| scholarly article | Q13442814 |
| P2093 | author name string | Camerini-Otero RD | |
| Romanienko PJ | |||
| P2860 | cites work | Cloning, characterization, and localization of mouse and human SPO11 | Q22010714 |
| Fibroblast growth factor receptor 3 is a negative regulator of bone growth | Q24322706 | ||
| An alternative splicing event which occurs in mouse pachytene spermatocytes generates a form of DNA ligase III with distinct biochemical properties that may function in meiotic recombination | Q24647280 | ||
| Meiosis-specific DNA double-strand breaks are catalyzed by Spo11, a member of a widely conserved protein family | Q27930009 | ||
| Meiotic chromosomes: it takes two to tango | Q27930023 | ||
| RecA homologs Dmc1 and Rad51 interact to form multiple nuclear complexes prior to meiotic chromosome synapsis. | Q27932144 | ||
| Saccharomyces cerevisiae recA homologues RAD51 and DMC1 have both distinct and overlapping roles in meiotic recombination | Q27936736 | ||
| The transcriptional program of sporulation in budding yeast | Q27938344 | ||
| New gene family defined by MORC, a nuclear protein required for mouse spermatogenesis | Q28115778 | ||
| Meiotic recombination in C. elegans initiates by a conserved mechanism and is dispensable for homologous chromosome synapsis | Q28279936 | ||
| Mammalian MutS homologue 5 is required for chromosome pairing in meiosis | Q28295022 | ||
| The murine SCP3 gene is required for synaptonemal complex assembly, chromosome synapsis, and male fertility | Q28505195 | ||
| Identification of morc (microrchidia), a mutation that results in arrest of spermatogenesis at an early meiotic stage in the mouse | Q28513262 | ||
| Mouse mutants from chemically mutagenized embryonic stem cells | Q28593735 | ||
| An atypical topoisomerase II from Archaea with implications for meiotic recombination | Q29618230 | ||
| Meiotic prophase arrest with failure of chromosome synapsis in mice deficient for Dmc1, a germline-specific RecA homolog | Q29618405 | ||
| Atm-deficient mice: a paradigm of ataxia telangiectasia | Q29619532 | ||
| The association of ATR protein with mouse meiotic chromosome cores | Q30724277 | ||
| Toprim--a conserved catalytic domain in type IA and II topoisomerases, DnaG-type primases, OLD family nucleases and RecR proteins | Q32030823 | ||
| Hanging on to your homolog: the roles of pairing, synapsis and recombination in the maintenance of homolog adhesion | Q33943969 | ||
| High rate of recombination and double crossovers in the mouse pseudoautosomal region during male meiosis | Q34354262 | ||
| Isolation, DNA sequence, and regulation of a meiosis-specific eukaryotic recombination gene | Q34365937 | ||
| Mouse MutS-like protein Msh5 is required for proper chromosome synapsis in male and female meiosis | Q35190411 | ||
| The tumor suppressor SMAD4/DPC4 is essential for epiblast proliferation and mesoderm induction in mice | Q36008239 | ||
| Multiple roles of Spo11 in meiotic chromosome behavior | Q36246137 | ||
| Cisplatin increases meiotic crossing-over in mice | Q36554672 | ||
| Evidence for close contact between recombination nodules and the central element of the synaptonemal complex | Q38551724 | ||
| Identification and characterization of an SPO11 homolog in the mouse | Q40873645 | ||
| Synaptonemal complexes: structure and function | Q41066968 | ||
| RAD51 and DMC1 form mixed complexes associated with mouse meiotic chromosome cores and synaptonemal complexes | Q42918693 | ||
| Meiotic synapsis in the absence of recombination. | Q46794994 | ||
| Evidence for the evolution of bdelloid rotifers without sexual reproduction or genetic exchange | Q47673378 | ||
| Meiotic DNA breaks associated with recombination in S. pombe | Q47847394 | ||
| The mouse RecA-like gene Dmc1 is required for homologous chromosome synapsis during meiosis | Q47858327 | ||
| Differential gene expression of mammalian SPO11/TOP6A homologs during meiosis | Q47895242 | ||
| A mouse homolog of the Saccharomyces cerevisiae meiotic recombination DNA transesterase Spo11p. | Q47917592 | ||
| Chromosome synapsis defects and sexually dimorphic meiotic progression in mice lacking Spo11. | Q50720785 | ||
| THE LEPTOTENE-ZYGOTENE TRANSITION OF MEIOSIS | Q56136641 | ||
| Genetic control of chromosome synapsis in yeast meiosis | Q69557796 | ||
| The differential expression of the actins and tubulins during spermatogenesis in the mouse | Q71390702 | ||
| Chromosome pairing via multiple interstitial interactions before and during meiosis in yeast | Q72034931 | ||
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 975-87 | |
| P577 | publication date | 2000-11-01 | |
| P1433 | published in | Molecular Cell | Q3319468 |
| P1476 | title | The mouse Spo11 gene is required for meiotic chromosome synapsis | |
| P478 | volume | 6 |
| Q54386874 | A DNA-binding surface of SPO11-1, an Arabidopsis SPO11 orthologue required for normal meiosis. |
| Q34099632 | A crucial role for the putative Arabidopsis topoisomerase VI in plant growth and development |
| Q33281668 | A dominant, recombination-defective allele of Dmc1 causing male-specific sterility |
| Q34591098 | A genome-wide distribution of 8-oxoguanine correlates with the preferred regions for recombination and single nucleotide polymorphism in the human genome |
