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Annals of Medicine Volume 29, 1997 - Issue 6
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Original Article

Animal Model for Fragile X Syndrome

Ben A. Oostra MGC Department of Clinical Genetics, Erasmus University, Rotterdam, The NetherlandsCorrespondence[email protected]
&
Andre T. Hoogeveen MGC Department of Clinical Genetics, Erasmus University, Rotterdam, The Netherlands
Pages 563-567 | Published online: 08 Jul 2009

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Mary Sourial, Connie Cheng & Laurie C Doering. (2013) Progress toward therapeutic potential for AFQ056 in Fragile X syndrome. Journal of Experimental Pharmacology 5, pages 45-54.
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Katriina Aalto-setälä & Eero Vuorio. (1997) Gene Therapy of Single-gene Disorders: Preface to the. Annals of Medicine 29:6, pages 549-551.
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Articles from other publishers (12)

Dipashree Chatterjee & Jean Martin Beaulieu. (2022) Inhibition of glycogen synthase kinase 3 by lithium, a mechanism in search of specificity. Frontiers in Molecular Neuroscience 15.
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W M Kenkel, J R Yee, K Moore, D Madularu, P Kulkarni, K Gamber, M Nedelman & C F Ferris. (2016) Functional magnetic resonance imaging in awake transgenic fragile X rats: evidence of dysregulation in reward processing in the mesolimbic/habenular neural circuit. Translational Psychiatry 6:3, pages e763-e763.
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Jacob Ellegood, Laura K. Pacey, David R. Hampson, Jason P. Lerch & R. Mark Henkelman. (2010) Anatomical phenotyping in a mouse model of fragile X syndrome with magnetic resonance imaging. NeuroImage 53:3, pages 1023-1029.
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Susan M. Rivera & Allan L. Reiss. 2010. Neuroimaging in Developmental Clinical Neuroscience. Neuroimaging in Developmental Clinical Neuroscience 217 228 .
Julie C. Lauterborn, Christopher S. Rex, Eniko Kramár, Lulu Y. Chen, Vijay Pandyarajan, Gary Lynch & Christine M. Gall. (2007) Brain-Derived Neurotrophic Factor Rescues Synaptic Plasticity in a Mouse Model of Fragile X Syndrome. The Journal of Neuroscience 27:40, pages 10685-10694.
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Robert Gerlai & Julia Gerlai. (2004) Autism: a target of pharmacotherapies?. Drug Discovery Today 9:8, pages 366-374.
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Julia Gerlai & Robert Gerlai. (2003) Autism: a large unmet medical need and a complex research problem. Physiology & Behavior 79:3, pages 461-470.
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Jianxue Li, Marc R. Pelletier, Jose-Luis Perez Velazquez & Peter L. Carlen. (2002) Reduced Cortical Synaptic Plasticity and GluR1 Expression Associated with Fragile X Mental Retardation Protein Deficiency. Molecular and Cellular Neuroscience 19:2, pages 138-151.
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Christian Andres. (2002) Molecular genetics and animal models in autistic disorder. Brain Research Bulletin 57:1, pages 109-119.
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Yvonne Boyd, Helen J. Blair, Pamela Cunliffe, Walter K. Masson & Vivienne Reed. (2000) A Phenotype Map of the Mouse X Chromosome: Models for Human X-linked Disease. Genome Research 10:3, pages 277-292.
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Peter Steinbach. 2000. Monogen bedingte Erbkrankheiten 1. Monogen bedingte Erbkrankheiten 1 479 511 .
Edouard W Khandjian. (1999) Biology of the fragile X mental retardation protein, an RNA-binding protein. Biochemistry and Cell Biology 77:4, pages 331-342.
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