ARP-T1-associated Bazex–Dupré–Christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies
Park et al. characterise the interactome, localisation and function of Actin-Related Protein-Testis1 protein (ARP-T1), encoded by the ACTRT1 gene, associated with inherited basal cell cancer. They find that ARP-T1 is localised to the primary cilia basal body in epidermal cells, interacts with the ci...
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Nature Portfolio
2021
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oai:doaj.org-article:a0f02e7c75a741a59d63e638f24468512021-12-02T16:57:13ZARP-T1-associated Bazex–Dupré–Christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies10.1038/s42003-021-02054-92399-3642https://doaj.org/article/a0f02e7c75a741a59d63e638f24468512021-05-01T00:00:00Zhttps://doi.org/10.1038/s42003-021-02054-9https://doaj.org/toc/2399-3642Park et al. characterise the interactome, localisation and function of Actin-Related Protein-Testis1 protein (ARP-T1), encoded by the ACTRT1 gene, associated with inherited basal cell cancer. They find that ARP-T1 is localised to the primary cilia basal body in epidermal cells, interacts with the cilia machinery, and is needed for proper ciliogenesis.Hyun-Sook ParkEirini PapanastasiGabriela BlanchardElena ChiticariuDaniel BachmannMarkus PlomannFanny Morice-PicardPierre VabresAsma SmahiMarcel HuberChristine PichDaniel HohlNature PortfolioarticleBiology (General)QH301-705.5ENCommunications Biology, Vol 4, Iss 1, Pp 1-13 (2021) |
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DOAJ |
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Biology (General) QH301-705.5 |
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Biology (General) QH301-705.5 Hyun-Sook Park Eirini Papanastasi Gabriela Blanchard Elena Chiticariu Daniel Bachmann Markus Plomann Fanny Morice-Picard Pierre Vabres Asma Smahi Marcel Huber Christine Pich Daniel Hohl ARP-T1-associated Bazex–Dupré–Christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies |
description |
Park et al. characterise the interactome, localisation and function of Actin-Related Protein-Testis1 protein (ARP-T1), encoded by the ACTRT1 gene, associated with inherited basal cell cancer. They find that ARP-T1 is localised to the primary cilia basal body in epidermal cells, interacts with the cilia machinery, and is needed for proper ciliogenesis. |
format |
article |
author |
Hyun-Sook Park Eirini Papanastasi Gabriela Blanchard Elena Chiticariu Daniel Bachmann Markus Plomann Fanny Morice-Picard Pierre Vabres Asma Smahi Marcel Huber Christine Pich Daniel Hohl |
author_facet |
Hyun-Sook Park Eirini Papanastasi Gabriela Blanchard Elena Chiticariu Daniel Bachmann Markus Plomann Fanny Morice-Picard Pierre Vabres Asma Smahi Marcel Huber Christine Pich Daniel Hohl |
author_sort |
Hyun-Sook Park |
title |
ARP-T1-associated Bazex–Dupré–Christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies |
title_short |
ARP-T1-associated Bazex–Dupré–Christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies |
title_full |
ARP-T1-associated Bazex–Dupré–Christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies |
title_fullStr |
ARP-T1-associated Bazex–Dupré–Christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies |
title_full_unstemmed |
ARP-T1-associated Bazex–Dupré–Christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies |
title_sort |
arp-t1-associated bazex–dupré–christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/a0f02e7c75a741a59d63e638f2446851 |
work_keys_str_mv |
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1718382583178330112 |