sub.6 and n are as defined in claim 1, and the salts and stereoisomers of the compounds of formula I have good pre- and post-emergence selective herbicidal properties.The preparation of those compounds and their use as herbicidal active ingredients are described.

Abstract: Compounds of formula (I) ##STR1## in which the substituents W, R.sub.100, R.sub.101 and R.sub.102 are as defined 1; and the pyrazole N-oxides, salts, complexes and stereoisomer of the compounds of (I) have good pre- and post-emergence selective herbicidal properties. The preparation compounds and their use as herbicidal active compounds are described.

Abstract: Thiadiazabicyclodecanes of formula (I) wherein, Z is oxygen or sulfur; R is an optional substituent and W is an optionally condensed or substituted phenyl radical and the salts, complexes and stereisomers thereof, have good selective pre- and post-emergence herbicidal properties.

Abstract: Compounds of the formula I ##STR1## in which R is hydrogen, fluorine or chlorine;R.sub.1 is hydrogen, halogen, trifluoromethyl, C.sub.1 -C.sub.4 haloalkoxy, cyano, nitro or amino;A-B is a group ##STR2## in which the 2 carbon atom is bonded to the oxygen atom; W is a group ##STR3## R.sub.2 is hydrogen or C.sub.1 -C.sub.6 -alkyl; R.sub.3 is C.sub.1 -C.sub.6 alkyl, C.sub.1 -C.sub.6 haloalkyl, cyano-C.sub.1 -C.sub.4 alkyl, hydroxy-C.sub.1 -C.sub.6 alkyl, C.sub.1 -C.sub.6 alkoxy-C.sub.1 -C.sub.6 alkyl, C.sub.3 -C.sub.6 alkenyloxy-C.sub.1 -C.sub.4 -alkyl, C.sub.3 -C.sub.6 alkynyloxy-C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.6 alkylcarbonyloxy-C.sub.1 -C.sub.6 alkyl, carboxyl, C.sub.1 -C.sub.6 alkoxycarbonyl, C.sub.1 -C.sub.6 haloalkoxycarbonyl, C.sub.3 -C.sub.6 alkenyloxycarbonyl, C.sub.3 -C.sub.6 alkynyloxycarbonyl, C.sub.3 -C.sub.6 cycloalkoxycarbonyl, C.sub.1 -C.sub.4 alkoxy-C.sub.1 -C.sub.4 alkoxycarbonyl, C.sub.1 -C.sub.4 alkylaminocarbonyl, di-C.sub.1 -C.sub.