Index by Author

December 1994; 4 (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. Altschuler, M

  2. Aslanidis, C

    • Minimal length requirement of the single-stranded tails for ligation-independent cloning (LIC) of PCR products. Genome Res. December 1994 4: 172-177

B

  1. Bahramian, M B

    • Direct gene quantitation by PCR reveals differential accumulation of ectopic enzyme in rat-1 cells, v-fos transformants, and revertants. Genome Res. December 1994 4: 145-153

  2. Bartlett, J M

  3. Battistini, L

    • A comparison of methods for RNA extraction from lymphocytes for RT-PCR. Genome Res. December 1994 4: 185-187

  4. Benedetto, J P

  5. Blair, P

  6. Bonnet, J

  7. Borneman, J

  8. Brosnan, C F

    • A comparison of methods for RNA extraction from lymphocytes for RT-PCR. Genome Res. December 1994 4: 185-187

  9. Burdick, B A

C

  1. Cooke, T G

  2. Costa, G L

D

  1. de Jong, P J

    • Minimal length requirement of the single-stranded tails for ligation-independent cloning (LIC) of PCR products. Genome Res. December 1994 4: 172-177

  2. DeGrandis, P

  3. Dosch, H M

    • Quantitative analysis of gene expression in different tissues by template-calibrated RT-PCR and laser-induced fluorescence. Genome Res. December 1994 4: 154-159

F

  1. Fanburg, B L

    • A competitive deletion mutant quantitative PCR assay for angiotensin-converting enzyme mRNA in smooth muscle cells. Genome Res. December 1994 4: 167-171

  2. Fujita, K

G

  1. Gaedigk, R

    • Quantitative analysis of gene expression in different tissues by template-calibrated RT-PCR and laser-induced fluorescence. Genome Res. December 1994 4: 154-159

  2. Galasinski, S

  3. Garret, M

H

  1. Hamoui, S

  2. Hampel, A

J

  1. Jackson, J B

K

  1. Karges, W J

    • Quantitative analysis of gene expression in different tissues by template-calibrated RT-PCR and laser-induced fluorescence. Genome Res. December 1994 4: 154-159

  2. Kong, X J

    • A competitive deletion mutant quantitative PCR assay for angiotensin-converting enzyme mRNA in smooth muscle cells. Genome Res. December 1994 4: 167-171

  3. Kotze, M J

    • Improved heteroduplex detection of single-base substitutions in PCR-amplified DNA. Genome Res. December 1994 4: 188-190

L

  1. Lanzillo, J J

    • A competitive deletion mutant quantitative PCR assay for angiotensin-converting enzyme mRNA in smooth muscle cells. Genome Res. December 1994 4: 167-171

  2. Liedtke, W

    • A comparison of methods for RNA extraction from lymphocytes for RT-PCR. Genome Res. December 1994 4: 185-187

P

  1. Pease, L R

    • In vitro synthesis of novel genes: mutagenesis and recombination by PCR. Genome Res. December 1994 4: S123-S130

  2. Peeters, A V

    • Improved heteroduplex detection of single-base substitutions in PCR-amplified DNA. Genome Res. December 1994 4: 188-190

  3. Pogulis, R J

    • In vitro synthesis of novel genes: mutagenesis and recombination by PCR. Genome Res. December 1994 4: S123-S130

R

  1. Raine, C S

    • A comparison of methods for RNA extraction from lymphocytes for RT-PCR. Genome Res. December 1994 4: 185-187

  2. Ramanujam, R

  3. Reichelderfer, P S

S

  1. Schmitz, G

    • Minimal length requirement of the single-stranded tails for ligation-independent cloning (LIC) of PCR products. Genome Res. December 1994 4: 172-177

  2. Silver, J

  3. Siwkowski, A

U

  1. Underwood, M A

V

  1. Vallejo, A N

    • In vitro synthesis of novel genes: mutagenesis and recombination by PCR. Genome Res. December 1994 4: S123-S130

W

  1. Weiner, M P

Z

  1. Zarbl, H

    • Direct gene quantitation by PCR reveals differential accumulation of ectopic enzyme in rat-1 cells, v-fos transformants, and revertants. Genome Res. December 1994 4: 145-153

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