| Q21563335 | A high incidence of meiotic silencing of unsynapsed chromatin is not associated with substantial pachytene loss in heterozygous male mice carrying multiple simple robertsonian translocations |
| Q28505929 | A histone H3 methyltransferase controls epigenetic events required for meiotic prophase |
| Q61796323 | A meiosis-specific BRCA2 binding protein recruits recombinases to DNA double-strand breaks to ensure homologous recombination |
| Q35625730 | A molecular portrait of Arabidopsis meiosis |
| Q42699865 | A new meiosis-specific cohesin complex implicated in the cohesin code for homologous pairing |
| Q39645555 | A novel meiosis-specific protein of fission yeast, Meu13p, promotes homologous pairing independently of homologous recombination |
| Q28513683 | A novel mouse synaptonemal complex protein is essential for loading of central element proteins, recombination, and fertility |
| Q35416690 | A novel transcriptional factor Nkapl is a germ cell-specific suppressor of Notch signaling and is indispensable for spermatogenesis |
| Q27935770 | A role for MMS4 in the processing of recombination intermediates during meiosis in Saccharomyces cerevisiae |
| Q33751005 | A role for retrotransposon LINE-1 in fetal oocyte attrition in mice |
| Q36795932 | A surge of late-occurring meiotic double-strand breaks rescues synapsis abnormalities in spermatocytes of mice with hypomorphic expression of SPO11. |
| Q37343724 | A yeast two-hybrid screen for SYP-3 interactors identifies SYP-4, a component required for synaptonemal complex assembly and chiasma formation in Caenorhabditis elegans meiosis |
| Q28742900 | ATM controls meiotic double-strand-break formation |
| Q21145047 | ATM promotes the obligate XY crossover and both crossover control and chromosome axis integrity on autosomes |
| Q55506171 | ATR is a multifunctional regulator of male mouse meiosis. |
| Q55505997 | ATR is required to complete meiotic recombination in mice. |
| Q64389165 | Ablation of Ggnbp2 impairs meiotic DNA double-strand break repair during spermatogenesis in mice |
| Q36744928 | Activation-Induced Cytidine Deaminase Does Not Impact Murine Meiotic Recombination |
| Q28771502 | Alignment of Homologous Chromosomes and Effective Repair of Programmed DNA Double-Strand Breaks during Mouse Meiosis Require the Minichromosome Maintenance Domain Containing 2 (MCMDC2) Protein |
| Q46096099 | Altered nuclear distribution of recombination protein RAD51 in maize mutants suggests the involvement of RAD51 in meiotic homology recognition |
| Q38435173 | An Orchestrated Intron Retention Program in Meiosis Controls Timely Usage of Transcripts during Germ Cell Differentiation |
| Q36899631 | An ancient transcription factor initiates the burst of piRNA production during early meiosis in mouse testes |
| Q35205822 | An association study of SPO11 gene single nucleotide polymorphisms with idiopathic male infertility in Chinese Han population |
| Q37368057 | An essential role of DmRad51/SpnA in DNA repair and meiotic checkpoint control |
| Q47445150 | Analysis of factors decreasing testis weight in MRL mice |
| Q28588202 | Antagonistic roles of ubiquitin ligase HEI10 and SUMO ligase RNF212 regulate meiotic recombination |
| Q27931005 | Antiviral protein Ski8 is a direct partner of Spo11 in meiotic DNA break formation, independent of its cytoplasmic role in RNA metabolism |
| Q35557653 | Apoptosis in male germ cells in response to cyclin A1-deficiency and cell cycle arrest |
| Q42361116 | Arrested spermatogenesis and evidence for DNA damage in PTIP mutant testes |
| Q27936545 | Assembly of RecA-like recombinases: distinct roles for mediator proteins in mitosis and meiosis |
| Q33731257 | BRCA1 establishes DNA damage signaling and pericentric heterochromatin of the X chromosome in male meiosis |
| Q34079040 | Brain abnormalities, defective meiotic chromosome synapsis and female subfertility in HSF2 null mice |
| Q28589697 | CEP63 deficiency promotes p53-dependent microcephaly and reveals a role for the centrosome in meiotic recombination |
| Q36780664 | CHFR is important for the survival of male premeiotic germ cells |
| Q90701603 | CHTF18 ensures the quantity and quality of the ovarian reserve† |
| Q33340985 | CRA-1 uncovers a double-strand break-dependent pathway promoting the assembly of central region proteins on chromosome axes during C. elegans meiosis |
| Q42518081 | CRT1 is a nuclear-translocated MORC endonuclease that participates in multiple levels of plant immunity |
| Q48829348 | Caenorhabditis elegans Ce-rdh-1/rad-51 functions after double-strand break formation of meiotic recombination. |
| Q35787275 | Cancer predisposition and hematopoietic failure in Rad50(S/S) mice |
| Q44525185 | Cancer/Testis genes in relation to sperm biology and function |
| Q92153975 | Cannabinoid Receptors Signaling in the Development, Epigenetics, and Tumours of Male Germ Cells |
| Q35812251 | Centromere pairing--tethering partner chromosomes in meiosis I. |
| Q34429706 | Checkpoints: chromosome pairing takes an unexpected twist |
| Q37128128 | Chromatin remodeling finds its place in the DNA double-strand break response |
| Q34342179 | Chromatin remodeling, DNA damage repair and aging. |
| Q50727811 | Chromosome pairing and meiotic recombination in Neurospora crassa spo11 mutants. |
