Modeling autosomal recessive cutis laxa type 1C in mice reveals distinct functions for Ltbp-4 isoforms
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
In: Disease models & mechanisms : DMM, 8.2015, S. 403-415, doi:10.1242/dmm.018960
- Keyword
-
Krebs
Onkologie
- Event
-
Veröffentlichung
- (where)
-
Frankfurt am Main
- (who)
-
Universitätsbibliothek Johann Christian Senckenberg
- (when)
-
2015
- Creator
-
Bultmann-Mellin, Insa
Conradi, Anne
Maul, Alexandra C.
Dinger, Katharina
Wempe, Frank
Wohl, Alexander P.
Imhof, Thomas
Wunderlich, F. Thomas
Bunck, Alexander C.
Nakamura, Tomoyuki
Koli, Katri
Bloch, Wilhelm
Ghanem, Alexander
Heinz, Andrea
Melchner, Harald von
Sengle, Gerhard
Sterner-Kock, Anja
- URN
-
urn:nbn:de:hebis:30:3-373550
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
25.03.2025, 1:41 PM CET
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
- Bultmann-Mellin, Insa
- Conradi, Anne
- Maul, Alexandra C.
- Dinger, Katharina
- Wempe, Frank
- Wohl, Alexander P.
- Imhof, Thomas
- Wunderlich, F. Thomas
- Bunck, Alexander C.
- Nakamura, Tomoyuki
- Koli, Katri
- Bloch, Wilhelm
- Ghanem, Alexander
- Heinz, Andrea
- Melchner, Harald von
- Sengle, Gerhard
- Sterner-Kock, Anja
- Universitätsbibliothek Johann Christian Senckenberg
Time of origin
- 2015
Other Objects (12)
Investigation of the genetical basis of autosomal recessive Cutis Laxa
The role of Pycr1 in the pathomechanism of autosomal recessive cutis laxa
Distinct roles of PI4P 5-kinase isoforms in polar tip growth of pollen tubes
SPATA5 mutations cause a distinct autosomal recessive phenotype of intellectual disability, hypotonia and hearing loss
Cutis.
Cutis morbi.
Cutis Nigredo
El cutis
El cutis
Distinct
![Targeting δN-isoforms [Delta-isoforms] of the p53 family for cancer therapy](/assets/placeholder/searchResultMediaNoDigitisedMedia.png)
Targeting δN-isoforms [Delta-isoforms] of the p53 family for cancer therapy
Characterization of SKAP/Kinastrin isoforms
Investigation of the genetical basis of autosomal recessive Cutis Laxa
The role of Pycr1 in the pathomechanism of autosomal recessive cutis laxa
Distinct roles of PI4P 5-kinase isoforms in polar tip growth of pollen tubes
SPATA5 mutations cause a distinct autosomal recessive phenotype of intellectual disability, hypotonia and hearing loss
Cutis.
Cutis morbi.
Cutis Nigredo
El cutis
El cutis
Distinct
Targeting δN-isoforms [Delta-isoforms] of the p53 family for cancer therapy
Characterization of SKAP/Kinastrin isoforms
Investigation of the genetical basis of autosomal recessive Cutis Laxa
The role of Pycr1 in the pathomechanism of autosomal recessive cutis laxa
Distinct roles of PI4P 5-kinase isoforms in polar tip growth of pollen tubes
SPATA5 mutations cause a distinct autosomal recessive phenotype of intellectual disability, hypotonia and hearing loss
Cutis.
Cutis morbi.
Cutis Nigredo
El cutis
El cutis
Distinct
Targeting δN-isoforms [Delta-isoforms] of the p53 family for cancer therapy