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751.
Counterflow centrifugation with continuous monitoring of the output for cell number and cell scatter was used to separate low density (d less than 1.070 g/ml) human bone marrow cells in two fractions: one containing the majority of small size lymphocytes and the other the majority of the larger sized committed progenitor cells. The recovery of the pluripotent stem cells (CFU-GEMM) in the large cell fraction was complete. The mitogenic reactivity of this putative stem cell fraction had decreased to 6% and 11%, of the original value as measured with phytohemagglutinin stimulation and one way mixed lymphocytic culture respectively. Counterflow centrifugation offers a physical separation technique, by which the majority of the immunoreactive cells can be separated from the pluripotent hematopoietic stem cells.  相似文献   
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The advancement of recreational activities into wildlife habitat calls for a better knowledge about the effects of human-induced disturbances, particularly in systems where humans dominate wildlife mortality. We exposed nine adult free-ranging female moose repeatedly to off-trail backcountry skiing to study moose behavior and habituation using a controlled field experiment in Northern Sweden. Moose response was short-term, but distinct. Moose moved 33-fold faster during the first hour following disturbance, resulting in almost a doubling of the energetic usage per kilogram body weight. Movement rates increased 3 h following disturbances, came along with enlarged activity ranges at the day of disturbance, and resulted in moose leaving the original area. We found no evidence for habituation. Because of the short-term response, the effect of single skiing disturbance events on the overall energy budget of large-bodied animals in good body condition is likely to be negligible. We recommend off-trail skiers to avoid following wildlife tracks because such disturbances bear risk for more severe consequences on wildlife's energy budget if wildlife resists habituation, if an animal's risk perception is high, or when the frequency of disturbance increases.  相似文献   
755.
The pattern of protein synthesis in various coisogenic mycelial types of Schizophyllum commune, viz. monokaryon, dikaryon, and homokaryons carrying primary mutations in the A and the B factors, was studied by two-dimensional gel electrophoresis. After pulse-labeling with 35S-methionine, approximately 650 of 710 proteins analyzed were common to all mycelial types. Coisogenic monokaryons differed by only 2%, whereas the largest difference was found between these monokaryons and the dikaryon derived from them (6.6 and 7.7%). The majority of these differences fell into two about equally sized categories, i.e., proteins which were either specifically absent (“switched-off” proteins) or present (“switched-on” proteins) in the dikaryon. “Switched-on” proteins were on the average larger and slightly more acidic than “switched-off” proteins. The double factor mutant which best mimicked the dikaryon in morphology also best resembled the dikaryon in types of proteins synthesized. Unexpected, however, was the large overlap in proteins apparently controlled by each of the two incompatibility factors individually, despite the distinct morphological sequences directed by each of them.  相似文献   
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Summary Fruiting in the basidiomycete Schizophyllum commune readily occurs in a homokaryon with constitutive mutations in both the A and B mating-type genes. Such a homokaryon frequently expresses a mutation, fbf, which completely blocks fruiting and leads to a somewhat faster growth rate. The mutation is unlinked to the A and B genes, frequently reverts to its wild-type allele, and is recessive with respect to fruiting in matings with wild-type homokaryons. The mutation suppresses the accumulation of a number of mRNAs which are regulated by the mating-types genes and are specific for fruiting. The expression of the Sc-3 gene, structurally related to two of the fruiting genes (Sc-1 and Sc-4) but not regulated by the mating-type genes, is unaffected.  相似文献   
758.
Nonradioactive in situ hybridization (ISH) using biotinylated centromere probes for chromosomes 1, 6, 7, 10, 16, 17, 18, and the X, respectively, was combined with GTG-banding to study cytogenetic changes in two different ovarian cancer cell lines. ISH was performed after GTG-banding on the same metaphase. The use of a low trypsin concentration (0.01%) in the banding procedure was essential for subsequent ISH. This combined approach allows the detection of subtle chromosomal rearrangements and appears to aid the identification of marker chromosomes.  相似文献   
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