| Q50720785 | Chromosome synapsis defects and sexually dimorphic meiotic progression in mice lacking Spo11. |
| Q60927442 | Cisplatin-induced DNA double-strand breaks promote meiotic chromosome synapsis in PRDM9-controlled mouse hybrid sterility |
| Q37396828 | Clamping down on mammalian meiosis |
| Q92025174 | Combinatorial control of Spo11 alternative splicing by modulation of RNA polymerase II dynamics and splicing factor recruitment during meiosis |
| Q35385037 | Comprehensive, fine-scale dissection of homologous recombination outcomes at a hot spot in mouse meiosis. |
| 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 |
| Q30597286 | Contrasting behavior of heterochromatic and euchromatic chromosome portions and pericentric genome separation in pre-bouquet spermatocytes of hybrid mice |
| Q37104913 | Control of the meiotic cell division program in plants |
| Q33370539 | Corona is required for higher-order assembly of transverse filaments into full-length synaptonemal complex in Drosophila oocytes |
| Q34614838 | Crossover interference in Arabidopsis |
| Q33905905 | Crossover interference in humans |
| Q92901769 | Crossover recombination and synapsis are linked by adjacent regions within the N terminus of the Zip1 synaptonemal complex protein |
| Q97518601 | Cyclin N-Terminal Domain-Containing-1 Coordinates Meiotic Crossover Formation with Cell-Cycle Progression in a Cyclin-Independent Manner |
| Q48823384 | Cyclin-dependent kinase 2 is essential for meiosis but not for mitotic cell division in mice. |
| Q27323102 | DNA methylation restrains transposons from adopting a chromatin signature permissive for meiotic recombination |
| Q34814254 | DNA mismatch repair and infertility |
| Q33519489 | DNA polymerase beta is critical for mouse meiotic synapsis |
| Q34218073 | DNA repair: spot(light)s on chromatin. |
| Q36287506 | De novo mutations in PLXND1 and REV3L cause Möbius syndrome |
| Q31096075 | DeAnnIso: a tool for online detection and annotation of isomiRs from small RNA sequencing data |
| Q28506523 | Defective imprint resetting in carriers of Robertsonian translocation Rb (8.12) |
| Q89121896 | Defects in meiotic recombination delay progression through pachytene in Tex19.1-/- mouse spermatocytes |
| Q37713595 | Defying DNA double-strand break-induced death during prophase I meiosis by temporal TAp63α phosphorylation regulation in developing mouse oocytes |
| Q28513002 | Deletion of genes implicated in protecting the integrity of male germ cells has differential effects on the incidence of DNA breaks and germ cell loss |
| Q24337562 | Differential association of SMC1alpha and SMC3 proteins with meiotic chromosomes in wild-type and SPO11-deficient male mice |
| Q33646049 | Differential expression and sex chromosome association of CHD3/4 and CHD5 during spermatogenesis |
| Q38588876 | Differentiating the roles of microtubule-associated proteins at meiotic kinetochores during chromosome segregation |
| Q33296442 | Dissecting meiosis of rye using translational proteomics |
| Q35011478 | Dissecting plant meiosis using Arabidopsis thaliana mutants. |
| Q24557469 | Distinct DNA-damage-dependent and -independent responses drive the loss of oocytes in recombination-defective mouse mutants |
| Q24793276 | Distinct functions of S. pombe Rec12 (Spo11) protein and Rec12-dependent crossover recombination (chiasmata) in meiosis I; and a requirement for Rec12 in meiosis II |
| Q37334927 | Distinct histone modifications define initiation and repair of meiotic recombination in the mouse |
| Q35150490 | Distinct properties of the XY pseudoautosomal region crucial for male meiosis |
| Q51733900 | Distinct prophase arrest mechanisms in human male meiosis. |
| Q34241406 | Divergent kleisin subunits of cohesin specify mechanisms to tether and release meiotic chromosomes. |
| Q90365258 | Diverse roles for CDK-associated activity during spermatogenesis |
| Q34567177 | Does crossover interference count in Saccharomyces cerevisiae? |
| Q26830517 | Double-strand break repair on sex chromosomes: challenges during male meiotic prophase |
| Q36478227 | Double-stranded DNA breaks and gene functions in recombination and meiosis |
| Q24298683 | Dynamic regulation of p53 subnuclear localization and senescence by MORC3 |
| Q37671700 | Dynamics of DOT1L localization and H3K79 methylation during meiotic prophase I in mouse spermatocytes |
| Q37325397 | Dynamin 2 is essential for mammalian spermatogenesis. |
| Q36803534 | E-type cyclins modulate telomere integrity in mammalian male meiosis |
| Q40603482 | E2F1 controls germ cell apoptosis during the first wave of spermatogenesis |
| Q43117478 | Early meiotic-specific protein expression in post-natal rat ovaries |
| Q37393820 | Elucidation of the Fanconi Anemia Protein Network in Meiosis and Its Function in the Regulation of Histone Modifications |
| Q38322004 | Endonucleolytic processing of covalent protein-linked DNA double-strand breaks |
| Q38344293 | Epigenetic control of meiotic recombination in plants |
| Q28566542 | Evaluation of the Stag3 gene and the synaptonemal complex in a rat model (as/as) for male infertility |
| Q33913156 | Evolutionary conservation of meiotic DSB proteins: more than just Spo11 |
