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The Mechanism of Crossing-Over. II. IV. The Manner of Occurrence of Crossing-Over

1916; University of Chicago Press; Volume: 50; Issue: 593 Linguagem: Inglês

10.1086/279541

1537-5323

Hermann J. Müller,

Microbial Community Ecology and Physiology

Previous articleNext article FreeThe Mechanism of Crossing-Over. II. IV. The Manner of Occurrence of Crossing-OverHermann J. MullerHermann J. MullerPDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by The American Naturalist Volume 50, Number 593May, 1916 Published for The American Society of Naturalists Article DOIhttps://doi.org/10.1086/279541 Views: 257Total views on this site Citations: 35Citations are reported from Crossref PDF download Crossref reports the following articles citing this article:Andrew Lloyd Crossover patterning in plants, Plant Reproduction 102 (Jul 2022).https://doi.org/10.1007/s00497-022-00445-4Aurora Ruiz-Herrera, Paul D. Waters Fragile, unfaithful and persistent Ys—on how meiosis can shape sex chromosome evolution, Heredity 129, no.11 (Apr 2022): 22–30.https://doi.org/10.1038/s41437-022-00532-2Nila M. Pazhayam, Carolyn A. 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Saccheri, Samuel Whiteford, Carl J. Yung, Arjen E. van't Hof Recessive Z-linked lethals and the retention of haplotype diversity in a captive butterfly population, Heredity 125, no.1-21-2 (May 2020): 28–39.https://doi.org/10.1038/s41437-020-0316-xAndrew Lloyd, Eric Jenczewski Modelling Sex-Specific Crossover Patterning in Arabidopsis, Genetics 211, no.33 (Jan 2019): 847–859.https://doi.org/10.1534/genetics.118.301838Luoyan Zhang, Hongzhi Kong, Hong Ma, Ji Yang Phylogenomic detection and functional prediction of genes potentially important for plant meiosis, Gene 643 (Feb 2018): 83–97.https://doi.org/10.1016/j.gene.2017.12.005Parijat Chakraborty, Ajith V Pankajam, Gen Lin, Abhishek Dutta, G Nandanan Krishnaprasad, Manu M Tekkedil, Akira Shinohara, Lars M Steinmetz, K Thazath Nishant Modulating Crossover Frequency and Interference for Obligate Crossovers in Saccharomyces cerevisiae Meiosis, G3 Genes|Genomes|Genetics 7, no.55 (May 2017): 1511–1524.https://doi.org/10.1534/g3.117.040071Divya Pattabiraman, Baptiste Roelens, Alexander Woglar, Anne M. Villeneuve, Needhi Bhalla Meiotic recombination modulates the structure and dynamics of the synaptonemal complex during C. elegans meiosis, PLOS Genetics 13, no.33 (Mar 2017): e1006670.https://doi.org/10.1371/journal.pgen.1006670Gurukripa N. Krishnaprasad, Mayakonda T. Anand, Gen Lin, Manu M. Tekkedil, Lars M. Steinmetz, Koodali T. Nishant Variation in Crossover Frequencies Perturb Crossover Assurance Without Affecting Meiotic Chromosome Segregation in Saccharomyces cerevisiae, Genetics 199, no.22 (Dec 2014): 399–412.https://doi.org/10.1534/genetics.114.172320Liisa Kauppi Meiosis: SYP Up Firmly and Cross Over Evenly, Current Biology 24, no.11 (Jan 2014): R20–R23.https://doi.org/10.1016/j.cub.2013.11.007F. J. Bowring, P. J. Yeadon, D. E. A. Catcheside Residual recombination in Neurospora crassa spo11 deletion homozygotes occurs during meiosis, Molecular Genetics and Genomics 288, no.99 (Jun 2013): 437–444.https://doi.org/10.1007/s00438-013-0761-9A E Van't Hof, P Nguyen, M Dalíková, N Edmonds, F Marec, I J Saccheri Linkage map of the peppered moth, Biston betularia (Lepidoptera, Geometridae): a model of industrial melanism, Heredity 110, no.33 (Dec 2012): 283–295.https://doi.org/10.1038/hdy.2012.84Frederick