Search Results - "Mahadevaiah, S"
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Dissecting genomic regions and underlying candidate genes in groundnut MAGIC population for drought tolerance
Published in BMC plant biology (05-11-2024)“…Groundnut is mainly grown in the semi-arid tropic (SAT) regions worldwide, where abiotic stress like drought is persistent. However, a major research gap…”
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Genetic mapping identified three hotspot genomic regions and candidate genes controlling heat tolerance-related traits in groundnut
Published in Frontiers in plant science (23-05-2023)“…Groundnut productivity and quality have been impeded by rising temperatures in semi-arid environments. Hence, understanding the effects and molecular…”
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3
Genotyping-by-Sequencing Based Genetic Mapping Identified Major and Consistent Genomic Regions for Productivity and Quality Traits in Peanut
Published in Frontiers in plant science (23-09-2021)“…With an objective of identifying the genomic regions for productivity and quality traits in peanut, a recombinant inbred line (RIL) population developed from…”
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Mammalian meiotic silencing exhibits sexually dimorphic features
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
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
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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Mouse Homologues of the Human AZF Candidate Gene RBM Are Expressed in Spermatogonia and Spermatids, and Map to a Y Chromosome Deletion Interval Associated with a High Incidence of Sperm Abnormalities
Published in Human molecular genetics (01-04-1998)“…An RNA-binding motif (RBM) gene family has been identified on the human Y chromosome that maps to the same deletion interval as the ‘azoospermia factor’ (AZF)…”
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Recombinational DNA double-strand breaks in mice precede synapsis
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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Genetic mapping of drought tolerance traits phenotyped under varying drought stress environments in peanut (Arachis hypogaea L.)
Published in Euphytica (01-12-2022)“…Genomic regions governing water deficit stress tolerance were identified in peanut using a recombinant inbred line (RIL) population derived from an elite…”
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10
Meiotic sex chromosome inactivation in male mice with targeted disruptions of Xist
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
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
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
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
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
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
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?
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
Published in Proceedings of the National Academy of Sciences - PNAS (24-10-1995)“…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
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?
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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