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Titlebook: Nucleic Acids and Protein Synthesis in Plants; L. Bogorad,J. H. Weil Book 1977 Springer Science+Business Media New York 1977 biology.molec

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E. C. Cockinglementary shortenings of tableau-based derivations, without increasing the size of the tableaux in any case. These speedups are based on restrictions of the sets of variables on which the Skolem-functions depend, that are introduced by the quantifier elimination rules. The effect corresponds to the
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DNA Synthesis During Microsporogenesisof chromosome organization that are probably not required for vegetative growth and reproduction. Even where mitotic crossing over does occur, its frequency is rare presumably because a supportive organization is lacking. An apparently loose form of pairing between homologous chromosomes has been re
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Structure of Chloroplast DNA weight of 90×10. with no evidence of inter- or intramolecular heterogeneity. Recently we have extensively studied the size and structure of ctDNAs from pea, bean, spinach, lettuce, corn, and oats.. As much as 89% of the ctDNAs from these higher plants has been obtained in circular form. The DNA pre
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Transcription of the Nuclear Genome of ,Hämmerling was one of the very first who developed such a hypothesis and called these transmitters “ morphogenetische Substanzen” (Hämmerling, 1932). The existence of such “ morphogenetische Substanzen” was concluded from experiments which were performed on the unicellular and uninuclear green alga
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Mode of Synthesis of Ribosomal RNA in Various Plant Organismsin the nucleolus as components of a single large precursor molecule from which they are released through a succession of intermediates. This holds true for certain animal cells and yeast, In other eukaryotes, especially in higher and lower plants, details of rRNA synthesis are less well understood.
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