Random X Inactivation
Random X Inactivation is a genetic mechanism in female mammals whereby one of the two X chromosomes is transcriptionally silenced in a cell-specific manner during early embryonic development, with the choice of the inactivated X chromosome occurring randomly and independently in each cell, leading to a mosaic pattern of gene expression across tissues.
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Role of Histone H3 Lysine 27 Methylation in X Inactivation
Kathrin Plath, Jia Fang, Susanna Mlynarczyk‐Evans et al. · Science · 2003 · 1.2K citations
Epigenetic Dynamics of Imprinted X Inactivation During Early Mouse Development
Ikuhiro Okamoto, Arie P. Otte, C. David Allis et al. · Science · 2003 · 817 citations
Reactivation of the Paternal X Chromosome in Early Mouse Embryos
Winifred Mak, Tatyana B. Nesterova, Mariana de Napoles et al. · Science · 2004 · 545 citations
Targeted Mutagenesis of Tsix Leads to Nonrandom X Inactivation
Jeannie T. Lee, Naifang Lu · Cell · 1999 · 514 citations · Full text
GFAP promoter directs astrocyte-specific expression in transgenic mice
Michael Brenner, WC Kisseberth, Yuan Su et al. · Journal of Neuroscience · 1994 · 497 citations · Full text
Medicine, Genetics, Neuroscience +17
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Harvard University
Cambridge, United States
11 h-index
32 publications
4.4K citations

Howard Hughes Medical Institute
Chevy Chase, United States
10 h-index
34 publications
7.1K citations

Centre National de la Recherche Scientifique
Paris, France
9 h-index
31 publications
5.2K citations
Inserm
Paris, France
8 h-index
24 publications
1.3K citations
Erasmus MC
Rotterdam, The Netherlands
7 h-index
36 publications
3.2K citations

The University of Melbourne
Melbourne, Australia
7 h-index
7 publications
586 citations

Hokkaido University
Sapporo, Japan
7 h-index
15 publications
876 citations

Institut Curie
Paris, France
6 h-index
25 publications
5.4K citations
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PNAS · 12 publications · 930 citations
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11 publications · 595 citations
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11 publications · 480 citations
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11 publications · 734 citations
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9 publications · 542 citations
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