| 1. |
- Bremer, Kåre, et al.
(författare)
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An ordinal classification for the families of flowering plants
- 1998
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Ingår i: ANNALS OF THE MISSOURI BOTANICAL GARDEN. - : MISSOURI BOTANICAL GARDEN. - 0026-6493. ; 85:4, s. 531-553
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Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
- Recent cladistic analyses are revealing the phylogeny of flowering plants in increasing detail, and there is support for the monophyly of many major groups above the family level. With many elements of the major branching sequence of phylogeny established
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| 2. |
- Eudy, James D., et al.
(författare)
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Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa
- 1998
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Ingår i: Science. - : American Association for the Advancement of Science (AAAS). - 0036-8075 .- 1095-9203. ; 280:5370, s. 1753-1757
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Tidskriftsartikel (refereegranskat)abstract
- Usher syndrome type IIa (OMIM 276901), an autosomal recessive disorder characterized by moderate to severe sensorineural hearing loss and progressive retinitis pigmentosa, maps to the long arm of human chromosome 1q41 between markers AFM268ZD1 and AFM144XF2. Three biologically important mutations in Usher syndrome type IIa patients were identified in a gene (USH2A) isolated from this critical region. The USH2A gene encodes a protein with a predicted size of 171.5 kilodaltons that has laminin epidermal growth factor and fibronectin type III motifs; these motifs are most commonly observed in proteins comprising components of the basal lamina and extracellular matrixes and in cell adhesion molecules.
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| 3. |
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| 4. |
- Andersin, Michael, et al.
(författare)
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Subspace based estimation of the signal to interference ratio for TDMA cellular systems
- 1998
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Ingår i: Wireless networks. - : ACM/Kluwer Academic Publishers. - 1022-0038 .- 1572-8196. ; 4:4, s. 241-247
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Tidskriftsartikel (refereegranskat)abstract
- The Signal-to-Interference Ratio (SIR) has been highlighted in the literature to be a most efficient criterion for several methods aiming at reducing the effects of cochannel interference, e.g., diversity reception, dynamic channel allocation and power control. In this paper we address the problem of how to obtain fast and accurate measurements of this parameter in a practical context. We develop a general SIR estimation technique for narrow-band cellular systems that is based on a signal subspace approach using the sample covariance matrix of the received signal. Simulation results using the frame structure in the GSM system show that the SIR can be estimated to within an error of 0.3 dB after only 200 ms, or within an error of 0.1 dB after only 0.6 seconds.
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| 5. |
- Chang, W, et al.
(författare)
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Parathyroid Ca(2+)-conducting currents are modulated by muscarinic receptor agonists and antagonists.
- 1997
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Ingår i: The American journal of physiology. - 0002-9513. ; 273:5 Pt 1
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Tidskriftsartikel (refereegranskat)abstract
- Parathyroid cells express Ca(2+)-conducting cation currents, which are activated by raising the extracellular Ca2+ concentration ([Ca2+]o) and blocked by dihydropyridines. We found that acetylcholine (ACh) inhibited these currents in a reversible, dose-dependent manner (50% inhibitory concentration approximately equal to 10(-8) M). The inhibitory effects could be mimicked by the agonist (+)-muscarine. The effects of ACh were blunted by the antagonist atropine and reversed by removing ATP from the pipette solution (+)-Muscarine enhanced the adenosine 3',5'-cyclic monophosphate (cAMP) production by 30% but had no effect on inositol phosphate accumulation in parathyroid cells. Oligonucleotide primers, based on sequences of known muscarinic receptors (M1-M5), were used in reverse transcriptase-polymerase chain reaction (RT-PCR) to amplify receptor cDNA from parathyroid poly (A)+ RNA. RT-PCR products displayed > 90% nucleotide sequence identity to human M2- and M4-receptor cDNAs. Expression of M2-receptor protein was further confirmed by immunoblotting and immunocytochemistry. Thus parathyroid cells express muscarinic receptors of M2 and possibly M4 subtypes. These receptors may couple to dihydropyridine-sensitive, cation-selective currents through the activation of adenylate cyclase and ATP-dependent pathways in these cells.
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| 6. |
- Hallberg, Eva C., 1966, et al.
(författare)
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Chemical and lectin-gold electron microscopical studies of the expression of the Galalpha1-determinant in the pig aorta.
- 1998
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Ingår i: Xenotransplantation. - 0908-665X. ; 5:4, s. 246-56
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Tidskriftsartikel (refereegranskat)abstract
- In the xenotransplantation research field, pig aortic endothelial cells are frequently used in different model systems, e.g., for the study of the xenoantibody-antigen reaction. The Gal(alpha1),3Gal determinant is the major target for human xenoreactive antibodies in pig tissue. Characterisation of the Gal(alpha1)- distribution in pig aortic endothelial cells is thus important for understanding the reaction occurring at the endothelial cells during the xenorejection. We have determined the complete structure of the major Gal(alpha1),3Gal terminated glycolipid, Gal(alpha1),3nLc4Cer. Structural studies were performed on isolated glycosphingolipids by mass spectrometry and NMR spectroscopy. The results show a predominance of the pentasaccharide among the Gal(alpha1)-terminated glycolipids but also the presence of several Gal(alpha1)-terminated glycolipids with extended carbohydrate core chains. Ultrastructural localisation of the Galalpha1-antigen in pig aorta was done by lectin-gold electron microscopic studies of aortic wall sections using the Griffonia simplicifolia isolectin B4. Gal(alpha1)-determinants are predominantly localised on the luminal surface of pig aortic endothelial cells and endothelial cells of vasa vasorum and, to a lesser extent, vascular subendothelium.
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