SLC10A7, an orphan member of the SLC10 family involved in congenital disorders of glycosylation-Reference-Cited by-同舟云学术

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SLC10A7, an orphan member of the SLC10 family involved in congenital disorders of glycosylation

Published:2022-01-08 Issue:7 Volume:141 Page:1287-1298
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Durin Zoé,Dubail Johanne,Layotte Aurore,Legrand Dominique,Cormier-Daire Valérie,Foulquier François

Funder

Agence Nationale de la Recherche

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

https://link.springer.com/content/pdf/10.1007/s00439-021-02420-x.pdf

Reference40 articles.

1. Abe T, Kanemitu Y, Nakasone M et al (2013) SLC10A4 is a protease-activated transporter that transports bile acids. J Biochem 154:93–101. https://doi.org/10.1093/jb/mvt031

2. Alcalay M, Toniolo D (1988) CpG islands of the X chromosome are gene associated. Nucleic Acids Res 16:9527–9543. https://doi.org/10.1093/nar/16.20.9527

3. Ashikov A, Abu Bakar N, Wen X-Y et al (2018) Integrating glycomics and genomics uncovers SLC10A7 as essential factor for bone mineralization by regulating post-Golgi protein transport and glycosylation. Hum Mol Genet 27:3029–3045. https://doi.org/10.1093/hmg/ddy213

4. Bijsmans ITGW, Bouwmeester RAM, Geyer J et al (2012) Homo- and hetero-dimeric architecture of the human liver Na+-dependent taurocholate co-transporting protein. Biochem J 441:1007–1015. https://doi.org/10.1042/BJ20111234

5. Chen Y-H, Narimatsu Y, Clausen TM et al (2018) The GAGOme: a cell-based library of displayed glycosaminoglycans. Nat Methods 15:881–888. https://doi.org/10.1038/s41592-018-0086-z

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