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Items: 1 to 50 of 61

1.

Time dependent expression of the blood biomarkers EIF2D and TOX in patients with schizophrenia.

Gilabert-Juan J, López-Campos G, Sebastiá-Ortega N, Guara-Ciurana S, Ruso-Julve F, Prieto C, Crespo-Facorro B, Sanjuán J, Moltó MD.

Brain Behav Immun. 2019 Aug;80:909-915. doi: 10.1016/j.bbi.2019.05.015. Epub 2019 May 9.

PMID:
31078689
2.

The Role of Iron in Friedreich's Ataxia: Insights From Studies in Human Tissues and Cellular and Animal Models.

Llorens JV, Soriano S, Calap-Quintana P, Gonzalez-Cabo P, Moltó MD.

Front Neurosci. 2019 Feb 18;13:75. doi: 10.3389/fnins.2019.00075. eCollection 2019. Review.

3.

Phosphodiesterase Inhibitors Revert Axonal Dystrophy in Friedreich's Ataxia Mouse Model.

Mollá B, Muñoz-Lasso DC, Calap P, Fernandez-Vilata A, de la Iglesia-Vaya M, Pallardó FV, Moltó MD, Palau F, Gonzalez-Cabo P.

Neurotherapeutics. 2019 Apr;16(2):432-449. doi: 10.1007/s13311-018-00706-z.

PMID:
30761510
4.

Drosophila melanogaster Models of Friedreich's Ataxia.

Calap-Quintana P, Navarro JA, González-Fernández J, Martínez-Sebastián MJ, Moltó MD, Llorens JV.

Biomed Res Int. 2018 Apr 5;2018:5065190. doi: 10.1155/2018/5065190. eCollection 2018. Review.

5.

Drosophila melanogaster Models of Metal-Related Human Diseases and Metal Toxicity.

Calap-Quintana P, González-Fernández J, Sebastiá-Ortega N, Llorens JV, Moltó MD.

Int J Mol Sci. 2017 Jul 6;18(7). pii: E1456. doi: 10.3390/ijms18071456. Review.

6.

Early Social Isolation Stress and Perinatal NMDA Receptor Antagonist Treatment Induce Changes in the Structure and Neurochemistry of Inhibitory Neurons of the Adult Amygdala and Prefrontal Cortex.

Castillo-Gómez E, Pérez-Rando M, Bellés M, Gilabert-Juan J, Llorens JV, Carceller H, Bueno-Fernández C, García-Mompó C, Ripoll-Martínez B, Curto Y, Sebastiá-Ortega N, Moltó MD, Sanjuan J, Nacher J.

eNeuro. 2017 May 1;4(2). pii: ENEURO.0034-17.2017. doi: 10.1523/ENEURO.0034-17.2017. eCollection 2017 Mar-Apr.

7.

Identification of potential therapeutic compounds for Parkinson's disease using Drosophila and human cell models.

Sanz FJ, Solana-Manrique C, Muñoz-Soriano V, Calap-Quintana P, Moltó MD, Paricio N.

Free Radic Biol Med. 2017 Jul;108:683-691. doi: 10.1016/j.freeradbiomed.2017.04.364. Epub 2017 Apr 25.

PMID:
28455141
8.

Metal Homeostasis Regulators Suppress FRDA Phenotypes in a Drosophila Model of the Disease.

Soriano S, Calap-Quintana P, Llorens JV, Al-Ramahi I, Gutiérrez L, Martínez-Sebastián MJ, Botas J, Moltó MD.

PLoS One. 2016 Jul 19;11(7):e0159209. doi: 10.1371/journal.pone.0159209. eCollection 2016.

9.

Semaphorin and plexin gene expression is altered in the prefrontal cortex of schizophrenia patients with and without auditory hallucinations.

Gilabert-Juan J, Sáez AR, Lopez-Campos G, Sebastiá-Ortega N, González-Martínez R, Costa J, Haro JM, Callado LF, Meana JJ, Nacher J, Sanjuán J, Moltó MD.

