Mutations in the dynein assembly factor PF22 (DNAAF3) cause primary ciliary dyskinesia with absent dynein arms
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2046-2530
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Mutations in the dynein assembly factor PF22 (DNAAF3) cause primary ciliary dyskinesia with absent dynein arms ; 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
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Schmidts, M.
- Contributor
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Freshour, J.
Loges, NT
Dritsoula, A.
Antony, D.
Hirst, RA
O’Callaghan, C.
Blau, H.
Olbrich, H.
Yagi, T.
Mussaffi, H.
Chung, EMK
Omran, H.
Mitchell, DR
Mitchison, H.
SpringerLink (Online service)
- DOI
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10.1186/2046-2530-1-S1-P101
- URN
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urn:nbn:de:1111-2016072640520
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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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
- Schmidts, M.
- Freshour, J.
- Loges, NT
- Dritsoula, A.
- Antony, D.
- Hirst, RA
- O’Callaghan, C.
- Blau, H.
- Olbrich, H.
- Yagi, T.
- Mussaffi, H.
- Chung, EMK
- Omran, H.
- Mitchell, DR
- Mitchison, H.
- SpringerLink (Online service)
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Ciliary dyneins and dynein related ciliopathies
Molecular characterization of dynein arm defects in primary ciliary dyskinesia individuals with mutations in C11ORF70/CFAP300, PIH1D3 and DNAH9, [...]. [Band]
Novel genetic defects in primary ciliary dyskinesia affecting function of dynein arms and central pair apparatus
Immunofluorescence microscopy (IFM) analysis of primary ciliary dyskinesia (PCD) patients with suspected inner dynein arm defects (IDA)
Torque generating properties of Tetrahymena ciliary three-headed outer-arm dynein
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Conserved roles for the dynein intermediate chain and Ndel1 in assembly and activation of dynein
Schwann cell myelination requires Dynein function
Characterization of the Dynein-Dynactin Interaction
Primary ciliary dyskinesia with normal ciliary ultrastructure due to mutations in CCDC37/CFAP100
Mutations in PIH1D3 cause X-linked primary ciliary dyskinesia with outer and inner dynein arm defects
Ciliary dyneins and dynein related ciliopathies
Molecular characterization of dynein arm defects in primary ciliary dyskinesia individuals with mutations in C11ORF70/CFAP300, PIH1D3 and DNAH9, [...]. [Band]
Novel genetic defects in primary ciliary dyskinesia affecting function of dynein arms and central pair apparatus
Immunofluorescence microscopy (IFM) analysis of primary ciliary dyskinesia (PCD) patients with suspected inner dynein arm defects (IDA)
Torque generating properties of Tetrahymena ciliary three-headed outer-arm dynein
Primary Ciliary Dyskinesia
ZMYND10, ARMC4 and CCDC151 deficiencies in the ciliary axobeme cause primary cili primary ciliary dyskinesia by disruption of the outer dynein arm assembly through two different pathways
Conserved roles for the dynein intermediate chain and Ndel1 in assembly and activation of dynein
Schwann cell myelination requires Dynein function
Characterization of the Dynein-Dynactin Interaction