| Q36779032 | Expression profiling of mammalian male meiosis and gametogenesis identifies novel candidate genes for roles in the regulation of fertility |
| Q36790535 | Extensive meiotic asynapsis in mice antagonises meiotic silencing of unsynapsed chromatin and consequently disrupts meiotic sex chromosome inactivation |
| Q36036342 | Failure of homologous synapsis and sex-specific reproduction problems |
| Q36594499 | Fast forward to new genes in mammalian reproduction |
| Q24649866 | Female Lethality and Apoptosis of Spermatocytes in Mice Lacking the UBR2 Ubiquitin Ligase of the N-End Rule Pathway |
| Q33347072 | Filament formation and robust strand exchange activities of the rice DMC1A and DMC1B proteins |
| Q37288589 | Finding the correct partner: the meiotic courtship |
| Q24529074 | Fission yeast rad51 and dmc1, two efficient DNA recombinases forming helical nucleoprotein filaments |
| Q33883290 | Flow cytometry purification of mouse meiotic cells |
| Q36434484 | From early homologue recognition to synaptonemal complex formation |
| Q37656488 | From meiosis to postmeiotic events: homologous recombination is obligatory but flexible |
| Q36674059 | From primordial germ cell to primordial follicle: mammalian female germ cell development |
| Q38435029 | Functional Roles of Acetylated Histone Marks at Mouse Meiotic Recombination Hot Spots |
| Q28586489 | Functional conservation of Mei4 for meiotic DNA double-strand break formation from yeasts to mice |
| Q47873959 | Functional conservation of the meiotic genes SDS and RCK in male meiosis in the monocot rice |
| Q36190966 | Functional evaluation of BRCA2 variants mapping to the PALB2-binding and C-terminal DNA-binding domains using a mouse ES cell-based assay. |
| Q34614094 | Functional interactions between SPO11 and REC102 during initiation of meiotic recombination in Saccharomyces cerevisiae. |
| Q36526067 | Functions of the MRE11 complex in the development and maintenance of oocytes |
| Q36088344 | GPSy: a cross-species gene prioritization system for conserved biological processes--application in male gamete development |
| Q91854086 | Gametogenesis: A journey from inception to conception |
| Q34690840 | Gene expression analysis of parthenogenetic embryonic development of the pea aphid, Acyrthosiphon pisum, suggests that aphid parthenogenesis evolved from meiotic oogenesis |
| Q47069371 | Genetic and cytological characterization of the recombination protein RAD-51 in Caenorhabditis elegans |
| Q34961894 | Genetic circuits that govern bisexual and unisexual reproduction in Cryptococcus neoformans |
| Q35221514 | Genetic evidence that synaptonemal complex axial elements govern recombination pathway choice in mice |
| Q37669186 | Genetics of mammalian meiosis: regulation, dynamics and impact on fertility |
| Q26777164 | Genetics of the ovarian reserve |
| Q34778117 | Genome destabilization by homologous recombination in the germ line |
| Q47140078 | Genomic footprints of dryland stress adaptation in Egyptian fat-tail sheep and their divergence from East African and western Asia cohorts |
| Q28586137 | Germ cell differentiation and synaptonemal complex formation are disrupted in CPEB knockout mice |
| Q28592246 | Germ cell-specific transcriptional regulator sohlh2 is essential for early mouse folliculogenesis and oocyte-specific gene expression |
| Q53560094 | Germline stem cells and neo-oogenesis in the adult human ovary. |
| Q33770626 | Global gene expression in the human fetal testis and ovary |
| Q33965393 | H2AX is required for chromatin remodeling and inactivation of sex chromosomes in male mouse meiosis |
| Q28594947 | HORMAD1-dependent checkpoint/surveillance mechanism eliminates asynaptic oocytes |
| Q35034403 | High throughput sequencing reveals alterations in the recombination signatures with diminishing Spo11 activity |
| Q35824466 | Histone H2AFX Links Meiotic Chromosome Asynapsis to Prophase I Oocyte Loss in Mammals |
| Q33987524 | Homologous chromosome interactions in meiosis: diversity amidst conservation. |
| Q36581855 | Homologous pairing preceding SPO11-mediated double-strand breaks in mice |
| Q27345390 | Hormad1 mutation disrupts synaptonemal complex formation, recombination, and chromosome segregation in mammalian meiosis |
| Q48269909 | Human infertility: meiotic genes as potential candidates |
| Q30962381 | Huntington disease expansion mutations in humans can occur before meiosis is completed |
| Q27938442 | Identification of residues in yeast Spo11p critical for meiotic DNA double-strand break formation |
| Q34743783 | Ikbkap/Elp1 deficiency causes male infertility by disrupting meiotic progression |
| 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 |
| Q35903958 | Impairment of spermatogenesis leading to infertility |
| Q28513959 | In germ cells of mouse embryonic ovaries, the decision to enter meiosis precedes premeiotic DNA replication |
| Q37735506 | In vivo binding of PRDM9 reveals interactions with noncanonical genomic sites. |
| Q53183119 | Inactivation or non-reactivation: what accounts better for the silence of sex chromosomes during mammalian male meiosis? |
| Q53487384 | Increased frequency of asynapsis and associated meiotic silencing of heterologous chromatin in the presence of irradiation-induced extra DNA double strand breaks. |
