| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | Gearhart PJ | |
| Winter DB | |||
| P2860 | cites work | Accumulation of premutagenic DNA lesions in mice defective in removal of oxidative base damage | Q24651327 |
| Somatic hypermutation introduces insertions and deletions into immunoglobulin V genes | Q24652779 | ||
| Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over | Q28282791 | ||
| Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer | Q28294774 | ||
| Increased hypermutation at G and C nucleotides in immunoglobulin variable genes from mice deficient in the MSH2 mismatch repair protein | Q28505917 | ||
| Hot spot focusing of somatic hypermutation in MSH2-deficient mice suggests two stages of mutational targeting | Q28506440 | ||
| Mismatch repair deficiency interferes with the accumulation of mutations in chronically stimulated B cells and not with the hypermutation process | Q28507129 | ||
| Hypermutation of immunoglobulin genes in memory B cells of DNA repair-deficient mice | Q28507519 | ||
| Somatic hypermutation in MutS homologue (MSH)3-, MSH6-, and MSH3/MSH6-deficient mice reveals a role for the MSH2-MSH6 heterodimer in modulating the base substitution pattern | Q28510640 | ||
| Meiotic pachytene arrest in MLH1-deficient mice | Q28510650 | ||
| Different mismatch repair deficiencies all have the same effects on somatic hypermutation: intact primary mechanism accompanied by secondary modifications | Q28586687 | ||
| Female embryonic lethality in mice nullizygous for both Msh2 and p53 | Q28587400 | ||
| Hypermutation in Ig V genes from mice deficient in the MLH1 mismatch repair protein | Q28588513 | ||
| Altered spectra of hypermutation in antibodies from mice deficient for the DNA mismatch repair protein PMS2 | Q28910215 | ||
| A plethora of lesion-replicating DNA polymerases | Q33732359 | ||
| Patterns of somatic mutations in immunoglobulin variable genes | Q33952719 | ||
| Multiple ATM-dependent pathways: an explanation for pleiotropy | Q34388494 | ||
| Which DNA polymerases are used for DNA-repair in eukaryotes? | Q34422388 | ||
| Tissues of MSH2-deficient mice demonstrate hypermutability on exposure to a DNA methylating agent. | Q35795316 | ||
| 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 | ||
| 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 | ||
| Augmented expression of a human gene for 8-oxoguanine DNA glycosylase (MutM) in B lymphocytes of the dark zone in lymph node germinal centers | Q36380783 | ||
| Antibody diversity: somatic hypermutation of rearranged VH genes | Q36587415 | ||
| Clusters of point mutations are found exclusively around rearranged antibody variable genes | Q36593569 | ||
| High incidence of ultraviolet-B-or chemical-carcinogen-induced skin tumours in mice lacking the xeroderma pigmentosum group A gene | Q36694651 | ||
| Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis | Q38293261 | ||
| Life and death in germinal centers (redux). | Q40983825 | ||
| Three-dimensional structure determination of an anti-2-phenyloxazolone antibody: the role of somatic mutation and heavy/light chain pairing in the maturation of an immune response | Q41232426 | ||
| Defective mismatch repair in extracts of colorectal and endometrial cancer cell lines exhibiting microsatellite instability | Q41467421 | ||
| Di- and trinucleotide target preferences of somatic mutagenesis in normal and autoreactive B cells | Q42637489 | ||
| mRNA sequences define an unusually restricted IgG response to 2-phenyloxazolone and its early diversification | Q48397569 | ||
| Somatic mutation of immunoglobulin light-chain variable-region genes | Q48409137 | ||
| Differences between germ-line and rearranged immunoglobulin Vκ coding sequences suggest a localized mutation mechanism | Q48409267 | ||
| Somatic mutation and the maturation of immune response to 2-phenyl oxazolone | Q58019387 | ||
| Origin of Antibody Variation | Q59057486 | ||
| Somatic hypermutation of Ig genes in patients with xeroderma pigmentosum (XP-D) | Q71163077 | ||
| Mutator phenotype in Msh2-deficient murine embryonic fibroblasts | Q73677771 | ||
| The inactivation of the XP-C gene does not affect somatic hypermutation or class switch recombination of immunoglobulin genes | Q73864520 | ||
| Differential expression of DNA polymerase epsilon in resting and activated B lymphocytes is consistent with an in vivo role in replication and not repair | Q73920002 | ||
| P433 | issue | 1405 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | somatic hypermutation of immunoglobulin genes | Q14911681 |
| delta DNA polymerase complex | Q21117979 | ||
| P1104 | number of pages | 7 | |
| P304 | page(s) | 5-11 | |
| P577 | publication date | 2001-01-01 | |
| P1433 | published in | Philosophical Transactions of the Royal Society B | Q2153239 |
| P1476 | title | Altered spectra of hypermutation in DNA repair-deficient mice | |
| P478 | volume | 356 |
| Q34770418 | AID and mismatch repair in antibody diversification |
| Q36540495 | Antibody diversification caused by disrupted mismatch repair and promiscuous DNA polymerases |
| Q34994580 | Immunological disorders and DNA repair |
| Q36052347 | Inferring somatic mutation rates using the stop-enhanced green fluorescent protein mouse |
| Q40412801 | Somatic hypermutation and mismatch repair in non-B cells |
| Q34516540 | Somatic hypermutation in human B cell subsets |
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