| scholarly article | Q13442814 |
| P50 | author | Francis Collins | Q336658 |
| Eric D. Green | Q5386338 | ||
| P2093 | author name string | James Thomas | |
| Paula E. Cohen | |||
| Steven M. Lipkin | |||
| Jun Cheng | |||
| Victoria Wang | |||
| Peter B. Moens | |||
| Abigail Gilgeous | |||
| Dakshine Shanmugarajah | |||
| Jeffrey W. Touchman | |||
| Michelle Lenzi | |||
| Pam Schwartzberg | |||
| P2860 | cites work | Identification and characterization of the mouse MutS homolog 5: Msh5. | Q42613449 |
| Mutation of a meiosis-specific MutS homolog decreases crossing over but not mismatch correction | Q48076989 | ||
| Expression of a specific mouse germ cell nuclear antigen (GCNA1) by early embryonic testicular teratoma cells in 129/Sv-Sl/+ mice | Q71056174 | ||
| MSH5, a novel MutS homolog, facilitates meiotic reciprocal recombination between homologs in Saccharomyces cerevisiae but not mismatch repair | Q71919357 | ||
| MLH3: a DNA mismatch repair gene associated with mammalian microsatellite instability | Q22010995 | ||
| Cloning and expression analysis of a meiosis-specific MutS homolog: the human MSH4 gene | Q24312177 | ||
| The genomic region encompassing the nephropathic cystinosis gene (CTNS): complete sequencing of a 200-kb segment and discovery of a novel gene within the common cystinosis-causing deletion | Q24624725 | ||
| Mismatch repair deficiency associated with overexpression of the MSH3 gene | Q24681589 | ||
| Structure and function of the N-terminal 40 kDa fragment of human PMS2: a monomeric GHL ATPase | Q27635053 | ||
| Base-calling of automated sequencer traces using phred. I. Accuracy assessment | Q27860665 | ||
| The Saccharomyces cerevisiae MLH3 gene functions in MSH3-dependent suppression of frameshift mutations | Q27935158 | ||
| Eukaryotic DNA mismatch repair | Q27939116 | ||
| Functional specificity of MutL homologs in yeast: evidence for three Mlh1-based heterocomplexes with distinct roles during meiosis in recombination and mismatch correction | Q27939611 | ||
| Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over | Q28282791 | ||
| Mammalian MutS homologue 5 is required for chromosome pairing in meiosis | Q28295022 | ||
| Chromosomal influence on meiotic spindle assembly: abnormal meiosis I in female Mlh1 mutant mice | Q28506066 | ||
| Meiotic pachytene arrest in MLH1-deficient mice | Q28510650 | ||
| Mismatch repair in replication fidelity, genetic recombination, and cancer biology | Q29616483 | ||
| Strategies for the systematic sequencing of complex genomes | Q34325311 | ||
| Regulation of meiotic recombination and prophase I progression in mammals | Q34464620 | ||
| Comparative genomic sequence analysis of the human and mouse cystic fibrosis transmembrane conductance regulator genes | Q35009670 | ||
| Mouse MutS-like protein Msh5 is required for proper chromosome synapsis in male and female meiosis | Q35190411 | ||
| Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis | Q38293261 | ||
| Mlh1 is unique among mismatch repair proteins in its ability to promote crossing-over during meiosis | Q38344945 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | RAD51 recombinase | Q14907735 |
| MutL homolog 1 | Q14911713 | ||
| Replication protein A1 | Q21990541 | ||
| Synaptonemal complex protein 3 | Q21990670 | ||
| P304 | page(s) | 385–390 | |
| P577 | publication date | 2002-08-01 | |
| P1433 | published in | Nature Genetics | Q976454 |
| P1476 | title | Meiotic arrest and aneuploidy in MLH3-deficient mice | |
| P478 | volume | 31 |
| Q91917222 | A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21 |
| Q64928626 | A mutation in the endonuclease domain of mouse MLH3 reveals novel roles for MutLγ during crossover formation in meiotic prophase I. |
