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All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year Sort by creator [A → Z]' creator [Z → A]' publishing year ↑ (asc)' publishing year ↓ (desc)' title [A → Z]' title [Z → A]' Simple Search Hits 1 – 6 of 6 1 An Etiological Foxp2 Mutation Impairs Neuronal Gain in Layer VI Cortico-Thalamic Cells through Increased GABA(B)/GIRK Signaling Druart, Mélanie; Groszer, Matthias; Le Magueresse, Corentin In: J Neurosci (2020) BASE Show details 2 Humanized Foxp2 accelerates learning by enhancing transitions from declarative to procedural performance Schreiweis, Christiane; Bornschein, Ulrich; Burguière, Eric. - : National Academy of Sciences, 2014 BASE Show details 3 Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain. Vernes, Sonja,; Oliver, Peter,; Spiteri, Elizabeth... In: ISSN: 1553-7390 ; EISSN: 1553-7404 ; PLoS Genetics ; https://www.hal.inserm.fr/inserm-00715268 ; PLoS Genetics, Public Library of Science, 2011, 7 (7), pp.e1002145. ⟨10.1371/journal.pgen.1002145⟩ (2011) BASE Show details 4 An Aetiological Mutation Causes Aberrant Striatal Activity and Alters Plasticity during Skill Learning Costa, Rui M; French, Catherine Ann; Jin, Xin... In: ISSN: 1359-4184 ; EISSN: 1476-5578 ; Molecular Psychiatry ; https://hal.archives-ouvertes.fr/hal-00675395 ; Molecular Psychiatry, Nature Publishing Group, 2011, ⟨10.1038/mp.2011.105⟩ (2011) BASE Show details 5 Impaired Synaptic Plasticity and Motor Learning in Mice with a Point Mutation Implicated in Human Speech Deficits Groszer, Matthias; Keays, David A.; Deacon, Robert M.J.. - 2008 BASE Show details 6 High-Throughput Analysis of Promoter Occupancy Reveals Direct Neural Targets of FOXP2, a Gene Mutated in Speech and Language Disorders Vernes, Sonja C.; Spiteri, Elizabeth; Nicod, Jérôme. - : American Society of Human Genetics, 2007 BASE Show details

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