Gu weikuan (20 risultati)

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  • Lingua: Inglese

    Editore: Wiley, 2011

    047049946X / 9780470499467

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    Da: PBShop.store UK, Fairford, GLOS, Regno UnitoPBShop.store UK

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    EUR 138,53

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    Quantità: 9 disponibili

    HRD. Condizione: New. New Book. Shipped from UK. Established seller since 2000.

  • Lingua: Inglese

    Editore: Wiley, 2011

    047049946X / 9780470499467

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    Da: GreatBookPrices, Columbia, MD, U.S.A.GreatBookPrices

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    EUR 148,72

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    Condizione: New.

  • Lingua: Inglese

    Editore: Wiley, 2011

    047049946X / 9780470499467

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    Da: Brook Bookstore On Demand, Napoli, NA, ItaliaBrook Bookstore On Demand

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    EUR 138,45

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    Condizione: new.

  • Lingua: Inglese

    Editore: Wiley, 2011

    047049946X / 9780470499467

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    EUR 151,34

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    Condizione: As New. Unread book in perfect condition.

  • Lingua: Inglese

    Editore: Wiley, 2011

    047049946X / 9780470499467

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    EUR 138,52

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    Condizione: New.

  • Lingua: Inglese

    Editore: Wiley, 2011

    047049946X / 9780470499467

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    Da: GreatBookPricesUK, Woodford Green, Regno UnitoGreatBookPricesUK

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    Condizione: Usato - Come nuovo

    EUR 151,21

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    Condizione: As New. Unread book in perfect condition.

  • Lingua: Inglese

    Editore: Wiley 2011-04-12, 2011

    047049946X / 9780470499467

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    Da: Chiron Media, Wallingford, Regno UnitoChiron Media

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    EUR 167,97

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    Quantità: 9 disponibili

    Hardcover. Condizione: New. Brand new book, sourced directly from publisher. Dispatch time is 6-7 days from our warehouse. Book will be sent in robust, secure packaging to ensure it reaches you securely.

  • Lingua: Inglese

    Editore: John Wiley & Sons Inc, New York, 2011

    047049946X / 9780470499467

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    Da: Grand Eagle Retail, Bensenville, IL, U.S.A.Grand Eagle Retail

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    EUR 179,73

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    Hardcover. Condizione: new. Hardcover. This book provides readers with new paradigms on the mutation discovery in the post-genome era. The completion of human and other genome sequencing, along with other new technologies, such as mutation analysis and microarray, has dramatically accelerated the progress in positional cloning of genes from mutated models. In 2002, the Mouse Genome Sequencing Consortium stated that The availability of an annotated mouse genome sequence now provides the most efficient tool yet in the gene hunter's toolkit. One can move directly from genetic mapping to identification of candidate genes, and the experimental process is reduced to PCR amplification and sequencing of exons and other conserved elements in the candidate interval. With this streamlined protocol, it is anticipated that many decades-old mouse mutants will be understood precisely at the DNA level in the near future. The implication of such a statement should be similar to the identification of mutated genes from human diseases and animal models, when genome sequencing is completed for them. More than five years have passed, but genes in many human diseases and animal models have not yet been identified. In some cases, the identification of the mutated genes has been a bottleneck, because the genetic mechanism holds the key to understand the basis of the diseases. However, an integrative strategy, which is a combination of genetic mapping, genome resources, bioinformatics tools, and high throughput technologies, has been developed and tested. The classic paradigm of positional cloning has evolved with completely new concepts of genomic cloning and protocols. This book describes new concepts of gene discovery in the post-genome era and the use of streamlined protocols to identify genes of interest. This book helps identify not only large insertions/deletions but also single nucleotide mutations or polymorphisms that regulate quantitative trait loci (QTL). This book provides readers with new paradigms on the mutation discovery in the post-genome era. The completion of human and other genome sequencing, along with other new technologies, such as mutation analysis and microarray, has dramatically accelerated the progress in positional cloning of genes from mutated models. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.