Psychiatry Res. 2015 Oct 30;229(3):850-7. doi: 10.1016/j.psychres.2015.07.074. Epub 2015 Jul 29.

PMID:
26243375
10.

TORC1 Inhibition by Rapamycin Promotes Antioxidant Defences in a Drosophila Model of Friedreich's Ataxia.

Calap-Quintana P, Soriano S, Llorens JV, Al-Ramahi I, Botas J, Moltó MD, Martínez-Sebastián MJ.

PLoS One. 2015 Jul 9;10(7):e0132376. doi: 10.1371/journal.pone.0132376. eCollection 2015.

11.

Replication of previous genome-wide association studies of psychiatric diseases in a large schizophrenia case-control sample from Spain.

Ivorra JL, Rivero O, Costas J, Iniesta R, Arrojo M, Ramos-Ríos R, Carracedo A, Palomo T, Rodriguez-Jimenez R, Cervilla J, Gutiérrez B, Molina E, Arango C, Alvarez M, Pascual JC, Pérez V, Saiz PA, García-Portilla MP, Bobes J, González-Pinto A, Zorrilla I, Haro JM, Bernardo M, Baca-García E, González JC, Hoenicka J, Moltó MD, Sanjuán J.

Schizophr Res. 2014 Oct;159(1):107-13. doi: 10.1016/j.schres.2014.07.004. Epub 2014 Aug 12.

PMID:
25124521
12.

The genetic contribution of the NO system at the glutamatergic post-synapse to schizophrenia: further evidence and meta-analysis.

Weber H, Klamer D, Freudenberg F, Kittel-Schneider S, Rivero O, Scholz CJ, Volkert J, Kopf J, Heupel J, Herterich S, Adolfsson R, Alttoa A, Post A, Grußendorf H, Kramer A, Gessner A, Schmidt B, Hempel S, Jacob CP, Sanjuán J, Moltó MD, Lesch KP, Freitag CM, Kent L, Reif A.

Eur Neuropsychopharmacol. 2014 Jan;24(1):65-85. doi: 10.1016/j.euroneuro.2013.09.005. Epub 2013 Sep 27.

PMID:
24220657
13.

Sex-specific association of the ST8SIAII gene with schizophrenia in a Spanish population.

Gilabert-Juan J, Nacher J, Sanjuán J, Moltó MD.

Psychiatry Res. 2013 Dec 30;210(3):1293-5. doi: 10.1016/j.psychres.2013.09.001. Epub 2013 Sep 23.

PMID:
24070986
14.

Mesenchymal stromal-cell transplants induce oligodendrocyte progenitor migration and remyelination in a chronic demyelination model.

Jaramillo-Merchán J, Jones J, Ivorra JL, Pastor D, Viso-León MC, Armengól JA, Moltó MD, Geijo-Barrientos E, Martínez S.

Cell Death Dis. 2013 Aug 29;4:e779. doi: 10.1038/cddis.2013.304.

15.

A "double hit" murine model for schizophrenia shows alterations in the structure and neurochemistry of the medial prefrontal cortex and the hippocampus.

Gilabert-Juan J, Belles M, Saez AR, Carceller H, Zamarbide-Fores S, Moltó MD, Nacher J.

Neurobiol Dis. 2013 Nov;59:126-40. doi: 10.1016/j.nbd.2013.07.008. Epub 2013 Jul 26.

PMID:
23891727
16.

Deferiprone and idebenone rescue frataxin depletion phenotypes in a Drosophila model of Friedreich's ataxia.

Soriano S, Llorens JV, Blanco-Sobero L, Gutiérrez L, Calap-Quintana P, Morales MP, Moltó MD, Martínez-Sebastián MJ.

Gene. 2013 Jun 1;521(2):274-81. doi: 10.1016/j.gene.2013.02.049. Epub 2013 Mar 28.

PMID:
23542074
17.

Chronic stress alters inhibitory networks in the medial prefrontal cortex of adult mice.

Gilabert-Juan J, Castillo-Gomez E, Guirado R, Moltó MD, Nacher J.

