Index by Author

February 1993; 2 (3)
  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. Aalbers, K

    • Unwanted mutations in PCR mutagenesis: avoiding the predictable. Genome Res. February 1993 2: 253-257; doi:10.1101/gr.2.3.253

  2. Adriano, T

    • Synthesis and characterization of 5'-fluorescent-dye-labeled oligonucleotides. Genome Res. February 1993 2: 223-227; doi:10.1101/gr.2.3.223

B

  1. Bagnarelli, P

    • Quantitative PCR and RT-PCR in virology. Genome Res. February 1993 2: 191-196; doi:10.1101/gr.2.3.191

  2. Bambot, S B

    • Efficient total gene synthesis of 1.35-kb hybrid alpha-lytic protease gene using the polymerase chain reaction. Genome Res. February 1993 2: 266-271; doi:10.1101/gr.2.3.266

  3. Bickham, J W

    • Partial endonuclease digestion mapping of restriction sites using PCR-amplified DNA. Genome Res. February 1993 2: 228-233; doi:10.1101/gr.2.3.228

  4. Blanchard, M M

    • PCR buffer optimization with uniform temperature regimen to facilitate automation. Genome Res. February 1993 2: 234-240; doi:10.1101/gr.2.3.234

  5. Bradley, W G

    • Detection of the MAIDS virus using the polymerase chain reaction. Genome Res. February 1993 2: 272-274; doi:10.1101/gr.2.3.272

  6. Buell, R D

    • Detection of the MAIDS virus using the polymerase chain reaction. Genome Res. February 1993 2: 272-274; doi:10.1101/gr.2.3.272

C

  1. Chiang, L W

    • Mutagenic oligonucleotide-directed PCR amplification (Mod-PCR): an efficient method for generating random base substitution mutations in a DNA sequence element. Genome Res. February 1993 2: 210-217; doi:10.1101/gr.2.3.210

  2. Clementi, M

    • Quantitative PCR and RT-PCR in virology. Genome Res. February 1993 2: 191-196; doi:10.1101/gr.2.3.191

  3. Coriat, A M

    • PCR amplification of SRY-related gene sequences reveals evolutionary conservation of the SRY-box motif. Genome Res. February 1993 2: 218-222; doi:10.1101/gr.2.3.218

D

  1. Daniel, L J

    • An improved method for the detection of hepatitis C virus RNA in plasma utilizing heminested primers and internal control RNA. Genome Res. February 1993 2: 241-249; doi:10.1101/gr.2.3.241

  2. Day, N K

    • Detection of the MAIDS virus using the polymerase chain reaction. Genome Res. February 1993 2: 272-274; doi:10.1101/gr.2.3.272

F

  1. Falcinelli, C

    • Differential detection of colinear genes and RNA transcripts by modified reverse transcription and PCR. Genome Res. February 1993 2: 258-260; doi:10.1101/gr.2.3.258

  2. Froussard, P

    • rPCR: a powerful tool for random amplification of whole RNA sequences. Genome Res. February 1993 2: 185-190; doi:10.1101/gr.2.3.185

G

  1. Giusti, W G

    • Synthesis and characterization of 5'-fluorescent-dye-labeled oligonucleotides. Genome Res. February 1993 2: 223-227; doi:10.1101/gr.2.3.223

  2. Glickman, B W

  3. Good, R A

    • Detection of the MAIDS virus using the polymerase chain reaction. Genome Res. February 1993 2: 272-274; doi:10.1101/gr.2.3.272

  4. Gurvitz, A

    • Rapid preparation of limited biological samples for small-volume PCR. Genome Res. February 1993 2: 261-262; doi:10.1101/gr.2.3.261

H

  1. Harry, J L

    • PCR amplification of SRY-related gene sequences reveals evolutionary conservation of the SRY-box motif. Genome Res. February 1993 2: 218-222; doi:10.1101/gr.2.3.218

  2. Houge, G

    • Simplified construction of a subtracted cDNA library using asymmetric PCR. Genome Res. February 1993 2: 204-209; doi:10.1101/gr.2.3.204

  3. Howe, M M

    • Mutagenic oligonucleotide-directed PCR amplification (Mod-PCR): an efficient method for generating random base substitution mutations in a DNA sequence element. Genome Res. February 1993 2: 210-217; doi:10.1101/gr.2.3.210

I

  1. Ishaq, M

    • Effect of primer selection on spuriously generated deletion of a tandem repeat during PCR. Genome Res. February 1993 2: 263-265; doi:10.1101/gr.2.3.263

J

  1. Jones, D H

K

  1. Kovari, I

    • Mutagenic oligonucleotide-directed PCR amplification (Mod-PCR): an efficient method for generating random base substitution mutations in a DNA sequence element. Genome Res. February 1993 2: 210-217; doi:10.1101/gr.2.3.210

  2. Kusser, W C

L

  1. Lai, L Y

    • Rapid preparation of limited biological samples for small-volume PCR. Genome Res. February 1993 2: 261-262; doi:10.1101/gr.2.3.261

  2. Leigh, D A

    • Rapid preparation of limited biological samples for small-volume PCR. Genome Res. February 1993 2: 261-262; doi:10.1101/gr.2.3.261