  • Lingua: Inglese

    Editore: John Wiley and Sons Inc, US, 2011

    047049946X / 9780470499467

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    Da: Rarewaves.com USA, London, LONDO, Regno UnitoRarewaves.com USA

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    EUR 181,18

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    Quantità: 5 disponibili

    Hardback. Condizione: New. This book provides readers with new paradigms on the mutation discovery in the post-genome era. The completion of human and other genome sequencing, along with other new technologies, such as mutation analysis and microarray, has dramatically accelerated the progress in positional cloning of genes from mutated models. In 2002, the Mouse Genome Sequencing Consortium stated that "The availability of an annotated mouse genome sequence now provides the most efficient tool yet in the gene hunter's toolkit. One can move directly from genetic mapping to identification of candidate genes, and the experimental process is reduced to PCR amplification and sequencing of exons and other conserved elements in the candidate interval. With this streamlined protocol, it is anticipated that many decades-old mouse mutants will be understood precisely at the DNA level in the near future." The implication of such a statement should be similar to the identification of mutated genes from human diseases and animal models, when genome sequencing is completed for them. More than five years have passed, but genes in many human diseases and animal models have not yet been identified. In some cases, the identification of the mutated genes has been a bottleneck, because the genetic mechanism holds the key to understand the basis of the diseases. However, an integrative strategy, which is a combination of genetic mapping, genome resources, bioinformatics tools, and high throughput technologies, has been developed and tested. The classic paradigm of positional cloning has evolved with completely new concepts of genomic cloning and protocols. This book describes new concepts of gene discovery in the post-genome era and the use of streamlined protocols to identify genes of interest. This book helps identify not only large insertions/deletions but also single nucleotide mutations or polymorphisms that regulate quantitative trait loci (QTL).

  • Lingua: Inglese

    Editore: Wiley, 2011

    047049946X / 9780470499467

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    Da: Ria Christie Collections, Uxbridge, Regno UnitoRia Christie Collections

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    EUR 166,41

    EUR 17,39 spedizione 
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    Quantità: 9 disponibili

    Condizione: New. In English.

  • Lingua: Inglese

    Editore: John Wiley & Sons, 2011

    047049946X / 9780470499467

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    Da: Majestic Books, Hounslow, Regno UnitoMajestic Books

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    EUR 183,59

    EUR 7,57 spedizione 
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    Quantità: 3 disponibili

    Condizione: New. pp. 552.

  • Lingua: Inglese

    Editore: John Wiley & Sons Inc, 2011

    047049946X / 9780470499467

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    Da: THE SAINT BOOKSTORE, Southport, Regno UnitoTHE SAINT BOOKSTORE

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    EUR 167,49

    EUR 24,50 spedizione 
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    Quantità: 9 disponibili

    Hardback. Condizione: New. New copy - Usually dispatched within 4 working days.

  • Lingua: Inglese

    Editore: Wiley, 2011

    047049946X / 9780470499467

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    Da: Ubiquity Trade, Miami, FL, U.S.A.Ubiquity Trade

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    EUR 191,67

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    Quantità: Più di 20 disponibili

    Condizione: New. Brand new! Please provide a physical shipping address.

  • Lingua: Inglese

    Editore: John Wiley & Sons Inc, 2011

    047049946X / 9780470499467

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    • Prima edizione

    Da: Kennys Bookshop and Art Galleries Ltd., Galway, GY, IrlandaKennys Bookshop and Art Galleries Ltd.

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    Condizione: Nuovo

    EUR 179,50

    EUR 9,50 spedizione 
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    Quantità: 1 disponibili

    Condizione: New. This book provides readers with new paradigms on the mutation discovery in the post-genome era. The completion of human and other genome sequencing, along with other new technologies, such as mutation analysis and microarray, has dramatically accelerated the progress in positional cloning of genes from mutated models. Editor(s): Gu, Weikuan; Yongjun, Wang. Num Pages: 552 pages, Illustrations. BIC Classification: MFN; PN; PS; TCB. Category: (P) Professional & Vocational. Dimension: 239 x 164 x 36. Weight in Grams: 996. . 2011. 1st Edition. Hardcover. . . . .

