pGEX6P1-mCherry-Nanobody (LaM-2) Citations (1)

Originally described in: Molecular basis of ciliary defects caused by compound heterozygous IFT144/WDR19 mutations found in cranioectodermal dysplasia.
Ishida Y, Kobayashi T, Chiba S, Katoh Y, Nakayama K Hum Mol Genet. 2021 Apr 26;30(3-4):213-225. doi: 10.1093/hmg/ddab034. PubMed Journal

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Articles Citing pGEX6P1-mCherry-Nanobody (LaM-2)

Articles
Solo regulates the localization and activity of PDZ-RhoGEF for actin cytoskeletal remodeling in response to substrate stiffness. Kunitomi A, Chiba S, Higashitani N, Higashitani A, Sato S, Mizuno K, Ohashi K. Mol Biol Cell. 2024 Jun 1;35(6):ar87. doi: 10.1091/mbc.E23-11-0421. Epub 2024 Apr 24. PubMed

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