- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2046-2530
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Reciprocal rescue of sensory cell cilia defects by Cep290 and Mkks alleles ; volume:1 ; number:1 ; day:16 ; month:11 ; year:2012 ; pages:1 ; date:11.2012
Cilia ; 1, Heft 1 (16.11.2012), 1, 11.2012
- Creator
-
May-Simera, H.
- Contributor
-
Rachel, R.
Choi, B.
Li, T.
Friedman, T.
Swaroop, A.
Kelley, M.
SpringerLink (Online service)
- DOI
-
10.1186/2046-2530-1-S1-P94
- URN
-
urn:nbn:de:1111-2016072640950
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:55 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
- May-Simera, H.
- Rachel, R.
- Choi, B.
- Li, T.
- Friedman, T.
- Swaroop, A.
- Kelley, M.
- SpringerLink (Online service)
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In vitro Dissection of Intraflagellar Transport in <i>C. elegans</i> Sensory Cilia
Our thanks to Cilia’s reviewers
IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans
IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans
Acknowledgement of Cilia’s reviewers in 2013
Cilia develop long-lasting contacts, with other cilia
Primary cilia utilize glycoprotein-dependent adhesion mechanisms to stabilize long-lasting cilia-cilia contacts
Environmental responsiveness of tubulin glutamylation in sensory cilia is regulated by the p38 MAPK pathway
Cilia defects upon loss of WDR4 are linked to proteasomal hyperactivity and ubiquitin shortage
Maternal effects shape the alternative splicing of parental alleles in reciprocal cross hybrids of Megalobrama amblycephala × Culter alburnus
Cilia
Photoreceptor sensory cilia and ciliopathies: focus on CEP290, RPGR and their interacting proteins
In vitro Dissection of Intraflagellar Transport in <i>C. elegans</i> Sensory Cilia
Our thanks to Cilia’s reviewers
IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans
IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans
Acknowledgement of Cilia’s reviewers in 2013
Cilia develop long-lasting contacts, with other cilia
Primary cilia utilize glycoprotein-dependent adhesion mechanisms to stabilize long-lasting cilia-cilia contacts
Environmental responsiveness of tubulin glutamylation in sensory cilia is regulated by the p38 MAPK pathway
Cilia defects upon loss of WDR4 are linked to proteasomal hyperactivity and ubiquitin shortage