| Q52565680 | Induction of apoptosis involving multiple pathways is a primary response to cyclin A1-deficiency in male meiosis. |
| Q34163622 | Infertility associated with meiotic failure in the tremor rat (tm/tm) is caused by the deletion of spermatogenesis associated 22. |
| Q37664062 | Initiation of meiotic recombination in mammals |
| Q27935897 | Interactions between Mei4, Rec114, and other proteins required for meiotic DNA double-strand break formation in Saccharomyces cerevisiae |
| Q34325568 | Interplay between synaptonemal complex, homologous recombination, and centromeres during mammalian meiosis |
| Q52718185 | Interrogating the Functions of PRDM9 Domains in Meiosis. |
| Q52611222 | Isolation and cytogenetic characterization of zebrafish meiotic prophase I mutants. |
| Q61814678 | It starts at the ends: The zebrafish meiotic bouquet is where it all begins |
| Q35713281 | Key mediators of somatic ATR signaling localize to unpaired chromosomes in spermatocytes |
| Q37459212 | LMTK2 and PARP-2 gene polymorphism and azoospermia secondary to meiotic arrest |
| Q37261499 | Lim homeobox gene, lhx8, is essential for mouse oocyte differentiation and survival |
| Q52340801 | Live cell analyses of synaptonemal complex dynamics and chromosome movements in cultured mouse testis tubules and embryonic ovaries. |
| Q28587200 | Loss of HR6B ubiquitin-conjugating activity results in damaged synaptonemal complex structure and increased crossing-over frequency during the male meiotic prophase |
| Q34879712 | MDC1 directs chromosome-wide silencing of the sex chromosomes in male germ cells |
| Q28589490 | MEIOB targets single-strand DNA and is necessary for meiotic recombination |
| Q48252993 | MORC2B is essential for meiotic progression and fertility |
| Q64387589 | Mammalian meiosis involves DNA double-strand breaks with 3' overhangs |
| Q36365224 | Manipulation of Karyotype in Caenorhabditis elegans Reveals Multiple Inputs Driving Pairwise Chromosome Synapsis During Meiosis |
| Q33310052 | Mapping meiotic single-strand DNA reveals a new landscape of DNA double-strand breaks in Saccharomyces cerevisiae |
| Q41023071 | Mcp7, a meiosis-specific coiled-coil protein of fission yeast, associates with Meu13 and is required for meiotic recombination |
| Q29618789 | Mechanism and control of meiotic recombination initiation |
| Q34931212 | Mechanism and regulation of meiotic recombination initiation |
| Q39135838 | Mechanisms controlling germline cyst breakdown and primordial follicle formation |
| Q26770859 | Mechanisms of Origin, Phenotypic Effects and Diagnostic Implications of Complex Chromosome Rearrangements |
| Q30535213 | Mechanistic basis of infertility of mouse intersubspecific hybrids. |
| Q64388742 | Mei1 is epistatic to Dmc1 during mouse meiosis |
| Q92265781 | Meiosis I progression in spermatogenesis requires a type of testis-specific 20S core proteasome |
| Q37033768 | Meiosis in oocytes: predisposition to aneuploidy and its increased incidence with age. |
| Q28591031 | Meiosis-specific cohesin mediates homolog recognition in mouse spermatocytes |
| Q36358073 | Meiosis-specific proteins MEIOB and SPATA22 cooperatively associate with the single-stranded DNA-binding replication protein A complex and DNA double-strand breaks |
| Q74045902 | Meiosis: Synapsis spoilt |
| Q35663976 | Meiosis: an overview of key differences from mitosis |
| Q35968483 | Meiosis: cell-cycle controls shuffle and deal. |
| Q28585141 | Meiotic DNA double-strand breaks and chromosome asynapsis in mice are monitored by distinct HORMAD2-independent and -dependent mechanisms |
| Q49315270 | Meiotic Knockdown and Complementation Reveals Essential Role of RAD51 in Mouse Spermatogenesis. |
| Q38618828 | Meiotic Recombination: The Essence of Heredity |
| Q92403963 | Meiotic chromosomes in motion: a perspective from Mus musculus and Caenorhabditis elegans |
| Q35079862 | Meiotic cohesin SMC1β provides prophase I centromeric cohesion and is required for multiple synapsis-associated functions. |
| Q37526323 | Meiotic cohesin subunits RAD21L and REC8 are positioned at distinct regions between lateral elements and transverse filaments in the synaptonemal complex of mouse spermatocytes |
| Q38000414 | Meiotic double strand breaks repair in sexually reproducing eukaryotes: we are not all equal |
| Q24646919 | Meiotic double-strand breaks at the interface of chromosome movement, chromosome remodeling, and reductional division |
| Q34423978 | Meiotic errors activate checkpoints that improve gamete quality without triggering apoptosis in male germ cells |
| Q35541520 | Meiotic functions of RAD18. |
| Q64065894 | Meiotic gatekeeper STRA8 suppresses autophagy by repressing Nr1d1 expression during spermatogenesis in mice |
| Q28594654 | Meiotic homologue alignment and its quality surveillance are controlled by mouse HORMAD1. |
| Q27314735 | Meiotic pairing and segregation of achiasmate sex chromosomes in eutherian mammals: the role of SYCP3 protein |
| Q37371435 | Meiotic recombination and the crossover assurance checkpoint in Caenorhabditis elegans |
| Q34238005 | Meiotic recombination hot spots and cold spots |
| Q34570845 | Meiotic recombination in Drosophila females depends on chromosome continuity between genetically defined boundaries |
