| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S1472-6483(10)60027-2 |
| P698 | PubMed publication ID | 19490782 |
| P50 | author | Lluís Cabero Roura | Q40472349 |
| Montserrat Garcia-caldes | Q43150111 | ||
| José Luis Barbero | Q58865084 | ||
| P2093 | author name string | M Martin | |
| R Garcia | |||
| P Robles | |||
| I Roig | |||
| M Brieño | |||
| P2860 | cites work | Patterns of meiotic recombination in human fetal oocytes | Q37217307 |
| Mlh1 is unique among mismatch repair proteins in its ability to promote crossing-over during meiosis | Q38344945 | ||
| DNA double-strand breaks and gamma-H2AX signaling in the testis | Q44281802 | ||
| Imposition of crossover interference through the nonrandom distribution of synapsis initiation complexes | Q47910491 | ||
| Pairing and synapsis in oocytes from female fetuses with euploid and aneuploid chromosome complements | Q48787947 | ||
| Synaptic process in the rat (Rattus norvegicus): Influence of methodology on results | Q48835769 | ||
| Crossing over analysis at pachytene in man. | Q50335535 | ||
| Relationship of recombination patterns and maternal age among non-disjoined chromosomes 21. | Q50646900 | ||
| Evolution of the meiotic prophase and of the chromosome pairing process during human fetal ovarian development. | Q50662113 | ||
| Chromosome 18 pairing behavior in human trisomic oocytes. Presence of an extra chromosome extends bouquet stage. | Q50663043 | ||
| Silencing of unsynapsed meiotic chromosomes in the mouse. | Q50668569 | ||
| Crossover frequency and synaptonemal complex length: their variability and effects on human male meiosis. | Q53638430 | ||
| Synapsis and meiotic recombination analyses: MLH1 focus in the XY pair as an indicator. | Q53676187 | ||
| γ-H2AX illuminates meiosis | Q58486287 | ||
| Defective recombination in infertile men | Q59944725 | ||
| Analysis of non-crossover bivalents in pachytene cells from 10 normal men | Q60674251 | ||
| Karyotyping of human synaptonemal complexes by cenM-FISH | Q60674265 | ||
| Covariation of synaptonemal complex length and mammalian meiotic exchange rates | Q74253817 | ||
| Extreme heterogeneity in the molecular events leading to the establishment of chiasmata during meiosis i in human oocytes | Q24530701 | ||
| Meiosis-specific DNA double-strand breaks are catalyzed by Spo11, a member of a widely conserved protein family | Q27930009 | ||
| Cohesin component dynamics during meiotic prophase I in mammalian oocytes | Q28260099 | ||
| The evolution of meiosis: recruitment and modification of somatic DNA-repair proteins | Q28261559 | ||
| Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over | Q28282791 | ||
| Novel and diverse functions of the DNA mismatch repair family in mammalian meiosis and recombination | Q28509276 | ||
| To err (meiotically) is human: the genesis of human aneuploidy | Q29618613 | ||
| Recombinational DNA double-strand breaks in mice precede synapsis | Q29618790 | ||
| DNA double-strand breaks, recombination and synapsis: the timing of meiosis differs in grasshoppers and flies. | Q30476412 | ||
| Correlation of meiotic events in testis sections and microspreads of mouse spermatocytes relative to the mid-pachytene checkpoint | Q30839173 | ||
| Male mouse recombination maps for each autosome identified by chromosome painting | Q30870380 | ||
| Female-specific features of recombinational double-stranded DNA repair in relation to synapsis and telomere dynamics in human oocytes. | Q31088185 | ||
| Homologous recombinational repair proteins in mouse meiosis | Q31118803 | ||
| Temporal progression of recombination in human males | Q33222301 | ||
| Two levels of interference in mouse meiotic recombination | Q33246417 | ||
| A phase of chromosome aggregation during meiosis in human oocytes | Q33294150 | ||
| Studies of non-disjunction in trisomies 2, 7, 15, and 22: does the parental origin of trisomy influence placental morphology? | Q33681527 | ||
| Down syndrome: genetic recombination and the origin of the extra chromosome 21. | Q33874300 | ||
| Human male recombination maps for individual chromosomes | Q33911027 | ||
| Nondisjunction in trisomy 21: origin and mechanisms | Q33933101 | ||
| Meiotic recombination hot spots and cold spots | Q34238005 | ||
| Cytological studies of meiotic recombination in human males | Q34356217 | ||
| Lack of checkpoint control at the metaphase/anaphase transition: a mechanism of meiotic nondisjunction in mammalian females | Q34450618 | ||
| Risk factors for nondisjunction of trisomy 21. | Q34455219 | ||
| Where the crossovers are: recombination distributions in mammals. | Q35778662 | ||
| Effect of meiotic recombination on the production of aneuploid gametes in humans | Q36271551 | ||
| Genetic analysis of chromosome pairing, recombination, and cell cycle control during first meiotic prophase in mammals | Q36423604 | ||
| The synaptonemal complex and meiotic recombination in humans: new approaches to old questions | Q36425570 | ||
| Meiotic errors in human oogenesis and spermatogenesis | Q37138710 | ||
| P433 | issue | 6 | |
| P304 | page(s) | 784-794 | |
| P577 | publication date | 2009-06-01 | |
| P1433 | published in | Reproductive BioMedicine Online | Q15762964 |
| P1476 | title | Analysis of recombination along chromosome 21 during human female pachytene stage | |
| P478 | volume | 18 |
| Q61818799 | A comparative study of the recombination pattern in three species of Platyrrhini monkeys (primates) |
| Q33951926 | Maternal age and chromosomally abnormal pregnancies: what we know and what we wish we knew |
| Q48708236 | Predicting gene networks in human oocyte meiosis. |
| Q51608115 | Predicting meiotic pathways in human fetal oogenesis. |
| Q34530899 | Presence of an extra chromosome alters meiotic double-stranded break repair dynamics and MLH1 foci distribution in human oocytes. |
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