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By Aydin Arici; William F Rayburn

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Am J Obstet Gynecol 1970;107:1168 – 73. Mashal RD, Fejzo ML, Friedman AJ, et al. Analysis of androgen receptor DNA reveals the independent clonal origins of uterine leiomyomata and the secondary nature of cytogenetic aberrations in the development of leiomyomata. Genes Chromosomes Cancer 1994;11:1 – 6. Hashimoto K, Azuma C, Kamiura S, et al. Clonal determination of uterine leiomyomas by analyzing differential inactivation of the X-chromosome-linked phosphoglycerokinase gene. Gynecol Obstet Invest 1995;40:204 – 8.

A housekeeping gene coding for an enzyme in the citric acid cycle, FH is important in energy metabolism and also appears to act as a tumor suppressor [48,159]. 008%) were observed; further, FH mutations were only observed in UL of white women [158,160]. Other research examined 123 families with at least one affected sister pair, and performed linkage analysis on patient DNA to evaluate the role of FH mutations in predisposition of UL. This analysis confirmed the involvement of FH in a subset of nonsyndromic UL, and also found evidence suggesting earlier age of onset of UL is correlated with FH gene mutations.

116] Gattas GJ, Quade BJ, Nowak RA, et al. HMGIC expression in human adult and fetal tissues and in uterine leiomyomata. Genes Chromosomes Cancer 1999;25:316 – 22. [117] Ligon AH, Morton CC. Genetics of uterine leiomyomata. Genes Chromosomes Cancer 2000;28:235 – 45. [118] Reeves R, Langan TA, Nissen MS. Phosphorylation of the DNA-binding domain of nonhistone high-mobility group I protein by cdc2 kinase: reduction of binding affinity. Proc Natl Acad Sci U S A 1991;88:1671 – 5. [119] Nissen MS, Langan TA, Reeves R.

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