Index by Author

November 1991; 1 (2)
  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. Allen, M

B

  1. Barany, F.

    • The ligase chain reaction in a PCR world Genome Res. November 1991 1: 149; doi:10.1101/gr.1.2.149

  2. Barry, T.

    • The 16s/23s ribosomal spacer region as a target for DNA probes to identify eubacteria Genome Res. November 1991 1: 149; doi:10.1101/gr.1.2.149-a

  3. Blankenstein, T

C

  1. Colleran, G.

    • The 16s/23s ribosomal spacer region as a target for DNA probes to identify eubacteria Genome Res. November 1991 1: 149; doi:10.1101/gr.1.2.149-a

  2. Cone, R W

    • Slow inactivation of dry PCR templates by UV light. Genome Res. November 1991 1: 142-143; doi:10.1101/gr.1.2.142

D

  1. Diamantstein, T

  2. Dunican, L.K.

    • The 16s/23s ribosomal spacer region as a target for DNA probes to identify eubacteria Genome Res. November 1991 1: 149; doi:10.1101/gr.1.2.149-a

F

  1. Fairfax, M R

    • Slow inactivation of dry PCR templates by UV light. Genome Res. November 1991 1: 142-143; doi:10.1101/gr.1.2.142

G

  1. Gannon, F.

    • The 16s/23s ribosomal spacer region as a target for DNA probes to identify eubacteria Genome Res. November 1991 1: 149; doi:10.1101/gr.1.2.149-a

  2. Glennon, F.

    • The 16s/23s ribosomal spacer region as a target for DNA probes to identify eubacteria Genome Res. November 1991 1: 149; doi:10.1101/gr.1.2.149-a

  3. Golay, J

    • A simple and rapid method to analyze specific mRNAs from few cells in a semi-quantitative way using the polymerase chain reaction. Genome Res. November 1991 1: 144-145; doi:10.1101/gr.1.2.144

  4. Green, E D

    • Sequence-tagged site (STS) content mapping of human chromosomes: theoretical considerations and early experiences. Genome Res. November 1991 1: 77-90; doi:10.1101/gr.1.2.77

  5. Green, P

    • Sequence-tagged site (STS) content mapping of human chromosomes: theoretical considerations and early experiences. Genome Res. November 1991 1: 77-90; doi:10.1101/gr.1.2.77
    • OSP: a computer program for choosing PCR and DNA sequencing primers. Genome Res. November 1991 1: 124-128; doi:10.1101/gr.1.2.124

  6. Gyllensten, U

H

  1. Hillier, L

    • OSP: a computer program for choosing PCR and DNA sequencing primers. Genome Res. November 1991 1: 124-128; doi:10.1101/gr.1.2.124

I

  1. Introna, M

    • A simple and rapid method to analyze specific mRNAs from few cells in a semi-quantitative way using the polymerase chain reaction. Genome Res. November 1991 1: 144-145; doi:10.1101/gr.1.2.144

J

  1. Jacobson, D R

    • Rapid, nonradioactive screening for activating ras oncogene mutations using PCR-primer introduced restriction analysis (PCR-PIRA) Genome Res. November 1991 1: 146-148; doi:10.1101/gr.1.2.146

L

  1. Lagerström, M

    • Capture PCR: efficient amplification of DNA fragments adjacent to a known sequence in human and YAC DNA. Genome Res. November 1991 1: 111-119; doi:10.1101/gr.1.2.111

  2. Landegren, U

    • Capture PCR: efficient amplification of DNA fragments adjacent to a known sequence in human and YAC DNA. Genome Res. November 1991 1: 111-119; doi:10.1101/gr.1.2.111

  3. Lorens, J B

    • Rapid and reliable cloning of PCR products. Genome Res. November 1991 1: 140-141; doi:10.1101/gr.1.2.140

M

  1. MacGregor, G R

    • Use of a simplified single-site PCR to facilitate cloning of genomic DNA sequences flanking a transgene integration site. Genome Res. November 1991 1: 129-135; doi:10.1101/gr.1.2.129

  2. Malmgren, H

    • Capture PCR: efficient amplification of DNA fragments adjacent to a known sequence in human and YAC DNA. Genome Res. November 1991 1: 111-119; doi:10.1101/gr.1.2.111

  3. McCabe, E R

    • Utility of PCR for DNA analysis from dried blood spots on filter paper blotters. Genome Res. November 1991 1: 99-106; doi:10.1101/gr.1.2.99

  4. Metcalf, M A

    • Slow inactivation of dry PCR templates by UV light. Genome Res. November 1991 1: 142-143; doi:10.1101/gr.1.2.142

  5. Moskovits, T

    • Rapid, nonradioactive screening for activating ras oncogene mutations using PCR-primer introduced restriction analysis (PCR-PIRA) Genome Res. November 1991 1: 146-148; doi:10.1101/gr.1.2.146

N

  1. Nisson, P E

    • Rapid and efficient cloning of Alu-PCR products using uracil DNA glycosylase. Genome Res. November 1991 1: 120-123; doi:10.1101/gr.1.2.120

O

  1. Overbeek, P A

    • Use of a simplified single-site PCR to facilitate cloning of genomic DNA sequences flanking a transgene integration site. Genome Res. November 1991 1: 129-135; doi:10.1101/gr.1.2.129

P

  1. Pääbo, S

    • Amplifying DNA from archeological remains: a meeting report. Genome Res. November 1991 1: 107-110; doi:10.1101/gr.1.2.107

  2. Parik, J

    • Capture PCR: efficient amplification of DNA fragments adjacent to a known sequence in human and YAC DNA. Genome Res. November 1991 1: 111-119; doi:10.1101/gr.1.2.111

  3. Passerini, F

    • A simple and rapid method to analyze specific mRNAs from few cells in a semi-quantitative way using the polymerase chain reaction. Genome Res. November 1991 1: 144-145; doi:10.1101/gr.1.2.144

  4. Pettersson, U

    • Capture PCR: efficient amplification of DNA fragments adjacent to a known sequence in human and YAC DNA. Genome Res. November 1991 1: 111-119; doi:10.1101/gr.1.2.111

  5. Platzer, C

R

  1. Rashtchian, A

    • Rapid and efficient cloning of Alu-PCR products using uracil DNA glycosylase. Genome Res. November 1991 1: 120-123; doi:10.1101/gr.1.2.120

S

  1. Stewart, J

    • Capture PCR: efficient amplification of DNA fragments adjacent to a known sequence in human and YAC DNA. Genome Res. November 1991 1: 111-119; doi:10.1101/gr.1.2.111

U

  1. Uberla, K

W

  1. Watkins, P C

    • Rapid and efficient cloning of Alu-PCR products using uracil DNA glycosylase. Genome Res. November 1991 1: 120-123; doi:10.1101/gr.1.2.120

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