  • Lingua: Inglese

    Editore: John Wiley & Sons, 2011

    047049946X / 9780470499467

    • Rilegato

    Da: Books Puddle, New York, NY, U.S.A.Books Puddle

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    Condizione: Nuovo

    EUR 205,49

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    Quantità: 3 disponibili

    Condizione: New. pp. 552 Index.

  • Lingua: Inglese

    Editore: John Wiley & Sons Inc, 2011

    047049946X / 9780470499467

    • Rilegato

    Da: Revaluation Books, Exeter, Regno UnitoRevaluation Books

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    Condizione: Nuovo

    EUR 197,83

    EUR 14,55 spedizione 
    Spedito da Regno Unito a U.S.A.

    Quantità: 2 disponibili

    Hardcover. Condizione: Brand New. 1st edition. 560 pages. 9.25x6.25x1.25 inches. In Stock.

  • Lingua: Inglese

    Editore: John Wiley & Sons Inc, New York, 2011

    047049946X / 9780470499467

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    • Prima edizione

    Da: CitiRetail, Stevenage, Regno UnitoCitiRetail

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    Condizione: Nuovo

    EUR 167,82

    EUR 43,06 spedizione 
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    Quantità: 1 disponibili

    Hardcover. Condizione: new. Hardcover. This book provides readers with new paradigms on the mutation discovery in the post-genome era. The completion of human and other genome sequencing, along with other new technologies, such as mutation analysis and microarray, has dramatically accelerated the progress in positional cloning of genes from mutated models. In 2002, the Mouse Genome Sequencing Consortium stated that The availability of an annotated mouse genome sequence now provides the most efficient tool yet in the gene hunter's toolkit. One can move directly from genetic mapping to identification of candidate genes, and the experimental process is reduced to PCR amplification and sequencing of exons and other conserved elements in the candidate interval. With this streamlined protocol, it is anticipated that many decades-old mouse mutants will be understood precisely at the DNA level in the near future. The implication of such a statement should be similar to the identification of mutated genes from human diseases and animal models, when genome sequencing is completed for them. More than five years have passed, but genes in many human diseases and animal models have not yet been identified. In some cases, the identification of the mutated genes has been a bottleneck, because the genetic mechanism holds the key to understand the basis of the diseases. However, an integrative strategy, which is a combination of genetic mapping, genome resources, bioinformatics tools, and high throughput technologies, has been developed and tested. The classic paradigm of positional cloning has evolved with completely new concepts of genomic cloning and protocols. This book describes new concepts of gene discovery in the post-genome era and the use of streamlined protocols to identify genes of interest. This book helps identify not only large insertions/deletions but also single nucleotide mutations or polymorphisms that regulate quantitative trait loci (QTL). This book provides readers with new paradigms on the mutation discovery in the post-genome era. The completion of human and other genome sequencing, along with other new technologies, such as mutation analysis and microarray, has dramatically accelerated the progress in positional cloning of genes from mutated models. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.

  • Lingua: Inglese

    Editore: John Wiley & Sons Inc, 2011

    047049946X / 9780470499467

    • Rilegato

    Da: Kennys Bookstore, Olney, MD, U.S.A.Kennys Bookstore

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    Condizione: Nuovo

    EUR 223,74

    EUR 9,15 spedizione 
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    Quantità: 1 disponibili

    Condizione: New. This book provides readers with new paradigms on the mutation discovery in the post-genome era. The completion of human and other genome sequencing, along with other new technologies, such as mutation analysis and microarray, has dramatically accelerated the progress in positional cloning of genes from mutated models. Editor(s): Gu, Weikuan; Yongjun, Wang. Num Pages: 552 pages, Illustrations. BIC Classification: MFN; PN; PS; TCB. Category: (P) Professional & Vocational. Dimension: 239 x 164 x 36. Weight in Grams: 996. . 2011. 1st Edition. Hardcover. . . . . Books ship from the US and Ireland.

