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Genetically modified mouse models for premature ovarian failure (POF)
Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics.
Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics.
Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics.
Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics.
2010 (English)In: Molecular and Cellular Endocrinology, ISSN 0303-7207, E-ISSN 1872-8057, Vol. 315, no 1-2, 1-10 p.Article in journal (Refereed) Published
Abstract [en]

Premature ovarian failure (POF) is a complex disorder that affects approximately 1% of women. POF is characterized by the depletion of functional ovarian follicles before the age of 40 years, and clinically, patients may present with primary amenorrhea or secondary amenorrhea. Although some genes have been hypothesized to be candidates responsible for POF, the etiology of most of the cases is idiopathic, with the underlying causes still unidentified because of the heterogeneity of the disease. In this review, we consider some mutant mouse models that exhibit phenotypes which are comparable to human POF, and we suggest that the use of these mouse models may help us to gain a better understanding of the molecular mechanisms underlying POF in humans.

Place, publisher, year, edition, pages
2010. Vol. 315, no 1-2, 1-10 p.
Keyword [en]
Premature ovarian failure (POF); Mouse models; Ovary; Follicular development
Identifiers
URN: urn:nbn:se:umu:diva-42925DOI: 10.1016/j.mce.2009.07.016ISI: 000274608900001PubMedID: 19643165OAI: oai:DiVA.org:umu-42925DiVA: diva2:410772
Available from: 2011-04-14 Created: 2011-04-14 Last updated: 2017-12-11Bibliographically approved

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Jagarlamudi, KrishnaReddy, PradeepAdhikari, DeepakLiu, Kui
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