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Novel MLH1 duplication identified in Colombian families with Lynch syndrome.
Alonso-Espinaco V, Giráldez MD, Trujillo C, van der Klift H, Muñoz J, Balaguer F, Ocaña T, Madrigal I, Jones AM, Echeverry MM, Velez A, Tomlinson I, Milà M, Wijnen J, Carvajal-Carmona L, Castells A, Castellví-Bel S. Alonso-Espinaco V, et al. Among authors: trujillo c. Genet Med. 2011 Feb;13(2):155-60. doi: 10.1097/GIM.0b013e318202e10b. Genet Med. 2011. PMID: 21233718 Free article.
Biallelic variants in NSUN6 cause an autosomal recessive neurodevelopmental disorder.
Mattioli F, Worpenberg L, Li CT, Ibrahim N, Naz S, Sharif S, Firouzabadi SG, Vosoogh S, Saraeva-Lamri R, Raymond L, Trujillo C, Guex N, Antonarakis SE, Ansar M, Darvish H, Liu RJ, Roignant JY, Reymond A. Mattioli F, et al. Among authors: trujillo c. Genet Med. 2023 Sep;25(9):100900. doi: 10.1016/j.gim.2023.100900. Epub 2023 May 21. Genet Med. 2023. PMID: 37226891 Free article.
Oxenoid Reactivity Enabled by Targeted Photoactivation of Periodate.
Bossonnet A, Garner RA, O'Brien J, Trujillo C, Trowbridge AD. Bossonnet A, et al. Among authors: trujillo c. Angew Chem Int Ed Engl. 2024 Oct 18:e202417402. doi: 10.1002/anie.202417402. Online ahead of print. Angew Chem Int Ed Engl. 2024. PMID: 39423248
Human microglial cells as a therapeutic target in a neurodevelopmental disease model.
Mesci P, LaRock CN, Jeziorski JJ, Nakashima H, Chermont N, Ferrasa A, Herai RH, Ozaki T, Saleh A, Snethlage CE, Sanchez S, Goldberg G, Trujillo CA, Nakashima K, Nizet V, Muotri AR. Mesci P, et al. Among authors: trujillo ca. Stem Cell Reports. 2024 Aug 13;19(8):1074-1091. doi: 10.1016/j.stemcr.2024.06.013. Epub 2024 Jul 25. Stem Cell Reports. 2024. PMID: 39059378 Free PMC article.
374 results