Brain Struct Funct. 2013 Nov;218(6):1591-605. doi: 10.1007/s00429-012-0479-1. Epub 2012 Nov 21.

PMID:
23179864
18.

Post-weaning social isolation rearing influences the expression of molecules related to inhibitory neurotransmission and structural plasticity in the amygdala of adult rats.

Gilabert-Juan J, Moltó MD, Nacher J.

Brain Res. 2012 Apr 11;1448:129-36. doi: 10.1016/j.brainres.2012.01.073. Epub 2012 Feb 4.

PMID:
22356888
19.

Chronic stress induces changes in the structure of interneurons and in the expression of molecules related to neuronal structural plasticity and inhibitory neurotransmission in the amygdala of adult mice.

Gilabert-Juan J, Castillo-Gomez E, Pérez-Rando M, Moltó MD, Nacher J.

Exp Neurol. 2011 Nov;232(1):33-40. doi: 10.1016/j.expneurol.2011.07.009. Epub 2011 Jul 28.

PMID:
21819983
20.

Overexpression of human and fly frataxins in Drosophila provokes deleterious effects at biochemical, physiological and developmental levels.

Navarro JA, Llorens JV, Soriano S, Botella JA, Schneuwly S, Martínez-Sebastián MJ, Moltó MD.

PLoS One. 2011;6(7):e21017. doi: 10.1371/journal.pone.0021017. Epub 2011 Jul 11.

21.

Association between neonatal temperament, SLC6A4, DRD4 and a functional polymorphism located in TFAP2B.

Ivorra JL, D'Souza UM, Jover M, Arranz MJ, Williams BP, Henry SE, Sanjuan J, Molto MD.

Genes Brain Behav. 2011 Jul;10(5):570-8. doi: 10.1111/j.1601-183X.2011.00696.x. Epub 2011 May 31.

22.

Impact of the AHI1 gene on the vulnerability to schizophrenia: a case-control association study.

Rivero O, Reif A, Sanjuán J, Moltó MD, Kittel-Schneider S, Nájera C, Töpner T, Lesch KP.

PLoS One. 2010 Aug 18;5(8):e12254. doi: 10.1371/journal.pone.0012254.

23.

Gene-environment interaction of child temperament.

Ivorra JL, Sanjuan J, Jover M, Carot JM, Frutos Rd, Molto MD.

J Dev Behav Pediatr. 2010 Sep;31(7):545-54. doi: 10.1097/DBP.0b013e3181ee4072.

PMID:
20729761
24.

Potential involvement of serotonin receptor genes with age of onset and gender in schizophrenia: a preliminary study in a Spanish sample.

Gilabert-Juan J, Ivorra JL, Tolosa A, Gratacòs M, Costas J, Sanjuán J, Moltó MD.

Psychiatry Res. 2011 Mar 30;186(1):153-4. doi: 10.1016/j.psychres.2010.07.005. Epub 2010 Aug 1. No abstract available.

PMID:
20674037
25.

FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies.

Tolosa A, Sanjuán J, Dagnall AM, Moltó MD, Herrero N, de Frutos R.

BMC Med Genet. 2010 Jul 22;11:114. doi: 10.1186/1471-2350-11-114.

26.

Altered lipid metabolism in a Drosophila model of Friedreich's ataxia.

Navarro JA, Ohmann E, Sanchez D, Botella JA, Liebisch G, Moltó MD, Ganfornina MD, Schmitz G, Schneuwly S.

Hum Mol Genet. 2010 Jul 15;19(14):2828-40. doi: 10.1093/hmg/ddq183. Epub 2010 May 10.

PMID:
20460268
27.

Serotonin transporter gene polymorphisms and auditory hallucinations in psychosis.

Rivero O, Sanjuan J, Aguilar EJ, Gonzalez JC, Molto MD, de Frutos R, Najera C.

Rev Neurol. 2010 Mar 16;50(6):325-32. English, Spanish.

28.

Association study of 44 candidate genes with depressive and anxiety symptoms in post-partum women.

