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Biomedical subjects

U Weber

Publications and source records attributed to U Weber.

At least 199 records · Page 11Linked to original sources

Developmental expression of the white locus of Drosophila melanogaster.

We have isolated several cDNA clones of the white locus which are derived from embryonic and pupal transcripts of Drosophila melanogaster. The cDNA sequences map within 7.5 kb (coordinates -3.0 to +4.6) of the genomic DNA and correspond mainly to sequences within the distal region of the gene (coordinates -0.2 to -3.0). A major RNA species of 2.6 kb was detected on Northerns of poly(A) RNA isolated from all developmental stages. The total accumulation of this transcript peaks in the mature third instar larva to a level of 0.003% which is about ten times higher than that observed in embryos. The spatial distribution of white locus transcripts was determined by in situ hybridization to tissue sections. In embryos, hybridization signals are restricted to the cells of the developing Malpighian tubules and the signal strength corresponds with 50 transcripts per cell. Before the termination of the third instar stage, hybridization signals are also detected at a comparable level in the eye antennal disks. At the same stage, a third site of labeling is observed over a small cluster of cells which seems to be associated with the larval photoreceptor organs. Thus, white locus expression is largely restricted to tissues which are known to be involved in the biosynthesis of eye pigments and these different cell types act in a temporally autonomous manner with respect to the induction of the white gene during development.

Journal Article↗

Mathematical kinematics in engineering of endoprostheses. Evaluation of the results of gait analysis.

Certain optical methods (photogrammetry) achieve great precision in analysis of body motion. However, this study clearly shows that the tracing of body surface movement is unsuitable for analysis of actual joint motion, at least in the knee joint, because of the soft tissue shifting which occurs. It is also shown that comparatively simple mathematical-kinematic techniques can be used to check the degree of error of methods of measurement in orthopedics. It is to be assumed that no currently available knee joint prostheses function in a kinematically perfect manner. If the movement of knee joint prostheses is to be optimized and implantation errors affecting kinematics avoided, it seems indispensable, at the current level of technology, to employ X-ray stereophotogrammetry to describe natural knee joint motion.

Biomechanical Phenomena↗

[Albescent punctate retinopathy with central pigment epithelium atrophy].

A 45-year-old Italian patient suffering from punctate retinopathy associated with a central atrophy of the retinal pigment epithelium is described. He has suffered from nyctalopia since early childhood, and over the last 3 years has become increasingly susceptible to dazzling. Funktion tests revealed pathologic monofunctional dark adaptation of cones, centrocecal scotoma, a pathologic electro-oculogram and residual a-waves at high light stimulus intensities in the electroretinogram. An autosomal-recessive mode of inheritance is assumed, as 4 of the patient's 9 siblings have the same signs.

Electrooculography↗

[Crystalline chorioretinopathy with marginal corneal involvement].

The authors describe central and peripapillary chorioretinal dystrophies seen in 3 patients. In 2 of them a crystalline chorioretinal dystrophy was found. This is compared to the "simple" chorioretinal dystrophy of the third patient. Crystalline deposits in the limbus corneae were found in both patients with crystalline chorioretinopathy. Higher serum cholesterol levels and more widespread chorioretinal dystrophy are associated with greater corneal involvement. Visual acuity, central scotomata and the changes in the electroretinograms correlate with the chorioretinal dystrophy. The crystalline chorioretinopathy found in these patients is associated with Fredriksen's phenotype II, whereas the "simple" form of chorioretinal dystrophy is associated with multiple lipoprotein-type hyperlipidemia.

Aged↗

Denervation reduces extractable Met-enkephalin-like immunoreactivity in guinea-pig lips.

Skin extracts of the upper lip of 18 guinea pigs were made and subjected to a Met-enkephalin radioimmunoassay 3-4 weeks, 8 weeks, and 12 weeks after transection of one infraorbital nerve. There was a significant reduction in the concentration of extractable Met-enkephalin-like immunoreactivity in the denervated half of the lip as compared to the innervated side. The reduction increased with time. These results show that the enkephalin content of the guinea pig upper lip depends on an intact innervation by the infraorbital nerve.

Animals↗

[Variability of iris fluorescence angiograms].

Fluorescein angiography of the iris vascular system is more difficult in heavily pigmented irides of the coloured races; in light skinned patients it is easy to perform and even more details are demonstrated in patients with atrophies of the mesodermal iris structure. In congenital albinism very fine vascular structures are demonstrated in younger patients; a similar picture is seen in pupillotonia if there is atrophy of the iris stroma. In senile iris atrophies, Adie's syndrome and congenital albinism the iris vascular structure is basically normal, but atrophy of the iris stroma may lead to increased fluorescein permeability in the elderly.

Adult↗

[Endothelial changes in posterior polymorphous corneal dystrophy].

