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Wang, W., Yang, J., Liu, H., Lu, D., Chen, X., Zenonos, Z., Campos, L.S., Rad, R., Guo, G., Zhang, S.J., Bradley, A. and Liu, P.T. (2011) Rapid and Efficient Reprogramming of Somatic Cells to Induced Pluripotent Stem Cells by Retinoic Acid Receptor Gamma and Liver Receptor Homolog 1. Proceedings of the National Academy of Sciences of the United States of America, 108, 18283-18288.
http://dx.doi.org/10.1073/pnas.1100893108

has been cited by the following article:

• TITLE: Revisiting the X-Chromosome Inactivation and Its Impact on Female Longevity

  AUTHORS: Lilian Chuaire-Noack, Magda Carolina Sánchez-Corredor, María Martínez-Agüero

  KEYWORDS: Sex Chromosomes, Epigenetic Inheritance, Heterochromatin, DNA Methylation, Gene Therapy

  JOURNAL NAME: Advances in Bioscience and Biotechnology, Vol.5 No.6, May 29, 2014

  ABSTRACT: X-chromosome inactivation is the genetic mechanism by which X-linked gene expression is equalized between the male and female genders of all placental mammal species. Given that the probability of mutant X-linked allele expression decreases as a result of the inactivation, it has been proposed that females have biological advantages relative to males. These advantages have grabbed the attention of the scientific community in recent years and have focused it on this topic and its clinical implications. To shed some new light on this intriguing phenomenon, this article reviews the most relevant molecular events involved in this process. These events include the role of Xist, the selection mechanism for future X-chromosome inactivation, the age-related inactivation skewing, and the relationship between inactivation and the emergence of X-linked diseases, possible treatments, and longevity.