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Journal Abstract Search

226 related items for PubMed ID: 10928988

  • 21. MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice.
    Kneitz B, Cohen PE, Avdievich E, Zhu L, Kane MF, Hou H, Kolodner RD, Kucherlapati R, Pollard JW, Edelmann W.
    Genes Dev; 2000 May 01; 14(9):1085-97. PubMed ID: 10809667
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  • 22. Variation in genome-wide levels of meiotic recombination is established at the onset of prophase in mammalian males.
    Baier B, Hunt P, Broman KW, Hassold T.
    PLoS Genet; 2014 Jan 01; 10(1):e1004125. PubMed ID: 24497841
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  • 23. Family of SRY/Sox proteins is involved in the regulation of the mouse Msh4 (MutS Homolog 4) gene expression.
    Santucci-Darmanin S, Vidal F, Scimeca JC, Turc-Carel C, Paquis-Flucklinger V.
    Mol Reprod Dev; 2001 Oct 01; 60(2):172-80. PubMed ID: 11553915
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  • 24. Discontinuities and unsynapsed regions in meiotic chromosomes have a trans effect on meiotic recombination of some chromosomes in human males.
    Sun F, Oliver-Bonet M, Liehr T, Starke H, Ko E, Rademaker A, Martin RH.
    Cytogenet Genome Res; 2007 Oct 01; 119(1-2):27-32. PubMed ID: 18160778
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  • 25. Temporal progression of recombination in human males.
    Oliver-Bonet M, Turek PJ, Sun F, Ko E, Martin RH.
    Mol Hum Reprod; 2005 Jul 01; 11(7):517-22. PubMed ID: 16123081
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  • 28. Genetic analysis of mlh3 mutations reveals interactions between crossover promoting factors during meiosis in baker's yeast.
    Sonntag Brown M, Lim E, Chen C, Nishant KT, Alani E.
    G3 (Bethesda); 2013 Jan 01; 3(1):9-22. PubMed ID: 23316435
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  • 29. ATP-dependent interaction of human mismatch repair proteins and dual role of PCNA in mismatch repair.
    Gu L, Hong Y, McCulloch S, Watanabe H, Li GM.
    Nucleic Acids Res; 1998 Mar 01; 26(5):1173-8. PubMed ID: 9469823
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  • 31. Loss of HR6B ubiquitin-conjugating activity results in damaged synaptonemal complex structure and increased crossing-over frequency during the male meiotic prophase.
    Baarends WM, Wassenaar E, Hoogerbrugge JW, van Cappellen G, Roest HP, Vreeburg J, Ooms M, Hoeijmakers JH, Grootegoed JA.
    Mol Cell Biol; 2003 Feb 01; 23(4):1151-62. PubMed ID: 12556476
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  • 34. Mouse Sycp1 functions in synaptonemal complex assembly, meiotic recombination, and XY body formation.
    de Vries FA, de Boer E, van den Bosch M, Baarends WM, Ooms M, Yuan L, Liu JG, van Zeeland AA, Heyting C, Pastink A.
    Genes Dev; 2005 Jun 01; 19(11):1376-89. PubMed ID: 15937223
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  • 35. Human MutL homolog (MLH1) function in DNA mismatch repair: a prospective screen for missense mutations in the ATPase domain.
    Ellison AR, Lofing J, Bitter GA.
    Nucleic Acids Res; 2004 Jun 01; 32(18):5321-38. PubMed ID: 15475387
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  • 36. Male mouse recombination maps for each autosome identified by chromosome painting.
    Froenicke L, Anderson LK, Wienberg J, Ashley T.
    Am J Hum Genet; 2002 Dec 01; 71(6):1353-68. PubMed ID: 12432495
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  • 37. Altered patterns of meiotic recombination in human fetal oocytes with asynapsis and/or synaptonemal complex fragmentation at pachytene.
    Tease C, Hartshorne G, Hultén M.
    Reprod Biomed Online; 2006 Jul 01; 13(1):88-95. PubMed ID: 16820117
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  • 38. The DNA helicase FANCJ (BRIP1) functions in Double Strand Break repair processing, but not crossover formation during Prophase I of meiosis in male mice.
    Horan TS, Ascenção CFR, Mellor CA, Wang M, Smolka MB, Cohen PE.
    bioRxiv; 2023 Oct 08. PubMed ID: 37873301
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  • 39. The Dmc1 recombinase physically interacts with and promotes the meiotic crossover functions of the Mlh1-Mlh3 endonuclease.
    Pannafino G, Chen JJ, Mithani V, Payero L, Gioia M, Crickard JB, Alani E.
    Genetics; 2024 Jul 08; 227(3):. PubMed ID: 38657110
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