Costas J, Gratacòs M, Escaramís G, Martín-Santos R, de Diego Y, Baca-García E, Canellas F, Estivill X, Guillamat R, Guitart M, Gutiérrez-Zotes A, García-Esteve L, Mayoral F, Moltó MD, Phillips C, Roca M, Carracedo A, Vilella E, Sanjuán J.

J Psychiatr Res. 2010 Aug;44(11):717-24. doi: 10.1016/j.jpsychires.2009.12.012. Epub 2010 Jan 22.

PMID:
20092830
29.

Friedreich ataxia: an update on animal models, frataxin function and therapies.

González-Cabo P, Llorens JV, Palau F, Moltó MD.

Adv Exp Med Biol. 2009;652:247-61. doi: 10.1007/978-90-481-2813-6_17. Review.

PMID:
20225031
30.

Recent adaptive selection at MAOB and ancestral susceptibility to schizophrenia.

Carrera N, Sanjuán J, Moltó MD, Carracedo A, Costas J.

Am J Med Genet B Neuropsychiatr Genet. 2009 Apr 5;150B(3):369-74. doi: 10.1002/ajmg.b.30823.

PMID:
18553363
31.

Rapid evolving RNA gene HAR1A and schizophrenia.

Tolosa A, Sanjuán J, Leal C, Costas J, Moltó MD, de Frutos R.

Schizophr Res. 2008 Feb;99(1-3):370-2. Epub 2007 Nov 28. No abstract available.

PMID:
18054202
32.

Association between CCK-AR gene and schizophrenia with auditory hallucinations.

Toirac I, Sanjuán J, Aguilar EJ, González JC, Artigas F, Rivero O, Nájera C, Moltó MD, de Frutos R.

Psychiatr Genet. 2007 Apr;17(2):47-53.

PMID:
17413443
33.

Association of schizophrenia with DTNBP1 but not with DAO, DAOA, NRG1 and RGS4 nor their genetic interaction.

Vilella E, Costas J, Sanjuan J, Guitart M, De Diego Y, Carracedo A, Martorell L, Valero J, Labad A, De Frutos R, Nájera C, Moltó MD, Toirac I, Guillamat R, Brunet A, Vallès V, Pérez L, Leon M, de Fonseca FR, Phillips C, Torres M.

J Psychiatr Res. 2008 Mar;42(4):278-88. Epub 2007 Apr 3.

PMID:
17408693
34.

Causative role of oxidative stress in a Drosophila model of Friedreich ataxia.

Llorens JV, Navarro JA, Martínez-Sebastián MJ, Baylies MK, Schneuwly S, Botella JA, Moltó MD.

FASEB J. 2007 Feb;21(2):333-44. Epub 2006 Dec 13.

PMID:
17167074
35.

A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation.

Martínez-Garay I, Tomás M, Oltra S, Ramser J, Moltó MD, Prieto F, Meindl A, Kutsche K, Martínez F.

Eur J Hum Genet. 2007 Jan;15(1):29-34. Epub 2006 Oct 11.

36.

The microcephaly ASPM gene and schizophrenia: A preliminary study.

Rivero O, Sanjuán J, Moltó MD, Aguilar EJ, Gonzalez JC, de Frutos R, Nájera C.

Schizophr Res. 2006 Jun;84(2-3):427-9. Epub 2006 May 2. No abstract available.

PMID:
16631353
37.

Association between FOXP2 polymorphisms and schizophrenia with auditory hallucinations.

Sanjuán J, Tolosa A, González JC, Aguilar EJ, Pérez-Tur J, Nájera C, Moltó MD, de Frutos R.

Psychiatr Genet. 2006 Apr;16(2):67-72.

PMID:
16538183
38.

Serotonin transporter gene polymorphism (5-HTTLPR) and emotional response to auditory hallucinations in schizophrenia.

Sanjuan J, Rivero O, Aguilar EJ, González JC, Moltó MD, de Frutos R, Lesch KP, Nájera C.

Int J Neuropsychopharmacol. 2006 Feb;9(1):131-3. Epub 2005 May 26. No abstract available.

PMID:
15916716
39.

FOXP2 polymorphisms in patients with schizophrenia.

