Index by Author

February 1995; 4 (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. Beyermann, B

    • Identification of the species origin of highly processed meat products by mitochondrial DNA sequences. Genome Res. February 1995 4: 241-243

  2. Bhatnagar, R K

    • Background-minimized cassette mutagenesis by PCR using cassette-specific selection markers: a useful general approach for studying structure-function relationships of multisubstrate enzymes. Genome Res. February 1995 4: 212-218

  3. Brandt, P

    • Identification of the species origin of highly processed meat products by mitochondrial DNA sequences. Genome Res. February 1995 4: 241-243

  4. Brookes, A J

    • Catch-linker + PCR labeling: a simple method to generate fluorescence in situ hybridization probes from yeast artificial chromosomes. Genome Res. February 1995 4: 209-211

C

  1. Cheng, J

    • Metastable single-strand DNA conformational polymorphism analysis results in enhanced polymorphism detection. Genome Res. February 1995 4: 227-233

  2. Choong, C S

    • An evaluation of competitor type and size for use in the determination of mRNA by competitive PCR. Genome Res. February 1995 4: 219-226

D

  1. Devon, R S

    • Catch-linker + PCR labeling: a simple method to generate fluorescence in situ hybridization probes from yeast artificial chromosomes. Genome Res. February 1995 4: 209-211

  2. Dries, C

    • The one-tube quantitative HIV-1 RNA NASBA: precision, accuracy, and application. Genome Res. February 1995 4: S177-S184

  3. Dussurget, O

    • Advances in PCR-based detection of mycoplasmas contaminating cell cultures. Genome Res. February 1995 4: 199-208

F

  1. Fattah, F A

    • Background-minimized cassette mutagenesis by PCR using cassette-specific selection markers: a useful general approach for studying structure-function relationships of multisubstrate enzymes. Genome Res. February 1995 4: 212-218

  2. Fujiwara, H

    • PCR with deoxyinosine-containing primers using DNA polymerases with proofreading activity. Genome Res. February 1995 4: 239-240

  3. Fujiwara, K

    • PCR with deoxyinosine-containing primers using DNA polymerases with proofreading activity. Genome Res. February 1995 4: 239-240

G

  1. Gosden, J R

    • Catch-linker + PCR labeling: a simple method to generate fluorescence in situ hybridization probes from yeast artificial chromosomes. Genome Res. February 1995 4: 209-211

H

  1. Hashimoto, K

    • PCR with deoxyinosine-containing primers using DNA polymerases with proofreading activity. Genome Res. February 1995 4: 239-240

  2. Hiesel, R

    • Identification of the species origin of highly processed meat products by mitochondrial DNA sequences. Genome Res. February 1995 4: 241-243

  3. Hurley, D M

    • An evaluation of competitor type and size for use in the determination of mRNA by competitive PCR. Genome Res. February 1995 4: 219-226

J

  1. Jurriaans, S

    • The one-tube quantitative HIV-1 RNA NASBA: precision, accuracy, and application. Genome Res. February 1995 4: S177-S184

K

  1. Kasuga, T

    • Metastable single-strand DNA conformational polymorphism analysis results in enhanced polymorphism detection. Genome Res. February 1995 4: 227-233

  2. Kievits, T

    • The one-tube quantitative HIV-1 RNA NASBA: precision, accuracy, and application. Genome Res. February 1995 4: S177-S184

  3. Kury, F

    • Quantitative detection of reverse transcriptase-PCR products by means of a novel and sensitive DNA stain. Genome Res. February 1995 4: 234-238

L

  1. Lönneborg, A

    • Construction of subtractive cDNA library using magnetic beads and PCR. Genome Res. February 1995 4: S168-S176

M

  1. Majumder, K

    • Background-minimized cassette mutagenesis by PCR using cassette-specific selection markers: a useful general approach for studying structure-function relationships of multisubstrate enzymes. Genome Res. February 1995 4: 212-218

  2. Maule, J C

    • Catch-linker + PCR labeling: a simple method to generate fluorescence in situ hybridization probes from yeast artificial chromosomes. Genome Res. February 1995 4: 209-211

  3. McCulloch, R K

    • An evaluation of competitor type and size for use in the determination of mRNA by competitive PCR. Genome Res. February 1995 4: 219-226

  4. Mitchelson, K R

    • Metastable single-strand DNA conformational polymorphism analysis results in enhanced polymorphism detection. Genome Res. February 1995 4: 227-233

N

  1. Nuovo, G J

P

  1. Porteous, D J

    • Catch-linker + PCR labeling: a simple method to generate fluorescence in situ hybridization probes from yeast artificial chromosomes. Genome Res. February 1995 4: 209-211

R

  1. Rawadi, G

    • Advances in PCR-based detection of mycoplasmas contaminating cell cultures. Genome Res. February 1995 4: 199-208

S

  1. Schneeberger, C

    • Quantitative detection of reverse transcriptase-PCR products by means of a novel and sensitive DNA stain. Genome Res. February 1995 4: 234-238

  2. Schoones, R

    • The one-tube quantitative HIV-1 RNA NASBA: precision, accuracy, and application. Genome Res. February 1995 4: S177-S184

  3. Selvapandiyan, A

    • Background-minimized cassette mutagenesis by PCR using cassette-specific selection markers: a useful general approach for studying structure-function relationships of multisubstrate enzymes. Genome Res. February 1995 4: 212-218

  4. Sharma, P

    • Construction of subtractive cDNA library using magnetic beads and PCR. Genome Res. February 1995 4: S168-S176

  5. Shibasaki, Y

    • Catch-linker + PCR labeling: a simple method to generate fluorescence in situ hybridization probes from yeast artificial chromosomes. Genome Res. February 1995 4: 209-211

  6. Sillekens, P

    • The one-tube quantitative HIV-1 RNA NASBA: precision, accuracy, and application. Genome Res. February 1995 4: S177-S184

  7. Slorach, E M

    • Catch-linker + PCR labeling: a simple method to generate fluorescence in situ hybridization probes from yeast artificial chromosomes. Genome Res. February 1995 4: 209-211

  8. Speiser, P

    • Quantitative detection of reverse transcriptase-PCR products by means of a novel and sensitive DNA stain. Genome Res. February 1995 4: 234-238

  9. Stougaard, P

    • Construction of subtractive cDNA library using magnetic beads and PCR. Genome Res. February 1995 4: S168-S176

U

  1. Unseld, M

    • Identification of the species origin of highly processed meat products by mitochondrial DNA sequences. Genome Res. February 1995 4: 241-243

V

  1. v d Wiel, P

    • The one-tube quantitative HIV-1 RNA NASBA: precision, accuracy, and application. Genome Res. February 1995 4: S177-S184

  2. van Beuningen, R

    • The one-tube quantitative HIV-1 RNA NASBA: precision, accuracy, and application. Genome Res. February 1995 4: S177-S184

  3. van Gemen, B

    • The one-tube quantitative HIV-1 RNA NASBA: precision, accuracy, and application. Genome Res. February 1995 4: S177-S184

Z

  1. Zeillinger, R

    • Quantitative detection of reverse transcriptase-PCR products by means of a novel and sensitive DNA stain. Genome Res. February 1995 4: 234-238

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