The nexin-dynein regulatory complex subunit DRC1 is essential for motile cilia function in algae and humans.
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CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formationHEATR2 plays a conserved role in assembly of the ciliary motile apparatusZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6Mutations in ZMYND10, a gene essential for proper axonemal assembly of inner and outer dynein arms in humans and flies, cause primary ciliary dyskinesiaLoss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defectsThe awesome power of dikaryons for studying flagella and basal bodies in Chlamydomonas reinhardtiiMutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human DiseaseCCDC65 mutation causes primary ciliary dyskinesia with normal ultrastructure and hyperkinetic ciliaUnexpected genetic heterogeneity for primary ciliary dyskinesia in the Irish Traveller population.The axoneme: the propulsive engine of spermatozoa and cilia and associated ciliopathies leading to infertilityDiagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art reviewLoss-of-Function GAS8 Mutations Cause Primary Ciliary Dyskinesia and Disrupt the Nexin-Dynein Regulatory ComplexTranscription Factor RFX2 Is a Key Regulator of Mouse SpermiogenesisThe coiled-coil domain containing protein CCDC151 is required for the function of IFT-dependent motile cilia in animalsChlamydomonas ODA10 is a conserved axonemal protein that plays a unique role in outer dynein arm assemblyThe N-DRC forms a conserved biochemical complex that maintains outer doublet alignment and limits microtubule sliding in motile axonemes.Founder mutation in RSPH4A identified in patients of Hispanic descent with primary ciliary dyskinesiaPrimary ciliary dyskinesia: critical evaluation of clinical symptoms and diagnosis in patients with normal and abnormal ultrastructure.Insights into the structure and function of ciliary and flagellar doublet microtubules: tektins, Ca2+-binding proteins, and stable protofilamentsMotility and more: the flagellum of Trypanosoma brucei.Cryo-electron tomography of motile cilia and flagellaDRC3 connects the N-DRC to dynein g to regulate flagellar waveform.DNAH11 Localization in the Proximal Region of Respiratory Cilia Defines Distinct Outer Dynein Arm ComplexesThe nexin link and B-tubule glutamylation maintain the alignment of outer doublets in the ciliary axoneme.Evolution of Cilia.The role of molecular genetic analysis in the diagnosis of primary ciliary dyskinesiaPrimary Ciliary Dyskinesia: An Update on Clinical Aspects, Genetics, Diagnosis, and Future Treatment StrategiesTCTE1 is a conserved component of the dynein regulatory complex and is required for motility and metabolism in mouse spermatozoa.Recent advances in primary ciliary dyskinesia genetics.Detailed structural and biochemical characterization of the nexin-dynein regulatory complexDiagnosis and management of primary ciliary dyskinesia.Ciliary genes are down-regulated in bronchial tissue of primary ciliary dyskinesia patients.In situ localization of N and C termini of subunits of the flagellar nexin-dynein regulatory complex (N-DRC) using SNAP tag and cryo-electron tomography.Unique among ciliopathies: primary ciliary dyskinesia, a motile cilia disorder.A NIMA-Related Kinase Suppresses the Flagellar Instability Associated with the Loss of Multiple Axonemal Structures.Mutation analysis in patients with total sperm immotilityRSPH3 Mutations Cause Primary Ciliary Dyskinesia with Central-Complex Defects and a Near Absence of Radial SpokesMutations in Dnaaf1 and Lrrc48 Cause Hydrocephalus, Laterality Defects, and Sinusitis in Mice.Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein arms.Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia.
P2860
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P2860
The nexin-dynein regulatory complex subunit DRC1 is essential for motile cilia function in algae and humans.
description
2013 nî lūn-bûn
@nan
2013 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
The nexin-dynein regulatory co ...... a function in algae and humans
@nl
The nexin-dynein regulatory co ...... function in algae and humans.
@ast
The nexin-dynein regulatory co ...... function in algae and humans.
@en
The nexin-dynein regulatory co ...... function in algae and humans.
@en-gb
type
label
The nexin-dynein regulatory co ...... a function in algae and humans
@nl
The nexin-dynein regulatory co ...... function in algae and humans.
@ast
The nexin-dynein regulatory co ...... function in algae and humans.
@en
The nexin-dynein regulatory co ...... function in algae and humans.
@en-gb
prefLabel
The nexin-dynein regulatory co ...... a function in algae and humans
@nl
The nexin-dynein regulatory co ...... function in algae and humans.
@ast
The nexin-dynein regulatory co ...... function in algae and humans.
@en
The nexin-dynein regulatory co ...... function in algae and humans.
@en-gb
P2093
P2860
P50
P3181
P356
P1433
P1476
The nexin-dynein regulatory co ...... function in algae and humans.
@en
P2093
Birgitta Carlén
Douglas Tritschler
Elisabeth Horak
Gabriele Köhler
Mary E Porter
Maureen Wirschell
Niki T Loges
Petra Pennekamp
Raqual Bower
Sven Lindberg
P2860
P2888
P304
P3181
P356
10.1038/NG.2533
P407
P577
2013-01-27T00:00:00Z
P6179
1019371250