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  • variation  (3)
  • Molecular Sequence Data  (2)
  • Springer  (3)
  • American Association for the Advancement of Science (AAAS)  (2)
  • Springer Nature
  • 2020-2022
  • 1985-1989  (5)
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  • Springer  (3)
  • American Association for the Advancement of Science (AAAS)  (2)
  • Springer Nature
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Entomologia experimentalis et applicata 44 (1987), S. 177-185 
    ISSN: 1570-7458
    Keywords: spotted alfalfa aphid ; Therioaphis trifolii ; aphid-resistant plants ; lucerne = alfalfa ; Medicago sativa ; variation ; bioassay ; antibiosis non-preference ; inter-plant movement
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Description / Table of Contents: Résumé L'étude de la multiplication initiale des effectifs de T. trifolii, élevés au laboratoire sur pousses de différents pieds de luzerne, a servi de test d'antibiose pour les cultures en plein champ. La distribution de l'antibiose, dans des échantillons importants de plantes appartenant à des cultivars sélectionnés pour leur résistance aux pucerons, a présenté une forme en J, c'est-à-dire que la majorité des plantes était très résistante, quelques unes apparemment sensibles, et un certain nombre intermédiaires entre ces deux extrêmes. Pour un niveau donné d'antibiose, la reproduction, la mortalité et ainsi la distribution initiale en âges dans les populations de pucerons ont été généralement identiques. La multiplication végétative de plantes présentant un gradient de résistance à l'intérieur d'un cultivar et l'utilisation d'un plan de distribution des boutures ont permis l'étude de ce qui semble être l'effet de l'hétérogénéité spatiale sur la résistance des cultures aux attaques de pucerons. La simulation d'une invasion de la culture par les pucerons en plaçant des adulte sur toutes les boutures d'un rang ne pouvait donner une explication de la croissance de la population que si les pucerons se déplacaient le long du rang pour découvrir et exploiter les pieds les plus sensibles. Une distribution par taches, comme on peut l'envisager dans un champ, ne devrait pas gêner les pucerons, car bien que les mouvements d'évasion soient stimulés par les niveaux de résistance élevés (de non-préférence), on peut en déduire que les pucerons se déplaceront sur des plantes très résistantes, eventuellement pour atteindre des plantes moins résistantes placées derriere.
    Notes: Abstract Initial population growth of spotted alfalfa aphid reared on shoots cut from individual lucerne plants, was tested and used as a realistic bioassay of antibiosis. Within cultivars selected for aphid-resistance there was a J-shaped distribution of antibiosis between plants of the crop, the majority being highly resistant, a few apparently susceptible and a proportion partly-resistant. For a given level of antibiosis, reproduction, mortality and thus initial age distribution of aphid populations were generally similar. Vegetative cloning of plants from the range of resistance available in a cultivar has allowed studies of the likely effect of spatial variation of resistance in crops on aphid infestations, using experimental arrays of cut shoots. Simulation of aphid invasion of crops by the placement of adults on all shoots of an array gave results explicable only if the aphids moved through the array to find and breed on the more susceptible plants. A patchy arrangement of these, as might be expected in a field crop, would not hinder the aphids, for although movement off a plant is stimulated by higher resistance (non-preference) levels, it was inferred that aphids will move onto higher resistance plants, eventually to reach lower resistance plants beyond.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-4927
    Keywords: amylase ; chicken ; variation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Amylase allozymic and activity variation was studied in three flocks of chickens (Gallus domesticus). Individuals from one flock were studied to assess the effects of sex, tissue, and genotype on amylase activity. Additionally, the allozymes were purified and their specific activities compared. Variation was observed within and among the flocks. Two alleles were found to be segregating in the flocks, one flock being polymorphic and the other two monomorphic. Mean amylase activities among the three flocks were significantly different. The relationship of this activity variation to regulatory variation is discussed. There were no significant effects of sex or genotype on amylase activity and, in most cases, no correlation between activities in the various tissues. However, in heterozygotes one of the alloamylases had much lower activity than the other.
