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Number of items: 23.

Guidi, Luiz G., Velayos-Baeza, Antonio, Martinez Garay, Isabel, Monaco, Anthony P., Paracchini, Silvia, Bishop, Dorothy V. M. and Molnár, Zoltán 2018. The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on. European Journal of Neuroscience 48 (10) , pp. 3212-3233. 10.1111/ejn.14149
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Eneritz, Rueda-Alana, Martinez Garay, Isabel, Manuel, Encinas Juan, Zoltan, Molnar and Fernando, Garcia-Moreno 2018. Dbx1-derived pyramidal neurons are generated locally in the developing murine neocortex. Frontiers in Enteric Neuroscience 12 , 792. 10.3389/fnins.2018.00792
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Guidi, Luiz, Mattley, Jane, Martinez-Garay, Isabel, Monaco, Anthony P, Linden, Jennifer F, Velayos-Baeza, Antonio and Molnár, Zoltán 2017. Knockout mice for dyslexia susceptibility gene homologs KIAA0319 and KIAA0319L have unaffected neuronal migration but display abnormal auditory processing. Cerebral Cortex 27 (12) , pp. 5831-5845. 10.1093/cercor/bhx269
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Diggle, Christine P, Martinez-Garay, Isabel, Molnar, Zoltan, Brinkworth, Martin H., White, Ed, Fowler, Ewan, Hughes, Ruth, Hayward, Bruce E., Carr, Ian M., Watson, Christopher M., Crinnion, Laura, Asipu, Aruna, Woodman, Ben, Coletta, P. Louise, Markham, Alexander F., Dear, T. Neil, Bonthron, David T., Peckham, Michelle, Morrison, Ewan E. and Sheridan, Eamonn 2017. A tubulin alpha 8 mouse knockout model indicates a likely role in spermatogenesis but not in brain development. PLoS ONE 12 (4) , e0174264. 10.1371/journal.pone.0174264
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Martinez Garay, Isabel, Guidi, Luiz G., Holloway, Zoe G., Bailey, Melissa A. G., Lyngholm, Daniel, Schneider, Tomasz, Donnison, Timothy, Butt, Simon J. B., Monaco, Anthony P., Molnár, Zoltán and Velayos-Baeza, Antonio 2017. Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice. Brain Structure and Function 222 (3) , pp. 1367-1384. 10.1007/s00429-016-1282-1
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Martinez Garay, Isabel, Gil-Sanz, Cristina, Franco, Santos J, Espinosa, Ana, Molnár, Zoltan and Mueller, Ulrich 2016. Cadherin2/4-signaling via PTP1B and catenins is critical for nucleokinesis during radial neuronal migration in the neocortex. Development 143 , pp. 2121-2134. 10.1242/dev.132456
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Martinez Garay, Isabel, García-Moreno, Fernando, Vasistha, Navneet, Marques-Smith, Andre and Molnár, Zoltán 2016. In utero electroporation methods in the study of cerebral cortical development. Prenatal and Postnatal Determinants of Development, Neuromethods, vol. 109. New York: Springer, pp. 21-39. (10.1007/978-1-4939-3014-2_2)

Gil-Sanz, Cristina, Espinosa, Ana, Fregoso, Santiago P., Bluske, Krista K., Cunningham, Christopher L., Martinez Garay, Isabel, Zeng, Hongkui, Franco, Santos J. and Müller, Ulrich 2015. Lineage tracing using cux2-Cre and cux2-creERT2 mice. Neuron 86 (4) , pp. 1091-1099. 10.1016/j.neuron.2015.04.019

Gil-Sanz, Cristina, Franco, Santos J., Martinez Garay, Isabel, Espinosa, Ana, Harkins-Perry, Sarah and Müller, Ulrich 2013. Cajal-Retzius cells instruct neuronal migration by coincidence signaling between secreted and contact-dependent guidance cues. Neuron 79 (3) , pp. 461-477. 10.1016/j.neuron.2013.06.040

Franco, S. J., Gil-Sanz, C., Martinez Garay, Isabel, Espinosa, A., Harkins-Perry, S. R., Ramos, C. and Muller, U. 2012. Fate-restricted neural progenitors in the mammalian cerebral cortex. Science 337 (6095) , pp. 746-749. 10.1126/science.1223616

Franco, Santos J., Martinez Garay, Isabel, Gil-Sanz, Cristina, Harkins-Perry, Sarah R. and Müller, Ulrich 2011. Reelin regulates cadherin function via Dab1/Rap1 to control neuronal migration and lamination in the neocortex. Neuron 69 (3) , pp. 482-497. 10.1016/j.neuron.2011.01.003

