| Q41264930 | A human follicular lymphoma B cell line hypermutates its functional immunoglobulin genes in vitro |
| Q48081204 | A lambda 1 transgene under the control of a heavy chain promoter and enhancer does not undergo somatic hypermutation |
| Q47771685 | A unifying hypothesis for the molecular mechanism of somatic mutation and gene conversion in rearranged immunoglobulin variable genes |
| Q34505084 | A well-differentiated B-cell line is permissive for somatic mutation of a transfected immunoglobulin heavy-chain gene. |
| Q41839580 | Acquisition of Genetic Aberrations by Activation-Induced Cytidine Deaminase (AID) during Inflammation-Associated Carcinogenesis |
| Q37994933 | Activation-induced cytidine deaminase in antibody diversification and chromosome translocation |
| Q40801731 | Affinity maturation of lymphocyte receptors and positive selection of T cells in the thymus |
| Q33584295 | An immunoglobulin mutator that targets G.C base pairs |
| Q33391280 | Analysis of patterns of DNA sequence variation in flanking and coding regions of murine germ-line immunoglobulin heavy-chain variable genes: evolutionary implications |
| Q34328629 | Analysis of somatic mutation in five B cell subsets of human tonsil |
| Q45872648 | Autologous T lymphocytes recognize the tumour-derived immunoglobulin VH-CDR3 region in patients with B-cell chronic lymphocytic leukaemia |
| Q38506144 | Chromatin domains and prediction of MAR sequences. |
| Q37120876 | Clonal evolution of a follicular lymphoma: evidence for antigen selection |
| Q37385073 | Clonal expansion and somatic hypermutation of V(H) genes of B cells from cerebrospinal fluid in multiple sclerosis. |
| Q42248453 | Comparison of somatic mutation frequency among immunoglobulin genes |
| Q35851102 | Differential V region mutation of two transfected Ig genes and their interaction in cultured B cell lines |
| Q33622342 | Diffuse large B-cell lymphoma: can genomics improve treatment options for a curable cancer? |
| Q36616139 | Effect of Helicobacter pylori eradication on ongoing mutation of immunoglobulin genes in gastric MALT lymphoma |
| Q57307991 | Effects of Sequence and Structure on the Hypermutability of Immunoglobulin Genes |
| Q34063681 | Elucidation of IgH intronic enhancer functions via germ-line deletion |
| Q40696086 | Generating the antibody repertoire in rabbit. |
| Q34310757 | Genesis of the strand-biased signature in somatic hypermutation of rearranged immunoglobulin variable genes |
| Q33960151 | Germ line variable regions that match hypermutated sequences in genes encoding murine anti-hapten antibodies |
| Q34310763 | Human DNA polymerase-eta, an A-T mutator in somatic hypermutation of rearranged immunoglobulin genes, is a reverse transcriptase |
| Q36361415 | Hypermutation is observed only in antibody H chain V region transgenes that have recombined with endogenous immunoglobulin H DNA: implications for the location of cis-acting elements required for somatic mutation |
| Q28507519 | Hypermutation of immunoglobulin genes in memory B cells of DNA repair-deficient mice |
| Q38318053 | Hypermutation of the MYC gene in diffuse large cell lymphomas with translocations involving band 8q24. |
| Q53665463 | Hypothesis: biological role for J-C intronic matrix attachment regions in the molecular mechanism of antigen-driven somatic hypermutation. |
| Q48037871 | Immunoglobulin gene hypermutation in germinal centers is independent of the RAG-1 V(D)J recombinase |
| Q34114760 | Immunoglobulin variable region hypermutation in hybrids derived from a pre-B- and a myeloma cell line |
| Q36362440 | In situ studies of the primary immune response to (4-hydroxy-3-nitrophenyl)acetyl. III. The kinetics of V region mutation and selection in germinal center B cells |
| Q40802589 | In vitro and in vivo expression of a nephritogenic Ig heavy chain determinant: pathogenic autoreactivity requires permissive light chains |
| Q33237877 | Increased negative selection impairs neonatal B cell repertoire but does not directly lead to generation of disease-associated IgM auto-antibodies |
| Q88293192 | JH6 downstream intronic sequence is dispensable for RNA polymerase II accumulation and somatic hypermutation of the variable gene in Ramos cells |
| Q40983825 | Life and death in germinal centers (redux). |
| Q37255156 | Ligation-anchored PCR: a simple amplification technique with single-sided specificity |
| Q41359348 | Mechanism of antigen-driven somatic hypermutation of rearranged immunoglobulin V(D)J genes in the mouse |
| Q40505615 | Mechanisms of antigenic variation in Borrelia hermsii and African trypanosomes |
| Q35939989 | Modifying the sequence of an immunoglobulin V-gene alters the resulting pattern of hypermutation |
