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Splicing Analysis of Exonic OCRL Mutations Causing Lowe Syndrome or Dent-2 Disease.
Genes (Basel). 2018 Jan 4;9(1):15. doi: 10.3390/genes9010015.
Genes (Basel). 2018.
PMID: 29300302
Free PMC article.
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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Using PrISMa to reveal the interactome of the human claudins family.
Perez-Hernandez D, Suarez-Artiles L, Jones MSO, Dittmar G.
Perez-Hernandez D, et al. Among authors: suarez artiles l.
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.
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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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