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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 Page: 1 2 Hits 1 – 20 of 23 1 Children's biobehavioral reactivity to challenge predicts DNA methylation in adolescence and emerging adulthood. Goodman, Sarah J; Roubinov, Danielle S; Bush, Nicole R... In: Developmental science, vol 22, iss 2 (2019) BASE Show details 2 Protein-Protein Interaction Among the FoxP Family Members and their Regulation of Two Target Genes, VLDLR and CNTNAP2 in the Zebra Finch Song System ... Mendoza, Ezequiel; Scharff, Constance. - : Freie Universität Berlin, 2017 BASE Show details 3 DAZL and CPEB1 regulate mRNA translation synergistically during oocyte maturation. Sousa Martins, Joao P; Liu, Xueqing; Oke, Ashwini... In: Journal of cell science, vol 129, iss 6 (2016) BASE Show details 4 DAZL and CPEB1 regulate mRNA translation synergistically during oocyte maturation. Sousa Martins, Joao P; Liu, Xueqing; Oke, Ashwini... In: Journal of cell science, vol 129, iss 6 (2016) BASE Show details 5 Genome-wide association study of shared components of reading disability and language impairment. Eicher, JD; Powers, NR; Miller, LL... In: Genes, brain, and behavior, vol 12, iss 8 (2013) BASE Show details 6 Cerebral asymmetry and language development: cause, correlate, or consequence? Bishop, DV In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2013) BASE Show details 7 Deletion of chromosome 12q21 affecting KCNC2 and ATXN7L3B in a family with neurodevelopmental delay and ataxia. Rajakulendran, S; Roberts, J; Koltzenburg, M... In: J Neurol Neurosurg Psychiatry , 84 (11) 1255 - 1257. (2013) (2013) BASE Show details 8 Genetic Variants of FOXP2 and KIAA0319/TTRAP/THEM2 Locus Are Associated with Altered Brain Activation in Distinct Language-Related Regions Pinel, P.; Fauchereau, F.; Moreno, A.... In: ISSN: 0270-6474 ; EISSN: 1529-2401 ; Journal of Neuroscience ; https://hal-pasteur.archives-ouvertes.fr/pasteur-01580207 ; Journal of Neuroscience, Society for Neuroscience, 2012, 32 (3), pp.817 - 825. ⟨10.1523/JNEUROSCI.5996-10.2012⟩ (2012) BASE Show details 9 Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level. Barber, JC; Maloney, V; Hollox, EJ... In: PubMed ; http://www.ncbi.nlm.nih.gov/pubmed/ (2012) BASE Show details 10 An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning. French, CA; Jin, X; Campbell, TG... In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2012) BASE Show details 11 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 12 Genetic advances in the study of speech and language disorders. Newbury, DF; Monaco, AP In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; CrossRef (2010) BASE Show details 13 FOXP2 as a molecular window into speech and language. Fisher, SE; Scharff, C In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2009) BASE Show details 14 Unravelling neurogenetic networks implicated in developmental language disorders. Vernes, SC; Fisher, SE In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2009) BASE Show details 15 A functional genetic link between distinct developmental language disorders. Vernes, SC; Newbury, DF; Abrahams, BS... In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2008) BASE Show details 16 Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits. Groszer, M; Keays, DA; Deacon, RM... In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2008) BASE Show details 17 High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders. Vernes, SC; Spiteri, E; Nicod, J... In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2007) BASE Show details 18 Functional genetic analysis of mutations implicated in a human speech and language disorder. Vernes, SC; Nicod, J; Elahi, FM... In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2006) BASE Show details 19 Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. MacDermot, KD; Bonora, E; Sykes, N... In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2005) BASE Show details 20 On genes, speech, and language. Fisher, SE In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2005) BASE Show details Page: 1 2

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