| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1111/J.1600-065X.1998.TB01430.X |
| P698 | PubMed publication ID | 9602353 |
| P2093 | author name string | N Maizels | |
| Q Kong | |||
| R S Harris | |||
| P2860 | cites work | Elevated levels of mutation in multiple tissues of mice deficient in the DNA mismatch repair gene Pms2 | Q22248073 |
| Homothallic switching of yeast mating type cassettes is initiated by a double-stranded cut in the MAT locus | Q27930817 | ||
| The double-strand-break repair model for recombination | Q28267259 | ||
| Conformations of immunoglobulin hypervariable regions | Q28273335 | ||
| Somatic mutation. From the dark zone to the light | Q72707873 | ||
| Preimmune diversification creates a repertoire while somatic hypermutation fine-tunes affinity--implications for the processes of mutation | Q72761221 | ||
| Evidence for a physical interaction between the transposed and the substituted sequences during mating type gene transposition in yeast | Q72867871 | ||
| Evaluation of the role of the 3'alpha heavy chain enhancer [3'alpha E(hs1,2)] in Vh gene somatic hypermutation | Q73689109 | ||
| The inactivation of the XP-C gene does not affect somatic hypermutation or class switch recombination of immunoglobulin genes | Q73864520 | ||
| Nuclear Rad51 foci induced by DNA damage are distinct from Rad51 foci associated with B cell activation and recombination | Q74000210 | ||
| Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over | Q28282791 | ||
| The origin of mutants | Q28288915 | ||
| Rad51 expression and localization in B cells carrying out class switch recombination | Q28508346 | ||
| Targeted disruption of the Rad51 gene leads to lethality in embryonic mice | Q29618278 | ||
| Genome-wide hypermutation in a subpopulation of stationary-phase cells underlies recombination-dependent adaptive mutation | Q33886793 | ||
| Hypothesis: somatic hypermutation by gene conversion via the error prone DNA----RNA----DNA information loop | Q34398630 | ||
| Modifying the sequence of an immunoglobulin V-gene alters the resulting pattern of hypermutation | Q35939989 | ||
| Boundaries of somatic mutation in rearranged immunoglobulin genes: 5' boundary is near the promoter, and 3' boundary is approximately 1 kb from V(D)J gene | Q36354162 | ||
| Point mutations cause the somatic diversification of IgM and IgG2a antiphosphorylcholine antibodies | Q36354592 | ||
| Molecular evolution of the human immunoglobulin E response: high incidence of shared mutations and clonal relatedness among epsilon VH5 transcripts from three unrelated patients with atopic dermatitis | Q36361154 | ||
| B lymphocytes of xeroderma pigmentosum or Cockayne syndrome patients with inherited defects in nucleotide excision repair are fully capable of somatic hypermutation of immunoglobulin genes | Q36380439 | ||
| Antibody diversity: somatic hypermutation of rearranged VH genes | Q36587415 | ||
| Heavy chain variable region contribution to the NPb family of antibodies: somatic mutation evident in a gamma 2a variable region | Q36630020 | ||
| The split-end model for homologous recombination at double-strand breaks and at Chi. | Q37361171 | ||
| Role of recombination enzymes in mammalian cell survival | Q37508951 | ||
| Might gene conversion be the mechanism of somatic hypermutation of mammalian immunoglobulin genes? | Q38622353 | ||
| Sequences of mouse immunoglobulin light chain genes before and after somatic changes | Q39638807 | ||
| Gene conversion: some implications for immunoglobulin genes | Q40309212 | ||
| Somatic hypermutation: how many mechanisms diversify V region sequences? | Q40410605 | ||
| Where transcription meets repair | Q40739628 | ||
| Discriminating intrinsic and antigen-selected mutational hotspots in immunoglobulin V genes | Q40858318 | ||
| Homologous recombination and the roles of double-strand breaks | Q40930013 | ||
| Somatic hypermutation of immunoglobulin genes | Q40955728 | ||
| The mechanism of somatic hypermutation studied with transgenic and transfected target genes | Q41062365 | ||
| Characterization of the cis-acting elements required for somatic hypermutation of murine antibody V genes using conventional transgenic and transgene homologous recombination approaches | Q41062370 | ||
| Gene conversion and homologous recombination in murine B cells | Q41062373 | ||
| The targeting of somatic hypermutation | Q41062380 | ||
| The germinal center: a crucible for lymphocyte selection | Q41062392 | ||
| Rearrangement/hypermutation/gene conversion: when, where and why? | Q41113095 | ||
| Genetic barriers among bacteria. | Q41120565 | ||
| Intraclonal generation of antibody mutants in germinal centres | Q41172275 | ||
| Meiotic recombination in yeast: coronation of the double-strand-break repair model | Q41285976 | ||
| Generation of antibody diversity in rabbits | Q41429681 | ||
| Mutation for survival | Q41703503 | ||
| Distribution of mutations around rearranged heavy-chain antibody variable-region genes | Q41966971 | ||
| Comparison of somatic mutation frequency among immunoglobulin genes | Q42248453 | ||
| Mapping the upstream boundary of somatic mutations in rearranged immunoglobulin transgenes and endogenous genes | Q48085081 | ||
| A hyperconversion mechanism generates the chicken light chain preimmune repertoire | Q48349399 | ||
| A single VH gene segment encodes the immune response to phosphorylcholine: somatic mutation is correlated with the class of the antibody | Q48409127 | ||
| Differences between germ-line and rearranged immunoglobulin Vκ coding sequences suggest a localized mutation mechanism | Q48409267 | ||
| The barrier to recombination between Escherichia coli and Salmonella typhimurium is disrupted in mismatch-repair mutants | Q50192890 | ||
| Introduction of homologous DNA sequences into mammalian cells induces mutations in the cognate gene. | Q54419614 | ||
| Microbial genetics. Hypermutation under stress. | Q54564293 | ||
| A direct role for DNA polymerase III in adaptive reversion of a frameshift mutation in Escherichia coli. | Q54567733 | ||
| Targeting of non-Ig sequences in place of the V segment by somatic hypermutation. | Q54608320 | ||
| Elements regulating somatic hypermutation of an immunoglobulin κ gene: Critical role for the intron enhancer/matrix attachment region | Q60370477 | ||
| Somatic hypermutation of immunoglobulin genes is linked to transcription initiation | Q70934062 | ||
| The appendix functions as a mammalian bursal equivalent in the developing rabbit | Q72140518 | ||
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 67-76 | |
| P577 | publication date | 1998-04-01 | |
| P1433 | published in | Immunological Reviews | Q15724582 |
| P1476 | title | Recombination-based mechanisms for somatic hypermutation | |
| P478 | volume | 162 |
| Q34094904 | Evolutionary changes in mutation rates and spectra and their influence on the adaptation of pathogens |
| Q35213276 | Immunoglobulin somatic hypermutation: double-strand DNA breaks, AID and error-prone DNA repair |
| Q33545735 | Somatic hypermutation and the three R's: repair, replication and recombination |
| Q40982321 | TdT-accessible breaks are scattered over the immunoglobulin V domain in a constitutively hypermutating B cell line |
| Q92963126 | The KT Jeang Prize 2019: Reuben S. Harris : Romancing the Mutator |
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