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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 2
2003 1
2004 1
2005 1
2006 2
2010 1
2011 1
2012 2
2013 2
2017 1
2018 4
2019 2
2020 1
2021 1
2022 5
2024 1

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26 results

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Page 1
Recent findings on genetics of systemic autoimmune diseases.
Delgado-Vega A, Sánchez E, Löfgren S, Castillejo-López C, Alarcón-Riquelme ME. Delgado-Vega A, et al. Among authors: castillejo lopez c. Curr Opin Immunol. 2010 Dec;22(6):698-705. doi: 10.1016/j.coi.2010.09.002. Epub 2010 Oct 20. Curr Opin Immunol. 2010. PMID: 20933377 Free PMC article. Review.
Organ-specific metabolic pathways distinguish prediabetes, type 2 diabetes, and normal tissues.
Diamanti K, Cavalli M, Pereira MJ, Pan G, Castillejo-López C, Kumar C, Mundt F, Komorowski J, Deshmukh AS, Mann M, Korsgren O, Eriksson JW, Wadelius C. Diamanti K, et al. Among authors: castillejo lopez c. Cell Rep Med. 2022 Oct 18;3(10):100763. doi: 10.1016/j.xcrm.2022.100763. Epub 2022 Oct 4. Cell Rep Med. 2022. PMID: 36198307 Free PMC article.
Glucose challenge metabolomics implicates medium-chain acylcarnitines in insulin resistance.
Nowak C, Hetty S, Salihovic S, Castillejo-Lopez C, Ganna A, Cook NL, Broeckling CD, Prenni JE, Shen X, Giedraitis V, Ärnlöv J, Lind L, Berne C, Sundström J, Fall T, Ingelsson E. Nowak C, et al. Among authors: castillejo lopez c. Sci Rep. 2018 Jun 6;8(1):8691. doi: 10.1038/s41598-018-26701-0. Sci Rep. 2018. PMID: 29875472 Free PMC article.
Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy.
Fatima A, Hoeber J, Schuster J, Koshimizu E, Maya-Gonzalez C, Keren B, Mignot C, Akram T, Ali Z, Miyatake S, Tanigawa J, Koike T, Kato M, Murakami Y, Abdullah U, Ali MA, Fadoul R, Laan L, Castillejo-López C, Liik M, Jin Z, Birnir B, Matsumoto N, Baig SM, Klar J, Dahl N. Fatima A, et al. Among authors: castillejo lopez c. Am J Hum Genet. 2022 Mar 3;109(3):542-546. doi: 10.1016/j.ajhg.2022.02.007. Am J Hum Genet. 2022. PMID: 35245475 Free PMC article. No abstract available.
Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy.
Fatima A, Hoeber J, Schuster J, Koshimizu E, Maya-Gonzalez C, Keren B, Mignot C, Akram T, Ali Z, Miyatake S, Tanigawa J, Koike T, Kato M, Murakami Y, Abdullah U, Ali MA, Fadoul R, Laan L, Castillejo-López C, Liik M, Jin Z, Birnir B, Matsumoto N, Baig SM, Klar J, Dahl N. Fatima A, et al. Among authors: castillejo lopez c. Am J Hum Genet. 2021 Apr 1;108(4):739-748. doi: 10.1016/j.ajhg.2021.02.015. Epub 2021 Mar 11. Am J Hum Genet. 2021. PMID: 33711248 Free PMC article.
SIDT1 plays a key role in type I IFN responses to nucleic acids in plasmacytoid dendritic cells and mediates the pathogenesis of an imiquimod-induced psoriasis model.
Morell M, Varela N, Castillejo-López C, Coppard C, Luque MJ, Wu YY, Martín-Morales N, Pérez-Cózar F, Gómez-Hernández G, Kumar R, O'Valle F, Alarcón-Riquelme ME, Marañón C. Morell M, et al. Among authors: castillejo lopez c. EBioMedicine. 2022 Feb;76:103808. doi: 10.1016/j.ebiom.2021.103808. Epub 2022 Jan 19. EBioMedicine. 2022. PMID: 35065421 Free PMC article.
26 results