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Using PrISMa to reveal the interactome of the human claudins family.
STAR Protoc. 2023 Dec 15;4(4):102549. doi: 10.1016/j.xpro.2023.102549. Epub 2023 Sep 26.
STAR Protoc. 2023.
PMID: 37756153
Free PMC article.
Pan-claudin family interactome analysis reveals shared and specific interactions.
Suarez-Artiles L, Breiderhoff T, Girardello R, Gonschior H, Rodius S, Lesur A, Reimer U, Ramberger E, Perez-Hernandez D, Müller D, Mertins P, Dittmar G.
Suarez-Artiles L, et al.
Cell Rep. 2022 Nov 8;41(6):111588. doi: 10.1016/j.celrep.2022.111588.
Cell Rep. 2022.
PMID: 36351382
Free article.
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A Universal Peptide Matrix Interactomics Approach to Disclose Motif-Dependent Protein Binding.
Ramberger E, Suarez-Artiles L, Perez-Hernandez D, Haji M, Popp O, Reimer U, Leutz A, Dittmar G, Mertins P.
Ramberger E, et al. Among authors: suarez artiles l.
Mol Cell Proteomics. 2021;20:100135. doi: 10.1016/j.mcpro.2021.100135. Epub 2021 Aug 13.
Mol Cell Proteomics. 2021.
PMID: 34391889
Free PMC article.
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Transcriptional and Translational Differences of Microglia from Male and Female Brains.
Guneykaya D, Ivanov A, Hernandez DP, Haage V, Wojtas B, Meyer N, Maricos M, Jordan P, Buonfiglioli A, Gielniewski B, Ochocka N, Cömert C, Friedrich C, Artiles LS, Kaminska B, Mertins P, Beule D, Kettenmann H, Wolf SA.
Guneykaya D, et al. Among authors: artiles ls.
Cell Rep. 2018 Sep 4;24(10):2773-2783.e6. doi: 10.1016/j.celrep.2018.08.001.
Cell Rep. 2018.
PMID: 30184509
Free article.
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Splicing Analysis of Exonic OCRL Mutations Causing Lowe Syndrome or Dent-2 Disease.
Suarez-Artiles L, Perdomo-Ramirez A, Ramos-Trujillo E, Claverie-Martin F.
Suarez-Artiles L, et al.
Genes (Basel). 2018 Jan 4;9(1):15. doi: 10.3390/genes9010015.
Genes (Basel). 2018.
PMID: 29300302
Free PMC article.
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Exonic CLDN16 mutations associated with familial hypomagnesemia with hypercalciuria and nephrocalcinosis can induce deleterious mRNA alterations.
Perdomo-Ramirez A, de Armas-Ortiz M, Ramos-Trujillo E, Suarez-Artiles L, Claverie-Martin F.
Perdomo-Ramirez A, et al. Among authors: suarez artiles l.
BMC Med Genet. 2019 Jan 8;20(1):6. doi: 10.1186/s12881-018-0713-7.
BMC Med Genet. 2019.
PMID: 30621608
Free PMC article.
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