201 results on '"Pintel, David J."'
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2. Activation of HIV-1 proviruses increases downstream chromatin accessibility
3. Mutation of a single amino acid of pregnane X receptor switches an antagonist to agonist by altering AF-2 helix positioning
4. The family Parvoviridae
5. The adeno-associated virus 2 genome and Rep 68/78 proteins interact with cellular sites of DNA damage
6. Rational engineering of a functional CpG-free ITR for AAV gene therapy
7. RNAse Mapping and Quantitation of RNA Isoforms
8. adeno-associated virus 2 genome and Rep 68/78 proteins interact with cellular sites of DNA damage.
9. Transfection of mammalian cells using linear polyethylenimine is a simple and effective means of producing recombinant adeno-associated virus vectors
10. Quantitation of encapsidated recombinant adeno-associated virus DNA in crude cell lysates and tissue culture medium by quantitative, real-time PCR
11. Binding of CCCTC-Binding Factor (CTCF) to the Minute Virus of Mice Genome Is Important for Proper Processing of Viral P4-Generated Pre-mRNAs
12. The NS1 protein of the parvovirus MVM Aids in the localization of the viral genome to cellular sites of DNA damage
13. Mutation of a single amino acid of pregnane X receptor switches an antagonist to agonist by altering AF-2 helix positioning
14. ICTV virus taxonomy profile: Parvoviridae
15. Minute Virus of Canines NP1 Protein Interacts with the Cellular Factor CPSF6 To Regulate Viral Alternative RNA Processing
16. The NS2 Protein Generated by the Parvovirus Minute Virus of Mice Is Degraded by the Proteasome in a Manner Independent of Ubiquitin Chain Elongation or Activation
17. Recombination within the Nonstructural Genes of the Parvovirus Minute Virus of Mice (MVM) Generates Functional Levels of Wild-type NS1, Which Can Be Detected in the Absence of Selective Pressure Following Transfection of Nonreplicating Plasmids
18. The Human Bocavirus 1 NP1 Protein Is a Multifunctional Regulator of Viral RNA Processing
19. Parvovirus minute virus of mice interacts with sites of cellular DNA damage to establish and amplify its lytic infection
20. Author response: Parvovirus minute virus of mice interacts with sites of cellular DNA damage to establish and amplify its lytic infection
21. Inclusion of the NS2-Specific Exon in Minute Virus of Mice mRNA Is Facilitated by an Intronic Splicing Enhancer That Affects Definition of the Downstream Small Intron
22. Minute Virus of Mice Inhibits Transcription of the Cyclin B1 Gene during Infection
23. Minute Virus of Canines NP1 Protein Governs the Expression of a Subset of Essential Nonstructural Proteins via Its Role in RNA Processing
24. Genetic engineering of CHO cells for viral resistance to minute virus of mice
25. NP1 Protein of the Bocaparvovirus Minute Virus of Canines Controls Access to the Viral Capsid Genes via Its Role in RNA Processing
26. Protoparvovirus Interactions with the Cellular DNA Damage Response.
27. Genetic engineering of CHO cells for viral resistance to minute virus of mice.
28. The ATR Signaling Pathway Is Disabled during Infection with the Parvovirus Minute Virus of Mice
29. Efficient Parvovirus Replication Requires CRL4Cdt2-Targeted Depletion of p21 to Prevent Its Inhibitory Interaction with PCNA
30. EXPRESSION OF VP2 PROTEIN OF RAT MINUTE VIRUS TYPE 1 (RMV-1) IN RECOMBINANT BACULOVIRUS AND ITS APPLICATION TO DIAGNOSIS OF RMV-1 INFECTION
31. Parvovirus-Induced Depletion of Cyclin B1 Prevents Mitotic Entry of Infected Cells
32. The family Parvoviridae
33. Characterization of the Nonstructural Proteins of the Bocavirus Minute Virus of Canines
34. The Adeno-Associated Virus Type 5 Small Rep Proteins Expressed via Internal Translation Initiation Are Functional
35. Replication of Minute Virus of Mice in Murine Cells Is Facilitated by Virally Induced Depletion of p21
36. Splicing of goose parvovirus pre-mRNA influences cytoplasmic translation of the processed mRNA
37. Parvovirus Minute Virus of Mice Induces a DNA Damage Response That Facilitates Viral Replication
38. Adeno-Associated Virus Small Rep Proteins Are Modified with at Least Two Types of Polyubiquitination
39. Adeno-Associated Virus Type 5 Utilizes Alternative Translation Initiation To Encode a Small Rep40-Like Protein
40. The Choice of Translation Initiation Site of the Rep Proteins from Goose Parvovirus P9-Generated mRNA Is Governed by Splicing and the Nature of the Excised Intron
41. Deaminase-Independent Inhibition of Parvoviruses by the APOBEC3A Cytidine Deaminase
42. Improved Splicing of Adeno-Associated Viral (AAV) Capsid Protein-Supplying Pre-mRNAs Leads to Increased Recombinant AAV Vector Production
43. Block to the Production of Full-Length B19 Virus Transcripts by Internal Polyadenylation Is Overcome by Replication of the Viral Genome
44. E4Orf6-E1B-55k-Dependent Degradation of De Novo-Generated Adeno-Associated Virus Type 5 Rep52 and Capsid Proteins Employs a Cullin 5-Containing E3 Ligase Complex
45. The transcription strategy of bovine adeno-associated virus (B-AAV) combines features of both adeno-associated virus type 2 (AAV2) and type 5 (AAV5)
46. Adeno-Associated Viruses Can Induce Phosphorylation of eIF2α via PKR Activation, Which Can Be Overcome by Helper Adenovirus Type 5 Virus-Associated RNA
47. Upstream AP1- and CREB-Binding Sites Confer High Basal Activity on the Adeno-Associated Virus Type 5 Capsid Gene Promoter
48. Positive and Negative Effects of Adenovirus Type 5 Helper Functions on Adeno-Associated Virus Type 5 (AAV5) Protein Accumulation Govern AAV5 Virus Production
49. Efficient Expression of the Adeno-Associated Virus Type 5 P41 Capsid Gene Promoter in 293 Cells Does Not Require Rep
50. Expression Profiles of Bovine Adeno-Associated Virus and Avian Adeno-Associated Virus Display Significant Similarity to That of Adeno-Associated Virus Type 5
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