Hochschulschrift
Creation and establishment of transgenic mouse models for Mecp2 gene, causing Rett syndrome
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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Göttingen, Univ., Diss., 2007
- Keyword
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Gehirn
Zentralnervensystem
Nucleinsäurestoffwechsel
Tierphysiologie
Maus
- Creator
- URN
-
urn:nbn:de:gbv:7-webdoc-1470-9
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:47 AM CEST
Data provider
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Object type
- Hochschulschrift
Associated
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MECP2 germline mosaicism plays an important part in the inheritance of Rett syndrome: a study of MECP2 germline mosaicism in males
Severe changes in colon epithelium in the Mecp2-null mouse model of Rett syndrome
Protective role of mirtazapine in adult female Mecp2 +/− mice and patients with Rett syndrome
Two sisters with Rett syndrome and non-identical paternally-derived microdeletions in the MECP2 gene
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MeCP2 mutations: progress towards understanding and treating Rett syndrome
Characterization of Rett Syndrome-like phenotypes in Mecp2-knockout rats
Spectrum of MECP2 mutations in Vietnamese patients with RETT syndrome
Rett syndrome due to mutation in the MECP2 gene and electroencephalographic findings
MECP2 mutations affect ciliogenesis: a novel perspective for Rett syndrome and related disorders
MECP2 germline mosaicism plays an important part in the inheritance of Rett syndrome: a study of MECP2 germline mosaicism in males
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