| Q36724317 | A mutation in the putative MLH3 endonuclease domain confers a defect in both mismatch repair and meiosis in Saccharomyces cerevisiae |
| Q42699865 | A new meiosis-specific cohesin complex implicated in the cohesin code for homologous pairing |
| Q36540457 | A personal historical view of DNA mismatch repair with an emphasis on eukaryotic DNA mismatch repair |
| Q36211150 | A role for the MutL mismatch repair Mlh3 protein in immunoglobulin class switch DNA recombination and somatic hypermutation |
| Q36795932 | A surge of late-occurring meiotic double-strand breaks rescues synapsis abnormalities in spermatocytes of mice with hypomorphic expression of SPO11. |
| Q35098176 | A-MYB (MYBL1) transcription factor is a master regulator of male meiosis |
| Q28506572 | AGO4 regulates entry into meiosis and influences silencing of sex chromosomes in the male mouse germline |
| Q49886701 | Age-Dependent Alterations in Meiotic Recombination Cause Chromosome Segregation Errors in Spermatocytes |
| Q24652699 | Alternative induction of meiotic recombination from single-base lesions of DNA deaminases |
| Q36614680 | An intact Pms2 ATPase domain is not essential for male fertility |
| Q54991104 | Analysis of Endocannabinoid System in Rat Testis During the First Spermatogenetic Wave. |
| Q37615474 | Analysis of MLH3 C2531T polymorphism in Iranian women with unexplained infertility |
| Q28588202 | Antagonistic roles of ubiquitin ligase HEI10 and SUMO ligase RNF212 regulate meiotic recombination |
| Q36231123 | Antibody class switch recombination: roles for switch sequences and mismatch repair proteins |
| Q36082370 | BLM ortholog, Sgs1, prevents aberrant crossing-over by suppressing formation of multichromatid joint molecules |
| Q27310690 | Cattle Sex-Specific Recombination and Genetic Control from a Large Pedigree Analysis |
| Q52716172 | Characterization of recombination features and the genetic basis in multiple cattle breeds. |
| Q79773199 | Characterization of the "mismatch repairosome" and its role in the processing of modified nucleosides in vitro |
| Q36429060 | Chiasma formation: chromatin/axis interplay and the role(s) of the synaptonemal complex |
| Q52725766 | Chromatin Spread Preparations for the Analysis of Mouse Oocyte Progression from Prophase to Metaphase II. |
| Q48512514 | Chromosomes, recombination and proteins at meiosis--a tribute to Peter Moens (1931-2008). |
| Q37313690 | Coding and noncoding variants in HFM1, MLH3, MSH4, MSH5, RNF212, and RNF212B affect recombination rate in cattle |
| Q34569381 | Competing crossover pathways act during meiosis in Saccharomyces cerevisiae |
| Q37157456 | Completion of meiosis in male zebrafish (Danio rerio) despite lack of DNA mismatch repair gene mlh1. |
| Q40806587 | Concerted action of the MutLβ heterodimer and Mer3 helicase regulates the global extent of meiotic gene conversion. |
| Q27324367 | Conditional inactivation of the DNA damage response gene Hus1 in mouse testis reveals separable roles for components of the RAD9-RAD1-HUS1 complex in meiotic chromosome maintenance |
| Q37656154 | Control of Meiotic Crossovers: From Double-Strand Break Formation to Designation. |
| Q79224497 | Coordinate variation in meiotic pachytene SC length and total crossover/chiasma frequency under conditions of constant DNA length |
| Q30839173 | Correlation of meiotic events in testis sections and microspreads of mouse spermatocytes relative to the mid-pachytene checkpoint |
| Q34441535 | Crossover formation during rice meiosis relies on interaction of OsMSH4 and OsMSH5. |
| Q97518601 | Cyclin N-Terminal Domain-Containing-1 Coordinates Meiotic Crossover Formation with Cell-Cycle Progression in a Cyclin-Independent Manner |
