Index by Author

February 1992; 1 (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. Abramow-Newerly, W

    • Analysis of transgenic animal pedigrees using the junction-polymerase chain reaction. Genome Res. February 1992 1: 208-209; doi:10.1101/gr.1.3.208

B

  1. Bej, A K

    • Applications of the polymerase chain reaction in environmental microbiology. Genome Res. February 1992 1: 151-159; doi:10.1101/gr.1.3.151

C

  1. Cheng, J

    • Sensitivity of detection of heterozygous point mutations in p53 cDNAs by direct PCR sequencing. Genome Res. February 1992 1: 199-201; doi:10.1101/gr.1.3.199

  2. Clapoff, S

    • Analysis of transgenic animal pedigrees using the junction-polymerase chain reaction. Genome Res. February 1992 1: 208-209; doi:10.1101/gr.1.3.208

  3. Collier, S

    • A method for specific amplification and PCR sequencing of individual members of multigene families: application to the study of steroid 21-hydroxylase deficiency. Genome Res. February 1992 1: 181-186; doi:10.1101/gr.1.3.181

D

  1. Dai, A

    • A sensitive, quantitative assay for measurement of allele-specific transcripts differing by a single nucleotide. Genome Res. February 1992 1: 160-163; doi:10.1101/gr.1.3.160

  2. Deng, S

    • Detection by PCR and differentiation by restriction fragment length polymorphism of Acholeplasma, Spiroplasma, Mycoplasma, and Ureaplasma, based upon 16S rRNA genes. Genome Res. February 1992 1: 202-204; doi:10.1101/gr.1.3.202

  3. Deragon, J M

    • RAPD and other PCR-based analyses of plant genomes using DNA extracted from small leaf disks. Genome Res. February 1992 1: 175-180; doi:10.1101/gr.1.3.175

  4. Dritschilo, A

    • Reliable and efficient direct sequencing of PCR-amplified double-stranded genomic DNA template. Genome Res. February 1992 1: 171-174; doi:10.1101/gr.1.3.171

G

  1. Grose, C

    • Site-directed mutagenesis of herpesvirus glycoprotein phosphorylation sites by recombination polymerase chain reaction. Genome Res. February 1992 1: 205-207; doi:10.1101/gr.1.3.205

H

  1. Haas, M

    • Sensitivity of detection of heterozygous point mutations in p53 cDNAs by direct PCR sequencing. Genome Res. February 1992 1: 199-201; doi:10.1101/gr.1.3.199

  2. Hiruki, C

    • Detection by PCR and differentiation by restriction fragment length polymorphism of Acholeplasma, Spiroplasma, Mycoplasma, and Ureaplasma, based upon 16S rRNA genes. Genome Res. February 1992 1: 202-204; doi:10.1101/gr.1.3.202

J

  1. Jacobson, D.R.

    • Rapid, nonradioactive screening for activating ras oncogene mutations using PCR-primer introduced restriction analysis (PCR-PIRA) Genome Res. February 1992 1: 210; doi:10.1101/gr.1.3.210

  2. Jones, D H

    • Site-directed mutagenesis of herpesvirus glycoprotein phosphorylation sites by recombination polymerase chain reaction. Genome Res. February 1992 1: 205-207; doi:10.1101/gr.1.3.205

  3. Jung, M

    • Reliable and efficient direct sequencing of PCR-amplified double-stranded genomic DNA template. Genome Res. February 1992 1: 171-174; doi:10.1101/gr.1.3.171

K

  1. Kasid, U

    • Reliable and efficient direct sequencing of PCR-amplified double-stranded genomic DNA template. Genome Res. February 1992 1: 171-174; doi:10.1101/gr.1.3.171

  2. Klemish, S W

    • A rapid PCR protocol for identification of differentially expressed genes from a cDNA library. Genome Res. February 1992 1: 195-198; doi:10.1101/gr.1.3.195

L

  1. Landry, B S

    • RAPD and other PCR-based analyses of plant genomes using DNA extracted from small leaf disks. Genome Res. February 1992 1: 175-180; doi:10.1101/gr.1.3.175

  2. LeBon, J M

    • A sensitive, quantitative assay for measurement of allele-specific transcripts differing by a single nucleotide. Genome Res. February 1992 1: 160-163; doi:10.1101/gr.1.3.160

  3. Lupski, J R

    • Rapid mapping of Escherichia coli::Tn5 insertion mutations by REP-Tn5 PCR. Genome Res. February 1992 1: 187-192; doi:10.1101/gr.1.3.187

