Literature DB >> 16551715

The role of X inactivation and cellular mosaicism in women's health and sex-specific diseases.

Barbara R Migeon1.   

Abstract

Sex-specific manifestations of disease are most often attributed to differences in the reproductive apparatus or in life experiences. However, a good deal of sex differences in health issues have their origins in the genes on the sex chromosomes themselves and in X inactivation-the developmental program that equalizes their expression in males and females. Most females are mosaics, having a mixture of cells expressing either their mother's or father's X-linked genes. Often, cell mosaicism is advantageous, ameliorating the deleterious effects of X-linked mutations and contributing to physiological diversity. As a consequence, most X-linked mutations produce male-only diseases. Yet, in some cases the dynamic interactions between cells in mosaic females lead to female-specific disease manifestations.

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Year:  2006        PMID: 16551715     DOI: 10.1001/jama.295.12.1428

Source DB:  PubMed          Journal:  JAMA        ISSN: 0098-7484            Impact factor:   56.272


  70 in total

1.  Exercise-induced left ventricular systolic dysfunction in women heterozygous for dystrophinopathy.

Authors:  Robert M Weiss; Richard E Kerber; Jane K Jones; Carrie M Stephan; Christina J Trout; Paul D Lindower; Kimberly S Staffey; Kevin P Campbell; Katherine D Mathews
Journal:  J Am Soc Echocardiogr       Date:  2010-06-19       Impact factor: 5.251

Review 2.  X chromosome inactivation and female predisposition to autoimmunity.

Authors:  Tayfun Ozcelik
Journal:  Clin Rev Allergy Immunol       Date:  2008-06       Impact factor: 8.667

Review 3.  X chromosome inactivation in clinical practice.

Authors:  Karen Helene Orstavik
Journal:  Hum Genet       Date:  2009-04-25       Impact factor: 4.132

4.  Supporting family adaptation to presymptomatic and "untreatable" conditions in an era of expanded newborn screening.

Authors:  Donald B Bailey; F Daniel Armstrong; Alex R Kemper; Debra Skinner; Steven F Warren
Journal:  J Pediatr Psychol       Date:  2008-03-30

5.  Human X-chromosome inactivation pattern distributions fit a model of genetically influenced choice better than models of completely random choice.

Authors:  Nisa K E Renault; Sonja M Pritchett; Robin E Howell; Wenda L Greer; Carmen Sapienza; Karen Helene Ørstavik; David C Hamilton
Journal:  Eur J Hum Genet       Date:  2013-05-08       Impact factor: 4.246

6.  Female X-chromosome mosaicism for NOX2 deficiency presents unique inflammatory phenotype and improves outcome in polymicrobial sepsis.

Authors:  Rachna Chandra; Stephanie Federici; Zoltán H Németh; Béla Horváth; Pál Pacher; György Haskó; Edwin A Deitch; Zoltán Spolarics
Journal:  J Immunol       Date:  2011-04-18       Impact factor: 5.422

7.  Respiratory failure, cleft palate and epilepsy in the mouse model of human Xq22.1 deletion syndrome.

Authors:  Jian Zhou; Ethan M Goldberg; N Adrian Leu; Lei Zhou; Douglas A Coulter; P Jeremy Wang
Journal:  Hum Mol Genet       Date:  2014-02-25       Impact factor: 6.150

Review 8.  Expression of the disease on female carriers of X-linked lysosomal disorders: a brief review.

Authors:  Louise L C Pinto; Taiane A Vieira; Roberto Giugliani; Ida V D Schwartz
Journal:  Orphanet J Rare Dis       Date:  2010-05-28       Impact factor: 4.123

Review 9.  Review: Male systemic lupus erythematosus: a review of sex disparities in this disease.

Authors:  L-J Lu; D J Wallace; M L Ishimori; R H Scofield; M H Weisman
Journal:  Lupus       Date:  2009-11-27       Impact factor: 2.911

10.  Influence of sex on gene expression in human corneal epithelial cells.

Authors:  Tomo Suzuki; Stephen M Richards; Shaohui Liu; Roderick V Jensen; David A Sullivan
Journal:  Mol Vis       Date:  2009-12-03       Impact factor: 2.367

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