Pages that link to "Q67280348"
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The following pages link to Extent of sequence homology required for bacteriophage lambda site-specific recombination (Q67280348):
Displaying 46 items.
- Directional cDNA library construction assisted by the in vitro recombination reaction (Q30978595) (← links)
- Mutations of the phage lambda attachment site alter the directionality of resolution of Holliday structures (Q33565595) (← links)
- Heteroduplex substrates for bacteriophage lambda site-specific recombination: cleavage and strand transfer products (Q33586416) (← links)
- Homology-dependent interactions determine the order of strand exchange by IntDOT recombinase (Q33633792) (← links)
- The effect of attachment site mutations on strand exchange in bacteriophage lambda site-specific recombination (Q33955556) (← links)
- Site-specific recombination of temperate Myxococcus xanthus phage Mx8: genetic elements required for integration. (Q33992470) (← links)
- Integration sites for genetic elements in prokaryotic tRNA and tmRNA genes: sublocation preference of integrase subfamilies (Q34528191) (← links)
- Role of homology in site-specific recombination of bacteriophage lambda: evidence against joining of cohesive ends (Q34630999) (← links)
- Integration and excision of a newly discovered bacteroides conjugative transposon, CTnBST. (Q35634460) (← links)
- Xis and Fis proteins prevent site-specific DNA inversion in lysogens of phage HK022 (Q35966880) (← links)
- Transposon Tn554 encodes three products required for transposition (Q36062472) (← links)
- CTnDOT integrase performs ordered homology-dependent and homology-independent strand exchanges (Q36082889) (← links)
- Roles of Exc protein and DNA homology in the CTnDOT excision reaction (Q36211727) (← links)
- Mutations in an integration host factor-binding site: effect on lambda site-specific recombination and regulatory implications (Q36262602) (← links)
- Holliday intermediates and reaction by-products in FLP protein-promoted site-specific recombination (Q36845129) (← links)
- Interactions of NBU1 IntN1 and Orf2x proteins with attachment site DNA. (Q37469777) (← links)
- Challenging a paradigm: the role of DNA homology in tyrosine recombinase reactions. (Q37504513) (← links)
- Specificity determinants in the attachment sites of bacteriophages HK022 and lambda (Q37608684) (← links)
- Dissecting the resolution reaction of lambda integrase using suicide Holliday junction substrates (Q37633216) (← links)
- Characterization of the bacteriophage lambda excisionase (Xis) protein: the C-terminus is required for Xis-integrase cooperativity but not for DNA binding (Q38325611) (← links)
- Attachment sites for bacteriophage P2 on the Escherichia coli chromosome: DNA sequences, localization on the physical map, and detection of a P2-like remnant in E. coli K-12 derivatives (Q38513986) (← links)
- The Integration and Excision of CTnDOT. (Q38536100) (← links)
- Excision of a conjugative transposon in vitro by the Int and Xis proteins of Tn916 (Q39721461) (← links)
- Secondary attachment site for bacteriophage lambda in the guaB gene of Escherichia coli (Q39961712) (← links)
- A mammalian artificial chromosome engineering system (ACE System) applicable to biopharmaceutical protein production, transgenesis and gene-based cell therapy (Q40483262) (← links)
- The Holliday junction intermediates of lambda integrative and excisive recombination respond differently to the bending proteins integration host factor and excisionase. (Q40805571) (← links)
- Synaptic intermediates in bacteriophage lambda site-specific recombination: integrase can align pairs of attachment sites. (Q40875010) (← links)
- Control of directionality in lambda site specific recombination (Q41853516) (← links)
- Site promiscuity of coliphage HK022 integrase as a tool for gene therapy (Q42155621) (← links)
- The N-terminus of IntDOT forms hydrophobic interactions during Holliday Junction resolution (Q42364175) (← links)
- Genomic analysis of Pseudomonas putida phage tf with localized single-strand DNA interruptions (Q42398484) (← links)
- Resolution of Holliday Junction Recombination Intermediates by Wild-Type and Mutant IntDOT Proteins (Q42706854) (← links)
- Resolution of Mismatched Overlap Holliday Junction Intermediates by the Tyrosine Recombinase IntDOT. (Q43107568) (← links)
- Analysis of insertion into secondary attachment sites by phage lambda and by int mutants with altered recombination specificity (Q43696558) (← links)
- Homology-dependent interactions in phage lambda site-specific recombination (Q44254975) (← links)
- A host factor absent from Lactococcus lactis subspecies lactis MG1363 is required for conjugative transposition (Q46623194) (← links)
- Swapping DNA strands and sensing homology without branch migration in lambda site-specific recombination (Q49320826) (← links)
- Junction mobility and resolution of Holliday structures by Flp site-specific recombinase. Testing partner compatibility during recombination. (Q52877878) (← links)
- Suicide substrates reveal properties of the homology-dependent steps during integrative recombination of bacteriophage lambda. (Q52887058) (← links)
- Uncoupling of the recombination and topoisomerase activities of the γδ resolvase by a mutation at the crossover point (Q58982893) (← links)
- Sensing homology at the strand-swapping step in λ excisive recombination (Q64389167) (← links)
- Sequence and spacing requirements of a retrovirus integration site (Q68294695) (← links)
- Proceedings of the British Pharmacological Society. 10th-18th September 1986. Abstracts (Q69659385) (← links)
- Topological analysis of the role of homology in Flp-mediated recombination (Q73174693) (← links)
- Recognition of core binding sites by bacteriophage integrases (Q74507032) (← links)
- Defining the structural and functional roles of the carboxyl region of the bacteriophage lambda excisionase (Xis) protein 1 1Edited by M. Gottesman (Q77116529) (← links)