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Fetal loss in homozygous mutant Norrie disease mice: a new role of Norrin in reproduction
Uppsala University, Disciplinary Domain of Science and Technology, Biology, Department of Physiology and Developmental Biology, Animal Development and Genetics.
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2005 (English)In: Genesis, ISSN 1526-954X, E-ISSN 1526-968X, Vol. 42, no 4, 253-62 p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2005. Vol. 42, no 4, 253-62 p.
Keyword [en]
Animals, Animals; Newborn, Deafness/genetics, Disease Models; Animal, Eye Diseases; Hereditary/*genetics, Eye Proteins/biosynthesis/*genetics, Female, Fertility/genetics, Fetal Death/*genetics, Gene Expression, Genetic Diseases; X-Linked/*genetics, Homozygote, Humans, In Situ Hybridization, Infertility; Female/*genetics, Male, Mental Retardation/genetics, Mice, Mice; Knockout, Nerve Tissue Proteins/biosynthesis/*genetics, Pregnancy, Reproduction/*genetics/physiology, Research Support; Non-U.S. Gov't, Reverse Transcriptase Polymerase Chain Reaction, Trophoblasts
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Developmental Biology
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URN: urn:nbn:se:uu:diva-78430DOI: 10.1002/gene.20141PubMedID: 16035034OAI: oai:DiVA.org:uu-78430DiVA: diva2:106343
Available from: 2007-02-08 Created: 2007-02-08 Last updated: 2017-12-14Bibliographically approved

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Fundele, Reinald

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