Index by Author

May 1993; 2 (4)
  1. A
  2. B
  3. C
  4. D
  5. E
  6. F
  7. G
  8. H
  9. I
  10. J
  11. K
  12. L
  13. M
  14. N
  15. O
  16. P
  17. Q
  18. R
  19. S
  20. T
  21. U
  22. V
  23. W
  24. X
  25. Y
  26. Z

A

  1. Abramson, R D

    • High-level expression, purification, and enzymatic characterization of full-length Thermus aquaticus DNA polymerase and a truncated form deficient in 5' to 3' exonuclease activity. Genome Res. May 1993 2: 275-287; doi:10.1101/gr.2.4.275

  2. Andersson, B

    • Rapid characterization of HIV-1 sequence diversity using denaturing gradient gel electrophoresis and direct automated DNA sequencing of PCR products. Genome Res. May 1993 2: 293-300; doi:10.1101/gr.2.4.293

B

  1. Benson, P D

    • PCR-based genetic analysis of DNA from autopsied prostate tissue. Genome Res. May 1993 2: 354-355; doi:10.1101/gr.2.4.354

  2. Bloch, W

    • Importance of different variables for enhancing in situ detection of PCR-amplified DNA. Genome Res. May 1993 2: 305-312; doi:10.1101/gr.2.4.305

  3. Bolander, M E

    • Restriction-site PCR: a direct method of unknown sequence retrieval adjacent to a known locus by using universal primers. Genome Res. May 1993 2: 318-322; doi:10.1101/gr.2.4.318

  4. Bush, A

    • Reproducibility of random amplified polymorphic DNA (RAPD) analysis among laboratories. Genome Res. May 1993 2: 341-345; doi:10.1101/gr.2.4.341

C

  1. Cassiman, J J

    • A rapid, semiautomated method for apolipoprotein E genotyping. Genome Res. May 1993 2: 348-350; doi:10.1101/gr.2.4.348

  2. Cattaneo, R

    • A rapid and simple method for reversing the inhibitory effect of heparin on PCR for HLA class II typing. Genome Res. May 1993 2: 356-358; doi:10.1101/gr.2.4.356

  3. Chang, S Y

    • High-level expression, purification, and enzymatic characterization of full-length Thermus aquaticus DNA polymerase and a truncated form deficient in 5' to 3' exonuclease activity. Genome Res. May 1993 2: 275-287; doi:10.1101/gr.2.4.275

  4. Chen, D

    • Use of stock solutions to simplify mRNA quantitation by reverse transcription--PCR assays. Genome Res. May 1993 2: 351-353; doi:10.1101/gr.2.4.351

  5. Crespiatico, L

    • A rapid and simple method for reversing the inhibitory effect of heparin on PCR for HLA class II typing. Genome Res. May 1993 2: 356-358; doi:10.1101/gr.2.4.356

D

  1. Da, Y

  2. Day, P J

    • Generation of cohesive ends on PCR products by UDG-mediated excision of dU, and application for cloning into restriction digest-linearized vectors. Genome Res. May 1993 2: 328-332; doi:10.1101/gr.2.4.328

  3. Desrosiers, R C

    • A PCR-derived library of random point mutations within the V3 region of simian immunodeficiency virus. Genome Res. May 1993 2: 301-304; doi:10.1101/gr.2.4.301

  4. Dias, C

    • Predominant mutations induced by the Thermococcus litoralis, vent DNA polymerase during DNA amplification in vitro. Genome Res. May 1993 2: 288-292; doi:10.1101/gr.2.4.288

  5. Domier, L

    • Reproducibility of random amplified polymorphic DNA (RAPD) analysis among laboratories. Genome Res. May 1993 2: 341-345; doi:10.1101/gr.2.4.341

F

  1. Fedak, G

    • Reproducibility of random amplified polymorphic DNA (RAPD) analysis among laboratories. Genome Res. May 1993 2: 341-345; doi:10.1101/gr.2.4.341

G

  1. Gallery, F

    • Importance of different variables for enhancing in situ detection of PCR-amplified DNA. Genome Res. May 1993 2: 305-312; doi:10.1101/gr.2.4.305

  2. Gelfand, D H

    • High-level expression, purification, and enzymatic characterization of full-length Thermus aquaticus DNA polymerase and a truncated form deficient in 5' to 3' exonuclease activity. Genome Res. May 1993 2: 275-287; doi:10.1101/gr.2.4.275

  3. Gibbs, R A

    • Rapid characterization of HIV-1 sequence diversity using denaturing gradient gel electrophoresis and direct automated DNA sequencing of PCR products. Genome Res. May 1993 2: 293-300; doi:10.1101/gr.2.4.293

  4. Guo, C

    • A rapid, semiautomated method for apolipoprotein E genotyping. Genome Res. May 1993 2: 348-350; doi:10.1101/gr.2.4.348