| Q35910256 | Meiotic recombination intermediates and mismatch repair proteins |
| Q34609362 | Meiotic recombination protein Rec12: functional conservation, crossover homeostasis and early crossover/non-crossover decision |
| Q58486284 | Meiotic recombination: Breaking the genome to save it |
| Q24597411 | Meiotic versus mitotic recombination: two different routes for double-strand break repair: the different functions of meiotic versus mitotic DSB repair are reflected in different pathway usage and different outcomes |
| Q33530120 | Microgravity promotes differentiation and meiotic entry of postnatal mouse male germ cells |
| Q27313888 | Mll5 is required for normal spermatogenesis |
| Q34067772 | Mnd1p: an evolutionarily conserved protein required for meiotic recombination |
| Q28081157 | Models of germ cell development and their application for toxicity studies |
| 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 |
| Q28586590 | Mouse HORMAD1 and HORMAD2, two conserved meiotic chromosomal proteins, are depleted from synapsed chromosome axes with the help of TRIP13 AAA-ATPase |
| Q33826136 | Mouse HORMAD1 is a meiosis i checkpoint protein that modulates DNA double- strand break repair during female meiosis |
| Q60045774 | Mouse REC114 is essential for meiotic DNA double-strand break formation and forms a complex with MEI4 |
| Q28512197 | Mouse TEX15 is essential for DNA double-strand break repair and chromosomal synapsis during male meiosis |
| Q28504811 | Mouse maelstrom, a component of nuage, is essential for spermatogenesis and transposon repression in meiosis |
| Q36391036 | Mouse models for genes involved in impaired spermatogenesis. |
| Q34932076 | Mouse models of male infertility. |
| Q28591450 | Mouse pachytene checkpoint 2 (trip13) is required for completing meiotic recombination but not synapsis |
| Q36233041 | Mouse strains with an active H2-Ea meiotic recombination hot spot exhibit increased levels of H2-Ea-specific DNA breaks in testicular germ cells |
| Q34558046 | Multiple opposing constraints govern chromosome interactions during meiosis |
| Q33324168 | MutL homologs in restriction-modification systems and the origin of eukaryotic MORC ATPases |
| 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 |
| Q28474807 | Mutation of the mouse Syce1 gene disrupts synapsis and suggests a link between synaptonemal complex structural components and DNA repair |
| Q28506028 | Mutations that affect meiosis in male mice influence the dynamics of the mid-preleptotene and bouquet stages |
| Q92825425 | NBS1 is required for SPO11-linked DNA double-strand break repair in male meiosis |
| Q61450769 | Narya, a RING finger domain-containing protein, is required for meiotic DNA double-strand break formation and crossover maturation in Drosophila melanogaster |
| Q64065581 | Noncanonical Contributions of MutLγ to VDE-Initiated Crossovers During Meiosis |
| Q34617124 | Nonrandom homolog segregation at meiosis I in Schizosaccharomyces pombe mutants lacking recombination |
| Q24543577 | Normal Synaptonemal Complex and Abnormal Recombination Nodules in Two Alleles of the Drosophila Meiotic Mutant mei-W68 |
| Q35998496 | Nuclear localization of PRDM9 and its role in meiotic chromatin modifications and homologous synapsis |
| Q36832176 | Numerical constraints and feedback control of double-strand breaks in mouse meiosis |
| Q34351172 | Oocyte differentiation is genetically dissociable from meiosis in mice |
| Q21129203 | OsRAD51C is essential for double-strand break repair in rice meiosis |
| Q35042146 | OsSDS is essential for DSB formation in rice meiosis |
| Q53312961 | OsSPO11-1 is essential for both homologous chromosome pairing and crossover formation in rice. |
| Q37217307 | Patterns of meiotic recombination in human fetal oocytes |
| Q47100071 | Periodic production of retinoic acid by meiotic and somatic cells coordinates four transitions in mouse spermatogenesis. |
| Q33629187 | Phenotyping male infertility in the mouse: how to get the most out of a 'non-performer' |
| Q34162317 | Phosphorylation of chromosome core components may serve as axis marks for the status of chromosomal events during mammalian meiosis |
| Q47108181 | Physiological Roles of DNA Double-Strand Breaks |
| Q57673146 | Point-of-care whole-exome sequencing of idiopathic male infertility |
| Q33653455 | Polo-like kinase-dependent phosphorylation of the synaptonemal complex protein SYP-4 regulates double-strand break formation through a negative feedback loop |
| Q28507685 | Polycomb protein SCML2 associates with USP7 and counteracts histone H2A ubiquitination in the XY chromatin during male meiosis |
| Q34523227 | Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest. |
| Q28512598 | Positional cloning and characterization of Mei1, a vertebrate-specific gene required for normal meiotic chromosome synapsis in mice |
| Q47358994 | Positive role of the mammalian TBPIP/HOP2 protein in DMC1-mediated homologous pairing. |
| Q64387595 | Prdm9 and Meiotic Cohesin Proteins Cooperatively Promote DNA Double-Strand Break Formation in Mammalian Spermatocytes |
| Q35020831 | Predicting human minisatellite polymorphism |
| Q35619405 | Prelude to a division |
| Q39155608 | Prophase I: Preparing Chromosomes for Segregation in the Developing Oocyte |