Sanjuan J, Tolosa A, González JC, Aguilar EJ, Moltó MD, Nájera C, de Frutos R.

Schizophr Res. 2005 Mar 1;73(2-3):253-6.

PMID:
15653268
40.

Localization of MRX82: a new nonsyndromic X-linked mental retardation locus to Xq24-q25 in a Basque family.

Martínez F, Martínez-Garay I, Oltra S, Moltó MD, Orellana C, Monfort S, Prieto F, Tejada I.

Am J Med Genet A. 2004 Dec 1;131(2):174-8.

PMID:
15526294
41.

A possible association between the CCK-AR gene and persistent auditory hallucinations in schizophrenia.

Sanjuan J, Toirac I, González JC, Leal C, Moltó MD, Nájera C, De Frutos R.

Eur Psychiatry. 2004 Sep;19(6):349-53.

PMID:
15363473
42.

Intronic L1 insertion and F268S, novel mutations in RPS6KA3 (RSK2) causing Coffin-Lowry syndrome.

Martínez-Garay I, Ballesta MJ, Oltra S, Orellana C, Palomeque A, Moltó MD, Prieto F, Martínez F.

Clin Genet. 2003 Dec;64(6):491-6.

PMID:
14986828
43.

Screening for microdeletions of the X-chromosome in non-specific mental retardation.

Martínez F, Oltra S, Berges M, Orellana C, Prieto F, Martínez-Garay I, Moltó MD.

Am J Med Genet A. 2004 Jan 1;124A(1):99-101. No abstract available.

PMID:
14679596
44.

Localization of non-specific X-linked mental retardation gene (MRX73) to Xp22.2.

Martínez F, Martínez-Garay I, Millán JM, Pérez-Aytes A, Moltó MD, Orellana C, Prieto F.

Am J Med Genet. 2001 Aug 1;102(2):200-4.

PMID:
11477616
45.

dfh is a Drosophila homolog of the Friedreich's ataxia disease gene.

Cañizares J, Blanca JM, Navarro JA, Monrós E, Palau F, Moltó MD.

Gene. 2000 Oct 3;256(1-2):35-42.

PMID:
11054533
46.

Genotype and phenotype analysis of Friedreich's ataxia compound heterozygous patients.

De Castro M, García-Planells J, Monrós E, Cañizares J, Vázquez-Manrique R, Vílchez JJ, Urtasun M, Lucas M, Navarro G, Izquierdo G, Moltó MD, Palau F.

Hum Genet. 2000 Jan;106(1):86-92.

PMID:
10982187
47.

Tirant is a new member of the gypsy family of retrotransposons in Drosophila melanogaster.

Cañizares J, Grau M, Paricio N, Moltó MD.

Genome. 2000 Feb;43(1):9-14.

PMID:
10701107
48.

Incipient GAA repeats in the primate Friedreich ataxia homologous genes.

González-Cabo P, Sánchez MI, Cañizares J, Blanca JM, Martínez-Arias R, De Castro M, Bertranpetit J, Palau F, Moltó MD, de Frutos R.

Mol Biol Evol. 1999 Jun;16(6):880-3. No abstract available.

PMID:
10368965
49.

Phenotype correlation and intergenerational dynamics of the Friedreich ataxia GAA trinucleotide repeat.

Monrós E, Moltó MD, Martínez F, Cañizares J, Blanca J, Vílchez JJ, Prieto F, de Frutos R, Palau F.

Am J Hum Genet. 1997 Jul;61(1):101-10.

50.

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.

Campuzano V, Montermini L, Moltò MD, Pianese L, Cossée M, Cavalcanti F, Monros E, Rodius F, Duclos F, Monticelli A, Zara F, Cañizares J, Koutnikova H, Bidichandani SI, Gellera C, Brice A, Trouillas P, De Michele G, Filla A, De Frutos R, Palau F, Patel PI, Di Donato S, Mandel JL, Cocozza S, Koenig M, Pandolfo M.

Science. 1996 Mar 8;271(5254):1423-7.

PMID:
8596916

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