Chromosome 1 in human colorectal tumors.
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Aged↗
Biomedical subjects
S Neubauer
Publications and source records attributed to S Neubauer.
[Effect of modified labor posture on oxygenation of the fetus--a pulse oximetry study].
BACKGROUND: The evaluation of the birth position and its effects on maternal and fetal wellbeing has been a topic of perinatal research over the last decades. The aim of our observational study was to determine the effects of a modified and vertical maternal position on fetal oxygen saturation measured by pulse oximetry. METHODS: Fetal oxygen saturation was measured by pulse oximetry in 56 labouring women randomly and successively adopting the supine position in 96.4%, the sitting position in 25.0%, the standing position in 14.3% and the prone position in 12.5%. The statistical analysis addressed the integrated 10 minutes period of SpO2 registrations before versus after adopting the modified position. Furthermore the mean values and the standard deviation (SD) for the total registration periods of different birth position was calculated. RESULTS: While the supine position induced a reduction in oxygen saturation, sitting and prone position were favorable for fetal oxygenation as compared to horizontal position. DISCUSSION: These findings implicate a clinical benefit of the modified birth position.
Adult↗
Chromosome and oncogene studies in human rectal and colon carcinomas.
Cytogenetic examinations of 48 rectal and 17 colon carcinomas and analyses of proto-oncogene activation on 67 of the former and 8 of the latter tumors were performed. Besides a general considerable heterogeneity of chromosome counts, some chromosomes were found to contribute non-randomly to hypersomies (# 2, 3, 7, 9, 19, 20 and 6) and to hyposomies (# 14, 15, Y, 21, and 18) in this material. Chromosomal markers non-randomly involved breakpoint clusters on 17p11, 13q11, 7p, 1p11, and 1p36 and on the centromeric regions of chromosomes 1, 8, 14, 15 and 21. Cytogenetic equivalents of gene amplification ("double minutes") were present in only rather small cell fractions (less than 20%) of 50% of the studied tumors. Using a cDNA technique and a battery of respective probes, proto-oncogene overexpression was screened for in the tumor samples, but also in 24 samples of inconspicuous mucosae of tumor patients and in two mucosae of healthy individuals. Simultaneous overexpression of several proto-oncogenes was the most characteristic finding in the tumor cells. However several of the mucosa samples obtained from tumor patients also just exhibited clear signals of proto-oncogene overexpression, which were not found in epithelial cells from non-tumor patients.
Adult↗