Human speech- and reading-related genes display partially overlapping expression patterns in the marmoset brain

Brain and Language

Volumn 133, Issue , 2014, Pages 26-38

  Kato, Masaki ^a,d   Okanoya, Kazuo ^a   Koike, Taku ^a   Sasaki, Erika ^b,c,d   Okano, Hideyuki ^c,d   Watanabe, Shigeru ^d   Iriki, Atsushi ^a,d  

^a RIKEN BRAIN SCIENCE INSTITUTE   (Japan)

^b CENTRAL INSTITUTE FOR EXPERIMENTAL ANIMALS   (Japan)

^c KEIO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^d KEIO UNIVERSITY   (Japan)

Author keywords

Common marmoset; Dyslexia; Gene expression; Language; Specific language impairment; Vocal communication

Indexed keywords

TRANSCRIPTION FACTOR FOXP2; CNTNAP2 PROTEIN, HUMAN; DCDC2 PROTEIN, HUMAN; FORKHEAD TRANSCRIPTION FACTOR; FOXP1 PROTEIN, HUMAN; FOXP2 PROTEIN, HUMAN; IMMUNOGLOBULIN RECEPTOR; KIAA0319 PROTEIN, HUMAN; MEMBRANE PROTEIN; MICROTUBULE ASSOCIATED PROTEIN; NERVE PROTEIN; REPRESSOR PROTEIN; ROUNDABOUT RECEPTOR;

ANIMAL TISSUE; ARTICLE; BASAL GANGLION; BRAIN FUNCTION; BRAIN REGION; CALLITHRIX; CMIP GENE; CNTNAP2 GENE; COCHLEAR NUCLEUS; CONTROLLED STUDY; DCDC2 GENE; DYSLEXIA; FEMALE; FOXP1 GENE; FOXP2 GENE; FUNCTIONAL ASSESSMENT; GENE; GENE EXPRESSION; GENE FUNCTION; GENE IDENTIFICATION; GENE LOCATION; GENETIC ASSOCIATION; KIAA0319 GENE; LANGUAGE ABILITY; MALE; MOLECULAR DYNAMICS; NONHUMAN; PRIMARY MOTOR CORTEX; READING RELATED GENE; ROBO1 GENE; SECONDARY VISUAL CORTEX; SIGNAL TRANSDUCTION; SPEECH DISORDER; SPEECH RELATED GENE; THALAMUS; VERBAL COMMUNICATION; AGE; ANIMAL; BRAIN; BRAIN LEVEL; DISEASE MODEL; GENE EXPRESSION PROFILING; GENETICS; HUMAN; IN SITU HYBRIDIZATION; LANGUAGE; LANGUAGE DISABILITY; PATHOPHYSIOLOGY; PHYSIOLOGY; READING; SPEECH;

AGE FACTORS; ANIMALS; BRAIN; BRAIN CHEMISTRY; CALLITHRIX; DISEASE MODELS, ANIMAL; DYSLEXIA; FEMALE; FORKHEAD TRANSCRIPTION FACTORS; GENE EXPRESSION PROFILING; HUMANS; IN SITU HYBRIDIZATION; LANGUAGE; LANGUAGE DISORDERS; MALE; MEMBRANE PROTEINS; MICROTUBULE-ASSOCIATED PROTEINS; NERVE TISSUE PROTEINS; READING; RECEPTORS, IMMUNOLOGIC; REPRESSOR PROTEINS; SPEECH; SPEECH DISORDERS;

EID: 84900428578     PISSN: 0093934X     EISSN: 10902155     Source Type: Journal    
DOI: 10.1016/j.bandl.2014.03.007     Document Type: Article

References (125)