  • Lingua: Inglese

    Editore: John Wiley and Sons Inc, US, 2011

    047049946X / 9780470499467

    • Rilegato

    Da: Rarewaves.com UK, London, Regno UnitoRarewaves.com UK

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    Condizione: Nuovo

    EUR 174,95

    EUR 75,65 spedizione 
    Spedito da Regno Unito a U.S.A.

    Quantità: 5 disponibili

    Hardback. Condizione: New. This book provides readers with new paradigms on the mutation discovery in the post-genome era. The completion of human and other genome sequencing, along with other new technologies, such as mutation analysis and microarray, has dramatically accelerated the progress in positional cloning of genes from mutated models. In 2002, the Mouse Genome Sequencing Consortium stated that "The availability of an annotated mouse genome sequence now provides the most efficient tool yet in the gene hunter's toolkit. One can move directly from genetic mapping to identification of candidate genes, and the experimental process is reduced to PCR amplification and sequencing of exons and other conserved elements in the candidate interval. With this streamlined protocol, it is anticipated that many decades-old mouse mutants will be understood precisely at the DNA level in the near future." The implication of such a statement should be similar to the identification of mutated genes from human diseases and animal models, when genome sequencing is completed for them. More than five years have passed, but genes in many human diseases and animal models have not yet been identified. In some cases, the identification of the mutated genes has been a bottleneck, because the genetic mechanism holds the key to understand the basis of the diseases. However, an integrative strategy, which is a combination of genetic mapping, genome resources, bioinformatics tools, and high throughput technologies, has been developed and tested. The classic paradigm of positional cloning has evolved with completely new concepts of genomic cloning and protocols. This book describes new concepts of gene discovery in the post-genome era and the use of streamlined protocols to identify genes of interest. This book helps identify not only large insertions/deletions but also single nucleotide mutations or polymorphisms that regulate quantitative trait loci (QTL).

  • Lingua: Inglese

    Editore: John Wiley & Sons Inc, New York, 2011

    047049946X / 9780470499467

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    • Prima edizione

    Da: AussieBookSeller, Truganina, VIC, AustraliaAussieBookSeller

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    Condizione: Nuovo

    EUR 268,52

    EUR 32,24 spedizione 
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    Quantità: 1 disponibili

    Hardcover. Condizione: new. Hardcover. This book provides readers with new paradigms on the mutation discovery in the post-genome era. The completion of human and other genome sequencing, along with other new technologies, such as mutation analysis and microarray, has dramatically accelerated the progress in positional cloning of genes from mutated models. In 2002, the Mouse Genome Sequencing Consortium stated that The availability of an annotated mouse genome sequence now provides the most efficient tool yet in the gene hunter's toolkit. One can move directly from genetic mapping to identification of candidate genes, and the experimental process is reduced to PCR amplification and sequencing of exons and other conserved elements in the candidate interval. With this streamlined protocol, it is anticipated that many decades-old mouse mutants will be understood precisely at the DNA level in the near future. The implication of such a statement should be similar to the identification of mutated genes from human diseases and animal models, when genome sequencing is completed for them. More than five years have passed, but genes in many human diseases and animal models have not yet been identified. In some cases, the identification of the mutated genes has been a bottleneck, because the genetic mechanism holds the key to understand the basis of the diseases. However, an integrative strategy, which is a combination of genetic mapping, genome resources, bioinformatics tools, and high throughput technologies, has been developed and tested. The classic paradigm of positional cloning has evolved with completely new concepts of genomic cloning and protocols. This book describes new concepts of gene discovery in the post-genome era and the use of streamlined protocols to identify genes of interest. This book helps identify not only large insertions/deletions but also single nucleotide mutations or polymorphisms that regulate quantitative trait loci (QTL). This book provides readers with new paradigms on the mutation discovery in the post-genome era. The completion of human and other genome sequencing, along with other new technologies, such as mutation analysis and microarray, has dramatically accelerated the progress in positional cloning of genes from mutated models. Shipping may be from our Sydney, NSW warehouse or from our UK or US warehouse, depending on stock availability.