H

  1. Haas, G P

    • PCR-based genetic analysis of DNA from autopsied prostate tissue. Genome Res. May 1993 2: 354-355; doi:10.1101/gr.2.4.354

  2. Hom, R

    • Importance of different variables for enhancing in situ detection of PCR-amplified DNA. Genome Res. May 1993 2: 305-312; doi:10.1101/gr.2.4.305

I

  1. Ishino, Y

    • Practical application of fluorescence-based image analyzer for PCR single-stranded conformation polymorphism analysis used in detection of multiple point mutations. Genome Res. May 1993 2: 323-327; doi:10.1101/gr.2.4.323

K

  1. Kasha, K

    • Reproducibility of random amplified polymorphic DNA (RAPD) analysis among laboratories. Genome Res. May 1993 2: 341-345; doi:10.1101/gr.2.4.341

  2. Kato, I

    • Practical application of fluorescence-based image analyzer for PCR single-stranded conformation polymorphism analysis used in detection of multiple point mutations. Genome Res. May 1993 2: 323-327; doi:10.1101/gr.2.4.323

  3. Keohavong, P

    • Predominant mutations induced by the Thermococcus litoralis, vent DNA polymerase during DNA amplification in vitro. Genome Res. May 1993 2: 288-292; doi:10.1101/gr.2.4.288

  4. Kim, W

    • Reproducibility of random amplified polymorphic DNA (RAPD) analysis among laboratories. Genome Res. May 1993 2: 341-345; doi:10.1101/gr.2.4.341

  5. Kirchhoff, F

    • A PCR-derived library of random point mutations within the V3 region of simian immunodeficiency virus. Genome Res. May 1993 2: 301-304; doi:10.1101/gr.2.4.301

  6. Klebe, R J

    • Use of stock solutions to simplify mRNA quantitation by reverse transcription--PCR assays. Genome Res. May 1993 2: 351-353; doi:10.1101/gr.2.4.351

  7. Knittel, T

    • PCR with degenerate primers containing deoxyinosine fails with Pfu DNA polymerase. Genome Res. May 1993 2: 346-347; doi:10.1101/gr.2.4.346

L

  1. Landre, P A

    • High-level expression, purification, and enzymatic characterization of full-length Thermus aquaticus DNA polymerase and a truncated form deficient in 5' to 3' exonuclease activity. Genome Res. May 1993 2: 275-287; doi:10.1101/gr.2.4.275

  2. Laroche, A

    • Reproducibility of random amplified polymorphic DNA (RAPD) analysis among laboratories. Genome Res. May 1993 2: 341-345; doi:10.1101/gr.2.4.341

  3. Lawyer, F C

    • High-level expression, purification, and enzymatic characterization of full-length Thermus aquaticus DNA polymerase and a truncated form deficient in 5' to 3' exonuclease activity. Genome Res. May 1993 2: 275-287; doi:10.1101/gr.2.4.275

  4. Lewin, H A

  5. Lewis, D E

    • Rapid characterization of HIV-1 sequence diversity using denaturing gradient gel electrophoresis and direct automated DNA sequencing of PCR products. Genome Res. May 1993 2: 293-300; doi:10.1101/gr.2.4.293

  6. Ling, L

    • Predominant mutations induced by the Thermococcus litoralis, vent DNA polymerase during DNA amplification in vitro. Genome Res. May 1993 2: 288-292; doi:10.1101/gr.2.4.288

M

  1. MacConnell, P

    • Importance of different variables for enhancing in situ detection of PCR-amplified DNA. Genome Res. May 1993 2: 305-312; doi:10.1101/gr.2.4.305

  2. Macoska, J A

    • PCR-based genetic analysis of DNA from autopsied prostate tissue. Genome Res. May 1993 2: 354-355; doi:10.1101/gr.2.4.354

  3. Magnuson, V L

    • Use of stock solutions to simplify mRNA quantitation by reverse transcription--PCR assays. Genome Res. May 1993 2: 351-353; doi:10.1101/gr.2.4.351

  4. Marynen, P

    • A rapid, semiautomated method for apolipoprotein E genotyping. Genome Res. May 1993 2: 348-350; doi:10.1101/gr.2.4.348

  5. Mirsky, M L

  6. Molnar, S J

    • Reproducibility of random amplified polymorphic DNA (RAPD) analysis among laboratories. Genome Res. May 1993 2: 341-345; doi:10.1101/gr.2.4.341

N

  1. Nocco, A

    • A rapid and simple method for reversing the inhibitory effect of heparin on PCR for HLA class II typing. Genome Res. May 1993 2: 356-358; doi:10.1101/gr.2.4.356

  2. Nuovo, G J

    • Importance of different variables for enhancing in situ detection of PCR-amplified DNA. Genome Res. May 1993 2: 305-312; doi:10.1101/gr.2.4.305

