| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0168-9525(03)00026-X |
| P698 | PubMed publication ID | 12615011 |
| P50 | author | Heymut Omran | Q28219707 |
| P2093 | author name string | Patrice Bouvagnet | |
| Loubna El Zein | |||
| P2860 | cites work | Randomization of left-right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein | Q22008584 |
| Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia. | Q22010856 | ||
| Homozygosity mapping of a gene locus for primary ciliary dyskinesia on chromosome 5p and identification of the heavy dynein chain DNAH5 as a candidate gene | Q24290475 | ||
| The human dynein intermediate chain 2 gene (DNAI2): cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesia | Q24290728 | ||
| Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome) | Q24290886 | ||
| Disruption of an inner arm dynein heavy chain gene results in asthenozoospermia and reduced ciliary beat frequency | Q24291253 | ||
| Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry | Q24292162 | ||
| Identification of dynein heavy chain 7 as an inner arm component of human cilia that is synthesized but not assembled in a case of primary ciliary dyskinesia | Q24292401 | ||
| Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia | Q24302250 | ||
| X-linked situs abnormalities result from mutations in ZIC3 | Q24323307 | ||
| Assembly and motility of eukaryotic cilia and flagella. Lessons from Chlamydomonas reinhardtii | Q24679249 | ||
| Ciliogenesis and left-right axis defects in forkhead factor HFH-4-null mice | Q28511679 | ||
| Left-right asymmetry and kinesin superfamily protein KIF3A: new insights in determination of laterality and mesoderm induction by kif3A-/- mice analysis | Q28512332 | ||
| The Tctex1/Tctex2 class of dynein light chains. Dimerization, differential expression, and interaction with the LC8 protein family | Q28512595 | ||
| Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesia | Q30658274 | ||
| Identification, tissue specific expression, and chromosomal localisation of several human dynein heavy chain genes | Q33933177 | ||
| Radial spokes of Chlamydomonas flagella: genetic analysis of assembly and function | Q36204455 | ||
| Central-pair microtubular complex of Chlamydomonas flagella: polypeptide composition as revealed by analysis of mutants | Q36205422 | ||
| The 78,000 M(r) intermediate chain of Chlamydomonas outer arm dynein isa WD-repeat protein required for arm assembly | Q36235259 | ||
| The sup-pf-2 mutations of Chlamydomonas alter the activity of the outer dynein arms by modification of the gamma-dynein heavy chain | Q36257724 | ||
| Flagellar assembly in two hundred and fifty easy-to-follow steps | Q40372179 | ||
| DYNEINS: molecular structure and cellular function | Q40611459 | ||
| Expression of primary cilia in mammalian cells | Q40956036 | ||
| Mutations at twelve independent loci result in absence of outer dynein arms in Chylamydomonas reinhardtii | Q41582068 | ||
| Model for the motor component of dynein heavy chain based on homology to the AAA family of oligomeric ATPases | Q43543200 | ||
| X-linked transposition of the great arteries and incomplete penetrance among males with a nonsense mutation in ZIC3. | Q46354422 | ||
| Light chain 1 from the Chlamydomonas outer dynein arm is a leucine-rich repeat protein associated with the motor domain of the gamma heavy chain | Q47959169 | ||
| Abnormal nodal flow precedes situs inversus in iv and inv mice | Q51049412 | ||
| Isolation and expression of the human hPF20 gene orthologous to Chlamydomonas PF20: evaluation as a candidate for axonemal defects of respiratory cilia and sperm flagella. | Q51726068 | ||
| Conserved function for embryonic nodal cilia. | Q52117875 | ||
| Determination of left–right patterning of the mouse embryo by artificial nodal flow | Q59066359 | ||
| An extended microtubule-binding structure within the dynein motor domain | Q59096941 | ||
| Casein kinase I is anchored on axonemal doublet microtubules and regulates flagellar dynein phosphorylation and activity | Q73905834 | ||
| P433 | issue | 3 | |
| P921 | main subject | dyskinesia | Q629444 |
| P304 | page(s) | 162-167 | |
| P577 | publication date | 2003-03-01 | |
| P1433 | published in | Trends in Genetics | Q2451468 |
| P1476 | title | Lateralization defects and ciliary dyskinesia: lessons from algae | |
| P478 | volume | 19 |
| Q79711499 | Carrier status for 3 most frequent CFTR mutations in Polish PCD/KS patients: lack of association with the primary ciliary dyskinesia phenotype |
| Q34307853 | Cellular deflagellation |
| Q37530115 | Cilia gene mutations cause atrioventricular septal defects by multiple mechanisms |
| Q27312495 | Ciliary beating recovery in deficient human airway epithelial cells after lentivirus ex vivo gene therapy |
| Q34609964 | Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome |
| Q24318839 | DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defects |
| Q28768634 | Disruption of the A-kinase anchoring domain in flagellar radial spoke protein 3 results in unregulated axonemal cAMP-dependent protein kinase activity and abnormal flagellar motility |
| Q45201671 | Effect of bunching of cilia and their interplay on muco-ciliary transport |
| Q28585662 | Haploinsufficiency for the murine orthologue of Chlamydomonas PF20 disrupts spermatogenesis |
| Q28770082 | IC138 is a WD-repeat dynein intermediate chain required for light chain assembly and regulation of flagellar bending |
| Q28591871 | Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patients |
| Q43235661 | Identification of predicted human outer dynein arm genes: candidates for primary ciliary dyskinesia genes |
| Q36840844 | Keeping an eye on I1: I1 dynein as a model for flagellar dynein assembly and regulation |
| Q43168035 | Linkage analysis localises a Kartagener syndrome gene to a 3.5 cM region on chromosome 15q24-25. |
| Q24297464 | Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia |
| Q24306694 | Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia |
| Q24297678 | Mutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutation |
| Q46935657 | Primary ciliary dyskinesia presentation in 60 children according to ciliary ultrastructure |
| Q36920626 | Primary ciliary dyskinesia: recent advances in pathogenesis, diagnosis and treatment |
| Q45719311 | Psychological, cognitive and maternal stress assessment in children with primary ciliary dyskinesia |
| Q60389153 | Seeing cilia: imaging modalities for ciliary motion and clinical connections |
| Q41891497 | Select acetophenones modulate flagellar motility in chlamydomonas |
| Q34591779 | Situs ambiguus in a Brown Swiss cow with polysplenia: case report |
| Q41608112 | Structure of dimeric axonemal dynein in cilia suggests an alternative mechanism of force generation |
| Q31121485 | The LF1 gene of Chlamydomonas reinhardtii encodes a novel protein required for flagellar length control |
| Q28271824 | The flagellum of trypanosomes |
| Q29547198 | When cilia go bad: cilia defects and ciliopathies |
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