Index by Author

April 1994; 3 (5)
  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. Andrus, L

    • A simplified method for PCR detection of hepatitis C virus RNA from human serum. Genome Res. April 1994 3: 308-309

B

  1. Bentley, D R

  2. Biery, M

    • Issues of variability, carryover contamination, and detection in 3SR-based assays. Genome Res. April 1994 3: S83-S94

  3. Bockstahler, L E

C

  1. Callen, W

  2. Carcillo, J A

    • Comparison of the enzyme-linked oligonucleotide sorbent assay to the 32P-labeled PCR/Southern blotting technique in quantitative analysis of human and rat mRNA. Genome Res. April 1994 3: 292-297

  3. Cease, K B

  4. Costa, G L

    • Protocols for cloning and analysis of blunt-ended PCR-generated DNA fragments. Genome Res. April 1994 3: S95-S106

D

  1. de Caballero, O L

    • Low-stringency PCR provides an internal control for negative results in PCR-based diagnosis. Genome Res. April 1994 3: 305-307

  2. Dias Neto, E

    • Low-stringency PCR provides an internal control for negative results in PCR-based diagnosis. Genome Res. April 1994 3: 305-307

F

  1. Fahy, E

    • Issues of variability, carryover contamination, and detection in 3SR-based assays. Genome Res. April 1994 3: S83-S94

G

  1. Ghosh, S S

    • Issues of variability, carryover contamination, and detection in 3SR-based assays. Genome Res. April 1994 3: S83-S94

  2. Giannelli, F

  3. Gingeras, T R

    • Issues of variability, carryover contamination, and detection in 3SR-based assays. Genome Res. April 1994 3: S83-S94

  4. Goulden, M

    • Issues of variability, carryover contamination, and detection in 3SR-based assays. Genome Res. April 1994 3: S83-S94

  5. Green, P M

H

  1. Hall, J M

  2. Haris, I I

  3. Hedden, V

J

  1. Jenkins, F J

K

  1. Kotewicz, M L

    • The use of phosphorothioate primers and exonuclease hydrolysis for the preparation of single-stranded PCR products and their detection by solid-phase hybridization. Genome Res. April 1994 3: 285-291

  2. Koury, M C

    • Low-stringency PCR provides an internal control for negative results in PCR-based diagnosis. Genome Res. April 1994 3: 305-307

  3. Kretz, K

L

  1. Lai, J

    • A simplified method for PCR detection of hepatitis C virus RNA from human serum. Genome Res. April 1994 3: 308-309

  2. Liedtke, W

    • Different methods of sample preparation influence sensitivity of Mycobacterium tuberculosis and Borrelia burgdorferi PCR. Genome Res. April 1994 3: 301-304

  3. Lohff, C J

M

  1. Molesh, D A

N

  1. Nikiforov, T T

    • The use of phosphorothioate primers and exonuclease hydrolysis for the preparation of single-stranded PCR products and their detection by solid-phase hybridization. Genome Res. April 1994 3: 285-291

O

  1. Opalka, B

    • Different methods of sample preparation influence sensitivity of Mycobacterium tuberculosis and Borrelia burgdorferi PCR. Genome Res. April 1994 3: 301-304

P

  1. Parise, A

    • Comparison of the enzyme-linked oligonucleotide sorbent assay to the 32P-labeled PCR/Southern blotting technique in quantitative analysis of human and rat mRNA. Genome Res. April 1994 3: 292-297

  2. Potcova, C A

  3. Prince, A M

    • A simplified method for PCR detection of hepatitis C virus RNA from human serum. Genome Res. April 1994 3: 308-309

R

  1. Rendle, R B

    • The use of phosphorothioate primers and exonuclease hydrolysis for the preparation of single-stranded PCR products and their detection by solid-phase hybridization. Genome Res. April 1994 3: 285-291

  2. Rogers, Y H

    • The use of phosphorothioate primers and exonuclease hydrolysis for the preparation of single-stranded PCR products and their detection by solid-phase hybridization. Genome Res. April 1994 3: 285-291

  3. Romanha, A J

    • Low-stringency PCR provides an internal control for negative results in PCR-based diagnosis. Genome Res. April 1994 3: 305-307

  4. Romkes-Sparks, M

    • Comparison of the enzyme-linked oligonucleotide sorbent assay to the 32P-labeled PCR/Southern blotting technique in quantitative analysis of human and rat mRNA. Genome Res. April 1994 3: 292-297

S

  1. Schmid, E

    • Different methods of sample preparation influence sensitivity of Mycobacterium tuberculosis and Borrelia burgdorferi PCR. Genome Res. April 1994 3: 301-304

  2. Simpson, A J

    • Low-stringency PCR provides an internal control for negative results in PCR-based diagnosis. Genome Res. April 1994 3: 305-307

W

  1. Wahls, W P

    • RNA associated with a heterodimeric protein that activates a meiotic homologous recombination hot spot: RL/RT/PCR strategy for cloning any unknown RNA or DNA. Genome Res. April 1994 3: 272-277

  2. Weiner, M P

    • Protocols for cloning and analysis of blunt-ended PCR-generated DNA fragments. Genome Res. April 1994 3: S95-S106

  3. Wolfe, L

    • A simplified method for PCR detection of hepatitis C virus RNA from human serum. Genome Res. April 1994 3: 308-309

Z

  1. Zeigler, M E

  2. Zimmermann, C W

    • Different methods of sample preparation influence sensitivity of Mycobacterium tuberculosis and Borrelia burgdorferi PCR. Genome Res. April 1994 3: 301-304

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