Search Results - "Mahadevaiah, S"

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    Mammalian meiotic silencing exhibits sexually dimorphic features by Cloutier, J. M., Mahadevaiah, S. K., ElInati, E., Tóth, A., Turner, James

    Published in Chromosoma (01-06-2016)
    “…During mammalian meiotic prophase I, surveillance mechanisms exist to ensure that germ cells with defective synapsis or recombination are eliminated, thereby…”
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    ATR acts stage specifically to regulate multiple aspects of mammalian meiotic silencing by Royo, Hélène, Prosser, Haydn, Ruzankina, Yaroslava, Mahadevaiah, Shantha K, Cloutier, Jeffrey M, Baumann, Marek, Fukuda, Tomoyuki, Höög, Christer, Tóth, Attila, de Rooij, Dirk G, Bradley, Allan, Brown, Eric J, Turner, James M A

    Published in Genes & development (01-07-2013)
    “…In mammals, homologs that fail to synapse during meiosis are transcriptionally inactivated. This process, meiotic silencing, drives inactivation of the…”
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    H2AX Is Required for Chromatin Remodeling and Inactivation of Sex Chromosomes in Male Mouse Meiosis by Fernandez-Capetillo, Oscar, Mahadevaiah, Shantha K., Celeste, Arkady, Romanienko, Peter J., Camerini-Otero, R.Daniel, Bonner, William M., Manova, Katia, Burgoyne, Paul, Nussenzweig, André

    Published in Developmental cell (01-04-2003)
    “…During meiotic prophase in male mammals, the X and Y chromosomes condense to form a macrochromatin body, termed the sex, or XY, body, within which X- and…”
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    Recombinational DNA double-strand breaks in mice precede synapsis by Turner, James M.A, Jasin, Maria, Bonner, William M, Baudat, Frédéric, Blanco-Rodríguez, Josefa, Rogakou, Emmy P, de Boer, Peter, Mahadevaiah, Shantha K, Keeney, Scott, Burgoyne, Paul S

    Published in Nature genetics (01-03-2001)
    “…In Saccharomyces cerevisiae, meiotic recombination is initiated by Spo11-dependent double-strand breaks (DSBs), a process that precedes homologous synapsis…”
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    Meiotic sex chromosome inactivation in male mice with targeted disruptions of Xist by Turner, James M A, Mahadevaiah, Shantha K, Elliott, David J, Garchon, Henri-Jean, Pehrson, John R, Jaenisch, Rudolf, Burgoyne, Paul S

    Published in Journal of cell science (01-11-2002)
    “…X chromosome inactivation occurs twice during the life cycle of placental mammals. In normal females, one X chromosome in each cell is inactivated early in…”
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    A Y-encoded subunit of the translation initiation factor Eif2 is essential for mouse spermatogenesis by Mahadevaiah, Shantha K, Mazeyrat, Sophie, Burgoyne, Paul S, Mitchell, Michael J, Saut, Noëmie, Grigoriev, Vladimir, Ojarikre, Obah A, Bishop, Colin, Eicher, Eva M, Rattigan, Áine

    Published in Nature genetics (01-09-2001)
    “…In mouse and man, deletions of specific regions of the Y chromosome have been linked to early failure of spermatogenesis and consequent sterility; the Y…”
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    Fertility in mice requires X-Y pairing and a Y-chromosomal "spermiogenesis" gene mapping to the long arm by Burgoyne, P S, Mahadevaiah, S K, Sutcliffe, M J, Palmer, S J

    Published in Cell (30-10-1992)
    “…There is accumulating evidence that the mammalian Y chromosome, in addition to its testis-determining function, may have other male limited functions,…”
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    The Y rearrangement in mice: new insights into a perplexing PAR by Burgoyne, P S, Mahadevaiah, S K, Perry, J, Palmer, S J, Ashworth, A

    Published in Cytogenetics and cell genetics (01-01-1998)
    “…In essence, the Y* rearrangement in the mouse is a Y chromosome that has been hijacked by a non-Y centromere attached distal to the pseudoautosomal region…”
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    A protein encoded by a member of the multicopy Ssty gene family located on the long arm of the mouse Y chromosome is expressed during sperm development by Touré, Aminata, Grigoriev, Vladimir, Mahadevaiah, Shantha K., Rattigan, Áine, Ojarikre, Obah A., Burgoyne, Paul S.

    Published in Genomics (San Diego, Calif.) (2004)
    “…Multicopy Y-chromosomal genes in human and mouse have been postulated to play a role in spermatogenesis. The mouse Y long arm (Yq) carries hundreds of…”
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    An analysis of meiotic impairment and of sex chromosome associations throughout meiosis in XYY mice by Mahadevaiah, S K, Evans, E P, Burgoyne, P S

    Published in Cytogenetics and cell genetics (01-01-2000)
    “…The existing XYY meiotic data for mice present a very heterogeneous picture with respect to the relative frequencies of different sex chromosome associations,…”
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    Tdy-negative XY, XXY and XYY female mice: breeding data and synaptonemal complex analysis by Mahadevaiah, S K, Lovell-Badge, R, Burgoyne, P S

    Published in Journal of reproduction & fertility (01-01-1993)
    “…In this paper we have compared the breeding performance of Tdy -negative XY, XXY and XYY females to assess the relative importance of the lack of a second X…”
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    Does Rbmy have a role in sperm development in mice? by Szot, M, Grigoriev, V, Mahadevaiah, S K, Ojarikre, O A, Touré, A, von Glasenapp, E, Rattigan, A, Turner, J M A, Elliott, D J, Burgoyne, P S

    Published in Cytogenetic and genome research (01-01-2003)
    “…The Y(d1) deletion in mice removes most of the multi-copy Rbmy gene cluster that is located adjacent to the centromere on the Y short arm (Yp). XY(d1) mice…”
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    Y Chromosome Short Arm-Sxr Recombination in XSxr/Y Males Causes Deletion of Rbm and XY Female Sex Reversal by Laval, Steven H., Glenister, Peter H., Rasberry, Carol, Thornton, Claire E., Mahadevaiah, Shantha K., Cooke, Howard J., Burgoyne, Paul S., Cattanach, Bruce M.

    “…We earlier described three lines of sex-reversed XY female mice deleted for sequences believed close to the testes-determining gene (Sry) on the Y chromosome…”
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    Heterochromatin, HP1 and methylation at lysine 9 of histone H3 in animals by Cowell, Ian G, Aucott, Rebecca, Mahadevaiah, Shantha K, Burgoyne, Paul S, Huskisson, Neville, Bongiorni, Silvia, Prantera, Giorgio, Fanti, Laura, Pimpinelli, Sergio, Wu, Rong, Gilbert, David M, Shi, Wei, Fundele, Reinald, Morrison, Harris, Jeppesen, Peter, Singh, Prim B

    Published in Chromosoma (01-03-2002)
    “…We show that methylated lysine 9 of histone H3 (Me9H3) is a marker of heterochromatin in divergent animal species. It localises to both constitutive and…”
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    Unpaired chromosomes at meiosis: cause or effect of gametogenic insufficiency? by Mittwoch, U, Mahadevaiah, S K

    Published in Cytogenetics and cell genetics (01-01-1992)
    “…Pairing failure at meiosis has been postulated as a cause of gametogenic arrest in both heterozygous translocation carriers and males whose spermatocytes…”
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