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  • Crustal deformation (cf. Earthquake precursor: deformation or strain)  (4)
  • Male
  • Solar Physics
  • 1995-1999  (8)
  • 1950-1954
  • 1998  (8)
  • 1
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    In:  Geophys. Res. Lett., Amsterdam, Schweizerbart'sche Verlagsbuchhandlung, vol. 25, no. 18, pp. 3409-3412, pp. L07302, (ISSN 0016-8548, ISBN 3-510-50045-8)
    Publication Date: 1998
    Keywords: Crustal deformation (cf. Earthquake precursor: deformation or strain) ; Volcanology ; Geodesy ; GRL
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  • 2
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    In:  Geophys. Res. Lett., Luxembourg, Inst. Electrical & Electronics Engineers, vol. 25, no. 18, pp. 3413-3416, pp. B06303, (ISSN: 1340-4202)
    Publication Date: 1998
    Keywords: Crustal deformation (cf. Earthquake precursor: deformation or strain) ; Volcanology ; Geodesy ; GRL
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  • 3
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    In:  Phys. Earth Plan. Int., Potsdam, ZIPE, vol. 105, no. 3-4, pp. 167-181, pp. 2156, (ISBN: 0-12-018847-3)
    Publication Date: 1998
    Keywords: Geodesy ; Plate tectonics ; Seismicity ; Crustal deformation (cf. Earthquake precursor: deformation or strain) ; Review article ; PEPI
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  • 4
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    In:  Computers and Geosciences, Taipei, Academia Sinica, vol. 24, no. 2, pp. 173-182, pp. 2520, (ISSN: 1340-4202)
    Publication Date: 1998
    Keywords: Inversion ; Modelling ; Crustal deformation (cf. Earthquake precursor: deformation or strain) ; Dislocation ; Fault zone ; Source parameters ; Fernandez ; YuTT
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  • 5
    Publication Date: 1998-06-20
    Description: An efficient system for genetic modification and large-scale cloning of cattle is of importance for agriculture, biotechnology, and human medicine. Here, actively dividing fetal fibroblasts were genetically modified with a marker gene, a clonal line was selected, and the cells were fused to enucleated mature oocytes. Out of 28 embryos transferred to 11 recipient cows, three healthy, identical, transgenic calves were generated. Furthermore, the life-span of near senescent fibroblasts could be extended by nuclear transfer, as indicated by population doublings in fibroblast lines derived from a 40-day-old fetal clone. With the ability to extend the life-span of these primary cultured cells, this system would be useful for inducing complex genetic modifications in cattle.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cibelli, J B -- Stice, S L -- Golueke, P J -- Kane, J J -- Jerry, J -- Blackwell, C -- Ponce de Leon, F A -- Robl, J M -- New York, N.Y. -- Science. 1998 May 22;280(5367):1256-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Veterinary and Animal Sciences, University of Massachusetts, Amherst, MA 01003, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9596577" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Animals, Genetically Modified ; Blastocyst ; Cattle/embryology/*genetics ; Cell Aging ; Cell Division ; Cell Nucleus/genetics ; Cells, Cultured ; Clone Cells ; *Cloning, Organism ; Embryo Transfer ; Female ; Fetus/cytology ; Fibroblasts/*cytology ; G1 Phase ; Male ; Nuclear Transfer Techniques ; Oocytes/cytology ; Transfection ; Transgenes
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 6
    Publication Date: 1998-08-26
    Description: Experiences are remembered or forgotten, but the neural determinants for the mnemonic fate of experience are unknown. Event-related functional magnetic resonance imaging was used to identify specific brain activations that differentiated between visual experiences that were later remembered well, remembered less well, or forgotten. During scanning of medial temporal lobe and frontal lobe regions, subjects viewed complex, color photographs. Subjects later received a test of memory for the photographs. The magnitudes of focal activations in right prefrontal cortex and in bilateral parahippocampal cortex predicted which photographs were later remembered well, remembered less well, or forgotten.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Brewer, J B -- Zhao, Z -- Desmond, J E -- Glover, G H -- Gabrieli, J D -- New York, N.Y. -- Science. 1998 Aug 21;281(5380):1185-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Neuroscience Program and School of Medicine, Stanford University, Stanford, CA 94305, USA. brewer@psych.stanford.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9712581" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Brain/physiology ; Brain Mapping ; Female ; Humans ; Magnetic Resonance Imaging ; Male ; Memory/*physiology ; Memory, Short-Term ; Prefrontal Cortex/*physiology ; Temporal Lobe/*physiology ; Visual Perception
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 7
    Publication Date: 2019-07-10
    Description: We present a comparative analysis of the chromospheric solar limb prolateness, using strictly simultaneous H-alpha, ground-based observations and HeII space-based observations. The typical prolateness is found to be DeltaD/D = 5.5 x 10(exp -3) in HeII and 1.2 x 10(exp -3) in H-alpha. The first measurements in the 30.4 nm HeII line over a period of two years. as well as coronal data, are discussed to explore further the origin of the prolateness and its possible consequences.
    Keywords: Solar Physics
    Type: NOAO-Preprint-817 , Astronomy and Astrophysics
    Format: text
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  • 8
    Publication Date: 1998-07-04
    Description: Mutations in the gene encoding the homeobox transcription factor NKX2-5 were found to cause nonsyndromic, human congenital heart disease. A dominant disease locus associated with cardiac malformations and atrioventricular conduction abnormalities was mapped to chromosome 5q35, where NKX2-5, a Drosophila tinman homolog, is located. Three different NKX2-5 mutations were identified. Two are predicted to impair binding of NKX2-5 to target DNA, resulting in haploinsufficiency, and a third potentially augments target-DNA binding. These data indicate that NKX2-5 is important for regulation of septation during cardiac morphogenesis and for maturation and maintenance of atrioventricular node function throughout life.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schott, J J -- Benson, D W -- Basson, C T -- Pease, W -- Silberbach, G M -- Moak, J P -- Maron, B J -- Seidman, C E -- Seidman, J G -- New York, N.Y. -- Science. 1998 Jul 3;281(5373):108-11.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Genetics and Howard Hughes Medical Institute, Harvard Medical School, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9651244" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Atrioventricular Node/physiopathology ; Chromosome Mapping ; Chromosomes, Human, Pair 5 ; Codon ; Female ; Genes, Dominant ; Genetic Linkage ; Heart Block/*genetics/physiopathology ; Heart Septal Defects, Atrial/*genetics/physiopathology ; Homeodomain Proteins/*genetics/metabolism ; Humans ; Male ; Mice ; Molecular Sequence Data ; Mutation ; Pedigree ; Protein Biosynthesis ; Transcription Factors/*genetics/metabolism ; *Xenopus Proteins
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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