Centrosome and ciliary abnormalities in fetal akinesia deformation sequence human fibroblasts
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
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In: 10.1038/s41598-020-76192-1
- Event
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Veröffentlichung
- (where)
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Aachen
- (who)
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Universitätsbibliothek der RWTH Aachen
- (when)
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2020
- Creator
- DOI
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10.18154/RWTH-CONV-244296
- URN
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urn:nbn:de:101:1-2023112300373371491607
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:20 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
- Jühlen, Ramona
- Martinelli, Valérie
- Vinci, Chiara
- Breckpot, Jeroen
- Fahrenkrog, Birthe
- Universitätsbibliothek der RWTH Aachen
Time of origin
- 2020
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Centrosome and ciliary abnormalities in fetal akinesia deformation sequence human fibroblasts
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Centrosome and ciliary abnormalities in fetal akinesia deformation sequence human fibroblasts
Role of FBXW5-loss in Centrosome Abnormalities and Cell Physiology
Bronchiectasis, Bulla and Ciliary Dyskinesia (Pulmonary Structural/Functional Airway Abnormalities)
RB acute loss induces centrosome amplification and aneuploidy in murine primary fibroblasts
Isolated Fetal Cardiac Abnormalities: Are They Really Isolated?
The interaction between LC8 and LCA5 reveals a novel oligomerization function of LC8 in the ciliary-centrosome system
Application value of NIPT for uncommon fetal chromosomal abnormalities
A Capabilities Approach to Prenatal Screening for Fetal Abnormalities
Cellular abnormalities in Autosomal Dominant Polycystic Kidney Disease (ADPKD) fibroblasts
Human hyaluronic acid synthase-1 promotes malignant transformation via epithelial-to-mesenchymal transition, micronucleation and centrosome abnormalities
Mutations in PIK3C2A cause syndromic short stature, skeletal abnormalities, and cataracts associated with ciliary dysfunction
Fetal intestinal fibroblasts respond to insulin-like growth factor (IGF)-II better than adult intestinal fibroblasts
Centrosome and ciliary abnormalities in fetal akinesia deformation sequence human fibroblasts
Role of FBXW5-loss in Centrosome Abnormalities and Cell Physiology
Bronchiectasis, Bulla and Ciliary Dyskinesia (Pulmonary Structural/Functional Airway Abnormalities)
RB acute loss induces centrosome amplification and aneuploidy in murine primary fibroblasts
Isolated Fetal Cardiac Abnormalities: Are They Really Isolated?
The interaction between LC8 and LCA5 reveals a novel oligomerization function of LC8 in the ciliary-centrosome system
Application value of NIPT for uncommon fetal chromosomal abnormalities
A Capabilities Approach to Prenatal Screening for Fetal Abnormalities
Cellular abnormalities in Autosomal Dominant Polycystic Kidney Disease (ADPKD) fibroblasts
Human hyaluronic acid synthase-1 promotes malignant transformation via epithelial-to-mesenchymal transition, micronucleation and centrosome abnormalities
Mutations in PIK3C2A cause syndromic short stature, skeletal abnormalities, and cataracts associated with ciliary dysfunction