| Q34814254 | DNA mismatch repair and infertility |
| Q24647002 | DNA mismatch repair: molecular mechanism, cancer, and ageing |
| Q35062449 | DNA repair defects in colon cancer |
| Q36487307 | DNA-damage repair; the good, the bad, and the ugly |
| Q35803418 | Dgcr8 and Dicer are essential for sex chromosome integrity during meiosis in males. |
| Q22242924 | Differing patterns of genetic instability in mice deficient in the mismatch repair genes Pms2, Mlh1, Msh2, Msh3 and Msh6 |
| Q36371989 | Distinct DNA-binding surfaces in the ATPase and linker domains of MutLγ determine its substrate specificities and exert separable functions in meiotic recombination and mismatch repair |
| Q36670109 | Distinct effects of the recurrent Mlh1G67R mutation on MMR functions, cancer, and meiosis |
| Q36571740 | Distinct functions of MLH3 at recombination hot spots in the mouse. |
| Q33475117 | Effect of hydroxyurea on the promoter occupancy profiles of tumor suppressor p53 and p73. |
| Q37690783 | Embryological Results of Couples Undergoing ICSI-ET Treatments with Males Carrying the Single Nucleotide Polymorphism rs175080 of the MLH3 Gene. |
| Q37357503 | Epigenetic repression of DNA mismatch repair by inflammation and hypoxia in inflammatory bowel disease-associated colorectal cancer |
| Q34441207 | Evidence that hMLH3 functions primarily in meiosis and in hMSH2-hMSH3 mismatch repair. |
| Q36779032 | Expression profiling of mammalian male meiosis and gametogenesis identifies novel candidate genes for roles in the regulation of fertility |
| Q24530701 | Extreme heterogeneity in the molecular events leading to the establishment of chiasmata during meiosis i in human oocytes |
| Q28513158 | FancJ (Brip1) loss-of-function allele results in spermatogonial cell depletion during embryogenesis and altered processing of crossover sites during meiotic prophase I in mice |
| Q28589524 | Gonadotropin-regulated testicular RNA helicase (GRTH/Ddx25) is essential for spermatid development and completion of spermatogenesis |
| Q89517728 | Human MutLγ, the MLH1-MLH3 heterodimer, is an endonuclease that promotes DNA expansion |
| Q93211852 | Hybrid Sterility with Meiotic Metaphase Arrest in Intersubspecific Mouse Crosses |
| Q26795372 | Identification of Candidate Predictors of Lupus Flare |
| Q28074585 | Impact of DNA mismatch repair system alterations on human fertility and related treatments |
| Q38314307 | Impact of heat shock transcription factor 1 on global gene expression profiles in cells which induce either cytoprotective or pro-apoptotic response following hyperthermia |
| Q28585563 | Impaired placental trophoblast lineage differentiation in Alkbh1(-/-) mice |
| Q28182219 | Inactivation of Exonuclease 1 in mice results in DNA mismatch repair defects, increased cancer susceptibility, and male and female sterility |
| Q42700921 | Inhibition of colorectal cancer genomic copy number alterations and chromosomal fragile site tumor suppressor FHIT and WWOX deletions by DNA mismatch repair |
| Q24553992 | Interaction of mismatch repair protein PMS2 and the p53-related transcription factor p73 in apoptosis response to cisplatin |
| Q42191835 | Localization of MLH3 at the centrosomes |
| Q28505426 | Localization of MMR proteins on meiotic chromosomes in mice indicates distinct functions during prophase I |
| Q28505931 | Loss of YY1 impacts the heterochromatic state and meiotic double-strand breaks during mouse spermatogenesis |
| Q36246487 | Lynch syndrome genes |
| Q34617068 | MLH1 mutations differentially affect meiotic functions in Saccharomyces cerevisiae |
| Q34619470 | MLH1p and MLH3p localize to precociously induced chiasmata of okadaic-acid-treated mouse spermatocytes |