1. Bai J., Ramos R.L., Ackman J.B., Thomas A.M., Lee R.V., LoTurco J.J. RNAi reveals doublecortin is required for radial migration in rat neocortex. Nature Neuroscience 2003, 6(12):1277-1283.
2. Bates T.C., Luciano M., Medland S.E., Montgomery G.W., Wright M.J., Martin N.G. Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits. Behavior Genetics 2011, 41(1):50-57.
3. Belton E., Salmond C.H., Watkins K.E., Vargha-Khadem F., Gadian D.G. Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia. Human Brain Mapping 2003, 18(3):194-200.
4. Bezerra B.M., Souto A. Structure and usage of the vocal repertoire of Callithrix jacchus. International Journal of Primatology 2008, 29(3):671-701.
5. Bishop D.V., Hardiman M.J., Barry J.G. Lower-frequency event-related desynchronization: A signature of late mismatch responses to sounds, which is reduced or absent in children with specific language impairment. Journal of Neuroscience 2010, 30(46):15578-15584.
6. Bishop D.V., Snowling M.J. Developmental dyslexia and specific language impairment: Same or different?. Psychological Bulletin 2004, 130(6):858-886.
7. Bolhuis J.J., Okanoya K., Scharff C. Twitter evolution: Converging mechanisms in birdsong and human speech. Nature Reviews Neuroscience 2010, 11(11):747-759.
8. Brainard M.S., Doupe A.J. What songbirds teach us about learning. Nature 2002, 417(6886):351-358.
9. Brown S., Ngan E., Liotti M. A larynx area in the human motor cortex. Cerebral Cortex 2008, 18(4):837-845.
10. Bucci M.P., Nassibi N., Gerard C.L., Bui-Quoc E., Seassau M. Immaturity of the oculomotor saccade and vergence interaction in dyslexic children: Evidence from a reading and visual search study. PLoS One 2012, 7(3):e33458.
11. Campbell P., Reep R.L., Stoll M.L., Ophir A.G., Phelps S.M. Conservation and diversity of Foxp2 expression in muroid rodents: Functional implications. Journal of Comparative Neurology 2009, 512(1):84-100.
12. Carr C.W., Moreno-De-Luca D., Parker C., Zimmerman H.H., Ledbetter N., Martin C.L., et al. Chiari I malformation, delayed gross motor skills, severe speech delay, and epileptiform discharges in a child with FOXP1 haploinsufficiency. European Journal of Human Genetics 2010, 18(11):1216-1220.
13. Cope N., Harold D., Hill G., Moskvina V., Stevenson J., Holmans P., et al. Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. American Journal of Human Genetics 2005, 76(4):581-591.
14. Datson N.A., Morsink M.C., Atanasova S., Armstrong V.W., Zischler H., Schlumbohm C., et al. Development of the first marmoset-specific DNA microarray (EUMAMA): A new genetic tool for large-scale expression profiling in a non-human primate. BMC Genomics 2007, 8:190.
15. De Zeeuw C.I., Simpson J.I., Hoogenraad C.C., Galjart N., Koekkoek S.K., Ruigrok T.J. Microcircuitry and function of the inferior olive. Trends in Neurosciences 1998, 21(9):391-400.
16. Dennis M.Y., Paracchini S., Scerri T.S., Prokunina-Olsson L., Knight J.C., Wade-Martins R., et al. A common variant associated with dyslexia reduces expression of the KIAA0319 gene. PLoS Genetics 2009, 5(3):e1000436.
17. Doupe A.J., Kuhl P.K. Birdsong and human speech: Common themes and mechanisms. Annual Review of Neuroscience 1999, 22:567-631.
18. Enard W. FOXP2 and the role of cortico-basal ganglia circuits in speech and language evolution. Current Opinion in Neurobiology 2011, 21(3):415-424.
19. Falcaro M., Pickles A., Newbury D.F., Addis L., Banfield E., Fisher S.E., et al. Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment. Genes, Brain and Behavior 2008, 7(4):393-402.
20. Ferland R.J., Cherry T.J., Preware P.O., Morrisey E.E., Walsh C.A. Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain. Journal of Comparative Neurology 2003, 460(2):266-279.
21. Fisher S.E., DeFries J.C. Developmental dyslexia: Genetic dissection of a complex cognitive trait. Nature Reviews Neuroscience 2002, 3(10):767-780.