| Q37150956 | Proteins involved in meiotic recombination: a role in male infertility? |
| Q33779559 | Pseudosynapsis and decreased stringency of meiotic repair pathway choice on the hemizygous sex chromosome of Caenorhabditis elegans males |
| Q35080034 | Purification, folding, and characterization of Rec12 (Spo11) meiotic recombinase of fission yeast |
| Q36780816 | Quantitative analysis of male germline stem cell differentiation reveals a role for the p53-mTORC1 pathway in spermatogonial maintenance |
| Q28589265 | RAD51C deficiency in mice results in early prophase I arrest in males and sister chromatid separation at metaphase II in females |
| Q28509598 | RNF212 is a dosage-sensitive regulator of crossing-over during mammalian meiosis |
| Q36542150 | Rad50S alleles of the Mre11 complex: questions answered and questions raised |
| Q38071442 | RanBPM, a scaffolding protein for gametogenesis |
| Q35094244 | Rap1-independent telomere attachment and bouquet formation in mammalian meiosis |
| Q35058333 | Rec25 and Rec27, novel linear-element components, link cohesin to meiotic DNA breakage and recombination. |
| Q29618790 | Recombinational DNA double-strand breaks in mice precede synapsis |
| Q28505990 | Regulated CPEB phosphorylation during meiotic progression suggests a mechanism for temporal control of maternal mRNA translation |
| Q38824610 | Regulating the construction and demolition of the synaptonemal complex. |
| Q34464620 | Regulation of meiotic recombination and prophase I progression in mammals |
| Q51803054 | Relationship between incomplete synapsis and chiasma localization. |
| Q27012688 | Repair of strand breaks by homologous recombination |
| Q37096201 | Repeat expansion by homologous recombination in the mouse germ line at palindromic sequences |
| Q34015261 | Retinoic acid activates two pathways required for meiosis in mice |
| Q45808311 | Retinoic acid derived from the fetal ovary initiates meiosis in mouse germ cells. |
| Q36535367 | Retinol dehydrogenase 10 is indispensible for spermatogenesis in juvenile males |
| Q37769457 | Role of ubiquitination in meiotic recombination repair |
| Q55186299 | SHOC1 is a ERCC4-(HhH)2-like protein, integral to the formation of crossover recombination intermediates during mammalian meiosis. |
| Q39447587 | SOHLH1 and SOHLH2 coordinate spermatogonial differentiation |
| Q36758273 | SPO11-C631T Gene Polymorphism: Association With Male Infertility and an in Silico-Analysis |
| Q27322567 | SPO11-independent DNA repair foci and their role in meiotic silencing |
| Q36217378 | Saccharomyces cerevisiae Dmc1 and Rad51 proteins preferentially function with Tid1 and Rad54 proteins, respectively, to promote DNA strand invasion during genetic recombination |
| Q34786779 | Seeking new meiotic genes |
| Q34672035 | Senataxin plays an essential role with DNA damage response proteins in meiotic recombination and gene silencing |
| Q37098468 | Sex chromosome inactivation in germ cells: emerging roles of DNA damage response pathways |
| Q35205846 | Single nucleotide polymorphism in the UBR2 gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest. |
| Q24614084 | Single nucleotide polymorphisms in the SEPTIN12 gene may be associated with azoospermia by meiotic arrest in Japanese men |
| Q57162910 | Single-cell RNA-seq uncovers dynamic processes and critical regulators in mouse spermatogenesis |
| Q42589701 | Sister cohesion and structural axis components mediate homolog bias of meiotic recombination |
| Q28588839 | Spata22, a novel vertebrate-specific gene, is required for meiotic progress in mouse germ cells |
| Q35212439 | Spo11 and the Formation of DNA Double-Strand Breaks in Meiosis |
| Q35829344 | Stimulation of fission yeast and mouse Hop2-Mnd1 of the Dmc1 and Rad51 recombinases |
| Q36889785 | Stra8 and its inducer, retinoic acid, regulate meiotic initiation in both spermatogenesis and oogenesis in mice. |
| Q27933080 | Support for a meiotic recombination initiation complex: interactions among Rec102p, Rec104p, and Spo11p |
| Q34840536 | Suppression of genetic recombination in the pseudoautosomal region and at subtelomeres in mice with a hypomorphic Spo11 allele |
| Q24529923 | Surveillance of different recombination defects in mouse spermatocytes yields distinct responses despite elimination at an identical developmental stage |
| Q89857158 | Sycp2 is essential for synaptonemal complex assembly, early meiotic recombination and homologous pairing in zebrafish spermatocytes |
| Q104747937 | Synaptonemal Complex Formation Produces a Particular Arrangement of the Lateral Element-Associated DNA |
| Q45951757 | Synaptonemal complex assembly and H3K4Me3 demethylation determine DIDO3 localization in meiosis. |
| Q47069553 | Synaptonemal complex assembly in C. elegans is dispensable for loading strand-exchange proteins but critical for proper completion of recombination |
| Q36061063 | TAF4b Regulates Oocyte-Specific Genes Essential for Meiosis |
| Q28589015 | TOPAZ1, a germ cell specific factor, is essential for male meiotic progression |
| Q34403318 | Targeted JAM-C deletion in germ cells by Spo11-controlled Cre recombinase. |
| Q37493438 | Targeted gene knockout reveals a role in meiotic recombination for ZHP-3, a Zip3-related protein in Caenorhabditis elegans |
