Index by Author

August 1991; 1 (1)
  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. Arnold, C

B

  1. Baptist, E W

    • Degenerate oligonucleotide sequence-directed cross-species PCR cloning of the BCP 54/ALDH 3 cDNA: priming from inverted repeats and formation of tandem primer arrays. Genome Res. August 1991 1: 57-62; doi:10.1101/gr.1.1.57

  2. Barany, F

  3. Barry, T

    • The 16s/23s ribosomal spacer region as a target for DNA probes to identify eubacteria. Genome Res. August 1991 1: 51-56; doi:10.1101/gr.1.1.51
    • Direct genomic DNA amplification from autoclaved infectious microorganisms using PCR technology. Genome Res. August 1991 1: 75; doi:10.1101/gr.1.1.75

  4. Brian, D A

C

  1. Chang, Y F

    • RT-PCR artifacts from processed pseudogenes. Genome Res. August 1991 1: 70-71; doi:10.1101/gr.1.1.70

  2. Colleran, G

    • The 16s/23s ribosomal spacer region as a target for DNA probes to identify eubacteria. Genome Res. August 1991 1: 51-56; doi:10.1101/gr.1.1.51

  3. Cooper, D L

    • Degenerate oligonucleotide sequence-directed cross-species PCR cloning of the BCP 54/ALDH 3 cDNA: priming from inverted repeats and formation of tandem primer arrays. Genome Res. August 1991 1: 57-62; doi:10.1101/gr.1.1.57

D

  1. Dias, C

    • Optimization of the polymerase chain reaction with regard to fidelity: modified T7, Taq, and vent DNA polymerases. Genome Res. August 1991 1: 63-69; doi:10.1101/gr.1.1.63

  2. Dunican, L K

    • The 16s/23s ribosomal spacer region as a target for DNA probes to identify eubacteria. Genome Res. August 1991 1: 51-56; doi:10.1101/gr.1.1.51

E

  1. Eckert, K A

F

  1. Fahy, E

    • Self-sustained sequence replication (3SR): an isothermal transcription-based amplification system alternative to PCR. Genome Res. August 1991 1: 25-33; doi:10.1101/gr.1.1.25

G

  1. Gannon, F

    • The 16s/23s ribosomal spacer region as a target for DNA probes to identify eubacteria. Genome Res. August 1991 1: 51-56; doi:10.1101/gr.1.1.51
    • Direct genomic DNA amplification from autoclaved infectious microorganisms using PCR technology. Genome Res. August 1991 1: 75; doi:10.1101/gr.1.1.75

  2. Gingeras, T R

    • Self-sustained sequence replication (3SR): an isothermal transcription-based amplification system alternative to PCR. Genome Res. August 1991 1: 25-33; doi:10.1101/gr.1.1.25

  3. Glennon, M

    • The 16s/23s ribosomal spacer region as a target for DNA probes to identify eubacteria. Genome Res. August 1991 1: 51-56; doi:10.1101/gr.1.1.51

  4. Greer, C E

    • PCR amplification from paraffin-embedded tissues: recommendations on fixatives for long-term storage and prospective studies. Genome Res. August 1991 1: 46-50; doi:10.1101/gr.1.1.46

H

  1. Ham, R G

    • RT-PCR artifacts from processed pseudogenes. Genome Res. August 1991 1: 70-71; doi:10.1101/gr.1.1.70

  2. Hayashi, K

    • PCR-SSCP: a simple and sensitive method for detection of mutations in the genomic DNA. Genome Res. August 1991 1: 34-38; doi:10.1101/gr.1.1.34

  3. Hodgson, I J

  4. Hofmann, M A

K

  1. Keohavong, P

    • Optimization of the polymerase chain reaction with regard to fidelity: modified T7, Taq, and vent DNA polymerases. Genome Res. August 1991 1: 63-69; doi:10.1101/gr.1.1.63

  2. Kunkel, T A

  3. Kwoh, D Y

    • Self-sustained sequence replication (3SR): an isothermal transcription-based amplification system alternative to PCR. Genome Res. August 1991 1: 25-33; doi:10.1101/gr.1.1.25

L

  1. Ling, L L

    • Optimization of the polymerase chain reaction with regard to fidelity: modified T7, Taq, and vent DNA polymerases. Genome Res. August 1991 1: 63-69; doi:10.1101/gr.1.1.63

  2. Lund, J K

    • PCR amplification from paraffin-embedded tissues: recommendations on fixatives for long-term storage and prospective studies. Genome Res. August 1991 1: 46-50; doi:10.1101/gr.1.1.46

M

  1. Manos, M M

    • PCR amplification from paraffin-embedded tissues: recommendations on fixatives for long-term storage and prospective studies. Genome Res. August 1991 1: 46-50; doi:10.1101/gr.1.1.46

  2. Menon, R S

    • RT-PCR artifacts from processed pseudogenes. Genome Res. August 1991 1: 70-71; doi:10.1101/gr.1.1.70

  3. Mullis, Kary B.

    • The Polymerase Chain Reaction in an Anemic Mode: How to Avoid Cold Oligodeoxyribonuclear Fusion Genome Res. August 1991 1: 1-4; doi:10.1101/gr.1.1.1

S

  1. St Clair, J

    • RT-PCR artifacts from processed pseudogenes. Genome Res. August 1991 1: 70-71; doi:10.1101/gr.1.1.70

T

  1. Thilly, W G

    • Optimization of the polymerase chain reaction with regard to fidelity: modified T7, Taq, and vent DNA polymerases. Genome Res. August 1991 1: 63-69; doi:10.1101/gr.1.1.63

W

  1. Winberg, G

    • A rapid method for preparing DNA from blood, suited for PCR screening of transgenes in mice. Genome Res. August 1991 1: 72-74; doi:10.1101/gr.1.1.72

Current Issue

  1. February 2026, 36 (2)
  1. Current Issue
  1. Alert me to new issues of Genome Research