Cochlear Duct

"Cochlear Duct" 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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

A spiral tube that is firmly suspended in the bony shell-shaped part of the cochlea. This ENDOLYMPH-filled cochlear duct begins at the vestibule and makes 2.5 turns around a core of spongy bone (the modiolus) thus dividing the PERILYMPH-filled spiral canal into two channels, the SCALA VESTIBULI and the SCALA TYMPANI.

Descriptor ID

D003053

MeSH Number(s)

A09.246.631.246.292

Concept/Terms

Cochlear Duct

Below are MeSH descriptors whose meaning is more general than "Cochlear Duct".

Anatomy [A]
Sense Organs [A09]
Ear [A09.246]
Ear, Inner [A09.246.631]
Cochlea [A09.246.631.246]
Cochlear Duct [A09.246.631.246.292]

Below are MeSH descriptors whose meaning is related to "Cochlear Duct".

Below are MeSH descriptors whose meaning is more specific than "Cochlear Duct".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Cochlear Duct" by people in Harvard Catalyst Profiles by year, and whether "Cochlear Duct" was a major or minor topic of these publication.

Bar chart showing 11 publications over 10 distinct years, with a maximum of 2 publications in 2001

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1997	0	1	1
2001	1	1	2
2008	0	1	1
2010	0	1	1
2011	0	1	1
2014	1	0	1
2016	0	1	1
2019	0	1	1
2021	0	1	1
2023	0	1	1

Below are the most recent publications written about "Cochlear Duct" by people in Profiles.

Incomplete Partition Type II Cochlear Malformations: Delineating the Three-Dimensional Structure from Digitized Human Histopathological Specimens. Otol Neurotol. 2023 10 01; 44(9):881-889.

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Cochlear Pathomorphogenesis of Incomplete Partition Type II in Slc26a4-Null Mice. J Assoc Res Otolaryngol. 2021 12; 22(6):681-691.

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Computed Tomography-Based Measurements of the Cochlear Duct: Implications for Cochlear Implant Pitch Tuning. Ear Hear. 2021 May/Jun; 42(3):732-743.

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Morphological Immaturity of the Neonatal Organ of Corti and Associated Structures in Humans. J Assoc Res Otolaryngol. 2019 10; 20(5):461-474.

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Comprehensive Expression of Wnt Signaling Pathway Genes during Development and Maturation of the Mouse Cochlea. PLoS One. 2016; 11(2):e0148339.

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Water permeability of the mammalian cochlea: functional features of an aquaporin-facilitated water shunt at the perilymph-endolymph barrier. Pflugers Arch. 2014 Oct; 466(10):1963-85.

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All functional aquaporin-4 isoforms are expressed in the rat cochlea and contribute to the formation of orthogonal arrays of particles. Neuroscience. 2011 Aug 25; 189:79-92.

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Polygenic inheritance of sensorineural hearing loss (Snhl2, -3, and -4) and organ of Corti patterning defect in the ALR/LtJ mouse strain. Hear Res. 2011 May; 275(1-2):150-9.

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A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunction. Hum Mol Genet. 2008 Nov 01; 17(21):3426-34.

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Cellular growth and rearrangement during the development of the mammalian organ of Corti. Dev Dyn. 2004 Apr; 229(4):802-12.

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