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Nonrandom X Chromosome Inactivation Detection
Current Protocols in Human Genetics, 2014AbstractX chromosome inactivation patterns may be clinically useful in assessing tumor clonality, determining carrier status for certain X‐linked disorders and evaluating the pathogenicity of a genetic variant identified in an X‐linked gene. The protocols in this unit utilize the highly polymorphic trinucleotide repeat within the first exon of the ...
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X Chromosome Inactivation and Autoimmunity
Clinical Reviews in Allergy & Immunology, 2009Autoimmune diseases appear to have multiple contributing factors including genetics, epigenetics, environmental factors, and aging. The predominance of females among patients with autoimmune diseases suggests possible involvement of the X chromosome and X chromosome inactivation.
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Imprinting and X-Chromosome Inactivation
1999In normal female mammals one of the two X-chromosomes in every somatic cell is inactive i.e. it fails to transcribe RNA (reviews Gartler et al. 1992; Migeon 1994; Lyon 1996). The result of this is that chromosomally XX females and XY males both effectively have a single dosage of the products of X-linked genes.
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MAMMALIAN X-CHROMOSOME INACTIVATION
Annual Review of Genetics, 1983S M, Gartler, A D, Riggs
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Xg AND X CHROMOSOME INACTIVATION
The Lancet, 1971J, Ducos, Y, Marty, R, Sanger, R R, Race
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X‐chromosome inactivation in female patients with Fabry disease
Clinical Genetics, 2016L. Echevarría +9 more
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Phase separation drives X-chromosome inactivation: a hypothesis
Nature Structural & Molecular Biology, 2019A. Cerase +5 more
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