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Watson james dewey (18 Ergebnisse)

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  • Sprache: Englisch

    Verlag: PENGUIN BOOKS LTD (edition first penguin edition), 1971

    0140031421 / 9780140031423

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    Paperback. Zustand: Very Good. first penguin edition. It's a well-cared-for item that has seen limited use. The item may show minor signs of wear. All the text is legible, with all pages included. It may have slight markings and/or highlighting.

  • Sprache: Englisch

    Verlag: PENGUIN BOOKS LTD, 1971

    0140031421 / 9780140031423

    • Softcover

    Anbieter: Hay-on-Wye Booksellers, Hay-on-Wye, HEREF, Vereinigtes KönigreichHay-on-Wye Booksellers

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    Zustand: Good. Different cover design. Creases/fading/scuffs to spine. Scratches/creases/scuffs to cover. Marks/scratches to textblock edges. Tanning/some foxing to pages. Text good.

  • Verlag: Kagaku Dojin, Kyoto, 1973

    • Hardcover

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    Hardcover. Zustand: Fine. Octavo in dark turqoise cloth and while color ilus DJ; 291 + index, illus. ** Volume two only ** Second edition of Molecular Biology of the Gene, translated assumedly for the first time (the second ed.) into Japanese. Uncommon. Fine in near fine(-) to very good lightly soiled and redge-ubbed DJ with small chip to upper rear edge, about 1 x .25 inches.…

  • Sprache: Englisch

    Verlag: San Francisco: W. H. Freeman, 1981., 1981

    071671292X / 9780716712923

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    Hardcover. Zustand: Fine. Zustand des Schutzumschlags: Fine. 1st Edition. xvi, 1 leaf, 605 pp; illus. Original cloth, small 4to. Near Fine, in near fine dust jacket.

  • Sprache: Japanisch

    Verlag: Kodansha., 2012

    4062577925 / 9784062577922

    • Softcover

    Anbieter: Revaluation Books, Exeter, Vereinigtes KönigreichRevaluation Books

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    Paperback Shinsho. Zustand: Brand New. Japanese language. 6.93x4.41x0.71 inches. In Stock.

  • Verlag: Paris : R. Laffont, 1968

    • Softcover
    • Erstausgabe

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    In den Warenkorb

    soft cover. Zustand: very good. first edition. ln-8°broché, 179 pages.

  • Sprache: Französisch

    Verlag: Hachette Littératures, 1984

    2010099613 / 9782010099618

    • Softcover

    Anbieter: RECYCLIVRE, Paris, FrankreichRECYCLIVRE

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    Zustand: Assez bon. Merci, votre achat aide à financer des programmes de lutte contre l'illettrisme.

  • Sprache: Französisch

    Verlag: R. Laffont, 2003

    2221098978 / 9782221098974

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  • Sprache: Französisch

    Verlag: Hachette Littératures, 1999

    2012789757 / 9782012789753

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  • Sprache: Französisch

    Verlag: O. Jacob, 2003

    2738113362 / 9782738113368

    • Softcover

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    • Hardcover

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    In den Warenkorb

    Mit einer Einführung von H.Haber. - Hamburg 1971, 8°, 287 pp., zahlr. Abbildungen, orig. Leinenband.

  • Sprache: Französisch

    Verlag: ROBERT LAFFONT, 2003

    2221098978 / 9782221098974

    • Softcover

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    EUR 107,40

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    paperback. Zustand: Good. Good. Dust Jacket NOT present. CD WILL BE MISSING. . SHIPS FROM MULTIPLE LOCATIONS. book.