Posterior polymorphous dystrophy of the cornea (Schlichting) was found in a 51-year-old male. In addition, the patient had a cerulean cataract and myopia. The PPD, which was thought to have been caused by endothelial degeneration, exhibited extremely variable expressivity. Of the patient's 3 children only the 19-year-old son, who is also myopic, has cerulean cataract; on specular microscopic examination he was also found to be suffering from endothelial changes.

Adult↗

[Rubinstein-Taybi syndrome and juvenile glaucoma].

In a six-year-old girl with Rubinstein-Taybi syndrome the ophthalmological findings were as follows: bushy brows, hypertelorism, epicanthus, an antimongoloid slant to the eyelids and hyperopia with an alternating convergent squint. In the sixth year of life juvenile glaucoma with deep cupping of the disk was found.

Abnormalities, Multiple↗

[Iris angiography and endothelium microscopy in dysgenesis mesodermalis iridis et corneae].

Three patients with endothelialization of the anterior chamber - 2 with Chandler's syndrome and 1 with Cogan-Reese syndrome - were followed up by means of iris angiography and specular microscopy over a period of several years. The endothelial angiographic changes occurred simultaneously in all cases; the more pronounced the endothelial changes, the more severe the iris changes. Since iris stroma and corneal endothelium develop from a common mesenchymal origin, and the extent of the changes they undergo is similar in the course of the diseases in question, a close relationship between Rieger's mesodermal dysgenesis, Chandler's syndrome and Cogan-Reese syndrome is postulated.

Adult↗

[Clinical course in Bietti crystalline tapetoretinal degeneration].

The course of Bietti's crystalline retinopathy, which has an autosomal-recessive mode of inheritance, is described with reference to three families. Initially, crystals appear in the inner and middle layers of the retina; in the third decade of life atrophy of the retinal pigment epithelium and of the choroid sets in. Secondary degeneration of the center of the retina results in the disappearance of the crystals in the degenerated areas.

Adult↗

Met- and leu-enkephalin immuno- and bio-reactivity in human stomach and pancreas.

Acid extracts of human pancreas and gastric corpus and antral mucosa and muscularis were investigated for the presence of met-enkephalin and leu-enkephalin by radioimmunoassay, Sephadex chromatography and radioreceptor assay. As the assays for leu-enkephalin crossreacted with those for met-enkephalin, only cyanogen bromide-treated samples were used for the determination of leu enkephalin. Met-enkephalin immunoreactivity was destroyed by more than 94% when treated with cyanogen bromide. Serial extract dilutions displaced 125 I labelled met-enkephalin and 125 I leu-enkephalin in the respective enkephalin radioimmunoassay both roughly parallel to the standard curves. Sephadex chromatography of the extracts resulted in elution of met-enkephalin and leu-enkephalin immunoreactivity similar to the size of 3H-met-enkephalin, and these eluates displaced 3H-met-enkephalin from rat brain membranes in an opioid radioreceptor assay. The highest concentration of met-enkephalin and leu-enkephalin immunoreactivity in tissue obtained at surgery was in the mucosa of the body of the stomach. Met- and leu-enkephalin receptor bioreactivity concentrations exceeded immunoreactivity concentrations. These investigations provide evidence of the presence of met-enkephalin- and leu-enkephalin-like substances in human stomach and pancreas.

Chromatography, Gel↗

[Ultrasonic modelling of bone cement - (reoperation of total hip endoprosthesis) (author's transl)].

In medicine ultrasound is very common in diagnostic and therapeutic applications, in surgery especially as so-called ultrasonic lithotripsy. Up to now experiences in bone surgery are not very successful. Bone cement (PMMA) is a thermoplastic material. Therefore results of ultrasonic lithotripsy cannot be simply transmitted. Investigations show that, because of their thermoplastic quality, the ultrasonic method may be helpful in modelling bone cement, for example in changing endoprosthesis. The preconditions for the use of high frequent oscillating probes are examined experimentally. The necessary visual distinction of bone cement and natural bone may be intensified by fluorochrome labelling of cement.

Bone Cements↗

[Morphological and functional findings in a family with aniridia (author's transl)].

The history of a family with aniridia (11 patients) is presented. Morphologically the following changes were found: Ptosis, microcornea, anterior embryotoxon, defects of the iris ranging from corectopia and coloboma to hypoplasia of the iris and clinical aniridia cataracts and hypoplasia of the fovea. Functionally there was reduced visual acuity (best vision 0.2), nystagmus and strabismus. Dark adaptation, electrooculogram, photopic and scotopic electroretinogram were within normal limits. The patients were found to have a red-green color vision deficiency, which was perhaps caused by foveal hypoplasia and nystagmus, and a trito defect which could not be explained.

Adolescent↗