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

Year Number of Results
1996 1
1997 2
1998 2
2001 3
2002 7
2003 13
2004 3
2005 9
2006 3
2007 3
2008 1
2012 1
2013 2
2014 4
2015 1
2016 2
2017 2
2018 2
2021 1
2022 1
2023 1
2024 1

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62 results

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Page 1
A Neuroligin-1 mutation associated with Alzheimer's disease produces memory and age-dependent impairments in hippocampal plasticity.
Arias-Aragón F, Tristán-Clavijo E, Martínez-Gallego I, Robles-Lanuza E, Coatl-Cuaya H, Martín-Cuevas C, Sánchez-Hidalgo AC, Rodríguez-Moreno A, Martinez-Mir A, Scholl FG. Arias-Aragón F, et al. Among authors: martinez mir a. iScience. 2023 May 13;26(6):106868. doi: 10.1016/j.isci.2023.106868. eCollection 2023 Jun 16. iScience. 2023. PMID: 37260747 Free PMC article.
Genetic linkage studies in alopecia areata.
Martinez-Mir A, Zlotogorski A, Ott J, Gordon D, Christiano AM. Martinez-Mir A, et al. J Investig Dermatol Symp Proc. 2003 Oct;8(2):199-203. doi: 10.1046/j.1087-0024.2003.00809.x. J Investig Dermatol Symp Proc. 2003. PMID: 14582673 Free article. Review.
A novel MYH7 founder mutation causing Laing distal myopathy in Southern Spain.
Carbonell-Corvillo P, Tristán-Clavijo E, Cabrera-Serrano M, Servián-Morilla E, García-Martín G, Villarreal-Pérez L, Rivas-Infante E, Area-Gómez E, Chamorro-Muñoz MI, Gil-Gálvez A, Miranda-Vizuete A, Martinez-Mir A, Laing N, Paradas C. Carbonell-Corvillo P, et al. Among authors: martinez mir a. Neuromuscul Disord. 2018 Oct;28(10):828-836. doi: 10.1016/j.nmd.2018.07.006. Epub 2018 Jul 26. Neuromuscul Disord. 2018. PMID: 30166250 Free article.
A truncating mutation in Alzheimer's disease inactivates neuroligin-1 synaptic function.
Tristán-Clavijo E, Camacho-Garcia RJ, Robles-Lanuza E, Ruiz A, van der Zee J, Van Broeckhoven C, Hernandez I, Martinez-Mir A, Scholl FG. Tristán-Clavijo E, et al. Among authors: martinez mir a. Neurobiol Aging. 2015 Dec;36(12):3171-3175. doi: 10.1016/j.neurobiolaging.2015.09.004. Epub 2015 Sep 10. Neurobiol Aging. 2015. PMID: 26440732
Genetic study of neurexin and neuroligin genes in Alzheimer's disease.
Martinez-Mir A, González-Pérez A, Gayán J, Antúnez C, Marín J, Boada M, Lopez-Arrieta JM, Fernández E, Ramírez-Lorca R, Sáez ME, Ruiz A, Scholl FG, Real LM. Martinez-Mir A, et al. J Alzheimers Dis. 2013;35(2):403-12. doi: 10.3233/JAD-122257. J Alzheimers Dis. 2013. PMID: 23403532
Proteolytic Processing of Neurexins by Presenilins Sustains Synaptic Vesicle Release.
Servián-Morilla E, Robles-Lanuza E, Sánchez-Hidalgo AC, Camacho-Garcia RJ, Paez-Gomez JA, Mavillard F, Saura CA, Martinez-Mir A, Scholl FG. Servián-Morilla E, et al. Among authors: martinez mir a. J Neurosci. 2018 Jan 24;38(4):901-917. doi: 10.1523/JNEUROSCI.1357-17.2017. Epub 2017 Dec 11. J Neurosci. 2018. PMID: 29229705 Free PMC article.
Selective expression of the neurexin substrate for presenilin in the adult forebrain causes deficits in associative memory and presynaptic plasticity.
Sánchez-Hidalgo AC, Arias-Aragón F, Romero-Barragán MT, Martín-Cuevas C, Delgado-García JM, Martinez-Mir A, Scholl FG. Sánchez-Hidalgo AC, et al. Among authors: martinez mir a. Exp Neurol. 2022 Jan;347:113896. doi: 10.1016/j.expneurol.2021.113896. Epub 2021 Oct 15. Exp Neurol. 2022. PMID: 34662541 Free article.
Mutation prevalence of cerebral cavernous malformation genes in Spanish patients.
Mondéjar R, Solano F, Rubio R, Delgado M, Pérez-Sempere A, González-Meneses A, Vendrell T, Izquierdo G, Martinez-Mir A, Lucas M. Mondéjar R, et al. Among authors: martinez mir a. PLoS One. 2014 Jan 23;9(1):e86286. doi: 10.1371/journal.pone.0086286. eCollection 2014. PLoS One. 2014. PMID: 24466005 Free PMC article.
62 results