Index by Author

May 1992; 1 (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

B

  1. Balachandran, R

    • Introduction of multiple restriction enzyme sites by in vitro mutagenesis using the polymerase chain reaction.Genome Res. May 1992 1:277-278; doi:10.1101/gr.1.4.277

  2. Basile, A A

    • Analysis of gene expression: use of oligonucleotide primers for glyceraldehyde-3-phosphate dehydrogenase.Genome Res. May 1992 1:283-285; doi:10.1101/gr.1.4.283

  3. Baur, W

    • Effect of different laboratory techniques for guanidinium-phenol-chloroform RNA extraction on A260/A280 and on accuracy of mRNA quantitation by reverse transcriptase-PCR.Genome Res. May 1992 1:286-290; doi:10.1101/gr.1.4.286

  4. Belloni, E

    • Multiplex PCR for rapid detection of three mutations in the cystic fibrosis gene.Genome Res. May 1992 1:297-298; doi:10.1101/gr.1.4.297

  5. Betts, R F

    • Detection of influenza A and B in respiratory secretions with the polymerase chain reaction.Genome Res. May 1992 1:263-268; doi:10.1101/gr.1.4.263

  6. Bevan, I S

  7. Bos, J L

    • PCR-based approaches for detection of mutated ras genes.Genome Res. May 1992 1:211-216; doi:10.1101/gr.1.4.211

C

  1. Cariani, E

    • Direct PCR amplification of HCV RNA from human serum.Genome Res. May 1992 1:291-292; doi:10.1101/gr.1.4.291

  2. Claussen, U

    • PCR-mediated cloning of HpaII tiny fragments from microdissected human chromosomes.Genome Res. May 1992 1:229-233; doi:10.1101/gr.1.4.229

  3. Connolly, R

    • Effect of different laboratory techniques for guanidinium-phenol-chloroform RNA extraction on A260/A280 and on accuracy of mRNA quantitation by reverse transcriptase-PCR.Genome Res. May 1992 1:286-290; doi:10.1101/gr.1.4.286

  4. Coonrod, J D

    • Detection of influenza A and B in respiratory secretions with the polymerase chain reaction.Genome Res. May 1992 1:263-268; doi:10.1101/gr.1.4.263

  5. Cousins, D

    • Detection and identification of multiple mycobacterial pathogens by DNA amplification in a single tube.Genome Res. May 1992 1:269-273; doi:10.1101/gr.1.4.269

  6. Cremonesi, L

    • Multiplex PCR for rapid detection of three mutations in the cystic fibrosis gene.Genome Res. May 1992 1:297-298; doi:10.1101/gr.1.4.297

  7. Cruess, D F

    • Effect of different laboratory techniques for guanidinium-phenol-chloroform RNA extraction on A260/A280 and on accuracy of mRNA quantitation by reverse transcriptase-PCR.Genome Res. May 1992 1:286-290; doi:10.1101/gr.1.4.286

D

  1. Davidson, J N

    • Detection of influenza A and B in respiratory secretions with the polymerase chain reaction.Genome Res. May 1992 1:263-268; doi:10.1101/gr.1.4.263

  2. Dieffenbach, C W

    • Analysis of gene expression: use of oligonucleotide primers for glyceraldehyde-3-phosphate dehydrogenase.Genome Res. May 1992 1:283-285; doi:10.1101/gr.1.4.283
    • Effect of different laboratory techniques for guanidinium-phenol-chloroform RNA extraction on A260/A280 and on accuracy of mRNA quantitation by reverse transcriptase-PCR.Genome Res. May 1992 1:286-290; doi:10.1101/gr.1.4.286

  3. Dilworth, D D

    • Single-step elimination of contaminating DNA prior to reverse transcriptase PCR.Genome Res. May 1992 1:279-282; doi:10.1101/gr.1.4.279

  4. Donofrio, J C

    • Detection of influenza A and B in respiratory secretions with the polymerase chain reaction.Genome Res. May 1992 1:263-268; doi:10.1101/gr.1.4.263

  5. Dveksler, G S

    • Analysis of gene expression: use of oligonucleotide primers for glyceraldehyde-3-phosphate dehydrogenase.Genome Res. May 1992 1:283-285; doi:10.1101/gr.1.4.283

E

  1. Ehrlich, G D

    • Introduction of multiple restriction enzyme sites by in vitro mutagenesis using the polymerase chain reaction.Genome Res. May 1992 1:277-278; doi:10.1101/gr.1.4.277

  2. Erlich, H A

F

  1. Ferrari, M

    • Multiplex PCR for rapid detection of three mutations in the cystic fibrosis gene.Genome Res. May 1992 1:297-298; doi:10.1101/gr.1.4.297

  2. Ford-Lloyd, B V

    • The random amplification of polymorphic DNA for fingerprinting plants.Genome Res. May 1992 1:274-276; doi:10.1101/gr.1.4.274

G

  1. Gupta, K C

    • Facile PCR cloning of full-length Sendai virus mRNAs.Genome Res. May 1992 1:293-296; doi:10.1101/gr.1.4.293

  2. Gupta, P

    • Introduction of multiple restriction enzyme sites by in vitro mutagenesis using the polymerase chain reaction.Genome Res. May 1992 1:277-278; doi:10.1101/gr.1.4.277

H

  1. Hesse, S

    • PCR-mediated cloning of HpaII tiny fragments from microdissected human chromosomes.Genome Res. May 1992 1:229-233; doi:10.1101/gr.1.4.229

  2. Higuchi, R

  3. Holodniy, M

    • Quantitative RNA and DNA gene amplification can rapidly monitor HIV infection and antiviral activity in cell cultures.Genome Res. May 1992 1:257-262; doi:10.1101/gr.1.4.257

