Found: 11
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miR449 Protects Airway Regeneration by Controlling AURKA/HDAC6-Mediated Ciliary Disassembly.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 14, p. 7749, doi. 10.3390/ijms23147749
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- Article
Motility of efferent duct cilia aids passage of sperm cells through the male reproductive system.
- Published in:
- Molecular Human Reproduction, 2021, v. 27, n. 3, p. 1, doi. 10.1093/molehr/gaab009
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- Publication type:
- Article
Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia.
- Published in:
- Nature Genetics, 2014, v. 46, n. 6, p. 646, doi. 10.1038/ng.2961
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- Article
Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility.
- Published in:
- PLoS Genetics, 2018, v. 14, n. 8, p. 1, doi. 10.1371/journal.pgen.1007602
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- Article
Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and Bronchiectasis.
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- American Journal of Respiratory & Critical Care Medicine, 2024, v. 210, n. 1, p. 63, doi. 10.1164/rccm.202308-1370OC
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- Publication type:
- Article
Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility.
- Published in:
- PLoS Genetics, 2021, v. 17, n. 2, p. 1, doi. 10.1371/journal.pgen.1009306
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- Publication type:
- Article
Cyclin O ( Ccno) functions during deuterosome-mediated centriole amplification of multiciliated cells.
- Published in:
- EMBO Journal, 2015, v. 34, n. 8, p. 1078, doi. 10.15252/embj.201490805
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- Article
DNAH11 Localization in the Proximal Region of Respiratory Cilia Defines Distinct Outer Dynein Arm Complexes.
- Published in:
- American Journal of Respiratory Cell & Molecular Biology, 2016, v. 55, n. 2, p. 213, doi. 10.1165/rcmb.2015-0353OC
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- Publication type:
- Article
Ciliary function and motor protein composition of human fallopian tubes.
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- 2015
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- Publication type:
- journal article
Systematic Analysis of CCNO Variants in a Defined Population: Implications for Clinical Phenotype and Differential Diagnosis.
- Published in:
- Human Mutation, 2016, v. 37, n. 4, p. 396, doi. 10.1002/humu.22957
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- Publication type:
- Article
CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-19113-0
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- Publication type:
- Article