Pages that link to "Q28253487"
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The following pages link to Nonoverlapping functions of DNA polymerases mu, lambda, and terminal deoxynucleotidyltransferase during immunoglobulin V(D)J recombination in vivo (Q28253487):
Displaying 50 items.
- The mechanism of double-strand DNA break repair by the nonhomologous DNA end-joining pathway (Q22065419) (← links)
- VprBP binds full-length RAG1 and is required for B-cell development and V(D)J recombination fidelity (Q24299516) (← links)
- DNA polymerase family X: function, structure, and cellular roles (Q24612173) (← links)
- Cernunnos/XLF promotes the ligation of mismatched and noncohesive DNA ends (Q24676586) (← links)
- Structure-function studies of DNA polymerase λ (Q26849468) (← links)
- Increased learning and brain long-term potentiation in aged mice lacking DNA polymerase μ (Q27322746) (← links)
- Structural insight into the substrate specificity of DNA Polymerase mu (Q27643274) (← links)
- Role of the catalytic metal during polymerization by DNA polymerase lambda (Q27644681) (← links)
- Loop 1 modulates the fidelity of DNA polymerase (Q27661142) (← links)
- Sustained active site rigidity during synthesis by human DNA polymerase μ (Q27681565) (← links)
- Structural basis for the binding and incorporation of nucleotide analogs with L-stereochemistry by human DNA polymerase (Q27684663) (← links)
- XRCC4:DNA ligase IV can ligate incompatible DNA ends and can ligate across gaps (Q27919707) (← links)
- End-bridging is required for pol mu to efficiently promote repair of noncomplementary ends by nonhomologous end joining (Q27919720) (← links)
- Terminal deoxynucleotidyl transferase: the story of a misguided DNA polymerase (Q28251730) (← links)
- The mechanism of human nonhomologous DNA end joining (Q28257187) (← links)
- Flexibility in the order of action and in the enzymology of the nuclease, polymerases, and ligase of vertebrate non-homologous DNA end joining: relevance to cancer, aging, and the immune system (Q28261381) (← links)
- Role of non-homologous end joining in V(D)J recombination (Q28266265) (← links)
- Mutation of POLB causes lupus in mice (Q28513579) (← links)
- Expansion of the preimmune antibody repertoire by junctional diversity in Bos taurus. (Q31165460) (← links)
- Genetic evidence for single-strand lesions initiating Nbs1-dependent homologous recombination in diversification of Ig v in chicken B lymphocytes (Q33404063) (← links)
- Nonhomologous end joining: a good solution for bad ends (Q33625010) (← links)
- Essential factors for incompatible DNA end joining at chromosomal DNA double strand breaks in vivo (Q34110326) (← links)
- Identification of critical residues for the tight binding of both correct and incorrect nucleotides to human DNA polymerase λ (Q34213489) (← links)
- Modeling DNA polymerase μ motions: subtle transitions before chemistry (Q34306952) (← links)
- ATM influences the efficiency of TCRβ rearrangement, subsequent TCRβ-dependent T cell development, and generation of the pre-selection TCRβ CDR3 repertoire (Q34692873) (← links)
- "Gate-keeper" residues and active-site rearrangements in DNA polymerase μ help discriminate non-cognate nucleotides (Q34743729) (← links)
- Nonhomologous DNA end joining (NHEJ) and chromosomal translocations in humans (Q34813549) (← links)
- Modulation of Pleurodeles waltl DNA polymerase mu expression by extreme conditions encountered during spaceflight (Q34920700) (← links)
- Choosing the right path: Does DNA-PK help make the decision? (Q35029335) (← links)
- Essential role for polymerase specialization in cellular nonhomologous end joining. (Q35989901) (← links)
- Error-free bypass of 2-hydroxyadenine by human DNA polymerase lambda with Proliferating Cell Nuclear Antigen and Replication Protein A in different sequence contexts (Q35990879) (← links)
- The X family portrait: structural insights into biological functions of X family polymerases. (Q36248608) (← links)
- Terminal deoxynucleotidyl transferase is required for an optimal response to the polysaccharide α-1,3 dextran (Q36455593) (← links)
- Multiple functions of DNA polymerases (Q36667353) (← links)
- Silencing of human DNA polymerase λ causes replication stress and is synthetically lethal with an impaired S phase checkpoint (Q36668832) (← links)
- Control of DNA polymerase lambda stability by phosphorylation and ubiquitination during the cell cycle (Q36946963) (← links)
- Bacterial DNA repair by non-homologous end joining (Q36972411) (← links)
- A comparison of BRCT domains involved in nonhomologous end-joining: introducing the solution structure of the BRCT domain of polymerase lambda. (Q36974836) (← links)
- Exome Array Analysis of Susceptibility to Pneumococcal Meningitis (Q37076439) (← links)
- DNA polymerases and cancer. (Q37084895) (← links)
- Mechanistic flexibility as a conserved theme across 3 billion years of nonhomologous DNA end-joining (Q37087051) (← links)
- A role for DNA polymerase mu in the emerging DJH rearrangements of the postgastrulation mouse embryo. (Q37099950) (← links)
- DNA polymerases in adaptive immunity (Q37109944) (← links)
- Probing conformational changes of human DNA polymerase lambda using mass spectrometry-based protein footprinting (Q37298232) (← links)
- Limited terminal transferase in human DNA polymerase mu defines the required balance between accuracy and efficiency in NHEJ. (Q37334769) (← links)
- Repair of ionizing radiation-induced DNA double-strand breaks by non-homologous end-joining (Q37365625) (← links)
- DNA polymerases β and λ do not directly affect Ig variable region somatic hypermutation although their absence reduces the frequency of mutations (Q37724828) (← links)
- Polymerases in nonhomologous end joining: building a bridge over broken chromosomes (Q37774662) (← links)
- Ubiquitylation of DNA polymerase λ. (Q37864395) (← links)
- Translesion DNA synthesis in the context of cancer research (Q37952001) (← links)