| [SINEs in mammalian genomes can serve as additional signals in formation of facultative heterochromatin] [English Abstract, Journal Article]
Tsitologiia 2008; 50(3):256-60.
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| Mahadevaiah SK, Bourc'his D, de Rooij DG, et al.
Extensive meiotic asynapsis in mice antagonises meiotic silencing of unsynapsed chromatin and consequently disrupts meiotic sex chromosome inactivation. [Journal Article]
J Cell Biol 2008 Jul 28; 182(2):263-76.
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| Hayashi S, Mizuno S, Migita O, et al.
The CASK gene harbored in a deletion detected by array-CGH as a potential candidate for a gene causative of X-linked dominant mental retardation. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Jul 15.
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| Gitschier J
The exception that proves the rule: an interview with jenny graves. [Journal Article]
PLoS Genet 2008 Jun; 4(6):e1000063.
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| Elisaphenko EA, Kolesnikov NN, Shevchenko AI, et al.
A dual origin of the Xist gene from a protein-coding gene and a set of transposable elements. [Journal Article, Research Support, N.I.H., Intramural, Research Support, Non-U.S. Gov't]
PLoS ONE 2008; 3(6):e2521.
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| Shibata S, Wakayama T, Yokota T
X chromosome inactivation in nuclear transfer ES cells. [Journal Article]
Cytogenet Genome Res 2008; 121(2):96-101.
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| Amakawa Y, Sado T
[X chromosome inactivation and reactivation during mouse development] [Journal Article]
Tanpakushitsu Kakusan Koso 2008 Jun; 53(7):830-5.
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| Ogawa Y, Sun BK, Lee JT
Intersection of the RNA interference and X-inactivation pathways. [Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't]
Science 2008 Jun 6; 320(5881):1336-41.
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| Gono T, Yazaki M, Agematsu K, et al.
Adult Onset X-Linked Chronic Granulomatous Disease in a Woman Patient Caused by a de novo Mutation in Paternal-Origin CYBB Gene and Skewed Inactivation of Normal Maternal X Chromosome. [JOURNAL ARTICLE]
Intern Med 2008; 47(11):1053-1056.
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| Bedeschi MF, Novelli A, Bernardini L, et al.
Association of syndromic mental retardation with an Xq12q13.1 duplication encompassing the oligophrenin 1 gene. [JOURNAL ARTICLE]
Am J Med Genet A 2008 May 29.
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