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排序方式: 共有114条查询结果,搜索用时 31 毫秒
91.
DOMINIK LERMEN BRUNHILDE BLÖMEKE ROBERT BROWNE ANN CLARKE PAUL W. DYCE THOMAS FIXEMER GÜNTER R. FUHR WILLIAM V. HOLT KATARINA JEWGENOW RHIANNON E. LLOYD STEFAN LÖTTERS MARTIN PAULUS GORDON MCGREGOR REID DANIEL H. RAPOPORT DAVID RAWSON JENNIFER RINGLEB OLIVER A. RYDER GABRIELE SPÖRL THOMAS SCHMITT MICHAEL VEITH PAUL MÜLLER 《Molecular ecology》2009,18(6):1030-1033
Cryobanking, the freezing of biological specimens to maintain their integrity for a variety of anticipated and unanticipated uses, offers unique opportunities to advance the basic knowledge of biological systems and their evolution. Notably, cryobanking provides a crucial opportunity to support conservation efforts for endangered species. Historically, cryobanking has been developed mostly in response to human economic and medical needs — these needs must now be extended to biodiversity conservation. Reproduction technologies utilizing cryobanked gametes, embryos and somatic cells are already vital components of endangered species recovery efforts. Advances in modern biological research (e.g. stem cell research, genomics and proteomics) are already drawing heavily on cryobanked specimens, and future needs are anticipated to be immense. The challenges of developing and applying cryobanking for a broader diversity of species were addressed at an international conference held at Trier University (Germany) in June 2008. However, the magnitude of the potential benefits of cryobanking stood in stark contrast to the lack of substantial resources available for this area of strategic interest for biological science — and society at large. The meeting at Trier established a foundation for a strong global incentive to cryobank threatened species. The establishment of an Amphibian Ark cryobanking programme offers the first opportunity for global cooperation to achieve the cryobanking of the threatened species from an entire vertebrate class. 相似文献
92.
Sodium balance determines the extracellular fluid volume and sets arterial blood pressure (BP). Chronically raised BP (hypertension)
represents a major health risk in Western societies. The relationship between BP and renal sodium excretion (the pressure/natriuresis
relationship) represents the key element in defining the BP homeostatic set point. The renin–angiotensin–aldosterone system
(RAAS) makes major adjustments to the rates of renal sodium secretion, but this system works slowly over a period of hours
to days. More rapid adjustments can be made by the sympathetic nervous system, although the kidney can function well without
sympathetic nerves. Attention has now focussed on regulatory mechanisms within the kidney, including extracellular nucleotides
and the P2 receptor system. Here, we discuss how extracellular ATP can control renal sodium excretion by altering the activity
of epithelial sodium channels (ENaC) present in the apical membrane of principal cells. There remains considerable controversy
over the molecular targets for released ATP, although the P2Y2 receptor has received much attention. We review the available data and reflect on our own findings in which ATP-activated
P2Y and P2X receptors make adjustments to ENaC activity and therefore sodium excretion. 相似文献
93.
Tightly linked markers for the neurofibromatosis type 1 gene 总被引:15,自引:0,他引:15
Ray White Yusuke Nakamura Peter O''Connell Mark Leppert Jean-Marc Lalouel David Barker David Goldgar Mark Skolnick John Carey C. E. Wallis C. P. Slater Chris Mathew Bruce Ponder 《Genomics》1987,1(4):364-367
Relationships among genetic markers in the region of the neurofibromatosis type 1 (NF1) gene on chromosome 17 were investigated by linkage studies in a large sample set of affected families and in a panel of 58 normal families. A new marker, pHHH202 (D17S33), was included along with two markers known to be closely linked to NF. The maximum likelihood estimate of the recombination rate between the pHHH202 and NF1 loci was found to be O. Multilocus analysis suggested the following marker order: pA10-41-(p3-6, pHHH202); the NF1 gene fell with equal likelihood between either pA10-41-p3-6 or p3-6-pHHH202. The odds against NF1 being outside this cluster of tightly linked markers were greater than 15:1. 相似文献
94.
The role of iron in ferritin- and haemosiderin-mediated lipid peroxidation in liposomes. 总被引:7,自引:6,他引:1
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Ferritin and haemosiderin were shown, by the measurement of malondialdehyde production and loss of polyunsaturated fatty acids, to stimulate lipid peroxidation in liposomes. At pH 7.4 ascorbate was additionally required to achieve peroxidation; however, peroxidation occurred at pH 4.5 in the presence of iron-proteins alone. The damage was completely inhibited by the incorporation of chain-breaking antioxidants (alpha-tocopherol and butylated hydroxytoluene) into the liposomes. Metal chelators (desferrioxamine and EDTA) also completely inhibited lipid peroxidation. These and further results indicate that, at pH 4.5, even in the absence of a reducing agent, iron is released from haemosiderin and can mediate oxidative damage to a lipid membrane. 相似文献
95.
An extended genetic linkage map of markers for human chromosome 10 总被引:15,自引:0,他引:15
Yusuke Nakamura Mark Lathrop Tara Bragg Mark Leppert Peter O''Connell Carol Jones Jean-Marc Lalouel Ray White 《Genomics》1988,3(4):389-392
We have extended, in both directions, our recently published genetic map of markers for human chromosome 10 by the addition of 10 newly defined arbitrary loci. The map now covers 230 cM in males and 329 cM in females. In addition, three new markers, one of them a new RFLP at the IRBP gene locus, have been mapped in the vicinity of the locus responsible for multiple endocrine neoplasia type 2A (MEN2A). A significantly higher frequency of recombination in males than in females was observed near both ends of the new map. 相似文献
96.
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98.
The effects of L-tryptophan (50 mg/kg i.p.) on extracellular concentrations of tryptophan and the 5-hydroxytryptamine (5-HT) metabolite 5-hydroxyindoleacetic acid (5-HIAA) were determined in the rat striatum and cerebellum, regions with rich and poor 5-HT innervation, respectively. Determinations were on perfusates from dialysis probes in the brains of conscious, freely moving rats. The pharmacokinetic profiles of dialysate tryptophan after tryptophan load (peak concentration, time to peak concentration, area under curve, and half-life) in the two regions did not differ significantly. The dialysate 5-HIAA concentration in the striatum rose two- to threefold after the administration of tryptophan. Therefore, as 5-HIAA was undetectable in the cerebellum either before or after the administration of tryptophan, the increase of 5-HIAA in the striatum is unlikely to depend appreciably on its production within the cerebral vasculature or outside the brain or on its entering the striatum through a blood-brain barrier damaged by placement of the dialysis probe. Overall, the findings strengthen previous evidence that extracellular 5-HIAA concentrations determined by cerebral dialysis are a valid measure of the metabolism of 5-HT of brain neuronal origin. 相似文献
99.
Iron release from both human and horse spleen haemosiderin to desferrioxamine was substantially less than that released from ferritin samples. This finding contradicts a previous report [Kontoghiorges, Chambers & Hoffbrand (1987) Biochem. J. 241, 87-92]. Differences in phosphate content of cores and in core size between haemosiderin and ferritin did not account for the different iron-release rates. Iron released to acetate was found to stimulate lipid peroxidation in liposomes, whereas that released to stronger chelators such as citrate and desferal did not. Absorption spectra and gel-filtration studies suggest that the acetate-solubilized iron was in the form of low-molecular-mass (less than 5 kDa) ferrihydrite fragments. 相似文献
100.