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Aquatic models of human ciliary diseases
Author(s) -
Corkins Mark E.,
KrnetaStankic Vanja,
Kloc Malgorzata,
Miller Rachel K.
Publication year - 2021
Publication title -
genesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.093
H-Index - 110
eISSN - 1526-968X
pISSN - 1526-954X
DOI - 10.1002/dvg.23410
Subject(s) - ciliopathies , cilium , biology , zebrafish , neuroscience , model organism , xenopus , computational biology , microbiology and biotechnology , genetics , gene , phenotype
Cilia are microtubule‐based structures that either transmit information into the cell or move fluid outside of the cell. There are many human diseases that arise from malfunctioning cilia. Although mammalian models provide vital insights into the underlying pathology of these diseases, aquatic organisms such as Xenopus and zebrafish provide valuable tools to help screen and dissect out the underlying causes of these diseases. In this review we focus on recent studies that identify or describe different types of human ciliopathies and outline how aquatic organisms have aided our understanding of these diseases.

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