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Citations to this article

Cilia, mitochondria, and cardiac development
Bill Chaudhry, Deborah J. Henderson
Bill Chaudhry, Deborah J. Henderson
Published June 17, 2019
Citation Information: J Clin Invest. 2019;129(7):2666-2668. https://doi.org/10.1172/JCI129827.
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Commentary Article has an altmetric score of 4

Cilia, mitochondria, and cardiac development

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Abstract

Motile cilia provide propulsion, and immotile ones are enriched with receptors. Both are required to establish left-right identity in the developing embryo and are also implicated in a wide range of human diseases. Abnormalities in cilial function underlie heterotaxy congenital heart disease (CHD) occurring in individuals with laterality disturbance. Mitochondrial function and cellular energetics, through mTOR and autophagy, are now linked with cilial function, revealing new mechanisms and candidate genes for syndromic human disease. In the current issue of the JCI, Burkhalter et al. ask the question: Can mitochondrial disturbances produce ciliopathy and does this explain some cases of heterotaxy?

Authors

Bill Chaudhry, Deborah J. Henderson

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Total citations by year

Year: 2023 2022 2021 2020 2019 Total
Citations: 1 2 2 1 1 7
Citation information
This citation data is accumulated from CrossRef, which receives citation information from participating publishers, including this journal. Not all publishers participate in CrossRef, so this information is not comprehensive. Additionally, data may not reflect the most current citations to this article, and the data may differ from citation information available from other sources (for example, Google Scholar, Web of Science, and Scopus).

Citations to this article in year 2020 (1)

Title and authors Publication Year
Susceptibility to Heart Defects in Down Syndrome Is Associated with Single Nucleotide Polymorphisms in HAS 21 Interferon Receptor Cluster and VEGFA Genes
CR Balistreri, CL Ammoscato, L Scola, T Fragapane, RM Giarratana, D Lio, M Piccione
Genes & development 2020

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