22. Fisher S.E., Francks C. Genes, cognition and dyslexia: Learning to read the genome. Trends in Cognitive Sciences 2006, 10(6):250-257.
23. Fisher S.E., Vargha-Khadem F., Watkins K.E., Monaco A.P., Pembrey M.E. Localisation of a gene implicated in a severe speech and language disorder. Nature Genetics 1998, 18(2):168-170.
24. Francks C., Paracchini S., Smith S.D., Richardson A.J., Scerri T.S., Cardon L.R., et al. A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. American Journal of Human Genetics 2004, 75(6):1046-1058.
25. Fujita H., Sugihara I. FoxP2 expression in the cerebellum and inferior olive: Development of the transverse stripe-shaped expression pattern in the mouse cerebellar cortex. Journal of Comparative Neurology 2012, 520(3):656-677.
26. Fukuoka T., Sumida K., Yamada T., Higuchi C., Nakagaki K., Nakamura K., et al. Gene expression profiles in the common marmoset brain determined using a newly developed common marmoset-specific DNA microarray. Neuroscience Research 2010, 66(1):62-85.
27. Gibson C.J., Gruen J.R. The human lexinome: Genes of language and reading. Journal of Communication Disorders 2008, 41(5):409-420.
28. Goodchild A.K., Martin P.R. The distribution of calcium-binding proteins in the lateral geniculate nucleus and visual cortex of a New World monkey, the marmoset, Callithrix jacchus. Visual Neuroscience 1998, 15(4):625-642.
29. Grainger J., Dufau S., Montant M., Ziegler J.C., Fagot J. Orthographic processing in baboons (Papio papio). Science 2012, 336(6078):245-248.
30. Haber S.N., Calzavara R. The cortico-basal ganglia integrative network: The role of the thalamus. Brain Research Bulletin 2009, 78(2-3):69-74.
31. Haesler S., Rochefort C., Georgi B., Licznerski P., Osten P., Scharff C. Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X. PLoS Biology 2007, 5(12):e321.
32. Haesler S., Wada K., Nshdejan A., Morrisey E.E., Lints T., Jarvis E.D., et al. FoxP2 expression in avian vocal learners and non-learners. Journal of Neuroscience 2004, 24(13):3164-3175.
33. Hamdan F.F., Daoud H., Rochefort D., Piton A., Gauthier J., Langlois M., et al. De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment. American Journal of Human Genetics 2010, 87(5):671-678.
34. Hannula-Jouppi K., Kaminen-Ahola N., Taipale M., Eklund R., Nopola-Hemmi J., Kaariainen H., et al. The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia. PLoS Genetics 2005, 1(4):e50.
35. Harold D., Paracchini S., Scerri T., Dennis M., Cope N., Hill G., et al. Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. Molecular Psychiatry 2006, 11(12):1085-1091.
36. Hashikawa T., Van Lieshout D., Harting J.K. Projections from the parabigeminal nucleus to the dorsal lateral geniculate nucleus in the tree shrew Tupaia glis. Journal of Comparative Neurology 1986, 246(3):382-394.
37. Hikishima K., Quallo M.M., Komaki Y., Yamada M., Kawai K., Momoshima S., et al. Population-averaged standard template brain atlas for the common marmoset (Callithrix jacchus). Neuroimage 2011, 54(4):2741-2749.
38. Hikishima K., Sawada K., Murayama A.Y., Komaki Y., Kawai K., Sato N., et al. Atlas of the developing brain of the marmoset monkey constructed using magnetic resonance histology. Neuroscience 2013, 230:102-113.
39. Horn D., Kapeller J., Rivera-Brugues N., Moog U., Lorenz-Depiereux B., Eck S., et al. Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. Human Mutation 2010, 31(11):E1851-E1860.
40. Iles J., Walsh V., Richardson A. Visual search performance in dyslexia. Dyslexia 2000, 6(3):163-177.
41. Iwatsubo T., Kuzuhara S., Kanemitsu A., Shimada H., Toyokura Y. Corticofugal projections to the motor nuclei of the brainstem and spinal cord in humans. Neurology 1990, 40(2):309-312.
42. Jainta S., Kapoula Z. Dyslexic children are confronted with unstable binocular fixation while reading. PLoS One 2011, 6(4):e18694.