J. Bowring, P.Jane Yeadon, David E.A. Catcheside Use of fluorescent protein to analyse recombination at three loci in Neurospora crassa, Fungal Genetics and Biology 49, no.88 (Aug 2012): 619–625.https://doi.org/10.1016/j.fgb.2012.05.012Claudio J. Bidau, Dardo A. Martí 110 Years of Orthopteran Cytogenetics, the Chromosomal Evolutionary Viewpoint, and Michael White's Signal Contributions to the Field*, Journal of Orthoptera Research 19, no.22 (Dec 2010): 165–182.https://doi.org/10.1665/034.019.0202Esther de Boer, Franck G.P. Lhuissier, Christa Heyting Cytological Analysis of Interference in Mouse Meiosis, (Jun 2009): 355–382.https://doi.org/10.1007/978-1-60761-103-5_21Raphael Falk GENETIC ANALYSIS, (Jan 2007): 249–308.https://doi.org/10.1016/B978-044451543-8/50015-0P Jane Yeadon, F J Bowring, D E A Catcheside Alleles of the Hotspot cog Are Codominant in Effect on Recombination in the his-3 Region of Neurospora, Genetics 167, no.33 (Jul 2004): 1143–1153.https://doi.org/10.1534/genetics.103.025080Scott L. Page, R. Scott Hawley c(3)G encodes a Drosophila synaptonemal complex protein, Genes & Development 15, no.2323 (Dec 2001): 3130–3143.https://doi.org/10.1101/gad.935001A. W. F. EDWARDS The early history of the statistical estimation of linkage, Annals of Human Genetics 60, no.33 (May 1996): 237–249.https://doi.org/10.1111/j.1469-1809.1996.tb00427.xRaphael Falk The Manifest and the Scientific, (Jan 1995): 57–79.https://doi.org/10.1007/978-94-011-0673-3_4Caroline E. Garey, Alexander L. Schwarzman, Matthew L. Rise, Thomas N. Seyfried Ceruloplasmin gene defect associated with epilepsy in EL mice, Nature Genetics 6, no.44 (Apr 1994): 426–431.https://doi.org/10.1038/ng0494-426Peter J. Russell Genetik der Eukaryonten: Meiotische Analyse bei Diploiden, (Jan 1983): 134–146.https://doi.org/10.1007/978-3-642-68865-2_14R. C. Woodruff, J. N. Thompson Hybrid Release of Mutator Activity and the Genetic Structure of Natural Populations, (Jan 1980): 129–162.https://doi.org/10.1007/978-1-4615-6959-6_3James N. Thompson, R. C. Woodruff Mutator genes—pacemakers of evolution, Nature 274, no.56695669 (Jul 1978): 317–321.https://doi.org/10.1038/274317a0R C Woodruff, J N Thompson An analysis of spontaneous recombination in Drosophila melanogaster males, Heredity 38, no.33 (Jun 1977): 291–307.https://doi.org/10.1038/hdy.1977.92BODIL SØGAARD The localization of eceriferum loci in barley, Hereditas 76, no.11 (Feb 2009): 41–47.https://doi.org/10.1111/j.1601-5223.1974.tb01175.xKirk T. Ehmsen, Wolf-Dietrich Heyer Biochemistry of Meiotic Recombination: Formation, Processing, and Resolution of Recombination Intermediates, (): 91–164.https://doi.org/10.1007/7050_2008_039Hans Grüneberg The case for somatic crossing over in the mouse, Genetical Research 7, no.11 (Apr 2009): 58–75.https://doi.org/10.1017/S0016672300009472T. C. Carter A search for chromatid interference in the male house mouse, Zeitschrift f�r Induktive Abstammungs- und Vererbungslehre 86, no.22 (Jan 1954): 210–223.https://doi.org/10.1007/BF00444789H. G. Gallan, G. Montalenti Chiasma interference in mosquitoes, Journal of Genetics 48, no.22 (Aug 1947): 119–134.https://doi.org/10.1007/BF02989374C. D. Darlington The time, place and action of crossing-over, Journal of Genetics 31, no.22 (Aug 1935): 185–212.https://doi.org/10.1007/BF02982340 Berwind P. Kaufmann Chromosome Structure in Drosophila, The American Naturalist 65, no.701701 (Oct 2015): 555–558.https://doi.org/10.1086/280401