Genetics and the Development of Fibroids
- 1 June 2001
- journal article
- review article
- Published by Wolters Kluwer Health in Clinical Obstetrics and Gynecology
- Vol. 44 (2) , 335-349
- https://doi.org/10.1097/00003081-200106000-00020
Abstract
No abstract availableKeywords
This publication has 103 references indexed in Scilit:
- Transgenic Mice Expressing a Truncated Form of the High Mobility Group I-C Protein Develop Adiposity and an Abnormally High Prevalence of LipomasJournal of Biological Chemistry, 2000
- HMGIC expression in human adult and fetal tissues and in uterine leiomyomataGenes, Chromosomes and Cancer, 1999
- PMS2-Related Genes Flank the Rearrangement Breakpoints Associated with Williams Syndrome and Other Diseases on Human Chromosome 7Genomics, 1997
- Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancersNature Genetics, 1997
- ERβ: Identification and characterization of a novel human estrogen receptorFEBS Letters, 1996
- Familial predisposition to uterine leiomyomasInternational Journal of Gynecology & Obstetrics, 1995
- Expression and cDNA Cloning of Human HMGI-C PhosphoproteinBiochemical and Biophysical Research Communications, 1994
- Uterine fibroids: A clinical reviewBJOG: An International Journal of Obstetrics and Gynaecology, 1990
- Trisomy 12 in uterine leiomyomasCancer Genetics and Cytogenetics, 1990
- Ring formation and structural rearrangements of chromosome 1 as secondary changes in uterine leiomyomas with t(12;14)(q14–15;q23–24)Cancer Genetics and Cytogenetics, 1988