Ciliary Motility Disorders
"Ciliary Motility Disorders" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Conditions caused by abnormal CILIA movement in the body, usually causing KARTAGENER SYNDROME, chronic respiratory disorders, chronic SINUSITIS, and chronic OTITIS. Abnormal ciliary beating is likely due to defects in any of the 200 plus ciliary proteins, such as missing motor enzyme DYNEIN arms.
Descriptor ID |
D002925
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MeSH Number(s) |
C08.200 C09.150 C16.131.077.245.500 C16.320.184.500
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Concept/Terms |
Ciliary Motility Disorders- Ciliary Motility Disorders
- Ciliary Motility Disorder
- Disorder, Ciliary Motility
- Disorders, Ciliary Motility
- Ciliary Dyskinesia
- Ciliary Dyskinesias
- Dyskinesia, Ciliary
- Dyskinesias, Ciliary
- Immotile Cilia Syndrome
- Cilia Syndrome, Immotile
- Cilia Syndromes, Immotile
- Immotile Cilia Syndromes
- Syndrome, Immotile Cilia
- Syndromes, Immotile Cilia
|
Below are MeSH descriptors whose meaning is more general than "Ciliary Motility Disorders".
Below are MeSH descriptors whose meaning is more specific than "Ciliary Motility Disorders".
This graph shows the total number of publications written about "Ciliary Motility Disorders" by people in this website by year, and whether "Ciliary Motility Disorders" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2010 | 2 | 0 | 2 |
2011 | 1 | 0 | 1 |
2013 | 1 | 0 | 1 |
2019 | 0 | 2 | 2 |
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Below are the most recent publications written about "Ciliary Motility Disorders" by people in Profiles.
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Polydactyly. Am J Obstet Gynecol. 2019 12; 221(6):B13-B15.
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Congenital talipes equinovarus (clubfoot). Am J Obstet Gynecol. 2019 12; 221(6):B10-B12.
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Fuz mutant mice reveal shared mechanisms between ciliopathies and FGF-related syndromes. Dev Cell. 2013 Jun 24; 25(6):623-35.
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TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum. Nat Genet. 2011 Mar; 43(3):189-96.
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Unusual ciliary abnormalities in three 9/11 response workers. Ann Otol Rhinol Laryngol. 2011 Jan; 120(1):40-8.
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CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs. Nat Genet. 2011 Jan; 43(1):72-8.
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[A case of primary ciliary dyskinesia who had been treated as asthma]. Arerugi. 2010 Jul; 59(7):847-54.
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Tubulin tyrosine ligase-like 1 deficiency results in chronic rhinosinusitis and abnormal development of spermatid flagella in mice. Vet Pathol. 2010 Jul; 47(4):703-12.
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Analysis of genetic inheritance in a family quartet by whole-genome sequencing. Science. 2010 Apr 30; 328(5978):636-9.
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Situs inversus in Dpcd/Poll-/-, Nme7-/- , and Pkd1l1-/- mice. Vet Pathol. 2010 Jan; 47(1):120-31.