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1. Enabling adoption of 2D-NMR for the higher order structure assessment of monoclonal antibody therapeutics

2. Enabling adoption of 2D-NMR for the higher order structure assessment of monoclonal antibody therapeutics.

3. Carbohydrates protect protein against abiotic fragmentation by soil minerals.

4. Assessing Coupled Protein Folding and Binding Through Temperature-Dependent Isothermal Titration Calorimetry.

5. Role of Ordered Proteins in the Folding-Upon-Binding of Intrinsically Disordered Proteins.

6. Carbon-Detected (15)N NMR Spin Relaxation of an Intrinsically Disordered Protein: FCP1 Dynamics Unbound and in Complex with RAP74.

7. The disordered C-terminus of the RNA polymerase II phosphatase FCP1 is partially helical in the unbound state.

8. Following the RAD6 pathway.

9. The Saccharomyces cerevisiae rev6-1 mutation, which inhibits both the lesion bypass and the recombination mode of DNA damage tolerance, is an allele of POL30, encoding proliferating cell nuclear antigen.

10. The error-free component of the RAD6/RAD18 DNA damage tolerance pathway of budding yeast employs sister-strand recombination.

11. Binding of MutS mismatch repair protein to DNA containing UV photoproducts, "mismatched" opposite Watson--Crick and novel nucleotides, in different DNA sequence contexts.

12. Transient loss of MHC class I tetramer binding after CD8+ T cell activation reflects altered T cell effector function.

13. Frequency, specificity, and sites of expansion of CD8+ T cells during primary pulmonary influenza virus infection.

14. In vivo evidence for a recA-independent recombination process in Escherichia coli that permits completion of replication of DNA containing UV damage in both strands.

15. The relative roles in vivo of Saccharomyces cerevisiae Pol eta, Pol zeta, Rev1 protein and Pol32 in the bypass and mutation induction of an abasic site, T-T (6-4) photoadduct and T-T cis-syn cyclobutane dimer.

16. Activation, differentiation, and migration of naive virus-specific CD8+ T cells during pulmonary influenza virus infection.

17. Cellular functions of DNA polymerase zeta and Rev1 protein.

18. hREV3 is essential for error-prone translesion synthesis past UV or benzo[a]pyrene diol epoxide-induced DNA lesions in human fibroblasts.

19. Cellular roles of DNA polymerase zeta and Rev1 protein.

20. Escherichia coli DNA polymerase III can replicate efficiently past a T-T cis-syn cyclobutane dimer if DNA polymerase V and the 3' to 5' exonuclease proofreading function encoded by dnaQ are inactivated.

22. CD8(+) T cell-mediated injury in vivo progresses in the absence of effector T cells.

23. Eukaryotic DNA polymerases: proposal for a revised nomenclature.

24. The Y-family of DNA polymerases.

25. Eukaryotic mutagenesis and translesion replication dependent on DNA polymerase zeta and Rev1 protein.

26. Mutagenesis in eukaryotes dependent on DNA polymerase zeta and Rev1p.

27. Evidence for a second function for Saccharomyces cerevisiae Rev1p.

28. The function of the human homolog of Saccharomyces cerevisiae REV1 is required for mutagenesis induced by UV light.

29. Intrinsic polymerase activities of UmuD'(2)C and MucA'(2)B are responsible for their different mutagenic properties during bypass of a T-T cis-syn cyclobutane dimer.

30. UV lesions located on the leading strand inhibit DNA replication but do not inhibit SV40 T-antigen helicase activity.

31. Roles of DNA polymerase zeta and Rev1 protein in eukaryotic mutagenesis and translesion replication.

32. Specific binding of human MSH2.MSH6 mismatch-repair protein heterodimers to DNA incorporating thymine- or uracil-containing UV light photoproducts opposite mismatched bases.

33. Efficient translesion replication in the absence of Escherichia coli Umu proteins and 3'-5' exonuclease proofreading function.

34. A human homolog of the Saccharomyces cerevisiae REV3 gene, which encodes the catalytic subunit of DNA polymerase zeta.

35. Mutagenic properties of the T-C cyclobutane dimer.

36. Deoxycytidyl transferase activity of yeast REV1 protein.

37. Analysis of the mutagenic properties of the UmuDC, MucAB and RumAB proteins, using a site-specific abasic lesion.

38. Thymine-thymine dimer bypass by yeast DNA polymerase zeta.

39. Mutagenicity of a unique thymine-thymine dimer or thymine-thymine pyrimidine pyrimidone (6-4) photoproduct in mammalian cells.

40. Substitution of mucAB or rumAB for umuDC alters the relative frequencies of the two classes of mutations induced by a site-specific T-T cyclobutane dimer and the efficiency of translesion DNA synthesis.

41. Complete replication of plasmid DNA containing a single UV-induced lesion in human cell extracts.

42. DNA polymerase zeta and the control of DNA damage induced mutagenesis in eukaryotes.

43. Novel mutagenic properties of abasic sites in Saccharomyces cerevisiae.

44. The T-T pyrimidine (6-4) pyrimidinone UV photoproduct is much less mutagenic in yeast than in Escherichia coli.

45. Cloning and sequence of REV7, a gene whose function is required for DNA damage-induced mutagenesis in Saccharomyces cerevisiae.

46. Accuracy of replication past the T-C (6-4) adduct.

47. Repair by human cell extracts of single (6-4) and cyclobutane thymine-thymine photoproducts in DNA.

48. U-U and T-T cyclobutane dimers have different mutational properties.

49. Human non-secretory ribonucleases. I. Purification, peptide mapping and lectin blotting analysis of the kidney, liver and spleen enzymes.

50. Human non-secretory ribonucleases. II. Structural characterization of the N-glycans of the kidney, liver and spleen enzymes by NMR spectroscopy and electrospray mass spectrometry.

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