| Q36607600 | Targeting the Gdnf Gene in peritubular myoid cells disrupts undifferentiated spermatogonial cell development |
| Q38622778 | Telomere homeostasis in mammalian germ cells: a review. |
| Q33424478 | Temporally regulated traffic of HuR and its associated ARE-containing mRNAs from the chromatoid body to polysomes during mouse spermatogenesis |
| Q38678873 | Tex19.1 promotes Spo11-dependent meiotic recombination in mouse spermatocytes |
| Q35174765 | The ATM signaling cascade promotes recombination-dependent pachytene arrest in mouse spermatocytes. |
| Q24535915 | The Arabidopsis homologue of Xrcc3 plays an essential role in meiosis |
| Q34084136 | The Arabidopsis synaptonemal complex protein ZYP1 is required for chromosome synapsis and normal fidelity of crossing over. |
| Q95831637 | The BCL-2 pathway preserves mammalian genome integrity by eliminating recombination-defective oocytes |
| Q34282575 | The Hop2 protein has a direct role in promoting interhomolog interactions during mouse meiosis |
| Q27308664 | The Meiotic Recombination Activator PRDM9 Trimethylates Both H3K36 and H3K4 at Recombination Hotspots In Vivo |
| Q33939457 | The RNA-binding specificity of the mouse Dazl protein |
| Q28592802 | The TopoVIB-Like protein family is required for meiotic DNA double-strand break formation |
| Q36574666 | The cellular control of DNA double-strand breaks |
| Q37384277 | The consequences of asynapsis for mammalian meiosis |
| Q35781510 | The conserved transcriptome in human and rodent male gametogenesis |
| Q40952548 | The control of Spo11's interaction with meiotic recombination hotspots. |
| Q34613621 | The distribution of early recombination nodules on zygotene bivalents from plants |
| Q36416265 | The diverse roles of transverse filaments of synaptonemal complexes in meiosis |
| Q90728910 | The ectopic expression of meiCT genes promotes meiomitosis and may facilitate carcinogenesis |
| Q36013651 | The enigmatic meiotic dense body and its newly discovered component, SCML1, are dispensable for fertility and gametogenesis in mice. |
| Q34119672 | The expression profile of the major mouse SPO11 isoforms indicates that SPO11beta introduces double strand breaks and suggests that SPO11alpha has an additional role in prophase in both spermatocytes and oocytes |
| Q36429056 | The many facets of SC function during C. elegans meiosis |
| Q47446592 | The mouse X chromosome is enriched for sex-biased genes not subject to selection by meiotic sex chromosome inactivation |
| Q92529023 | The pericentromeric heterochromatin of homologous chromosomes remains associated after centromere pairing dissolves in mouse spermatocyte meiosis |
| Q36900929 | The role of spermatogonially expressed germ cell-specific genes in mammalian meiosis |
| Q61814681 | The telomere bouquet is a hub where meiotic double-strand breaks, synapsis, and stable homolog juxtaposition are coordinated in the zebrafish, Danio rerio |
| Q36781174 | The tricky path to recombining X and Y chromosomes in meiosis |
| Q37763943 | The use of transgenic mouse models in the study of male infertility |
| Q63344850 | Theatspo11-1 mutation rescues atxrcc3 meiotic chromosome fragmentation |
| Q37192086 | Thoc1 deficiency compromises gene expression necessary for normal testis development in the mouse |
| Q43259698 | Tid1/Rdh54 promotes dissociation of Dmc1 from nonrecombinogenic sites on meiotic chromatin |
| Q28508190 | TopBP1 and ATR colocalization at meiotic chromosomes: role of TopBP1/Cut5 in the meiotic recombination checkpoint |
| Q61812011 | Transition from a meiotic to a somatic-like DNA damage response during the pachytene stage in mouse meiosis |
| Q30438766 | Tuberoinfundibular Peptide of 39 residues is required for germ cell development |
| Q24650847 | Two single nucleotide polymorphisms in PRDM9 (MEISETZ) gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest |
| Q37358029 | Tying synaptonemal complex initiation to the formation and programmed repair of DNA double-strand breaks |
| Q34278026 | UBR2 of the N-end rule pathway is required for chromosome stability via histone ubiquitylation in spermatocytes and somatic cells |
| Q29615266 | Un ménage à quatre: the molecular biology of chromosome segregation in meiosis |
| Q90259369 | Variable Patterning of Chromatin Remodeling, Telomere Positioning, Synapsis, and Chiasma Formation of Individual Rye Chromosomes in Meiosis of Wheat-Rye Additions |
| Q35018030 | Variation in patterns of human meiotic recombination |
| Q36435635 | Vilya, a component of the recombination nodule, is required for meiotic double-strand break formation in Drosophila |
| Q35778662 | Where the crossovers are: recombination distributions in mammals. |
| Q62609015 | White-cap mutants and meiotic apoptosis in the basidiomycete Coprinus cinereus |
| Q90451189 | XRCC2 mutation causes meiotic arrest, azoospermia and infertility |
| Q33641006 | Zfy genes are required for efficient meiotic sex chromosome inactivation (MSCI) in spermatocytes |
| Q48185934 | ketu mutant mice uncover an essential meiotic function for the ancient RNA helicase YTHDC2. |
| Q33853843 | p53 and TAp63 participate in the recombination-dependent pachytene arrest in mouse spermatocytes |
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