| Q33369076 | MUS81 generates a subset of MLH1-MLH3-independent crossovers in mammalian meiosis |
| Q48256770 | Main steps in DNA double-strand break repair: an introduction to homologous recombination and related processes. |
| Q33751700 | Mammalian BLM helicase is critical for integrating multiple pathways of meiotic recombination |
| Q27340183 | Mammalian BTBD12 (SLX4) protects against genomic instability during mammalian spermatogenesis |
| Q28592214 | Mammalian CNTD1 is critical for meiotic crossover maturation and deselection of excess precrossover sites |
| Q36991032 | Mammalian Exo1 encodes both structural and catalytic functions that play distinct roles in essential biological processes |
| Q26740310 | Manipulation of DNA Repair Proficiency in Mouse Models of Colorectal Cancer |
| Q28262719 | Mechanisms and functions of DNA mismatch repair |
| Q33433256 | Meiosis genes in Daphnia pulex and the role of parthenogenesis in genome evolution |
| Q28506670 | Meiosis in mice without a synaptonemal complex |
| Q36358073 | Meiosis-specific proteins MEIOB and SPATA22 cooperatively associate with the single-stranded DNA-binding replication protein A complex and DNA double-strand breaks |
| Q38618828 | Meiotic Recombination: The Essence of Heredity |
| Q38000414 | Meiotic double strand breaks repair in sexually reproducing eukaryotes: we are not all equal |
| Q48661366 | Meiotic genetics moves forward with SPATA22 (repro42). |
| Q38153644 | Meiotic recombination in mammals: localization and regulation |
| Q33921194 | Meiotic recombination intermediates are resolved with minimal crossover formation during return-to-growth, an analogue of the mitotic cell cycle |
| Q35548710 | Mismatch repair and response to DNA-damaging antitumour therapies |
| Q35034398 | Mismatch repair genes Mlh1 and Mlh3 modify CAG instability in Huntington's disease mice: genome-wide and candidate approaches |
| Q35757682 | Mlh1 deficiency in zebrafish results in male sterility and aneuploid as well as triploid progeny in females. |
| Q28305501 | Mlh1-Mlh3, a meiotic crossover and DNA mismatch repair factor, is a Msh2-Msh3-stimulated endonuclease |
| Q26826949 | Modeling the study of DNA damage responses in mice |
| Q33667402 | Modulating Crossover Frequency and Interference for Obligate Crossovers in Saccharomyces cerevisiae Meiosis. |
| Q90451067 | Molecular evolution of the meiotic recombination pathway in mammals |
| Q28512386 | Mouse HFM1/Mer3 is required for crossover formation and complete synapsis of homologous chromosomes during meiosis |
| Q28588451 | Mouse Sycp1 functions in synaptonemal complex assembly, meiotic recombination, and XY body formation |
| Q37084734 | Mouse models in male fertility research |
| Q34932076 | Mouse models of male infertility. |
| Q28591450 | Mouse pachytene checkpoint 2 (trip13) is required for completing meiotic recombination but not synapsis |
| Q57472222 | MutLγ promotes repeat expansion in a Fragile X mouse model while EXO1 is protective |
| Q28594464 | Mutation in mouse hei10, an e3 ubiquitin ligase, disrupts meiotic crossing over |
| Q64387363 | Mutation of the ATPase Domain of MutS Homolog-5 (MSH5) Reveals a Requirement for a Functional MutSγ Complex for All Crossovers in Mammalian Meiosis |
| Q33343446 | Novel roles for MLH3 deficiency and TLE6-like amplification in DNA mismatch repair-deficient gastrointestinal tumorigenesis and progression. |
| Q24599477 | Oocyte maturation failure: a syndrome of bad eggs |
| Q35576326 | Oocyte-specific differences in cell-cycle control create an innate susceptibility to meiotic errors |
| Q55118944 | PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice. |
| Q24294615 | Polo-like kinase is required for synaptonemal complex disassembly and phosphorylation in mouse spermatocytes |