P

  1. Pacek, P

    • Determination of allele frequencies at loci with length polymorphism by quantitative analysis of DNA amplified from pooled samples. Genome Res. May 1993 2: 313-317; doi:10.1101/gr.2.4.313

  2. Penner, G A

    • Reproducibility of random amplified polymorphic DNA (RAPD) analysis among laboratories. Genome Res. May 1993 2: 341-345; doi:10.1101/gr.2.4.341

  3. Picard, D

    • PCR with degenerate primers containing deoxyinosine fails with Pfu DNA polymerase. Genome Res. May 1993 2: 346-347; doi:10.1101/gr.2.4.346

  4. Poli, F

    • A rapid and simple method for reversing the inhibitory effect of heparin on PCR for HLA class II typing. Genome Res. May 1993 2: 356-358; doi:10.1101/gr.2.4.356

S

  1. Saiki, R K

    • High-level expression, purification, and enzymatic characterization of full-length Thermus aquaticus DNA polymerase and a truncated form deficient in 5' to 3' exonuclease activity. Genome Res. May 1993 2: 275-287; doi:10.1101/gr.2.4.275

  2. Sajantila, A

    • Determination of allele frequencies at loci with length polymorphism by quantitative analysis of DNA amplified from pooled samples. Genome Res. May 1993 2: 313-317; doi:10.1101/gr.2.4.313

  3. Sakr, W

    • PCR-based genetic analysis of DNA from autopsied prostate tissue. Genome Res. May 1993 2: 354-355; doi:10.1101/gr.2.4.354

  4. Sarkar, G

    • Restriction-site PCR: a direct method of unknown sequence retrieval adjacent to a known locus by using universal primers. Genome Res. May 1993 2: 318-322; doi:10.1101/gr.2.4.318

  5. Scoles, G

    • Reproducibility of random amplified polymorphic DNA (RAPD) analysis among laboratories. Genome Res. May 1993 2: 341-345; doi:10.1101/gr.2.4.341

  6. Shimada, A

    • Practical application of fluorescence-based image analyzer for PCR single-stranded conformation polymorphism analysis used in detection of multiple point mutations. Genome Res. May 1993 2: 323-327; doi:10.1101/gr.2.4.323

  7. Sirchia, G

    • A rapid and simple method for reversing the inhibitory effect of heparin on PCR for HLA class II typing. Genome Res. May 1993 2: 356-358; doi:10.1101/gr.2.4.356

  8. Smith, C

    • Generation of cohesive ends on PCR products by UDG-mediated excision of dU, and application for cloning into restriction digest-linearized vectors. Genome Res. May 1993 2: 328-332; doi:10.1101/gr.2.4.328

  9. Steffensen, B

    • Use of stock solutions to simplify mRNA quantitation by reverse transcription--PCR assays. Genome Res. May 1993 2: 351-353; doi:10.1101/gr.2.4.351

  10. Stoffel, S

    • High-level expression, purification, and enzymatic characterization of full-length Thermus aquaticus DNA polymerase and a truncated form deficient in 5' to 3' exonuclease activity. Genome Res. May 1993 2: 275-287; doi:10.1101/gr.2.4.275

  11. Syvänen, A C

    • Determination of allele frequencies at loci with length polymorphism by quantitative analysis of DNA amplified from pooled samples. Genome Res. May 1993 2: 313-317; doi:10.1101/gr.2.4.313

T

  1. Takahashi-Fujii, A

    • Practical application of fluorescence-based image analyzer for PCR single-stranded conformation polymorphism analysis used in detection of multiple point mutations. Genome Res. May 1993 2: 323-327; doi:10.1101/gr.2.4.323

  2. Thilly, W G

    • Predominant mutations induced by the Thermococcus litoralis, vent DNA polymerase during DNA amplification in vitro. Genome Res. May 1993 2: 288-292; doi:10.1101/gr.2.4.288

  3. Turkeri, L N

    • PCR-based genetic analysis of DNA from autopsied prostate tissue. Genome Res. May 1993 2: 354-355; doi:10.1101/gr.2.4.354

  4. Turner, R T

    • Restriction-site PCR: a direct method of unknown sequence retrieval adjacent to a known locus by using universal primers. Genome Res. May 1993 2: 318-322; doi:10.1101/gr.2.4.318

W

  1. Walker, M R

    • Generation of cohesive ends on PCR products by UDG-mediated excision of dU, and application for cloning into restriction digest-linearized vectors. Genome Res. May 1993 2: 328-332; doi:10.1101/gr.2.4.328

  2. Wise, R

    • Reproducibility of random amplified polymorphic DNA (RAPD) analysis among laboratories. Genome Res. May 1993 2: 341-345; doi:10.1101/gr.2.4.341

Y

  1. Ying, J H

    • Rapid characterization of HIV-1 sequence diversity using denaturing gradient gel electrophoresis and direct automated DNA sequencing of PCR products. Genome Res. May 1993 2: 293-300; doi:10.1101/gr.2.4.293

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