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    Zustand: Gebraucht

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    First edition. The Molecule That Copies Itself. First edition, in the rare three-paper offprint issue - the author's separate that gathers the whole of the 25 April 1953 Nature announcement - of the discovery of the molecular structure of DNA, the double helix, and with it the mechanism by which living things copy their inheritance. The journal's printer reset the three papers of that issue into a single pamphlet for the authors to send to colleagues. This three-paper offprint is far scarcer than the journal itself. Watson and Crick conducted no experiments of their own. Working at the Cavendish Laboratory in Cambridge across eighteen months, they unified the scattered findings of others into a single structure - two helical sugar-phosphate chains wound about a common axis, running in opposite directions, with the four bases paired across the inside of the ladder. The pairing was the whole of it: adenine always to thymine, cytosine always to guanine, so that the sequence of one strand fixes the sequence of the other. From that single constraint followed the answer to the oldest question in biology - how a gene is copied, with near-perfect fidelity, generation upon generation. The structure the paper sets out is exact and spare. Two right-handed helical chains coil about a common axis, the sugar-phosphate backbones on the outside and the paired bases stacked flat within, perpendicular to the axis; a residue recurs every 3.4 ångström along each chain, the helix repeats after ten residues at intervals of 34 ångström, and the whole forms a cylinder some twenty ångström across. Because the phosphates face outward into the surrounding water, solvent and cations reach them freely, and the model so accounts for the high water content of the fibres that Franklin had measured. Crick's lone schematic - two ribbons winding about a vertical fibre axis, the base-pairs drawn as horizontal rods between them - expresses the entire proposal in a single figure; it is this drawing, since become one of the most reproduced diagrams in modern science, that fills the second page of the present pamphlet. Everything the structure asserts is checked against the X-ray evidence: the perpendicular bases, the regular backbones, the antiparallel chains, each a feature the diffraction pattern demanded rather than a freedom the model-builders allowed themselves. The problem they solved was eighty years in the making. In 1869 the Swiss physiological chemist Friedrich Miescher, washing the pus from used surgical bandages to isolate the proteins of white blood cells, instead struck a substance from the cell nucleus richer in phosphorus than any protein and resistant to protein digestion; he named it nuclein and guessed that a whole family of such molecules might exist. The guess was forgotten. By the early 1950s researchers spoke confidently of the gene as the unit of heredity yet could not say what one looked like or how it was copied. Oswald Avery had shown in 1944 that it was DNA, not protein, that carried hereditary character in pneumococcus, but many held the molecule too monotonous - a backbone of four repeating units - to encode the intricacy of a living thing; the genetic material, they reasoned, surely had to be protein, with its twenty amino acids and endless variety. Crick and Watson grasped early that the three-dimensional shape of the gene was the central problem of the new biology, and that without it heredity could not be understood. They seized it at their first meeting, in 1951, and held to it with a single-mindedness that required them to absorb genetics, biochemistry, physical chemistry, and X-ray crystallography at once. Several disconnected results lay waiting to be joined. Alexander Todd had established that the molecular backbone was a regular chain of alternating phosphate and deoxyribose sugar. Erwin Chargaff had found that, however widely the proportions of the four bases varied between species, adenine and thymine always occurred in equal amounts, as did cytosine and guanine. Maurice Wilkins and Rosalind Franklin, at King's College London, had obtained X-ray fibre photographs pointing to a regular helical form. And Linus Pauling, the foremost structural chemist of the age, had not only discovered the single-stranded alpha helix in proteins but pioneered the method - building scale models constrained by known bond lengths and angles - by which Watson and Crick would work. Pauling supplied the spur as well as the tool: in February 1953 he proposed his own structure for DNA, a three-stranded helix with the phosphates at the core, and Watson and Crick, who could see at once that it was electrostatically impossible, feared being overtaken by the only rival capable of beating them. The paper opens by dismissing it, and sets aside in passing a further three-chain model that Bruce Fraser had drafted at King's but never properly published. The decisive correction came from across the office. Jerry Donohue, a visiting American physical chemist sharing the room, told Watson that the textbook forms of two of the bases were wrong: thymine and guanine should be drawn in their keto, not their enol, configuration. Shifting a single hydrogen atom on each accordingly, Watson cut fresh cardboard models and, moving them about his desktop in late February 1953, saw that an adenine-thymine pair and a cytosine-guanine pair had the very same shape and could be held together by hydrogen bonds. At a stroke this accounted for Chargaff's equalities, fitted the bases neatly between the two backbones demanded by the X-ray evidence, and required the chains to run antiparallel. The published paper states its central implication with a now-celebrated restraint - it had 'not escaped our notice' that the pairing at once suggested how the molecule might be copied: part the two strands, and each serves as the template for a new partner. By the account of Watson's memoir, Crick announced to the lunchtime drinkers at The Eagle that they had found the.…