| Q37587941 | Molecular characterization of five human anti-human immunodeficiency virus type 1 antibody heavy chains reveals extensive somatic mutation typical of an antigen-driven immune response |
| Q37525213 | Mutation in a reporter gene depends on proximity to and transcription of immunoglobulin variable transgenes |
| Q41083928 | Mutation pattern of immunoglobulin transgenes is compatible with a model of somatic hypermutation in which targeting of the mutator is linked to the direction of DNA replication |
| Q35953749 | On the molecular mechanism of somatic hypermutation of rearranged immunoglobulin genes |
| Q72875088 | Origin and maintenance of germ-line V genes |
| Q45025354 | PCR amplification of murine immunoglobulin germline V genes: strategies for minimization of recombination artefacts |
| Q46279727 | PIWIs, piRNAs and Retrotransposons: Complex battles during reprogramming in gametes and early embryos |
| Q36172034 | Passenger transgenes reveal intrinsic specificity of the antibody hypermutation mechanism: clustering, polarity, and specific hot spots |
| Q44870111 | Predicted and inferred waiting times for key mutations in the germinal centre reaction: evidence for stochasticity in selection |
| Q28087424 | RNA Exosome Regulates AID DNA Mutator Activity in the B Cell Genome |
| Q39720046 | Rapid methods for the analysis of immunoglobulin gene hypermutation: application to transgenic and gene targeted mice |
| Q47996615 | Recombination signature of germline immunoglobulin variable genes |
| Q64389096 | Recombination-based mechanisms for somatic hypermutation |
| Q47108323 | Reverse Transcriptase Mechanism of Somatic Hypermutation: 60 Years of Clonal Selection Theory |
| Q57295484 | Sequencing HIV-neutralizing antibody exons and introns reveals detailed aspects of lineage maturation |
| Q34468679 | Soma-to-germline feedback is implied by the extreme polymorphism at IGHV relative to MHC: The manifest polymorphism of the MHC appears greatly exceeded at Immunoglobulin loci, suggesting antigen-selected somatic V mutants penetrate Weismann's Barrie |
| Q41222940 | Somatic diversification of antibody responses |
| Q48103170 | Somatic hypermutation in 5' flanking regions of heavy chain antibody variable regions |
| Q24652779 | Somatic hypermutation introduces insertions and deletions into immunoglobulin V genes |
| Q36399510 | Somatic hypermutation is limited by CRM1-dependent nuclear export of activation-induced deaminase |
| Q36361238 | Somatic hypermutation of an immunoglobulin mu heavy chain transgene |
| Q70934062 | Somatic hypermutation of immunoglobulin genes is linked to transcription initiation |
| Q41081725 | Somatic hypermutation of immunoglobulin kappa may depend on sequences 3' of C kappa and occurs on passenger transgenes. |
| Q34922043 | Somatic hypermutation of the B cell receptor genes B29 (Igbeta, CD79b) and mb1 (Igalpha, CD79a). |
| Q33367730 | Somatic hypermutation: Another piece in the hypermutation puzzle |
| Q55034838 | Somatic mutation hotspots correlate with DNA polymerase eta error spectrum. |
| Q37591443 | Somatic mutation in constant regions of mouse lambda 1 light chains |
| Q40771425 | Somatic point mutations in the translocated bcl-2 genes of non-Hodgkin's lymphomas and lymphocytic leukemias: implications for mechanisms of tumor progression |
| Q40527478 | Targeting and regulation of immunoglobulin gene somatic hypermutation and isotype switch recombination |
| Q54608320 | Targeting of non-Ig sequences in place of the V segment by somatic hypermutation. |
| Q48081907 | The 5' boundary of somatic hypermutation in a V kappa gene is in the leader intron |
| Q50111104 | The 5' hypermutation boundary of kappa chains is independent of local and neighbouring sequences and related to the distance from the initiation of transcription. |
| Q35734132 | The boundaries of the distribution of somatic hypermutation of rearranged immunoglobulin variable genes |
| Q39645618 | The intrinsic hypermutability of antibody heavy and light chain genes decays exponentially |
| Q41049026 | The molecular basis of somatic hypermutation of immunoglobulin genes |
| Q33770284 | The reverse transcriptase model of somatic hypermutation |
| Q28592120 | The specificity and orientation of a TCR to its peptide-MHC class II ligands |
| Q28190690 | Transcription enhances AID-mediated cytidine deamination by exposing single-stranded DNA on the nontemplate strand |
| Q42799816 | Variable region gene selection of immunoglobulin G‐expressing B cells with specificity for a defined epitope on type II collagen |
| Q35219287 | c-mycHypermutation in Burkitt's Lymphoma |