  3. Levin, D B

  4. Lutz, C T

    • Unwanted mutations in PCR mutagenesis: avoiding the predictable. Genome Res. February 1993 2: 253-257; doi:10.1101/gr.2.3.253

M

  1. Manzin, A

    • Quantitative PCR and RT-PCR in virology. Genome Res. February 1993 2: 191-196; doi:10.1101/gr.2.3.191

  2. McDonald, B

    • Rapid preparation of limited biological samples for small-volume PCR. Genome Res. February 1993 2: 261-262; doi:10.1101/gr.2.3.261

  3. Menzo, S

    • Quantitative PCR and RT-PCR in virology. Genome Res. February 1993 2: 191-196; doi:10.1101/gr.2.3.191

  4. Morales, J C

    • Partial endonuclease digestion mapping of restriction sites using PCR-amplified DNA. Genome Res. February 1993 2: 228-233; doi:10.1101/gr.2.3.228

  5. Müller, U

    • PCR amplification of SRY-related gene sequences reveals evolutionary conservation of the SRY-box motif. Genome Res. February 1993 2: 218-222; doi:10.1101/gr.2.3.218

N

  1. Neilan, B A

    • Rapid preparation of limited biological samples for small-volume PCR. Genome Res. February 1993 2: 261-262; doi:10.1101/gr.2.3.261

  2. Nowotny, P

    • PCR buffer optimization with uniform temperature regimen to facilitate automation. Genome Res. February 1993 2: 234-240; doi:10.1101/gr.2.3.234

  3. Nowotny, V

    • PCR buffer optimization with uniform temperature regimen to facilitate automation. Genome Res. February 1993 2: 234-240; doi:10.1101/gr.2.3.234

O

  1. Ogata, N

    • Detection of the MAIDS virus using the polymerase chain reaction. Genome Res. February 1993 2: 272-274; doi:10.1101/gr.2.3.272

P

  1. Patton, J C

    • Partial endonuclease digestion mapping of restriction sites using PCR-amplified DNA. Genome Res. February 1993 2: 228-233; doi:10.1101/gr.2.3.228

Q

  1. Quint, W

    • Differential detection of colinear genes and RNA transcripts by modified reverse transcription and PCR. Genome Res. February 1993 2: 258-260; doi:10.1101/gr.2.3.258

R

  1. Romeo, J M

    • An improved method for the detection of hepatitis C virus RNA in plasma utilizing heminested primers and internal control RNA. Genome Res. February 1993 2: 241-249; doi:10.1101/gr.2.3.241

  2. Russell, A J

    • Efficient total gene synthesis of 1.35-kb hybrid alpha-lytic protease gene using the polymerase chain reaction. Genome Res. February 1993 2: 266-271; doi:10.1101/gr.2.3.266

S

  1. Sharpe, P T

    • PCR amplification of SRY-related gene sequences reveals evolutionary conservation of the SRY-box motif. Genome Res. February 1993 2: 218-222; doi:10.1101/gr.2.3.218

  2. Smith, K D

    • Unwanted mutations in PCR mutagenesis: avoiding the predictable. Genome Res. February 1993 2: 253-257; doi:10.1101/gr.2.3.253

  3. Stoner, G L

    • Effect of primer selection on spuriously generated deletion of a tandem repeat during PCR. Genome Res. February 1993 2: 263-265; doi:10.1101/gr.2.3.263

T

  1. Taillon-Miller, P

    • PCR buffer optimization with uniform temperature regimen to facilitate automation. Genome Res. February 1993 2: 234-240; doi:10.1101/gr.2.3.234

U

  1. Ulrich, P P

    • An improved method for the detection of hepatitis C virus RNA in plasma utilizing heminested primers and internal control RNA. Genome Res. February 1993 2: 241-249; doi:10.1101/gr.2.3.241

  2. Uwanogho, D

    • PCR amplification of SRY-related gene sequences reveals evolutionary conservation of the SRY-box motif. Genome Res. February 1993 2: 218-222; doi:10.1101/gr.2.3.218

V

  1. Valenza, A

    • Quantitative PCR and RT-PCR in virology. Genome Res. February 1993 2: 191-196; doi:10.1101/gr.2.3.191

  2. Valenzuela, A

    • Unwanted mutations in PCR mutagenesis: avoiding the predictable. Genome Res. February 1993 2: 253-257; doi:10.1101/gr.2.3.253

  3. van Belkum, A

    • Differential detection of colinear genes and RNA transcripts by modified reverse transcription and PCR. Genome Res. February 1993 2: 258-260; doi:10.1101/gr.2.3.258

  4. van Doorn, L J

    • Differential detection of colinear genes and RNA transcripts by modified reverse transcription and PCR. Genome Res. February 1993 2: 258-260; doi:10.1101/gr.2.3.258

  5. Varaldo, P E

    • Quantitative PCR and RT-PCR in virology. Genome Res. February 1993 2: 191-196; doi:10.1101/gr.2.3.191

  6. Vigna, J L

    • Unwanted mutations in PCR mutagenesis: avoiding the predictable. Genome Res. February 1993 2: 253-257; doi:10.1101/gr.2.3.253

  7. Vyas, G N

    • An improved method for the detection of hepatitis C virus RNA in plasma utilizing heminested primers and internal control RNA. Genome Res. February 1993 2: 241-249; doi:10.1101/gr.2.3.241

W

  1. Winistorfer, S C

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