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Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain.
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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)
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Auditory cortical N100 in pre- and post-synaptic auditory neuropathy to frequency or intensity changes of continuous tones.
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In: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology, vol 122, iss 3 (2011)
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Founder effect and estimation of the age of the Progranulin Thr272fs mutation in 14 Italian pedigrees with frontotemporal lobar degeneration
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Triagem auditiva neonatal: das alterações auditivas à análise molecular Newborn hearing screening: from audiological alterations to molecular analyses
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In: Revista CEFAC, Vol 13, Iss 5, Pp 909-916 (2011) (2011)
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Semantic Mutation Testing
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In: http://www.cs.york.ac.uk/%7Ejac/PublishedPapers/semantic_journal4.pdf (2010)
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Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders.
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In: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, vol 153B, iss 4 (2010)
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Kırgız Türkçesindeki Rusça Alıntı Sözcükler ve Bu Sözcüklerdeki Ünsüz Olayları
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In: Zeitschrift für die Welt der Türken / Journal of World of Turks; Vol 2, No 2 (2010): [ZfWT] Vol. 2, No. 2 (2010); 227-241 (2010)
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Syndromes of nonfluent primary progressive aphasia A clinical and neurolinguistic analysis
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In: NEUROLOGY , 75 (7) 603 - 610. (2010) (2010)
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Phonology Shaped by Phonetics: The Case of Intervocalic Lenition
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Nucleotide modifications in three functionally important regions of the Saccharomyces cerevisiae ribosome affect translation accuracy.
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In: ISSN: 0305-1048 ; EISSN: 1362-4962 ; Nucleic Acids Research ; https://hal.archives-ouvertes.fr/hal-00527402 ; Nucleic Acids Research, Oxford University Press, 2009, 37 (22), pp.7665-77. ⟨10.1093/nar/gkp816⟩ (2009)
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ХАРАКТЕР ОБУСЛОВЛЕННОСТИ СТЕПЕНИ СЕМАНТИЧЕСКОГО ОТРЫВА ОМОНИМОВ В АДЪЕКТИВНЫХ СЛОВООБРАЗОВАТЕЛЬНЫХ ОМОНИМИЧЕСКИХ РЯДАХ
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Abstract:
В статье рассматриваются факторы, обусловливающие характер омонимичности словообразовательных омонимов. В основе степени омонимического отрыва языковых единиц лежат структурно-семантические особенности словообразовательного омонимического ряда, в частности, полнота словообразовательных цепей, характер мотивации, тип словообразовательного значения, семантический характер словообразовательных шагов. ; This article is devoted to the factors that stipulate the homonymy nature of the derivational homonyms. In the basis of the degree of linguistic units' homonymous diversity lie the derivational models' completeness, the motivation nature, the derivational meaning type, and the semantic nature of the derivational successions.
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Keyword:
СЛОВООБРАЗОВАТЕЛЬНЫЕ ОМОНИМЫ,СТЕПЕНЬ ОМОНИМИЧЕСКОГО ОТРЫВА,ТИП СЛОВООБРАЗОВАТЕЛЬНОГО ЗНАЧЕНИЯ ТРАНСПОЗИЦИЯ,МОДИФИКАЦИЯ,СЛОВООБРАЗОВАТЕЛЬНАЯ ПОСЛЕДОВАТЕЛЬНОСТЬ,DERIVATIONAL HOMONYMS,DEGREE OF HOMONYMOUS DIVERSITY,DERIVATIONAL MEANING TYPE,TRANSPOSITION,MODIFICATION,MUTATION,DERIVATIONAL SUCCESSIONS
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URL: http://cyberleninka.ru/article/n/harakter-obuslovlennosti-stepeni-semanticheskogo-otryva-omonimov-v-adektivnyh-slovoobrazovatelnyh-omonimicheskih-ryadah http://cyberleninka.ru/article_covers/14126562.png
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Mutation of OPA1 gene causes deafness by affecting function of auditory nerve terminals.
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In: Brain research, vol 1300 (2009)
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FOXP2 as a molecular window into speech and language.
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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)
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Unravelling neurogenetic networks implicated in developmental language disorders.
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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)
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Investigação genética da surdez hereditária: mutação do gene da Conexina 26 Genetic investigation of hereditary deafness: connexin 26 gene mutation
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In: Revista da Sociedade Brasileira de Fonoaudiologia, Vol 14, Iss 1, Pp 142-147 (2009) (2009)
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Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits.
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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)
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Mapping cortical thickness in children with 22q11.2 deletions
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In: http://cercor.oxfordjournals.org/content/17/8/1889.full.pdf (2007)
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Mapping cortical thickness in children with 22q11.2 deletions
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In: http://cercor.oxfordjournals.org/content/early/2006/10/20/cercor.bhl097.full.pdf (2007)
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Mapping cortical thickness in children with 22q11.2 deletions
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In: http://www.ucdmc.ucdavis.edu/mindinstitute/research/cabil/publications/simon22q-cort-thickness.pdf (2007)
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