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    Verlag: Journal of Bacteriology, Vol. 60, No. 6, pp. 697-718, December 1950., Offprint:, 1950

    • Softcover
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    Tall 8vo. 3 figs., 10 tables, refs., pencil notation on fig. 3 (presumably by DeMars). Self-wraps; two rusted (original) staples, slight stain from rust. Signature of Robert DeMars and author's name notation on cover. Fine. [with:] WATSON, James Dewey. The Properties of X-Ray-Inactivated Bacteriophage. II. Inactivation by Indirect Effects. Offprint: Journal of Bacteriology, Vol. 63, No. 4, pp. 473-485, April 1952. 3 figs., 6 tables, refs. Self-wraps; two rusted (original) staples, slight stain from rust. Signature of Robert DeMars and author's name notation on cover. Fine. FIRST EDITION(s) of James D. Watson's first published research papers, in support of his doctoral candidacy, dealing with inactivation of T2 bacteriophage with X-Rays. Luria and Dulbecco had previously discovered (1949) that bacteriophage could be inactivated by ultraviolet irradiation, and in this paper Watson describes similar effects obtained by X-Ray exposure. A result of this investigation was that the required "killing" dosage or "hits" is logarithmically related to the intensity of the exposure, unlike ultraviolet irradiation. Through a sophisticated technique using heat-inactivated E. coli, Watson was able to measure the adsorptive capacities of various T-phages and postulate the damage done to a phage's ability to adsorb and infect a host bacterium, resulting in subsequent lysis. In his second paper, Watson demonstrates the indirect effect of "hyperprotection" of X-Ray inactivated phage by concentrations of cysteine. "The struggle in the spring of 1950 was 'to write up minor results' for his thesis. He thought of it as 'torture.' He wrote the thesis in a month, but Salva 'did not like is' and took it home for rewriting. 'Not surprisingly,' Watson recalled, 'the thesis was accepted without fuss at my Ph.D. exam in late May.' He later reflected that he got his degree fast, 'not because I was really that bright, but because there was very much less to learn.'" [McElheny]. Provenance: Robert DeMars' copies of these papers. As the third graduate student mentored by Salvador Luria, DeMars went on to positions at Washington University (St. Louis) and the University of Wisconsin (Madison). His genetic research also involved investigations using strains of T bacteriophage. As a personal friend and colleague of the author, Watson gave copies of all his papers to DeMars as they were published. McElheny, Watson and DNA Making a Scientific Revolution, pp. 25-28.…

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    In original cloth with the illustrated paper wrapper. 176 p. Signed Hungarian edition. The wrapper is chipped. A very good copy. In original cloth with the illustrated paper wrapper.

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    In den Warenkorb

    1968 BROCHE.

  • Verlag: O. O., 18. September 1975., 1975

    • Manuskript/Papierantiquität

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    1 S. Qu.-kl.-schmal-8vo. James D. Watson hatte 1962 zusammen mit F. H. C. Crick und Maurice Wilkins den Nobelpreis für Physiologie oder Medizin erhalten für ihre Entdeckungen über die Molekularstruktur der Nukleinsäuren und ihre Bedeutung für die Informationsübertragung in lebender Substanz".

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    Verlag: Cold Spring Harbor, 7. XI. 2006., 2006

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    4to. 1/2 p. Printed letterhead "Cold Spring Harbor Laboratory". My day to day, if not hour to hour, existence is too crowded to let me seriously review your manuscript over the foreseeable future. Without reading it, I would not be able to write the appropriate foreword.".