Index by Author

June 1995; 4 (6)
  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. Altwegg, M

    • A simple "universal" DNA extraction procedure using SDS and proteinase K is compatible with direct PCR amplification. Genome Res. June 1995 4: 368-370

B

  1. Buzás, Z

    • Rapid method for separation of microsatellite alleles by the PhastSystem. Genome Res. June 1995 4: 380-381

C

  1. Callis, M

    • Nonradioactive multiplex PCR screening strategy for the simultaneous detection of multiple low-density lipoprotein receptor gene mutations. Genome Res. June 1995 4: 352-356

  2. Cheifetz, S

D

  1. De Grandis, S A

  2. Deetz, K

    • Oligonucleotides with fluorescent dyes at opposite ends provide a quenched probe system useful for detecting PCR product and nucleic acid hybridization. Genome Res. June 1995 4: 357-362

  3. DeSilva, U

E

  1. Eggerding, F A

    • A one-step coupled amplification and oligonucleotide ligation procedure for multiplex genetic typing. Genome Res. June 1995 4: 337-345

F

  1. Flood, S J

    • Oligonucleotides with fluorescent dyes at opposite ends provide a quenched probe system useful for detecting PCR product and nucleic acid hybridization. Genome Res. June 1995 4: 357-362

G

  1. Giusti, W

    • Oligonucleotides with fluorescent dyes at opposite ends provide a quenched probe system useful for detecting PCR product and nucleic acid hybridization. Genome Res. June 1995 4: 357-362

  2. Goldenberger, D

    • A simple "universal" DNA extraction procedure using SDS and proteinase K is compatible with direct PCR amplification. Genome Res. June 1995 4: 368-370

  3. Green, E D

H

  1. Heroux, J A

    • Quantitative analysis of specific mRNA transcripts using a competitive PCR assay with electrochemiluminescent detection. Genome Res. June 1995 4: 327-330

  2. Hofmann, T A

  3. Hörnschemeyer, D

  4. Hu, J

K

  1. Kleesiek, K

  2. Kleiz, R

    • A method for rapid generation of competitive standard molecules for RT-PCR avoiding the problem of competitor/probe cross-reactions. Genome Res. June 1995 4: 371-375

  3. Kotze, M J

    • Nonradioactive multiplex PCR screening strategy for the simultaneous detection of multiple low-density lipoprotein receptor gene mutations. Genome Res. June 1995 4: 352-356

  4. Krizman, D B

L

  1. Langenhoven, E

    • Nonradioactive multiplex PCR screening strategy for the simultaneous detection of multiple low-density lipoprotein receptor gene mutations. Genome Res. June 1995 4: 352-356

  2. LeDuc, C

  3. Lichter, J

  4. Livak, K J

    • Oligonucleotides with fluorescent dyes at opposite ends provide a quenched probe system useful for detecting PCR product and nucleic acid hybridization. Genome Res. June 1995 4: 357-362

M

  1. Marmaro, J

    • Oligonucleotides with fluorescent dyes at opposite ends provide a quenched probe system useful for detecting PCR product and nucleic acid hybridization. Genome Res. June 1995 4: 357-362

  2. Meltzer, P S

  3. Miller, P

P

  1. Parry, P

  2. Peeters, A V

    • Nonradioactive multiplex PCR screening strategy for the simultaneous detection of multiple low-density lipoprotein receptor gene mutations. Genome Res. June 1995 4: 352-356

  3. Perschil, I

    • A simple "universal" DNA extraction procedure using SDS and proteinase K is compatible with direct PCR amplification. Genome Res. June 1995 4: 368-370

Q

  1. Quiros, C F

R

  1. Reske-Kunz, A B

    • A method for rapid generation of competitive standard molecules for RT-PCR avoiding the problem of competitor/probe cross-reactions. Genome Res. June 1995 4: 371-375

  2. Ritzler, M

    • A simple "universal" DNA extraction procedure using SDS and proteinase K is compatible with direct PCR amplification. Genome Res. June 1995 4: 368-370

  3. Ross, R

    • A method for rapid generation of competitive standard molecules for RT-PCR avoiding the problem of competitor/probe cross-reactions. Genome Res. June 1995 4: 371-375

S

  1. Sallés, F J

  2. Strickland, S

  3. Szczepanik, A M

    • Quantitative analysis of specific mRNA transcripts using a competitive PCR assay with electrochemiluminescent detection. Genome Res. June 1995 4: 327-330

T

  1. Theart, L

    • Nonradioactive multiplex PCR screening strategy for the simultaneous detection of multiple low-density lipoprotein receptor gene mutations. Genome Res. June 1995 4: 352-356

  2. Thiart, R

    • Nonradioactive multiplex PCR screening strategy for the simultaneous detection of multiple low-density lipoprotein receptor gene mutations. Genome Res. June 1995 4: 352-356

  3. Trent, J M

V

  1. van Eysden, J

  2. Varga, L

    • Rapid method for separation of microsatellite alleles by the PhastSystem. Genome Res. June 1995 4: 380-381

W

  1. Wilkinson, E T

  2. Wolff, C

  3. Wolff, D

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