| Q27690911 | Postreplicative mismatch repair |
| Q96576851 | Proline-rich protein PRR19 functions with cyclin-like CNTD1 to promote meiotic crossing over in mouse |
| Q39155608 | Prophase I: Preparing Chromosomes for Segregation in the Developing Oocyte |
| Q28509598 | RNF212 is a dosage-sensitive regulator of crossing-over during mammalian meiosis |
| Q90662845 | Rare mutations in the complement regulatory gene CSMD1 are associated with male and female infertility |
| Q37129931 | Reassessment of the role of Mut S homolog 5 in Ig class switch recombination shows lack of involvement in cis- and trans-switching. |
| Q46430833 | Recombination correlates with synaptonemal complex length and chromatin loop size in bovids-insights into mammalian meiotic chromosomal organization. |
| Q34500851 | Reduced meiotic crossovers and delayed prophase I progression in AtMLH3-deficient Arabidopsis |
| Q34131555 | Reproductive isolation in hybrid mice due to spermatogenesis defects at three meiotic stages |
| Q36540776 | Roles for mismatch repair family proteins in promoting meiotic crossing over |
| Q36117975 | SYCE2 is required for synaptonemal complex assembly, double strand break repair, and homologous recombination |
| Q64095486 | Shugoshin protects centromere pairing and promotes segregation of nonexchange partner chromosomes in meiosis |
| Q35027619 | Single molecule studies of DNA mismatch repair |
| Q35647368 | Spindles, mitochondria and redox potential in ageing oocytes |
| Q36751491 | Stage-specific gene expression is a fundamental characteristic of rat spermatogenic cells and Sertoli cells |
| Q24529923 | Surveillance of different recombination defects in mouse spermatocytes yields distinct responses despite elimination at an identical developmental stage |
| Q50667599 | Synapsis or silence. |
| Q28301386 | Temporally and biochemically distinct activities of Exo1 during meiosis: double-strand break resection and resolution of double Holliday junctions |
| Q36119914 | The Arabidopsis HEI10 is a new ZMM protein related to Zip3 |
| Q28592328 | The Mre11 complex influences DNA repair, synapsis, and crossing over in murine meiosis |
| Q28306188 | The Saccharomyces cerevisiae Mlh1-Mlh3 heterodimer is an endonuclease that preferentially binds to Holliday junctions |
| Q64389575 | The capacity of oocytes for DNA repair |
| Q36416265 | The diverse roles of transverse filaments of synaptonemal complexes in meiosis |
| Q38246275 | The dual nature of mismatch repair as antimutator and mutator: for better or for worse |
| Q48081095 | The mismatch repair protein MLH1 marks a subset of strongly interfering crossovers in tomato |
| Q36448284 | The multifaceted mismatch-repair system |
| Q34335536 | The role of rice HEI10 in the formation of meiotic crossovers |
| Q36781174 | The tricky path to recombining X and Y chromosomes in meiosis |
| Q61812011 | Transition from a meiotic to a somatic-like DNA damage response during the pachytene stage in mouse meiosis |
| Q83231314 | Unified single-cell analysis of testis gene regulation and pathology in five mouse strains |
| Q28253087 | Variation in crossover frequencies perturb crossover assurance without affecting meiotic chromosome segregation in Saccharomyces cerevisiae |
| Q62609015 | White-cap mutants and meiotic apoptosis in the basidiomycete Coprinus cinereus |
| Q24622206 | hMSH4-hMSH5 adenosine nucleotide processing and interactions with homologous recombination machinery |
| Q51791906 | miRNA and piRNA localization in the male mammalian meiotic nucleus. |
| Q42352313 | mlh3 mutations in baker's yeast alter meiotic recombination outcomes by increasing noncrossover events genome-wide. |
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