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  • 3
    ISSN: 1573-4927
    Keywords: amylase ; chicken ; variation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Amylase allozymic and activity variation was studied in three flocks of chickens (Gallus domesticus). Individuals from one flock were studied to assess the effects of sex, tissue, and genotype on amylase activity. Additionally, the allozymes were purified and their specific activities compared. Variation was observed within and among the flocks. Two alleles were found to be segregating in the flocks, one flock being polymorphic and the other two monomorphic. Mean amylase activities among the three flocks were significantly different. The relationship of this activity variation to regulatory variation is discussed. There were no significant effects of sex or genotype on amylase activity and, in most cases, no correlation between activities in the various tissues. However, in heterozygotes one of the alloamylases had much lower activity than the other.
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  • 4
    Publication Date: 1989-11-03
    Description: A complementary DNA (cDNA) for ubiquitin carboxyl-terminal hydrolase isozyme L3 was cloned from human B cells. The cDNA encodes a protein of 230 amino acids with a molecular mass of 26.182 daltons. The human protein is very similar to the bovine homolog, with only three amino acids differing in over 100 residues compared. The amino acid sequence deduced from the cDNA was 54% identical to that of the neuron-specific protein PGP 9.5. Purification of bovine PGP 9.5 confirmed that it is also a ubiquitin carboxyl-terminal hydrolase. These results suggest that a family of such related proteins exists and that their expression is tissue-specific.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wilkinson, K D -- Lee, K M -- Deshpande, S -- Duerksen-Hughes, P -- Boss, J M -- Pohl, J -- New York, N.Y. -- Science. 1989 Nov 3;246(4930):670-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry, Emory University School of Medicine, Atlanta, GA 30322.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2530630" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; B-Lymphocytes/enzymology ; Base Sequence ; Cattle ; DNA/genetics ; Humans ; Isoenzymes/genetics ; Molecular Sequence Data ; Neuropeptides/*genetics/isolation & purification ; Sequence Homology, Nucleic Acid ; Thiolester Hydrolases/*genetics/isolation & purification ; Ubiquitin Thiolesterase
    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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  • 5
    Publication Date: 1988-12-23
    Description: Hypocalcemic vitamin D-resistant rickets is a human genetic disease resulting from target organ resistance to the action of 1,25-dihydroxyvitamin D3. Two families with affected children homozygous for this autosomal recessive disorder were studied for abnormalities in the intracellular vitamin D receptor (VDR) and its gene. Although the receptor displays normal binding of 1,25-dihydroxyvitamin D3 hormone, VDR from affected family members has a decreased affinity for DNA. Genomic DNA isolated from these families was subjected to oligonucleotide-primed DNA amplification, and each of the nine exons encoding the receptor protein was sequenced for a genetic mutation. In each family, a different single nucleotide mutation was found in the DNA binding domain of the protein; one family near the tip of the first zinc finger (Gly----Asp) and one at the tip of the second zinc finger (Arg----Gly). The mutant residues were created in vitro by oligonucleotide directed point mutagenesis of wild-type VDR complementary DNA and this cDNA was transfected into COS-1 cells. The produced protein is biochemically indistinguishable from the receptor isolated from patients.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hughes, M R -- Malloy, P J -- Kieback, D G -- Kesterson, R A -- Pike, J W -- Feldman, D -- O'Malley, B W -- New York, N.Y. -- Science. 1988 Dec 23;242(4886):1702-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Cell Biology, Baylor College of Medicine, Houston, TX 77030.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2849209" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Binding Sites ; Calcitriol/metabolism ; Cell Line ; Cell Line, Transformed ; Codon ; DNA/genetics/metabolism ; Exons ; Female ; Gene Amplification ; Homozygote ; Humans ; Hypocalcemia/*genetics ; Immunoblotting ; Male ; Molecular Sequence Data ; *Mutation ; Receptors, Calcitriol ; Receptors, Steroid/*genetics/metabolism ; Rickets/*genetics ; Transfection
    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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