M

  1. Mahbubani, M H

    • Applications of the polymerase chain reaction in environmental microbiology. Genome Res. February 1992 1: 151-159; doi:10.1101/gr.1.3.151

  2. McCabe, E R

    • Rapid mapping of Escherichia coli::Tn5 insertion mutations by REP-Tn5 PCR. Genome Res. February 1992 1: 187-192; doi:10.1101/gr.1.3.187

  3. Mischke, D

    • Avoiding strand reassociation in direct sequencing of double-stranded PCR products with thermolabile polymerases. Genome Res. February 1992 1: 193-194; doi:10.1101/gr.1.3.193

  4. Moskovitz, T.

    • Rapid, nonradioactive screening for activating ras oncogene mutations using PCR-primer introduced restriction analysis (PCR-PIRA) Genome Res. February 1992 1: 210; doi:10.1101/gr.1.3.210

  5. Mutchler, K J

    • A rapid PCR protocol for identification of differentially expressed genes from a cDNA library. Genome Res. February 1992 1: 195-198; doi:10.1101/gr.1.3.195

N

  1. Nabholz, M

R

  1. Reichenbach, P

  2. Riggs, A D

    • A sensitive, quantitative assay for measurement of allele-specific transcripts differing by a single nucleotide. Genome Res. February 1992 1: 160-163; doi:10.1101/gr.1.3.160

  3. Robertson, J A

    • Detection by PCR and differentiation by restriction fragment length polymorphism of Acholeplasma, Spiroplasma, Mycoplasma, and Ureaplasma, based upon 16S rRNA genes. Genome Res. February 1992 1: 202-204; doi:10.1101/gr.1.3.202

  4. Roder, J C

    • Analysis of transgenic animal pedigrees using the junction-polymerase chain reaction. Genome Res. February 1992 1: 208-209; doi:10.1101/gr.1.3.208

  5. Russo, A F

    • A rapid PCR protocol for identification of differentially expressed genes from a cDNA library. Genome Res. February 1992 1: 195-198; doi:10.1101/gr.1.3.195

S

  1. Singer-Sam, J

    • A sensitive, quantitative assay for measurement of allele-specific transcripts differing by a single nucleotide. Genome Res. February 1992 1: 160-163; doi:10.1101/gr.1.3.160

  2. Sperisen, P

  3. Stemke, G W

    • Detection by PCR and differentiation by restriction fragment length polymorphism of Acholeplasma, Spiroplasma, Mycoplasma, and Ureaplasma, based upon 16S rRNA genes. Genome Res. February 1992 1: 202-204; doi:10.1101/gr.1.3.202

  4. Strachan, T

    • A method for specific amplification and PCR sequencing of individual members of multigene families: application to the study of steroid 21-hydroxylase deficiency. Genome Res. February 1992 1: 181-186; doi:10.1101/gr.1.3.181

  5. Subramanian, P S

    • Rapid mapping of Escherichia coli::Tn5 insertion mutations by REP-Tn5 PCR. Genome Res. February 1992 1: 187-192; doi:10.1101/gr.1.3.187

T

  1. Tassabehji, M

    • A method for specific amplification and PCR sequencing of individual members of multigene families: application to the study of steroid 21-hydroxylase deficiency. Genome Res. February 1992 1: 181-186; doi:10.1101/gr.1.3.181

  2. Tilmans, I

    • Avoiding strand reassociation in direct sequencing of double-stranded PCR products with thermolabile polymerases. Genome Res. February 1992 1: 193-194; doi:10.1101/gr.1.3.193

V

  1. Versalovic, J

    • Rapid mapping of Escherichia coli::Tn5 insertion mutations by REP-Tn5 PCR. Genome Res. February 1992 1: 187-192; doi:10.1101/gr.1.3.187

W

  1. Wang, S M

  2. Wanner, R

    • Avoiding strand reassociation in direct sequencing of double-stranded PCR products with thermolabile polymerases. Genome Res. February 1992 1: 193-194; doi:10.1101/gr.1.3.193

  3. Ward, M

    • Analysis of transgenic animal pedigrees using the junction-polymerase chain reaction. Genome Res. February 1992 1: 208-209; doi:10.1101/gr.1.3.208

Y

  1. Yao, Z

    • Site-directed mutagenesis of herpesvirus glycoprotein phosphorylation sites by recombination polymerase chain reaction. Genome Res. February 1992 1: 205-207; doi:10.1101/gr.1.3.205

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