Publisher Correction: Female mice lacking Ftx lncRNA exhibit impaired X-chromosome inactivation and a microphthalmia-like phenotype
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2041-1723
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Publisher Correction: Female mice lacking Ftx lncRNA exhibit impaired X-chromosome inactivation and a microphthalmia-like phenotype ; volume:9 ; number:1 ; day:31 ; month:10 ; year:2018 ; pages:1 ; date:12.2018
Nature Communications ; 9, Heft 1 (31.10.2018), 1, 12.2018
- Creator
-
Hosoi, Yusuke
Soma, Miki
Shiura, Hirosuke
Sado, Takashi
Hasuwa, Hidetoshi
Abe, Kuniya
Kohda, Takashi
Ishino, Fumitoshi
Kobayashi, Shin
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1038/s41467-018-07100-5
- URN
-
urn:nbn:de:101:1-2018121822260501176807
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:52 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Hosoi, Yusuke
- Soma, Miki
- Shiura, Hirosuke
- Sado, Takashi
- Hasuwa, Hidetoshi
- Abe, Kuniya
- Kohda, Takashi
- Ishino, Fumitoshi
- Kobayashi, Shin
- SpringerLink (Online service)
Other Objects (12)
Female mice lacking Ftx lncRNA exhibit impaired X-chromosome inactivation and a microphthalmia-like phenotype
Drosophila mutants lacking the glial neurotransmitter-modifying enzyme Ebony exhibit low neurotransmitter levels and altered behavior
Publisher Correction: Vesicles driven by dynein and kinesin exhibit directional reversals without regulators
Arabidopsis thaliana mutants lacking cpFtsY or cpSRP54 exhibit different defects in photosystem II repair
Mice lacking Casp1, Ifngr and Nos2 genes exhibit altered depressive- and anxiety-like behaviour, and gut microbiome composition
Mice lacking DIO3 exhibit sex-specific alterations in circadian patterns of corticosterone and gene expression in metabolic tissues
EC policy: Lacking solidarity
LncRNA LYPLAL1-AS1 rejuvenates human adipose-derived mesenchymal stem cell senescence via transcriptional MIRLET7B inactivation
Exhibit 183
Exhibit 198
Exhibit 136
Exhibit 195
Female mice lacking Ftx lncRNA exhibit impaired X-chromosome inactivation and a microphthalmia-like phenotype
Drosophila mutants lacking the glial neurotransmitter-modifying enzyme Ebony exhibit low neurotransmitter levels and altered behavior
Publisher Correction: Vesicles driven by dynein and kinesin exhibit directional reversals without regulators
Arabidopsis thaliana mutants lacking cpFtsY or cpSRP54 exhibit different defects in photosystem II repair
Mice lacking Casp1, Ifngr and Nos2 genes exhibit altered depressive- and anxiety-like behaviour, and gut microbiome composition
Mice lacking DIO3 exhibit sex-specific alterations in circadian patterns of corticosterone and gene expression in metabolic tissues
EC policy: Lacking solidarity
LncRNA LYPLAL1-AS1 rejuvenates human adipose-derived mesenchymal stem cell senescence via transcriptional MIRLET7B inactivation
Exhibit 183
Exhibit 198
Exhibit 136
Exhibit 195
Female mice lacking Ftx lncRNA exhibit impaired X-chromosome inactivation and a microphthalmia-like phenotype
Drosophila mutants lacking the glial neurotransmitter-modifying enzyme Ebony exhibit low neurotransmitter levels and altered behavior
Publisher Correction: Vesicles driven by dynein and kinesin exhibit directional reversals without regulators
Arabidopsis thaliana mutants lacking cpFtsY or cpSRP54 exhibit different defects in photosystem II repair
Mice lacking Casp1, Ifngr and Nos2 genes exhibit altered depressive- and anxiety-like behaviour, and gut microbiome composition
Mice lacking DIO3 exhibit sex-specific alterations in circadian patterns of corticosterone and gene expression in metabolic tissues
EC policy: Lacking solidarity
LncRNA LYPLAL1-AS1 rejuvenates human adipose-derived mesenchymal stem cell senescence via transcriptional MIRLET7B inactivation
Exhibit 183
Exhibit 198
Exhibit 136