111C Gamper, Jr., Howard - Jefferson Medical College - Thomas Jefferson University
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Howard Gamper, Jr., PhD

Contact Dr. Gamper, Jr.

233 South 10th Street
Philadelphia, PA 19107

(215) 503-9798
(215) 503-4954 fax

Most Recent Peer-reviewed Publications

  1. Potential for interdependent development of tRNA determinants for aminoacylation and ribosome decoding.
  2. Distinct kinetic determinants for the stepwise CCA addition to tRNA
  3. RecA-mediated strand invasion of DNA by oligonucleotides substituted with 2-aminoadenine and 2-thiothymine
  4. Properties of pseudo-complementary DNA substituted with weakly pairing analogs of guanine or cytosine
  5. Pyrrolo-C as a molecular probe for monitoring conformations of the tRNA 3′ end
  6. tRNA Integrity Is a Prerequisite for Rapid CCA Addition: Implication for Quality Control
  7. Enzymatic synthesis of structure-free DNA with pseudo-complementary properties
  8. Fluorescent labeling of tRNAs for dynamics experiments
  9. Kinetic Quality Control of Anticodon Recognition by a Eukaryotic Aminoacyl-tRNA Synthetase
  10. Unrestricted hybridization of oligonucleotides to structure-free DNA
  11. Isolation of a site-specifically modified RNA from an unmodified transcript
  12. Unrestricted accessibility of short oligonucleotides to RNA
  13. Modified bases in RNA reduce secondary structure and enhance hybridization
  14. Erratum: Strand bias in targeted gene repair is influenced by transcriptional activity (Molecular and Cellular Biology (2002) 22:11 (3852-3863))
  15. The synaptic complex of RecA protein participates in hybridization and inverse strand exchange reactions
  16. Nucleotide replacement at two sites can be directed by modified single-stranded oligonucleotides in vitro and in vivo
  17. Strand bias in targeted gene repair is influenced by transcriptional activity
  18. Evidence for a four-strand exchange catalyzed by the RecA protein
  19. The DNA strand of chimeric RNA/DNA oligonucleotides can direct gene repair/conversion activity in mammalian and plant cell-free extracts
  20. A plausible mechanism for gene correction by chimeric oligonucleotides
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