Gil-Sanz, Cristina and Martinez Garay, Isabel 2010. VISIONS: the art of science. Molecular Reproduction and Development 77 (3) , p. 195. 10.1002/mrd.21159

Llorens, Jose V., Clark, Jonathan B., Martinez Garay, Isabel, Soriano, Sirena, de Frutos, Rosa and Martínez-Sebastián, María J. 2008. Gypsy endogenous retrovirus maintains potential infectivity in several species of Drosophilids. BMC Evolutionary Biology 8 (1) , 302. 10.1186/1471-2148-8-302
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Rosello, M., Monfort, S., Orellana, O., Oltra, S., Martinez Garay, Isabel and Martinez, F. 2007. Subtelomeric deletion 9qter: definition of the syndrome and parental origin in 2 patients. Medical Clinics 128 (11) , pp. 419-421.

Orellana, C., Bernabeu, J., Monfort, S., Rosello, M., Oltra, S., Ferrer, I., Quiroga, R., Martinez Garay, Isabel and Martinez, F. 2007. Duplication of the Williams-Beuren critical region: case report and further delineation of the phenotypic spectrum. Journal of Medical Genetics 45 (3) , pp. 187-189. 10.1136/jmg.2007.054064

Martinez Garay, Isabel, Tomás, Miguel, Oltra, Silvestre, Ramser, Juliane, Moltó, Maria D, Prieto, Félix, Meindl, Alfons, Kutsche, Kerstin and Martínez, Francisco 2006. A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation. European Journal of Human Genetics 15 (1) , pp. 29-34. 10.1038/sj.ejhg.5201717

Martinez Garay, Isabel, Rustom, Amin, Gerdes, Hans-Hermann and Kutsche, Kerstin 2006. The novel centrosomal associated protein CEP55 is present in the spindle midzone and the midbody. Genomics 87 (2) , pp. 243-253. 10.1016/j.ygeno.2005.11.006

Martinez, Francisco, Martinez Garay, Isabel, Oltra, Silvestre, Molto, Maria Dolores, Orellana, Carmen, Monfort, Sandra, Prieto, Felix and Tejada, Isabel 2004. Localization of MRX82: A new nonsyndromic X-linked mental retardation locus to Xq24-q25 in a Basque family. American Journal of Medical Genetics 131A (2) , pp. 174-178. 10.1002/ajmg.a.30352

Sarafidou, Theologia, Kahl, Christina, Martinez Garay, Isabel, Mangelsdorf, Marie, Gesk, Stefan, Baker, Elizabeth, Kokkinaki, Maria, Talley, Polly, Maltby, Edna L., French, Lisa, Harder, Lana, Hinzmann, Bernd, Nobile, Carlo, Richkind, Kathy, Finnis, Merran, Deloukas, Panagiotis, Sutherland, Grant R., Kutsche, Kerstin, Moschonas, Nicholas K., Siebert, Reiner and Gécz, Jozef 2004. Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein. Genomics 84 (1) , pp. 69-81. 10.1016/j.ygeno.2003.12.017

Martinez, Felix, Oltra, S., Berges, V., Orellana, C., Prieto, F., Martinez Garay, Isabel and Molto, Maria Dolores 2004. Screening for microdeletions of the X-chromosome in non-specific mental retardation [Letter]. American Journal of Medical Genetics 124A , pp. 99-101.

Martinez Garay, Isabel, Ballesta, M. J., Oltra, S., Orellana, C., Palomeque, A., Moltó, M. D., Prieto, F. and Martínez, F. 2003. Intronic L1 insertion and F268S, novel mutations in RPS6KA3 (RSK2) causing Coffin-Lowry syndrome. Clinical Genetics 64 (6) , pp. 491-496. 10.1046/j.1399-0004.2003.00166.x

Martinez Garay, Isabel, Jablonka, Sibylle, Sutajova, Marketa, Steuernagel, Peter, Gal, Andreas and Kutsche, Kerstin 2002. A new gene family (FAM9) of low-copy repeats in Xp22.3 expressed exclusively in testis: Implications for R recombinations in this region. Genomics 80 (3) , pp. 259-267. 10.1006/geno.2002.6834

Martinez, F., Martinez Garay, Isabel, Milan, J. M., Perez-Aytes, A., Molto, M. D., Orellano, C. and Prieto, F. 2001. Localization of non specific x-linked mental retardation gene (MRX73) to Xp22.2. American Journal of Medical Genetics 102 (2) , pp. 200-204. 10.1002/ajmg.1416

This list was generated on Thu Oct 17 08:58:56 2019 BST.