  4. Horsthemke, B

    • PCR-mediated cloning of HpaII tiny fragments from microdissected human chromosomes.Genome Res. May 1992 1:229-233; doi:10.1101/gr.1.4.229

  5. Hulla, J E

    • The rat genome contains a p53 pseudogene: detection of a processed pseudogene using PCR.Genome Res. May 1992 1:251-254; doi:10.1101/gr.1.4.251

I

  1. Ikonen, E

    • Quantitative determination of rare mRNA species by PCR and solid-phase minisequencing.Genome Res. May 1992 1:234-240; doi:10.1101/gr.1.4.234

K

  1. Katzenstein, D A

    • Quantitative RNA and DNA gene amplification can rapidly monitor HIV infection and antiviral activity in cell cultures.Genome Res. May 1992 1:257-262; doi:10.1101/gr.1.4.257

  2. Kere, J

    • Simplified template preparation and improved direct sequencing using Taq polymerase.Genome Res. May 1992 1:255-256; doi:10.1101/gr.1.4.255

  3. Kocher, T D

    • PCR, direct sequencing, and the comparative approach.Genome Res. May 1992 1:217-221; doi:10.1101/gr.1.4.217

L

  1. Lüdecke, H J

    • PCR-mediated cloning of HpaII tiny fragments from microdissected human chromosomes.Genome Res. May 1992 1:229-233; doi:10.1101/gr.1.4.229

M

  1. Magnani, C

    • Multiplex PCR for rapid detection of three mutations in the cystic fibrosis gene.Genome Res. May 1992 1:297-298; doi:10.1101/gr.1.4.297

  2. Manninen, T

    • Quantitative determination of rare mRNA species by PCR and solid-phase minisequencing.Genome Res. May 1992 1:234-240; doi:10.1101/gr.1.4.234

  3. McCarrey, J R

    • Single-step elimination of contaminating DNA prior to reverse transcriptase PCR.Genome Res. May 1992 1:279-282; doi:10.1101/gr.1.4.279

  4. Merigan, T C

    • Quantitative RNA and DNA gene amplification can rapidly monitor HIV infection and antiviral activity in cell cultures.Genome Res. May 1992 1:257-262; doi:10.1101/gr.1.4.257

  5. Montanaro, V

    • Simplified template preparation and improved direct sequencing using Taq polymerase.Genome Res. May 1992 1:255-256; doi:10.1101/gr.1.4.255

  6. Munthali, M

    • The random amplification of polymorphic DNA for fingerprinting plants.Genome Res. May 1992 1:274-276; doi:10.1101/gr.1.4.274

N

  1. Newbury, H J

    • The random amplification of polymorphic DNA for fingerprinting plants.Genome Res. May 1992 1:274-276; doi:10.1101/gr.1.4.274

P

  1. Peltonen, L

    • Quantitative determination of rare mRNA species by PCR and solid-phase minisequencing.Genome Res. May 1992 1:234-240; doi:10.1101/gr.1.4.234

  2. Primi, D

    • Direct PCR amplification of HCV RNA from human serum.Genome Res. May 1992 1:291-292; doi:10.1101/gr.1.4.291

R

  1. Rapley, R

  2. Ravaggi, A

    • Direct PCR amplification of HCV RNA from human serum.Genome Res. May 1992 1:291-292; doi:10.1101/gr.1.4.291

S

  1. Seia, M

    • Multiplex PCR for rapid detection of three mutations in the cystic fibrosis gene.Genome Res. May 1992 1:297-298; doi:10.1101/gr.1.4.297

  2. Shankarappa, B

    • Introduction of multiple restriction enzyme sites by in vitro mutagenesis using the polymerase chain reaction.Genome Res. May 1992 1:277-278; doi:10.1101/gr.1.4.277

  3. Sharefkin, J B

    • Effect of different laboratory techniques for guanidinium-phenol-chloroform RNA extraction on A260/A280 and on accuracy of mRNA quantitation by reverse transcriptase-PCR.Genome Res. May 1992 1:286-290; doi:10.1101/gr.1.4.286

  4. Srivastava, A K

    • Simplified template preparation and improved direct sequencing using Taq polymerase.Genome Res. May 1992 1:255-256; doi:10.1101/gr.1.4.255

  5. Syvänen, A C

    • Quantitative determination of rare mRNA species by PCR and solid-phase minisequencing.Genome Res. May 1992 1:234-240; doi:10.1101/gr.1.4.234

V

  1. van Mansfeld, A D

    • PCR-based approaches for detection of mutated ras genes.Genome Res. May 1992 1:211-216; doi:10.1101/gr.1.4.211

W

  1. Walker, M R

  2. Walsh, P S

  3. Wilton, S

    • Detection and identification of multiple mycobacterial pathogens by DNA amplification in a single tube.Genome Res. May 1992 1:269-273; doi:10.1101/gr.1.4.269

  4. Winters, M A

    • Quantitative RNA and DNA gene amplification can rapidly monitor HIV infection and antiviral activity in cell cultures.Genome Res. May 1992 1:257-262; doi:10.1101/gr.1.4.257

X

  1. Xu, X

    • Facile PCR cloning of full-length Sendai virus mRNAs.Genome Res. May 1992 1:293-296; doi:10.1101/gr.1.4.293

Y

  1. Yamaguchi, M

    • Effect of different laboratory techniques for guanidinium-phenol-chloroform RNA extraction on A260/A280 and on accuracy of mRNA quantitation by reverse transcriptase-PCR.Genome Res. May 1992 1:286-290; doi:10.1101/gr.1.4.286

Current Issue

  1. December 2008, 18 (12)
  1. Current Issue
  1. Alert me to new issues of Genome Research