43. Jarvis E.D. Learned birdsong and the neurobiology of human language. Annals of the New York Academy of Sciences 2004, 1016:749-777.
44. Jarvis E.D., Gunturkun O., Bruce L., Csillag A., Karten H., Kuenzel W., et al. Avian brains and a new understanding of vertebrate brain evolution. Nature Reviews Neuroscience 2005, 6(2):151-159.
45. Jurgens U. Projections from the cortical larynx area in the squirrel monkey. Experimental Brain Research 1976, 25(4):401-411.
46. Jurgens U. Neural pathways underlying vocal control. Neuroscience and biobehavioral reviews 2002, 26(2):235-258.
47. Jurgens U., Richter K. Glutamate-induced vocalization in the squirrel monkey. Brain Research 1986, 373(1-2):349-358.
48. Kato M., Okanoya K. Molecular characterization of the song control nucleus HVC in Bengalese finch brain. Brain Research 2010, 1360:56-76.
49. Kidd T., Bland K.S., Goodman C.S. Slit is the midline repellent for the robo receptor in Drosophila. Cell 1999, 96(6):785-794.
50. Kidd T., Brose K., Mitchell K.J., Fetter R.D., Tessier-Lavigne M., Goodman C.S., et al. Roundabout controls axon crossing of the CNS midline and defines a novel subfamily of evolutionarily conserved guidance receptors. Cell 1998, 92(2):205-215.
51. Kuypers H.G. Corticobular connexions to the pons and lower brain-stem in man: An anatomical study. Brain 1958, 81(3):364-388.
52. Kuypers H.G. Some projections from the peri-central cortex to the pons and lower brain stem in monkey and chimpanzee. Journal of Comparative Neurology 1958, 110(2):221-255.
53. Lai C.S., Fisher S.E., Hurst J.A., Vargha-Khadem F., Monaco A.P. A forkhead-domain gene is mutated in a severe speech and language disorder. Nature 2001, 413(6855):519-523.
54. Lai C.S., Gerrelli D., Monaco A.P., Fisher S.E., Copp A.J. FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder. Brain 2003, 126(Pt 11):2455-2462.
55. Lamminmaki S., Massinen S., Nopola-Hemmi J., Kere J., Hari R. Human ROBO1 regulates interaural interaction in auditory pathways. Journal of Neuroscience 2012, 32(3):966-971.
56. Liegeois F., Baldeweg T., Connelly A., Gadian D.G., Mishkin M., Vargha-Khadem F. Language fMRI abnormalities associated with FOXP2 gene mutation. Nature Neuroscience 2003, 6(11):1230-1237.
57. Lind P.A., Luciano M., Wright M.J., Montgomery G.W., Martin N.G., Bates T.C. Dyslexia and DCDC2: Normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample. European Journal of Human Genetics 2010, 18(6):668-673.
58. Marillat V., Cases O., Nguyen-Ba-Charvet K.T., Tessier-Lavigne M., Sotelo C., Chedotal A. Spatiotemporal expression patterns of slit and robo genes in the rat brain. Journal of Comparative Neurology 2002, 442(2):130-155.
59. Mashiko H., Yoshida A.C., Kikuchi S.S., Niimi K., Takahashi E., Aruga J., et al. Comparative anatomy of marmoset and mouse cortex from genomic expression. Journal of Neuroscience 2012, 32(15):5039-5053.
60. Matsunaga E., Okanoya K. Expression analysis of cadherins in the songbird brain: Relationship to vocal system development. Journal of Comparative Neurology 2008, 508(2):329-342.
61. McFarland N.R., Haber S.N. Convergent inputs from thalamic motor nuclei and frontal cortical areas to the dorsal striatum in the primate. Journal of Neuroscience 2000, 20(10):3798-3813.
62. McFarland N.R., Haber S.N. Thalamic relay nuclei of the basal ganglia form both reciprocal and nonreciprocal cortical connections, linking multiple frontal cortical areas. Journal of Neuroscience 2002, 22(18):8117-8132.
63. McGrath L.M., Smith S.D., Pennington B.F. Breakthroughs in the search for dyslexia candidate genes. Trends in Molecular Medicine 2006, 12(7):333-341.
64. Meng H., Smith S.D., Hager K., Held M., Liu J., Olson R.K., et al. DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proceedings of the National Academy of Sciences of the United States of America 2005, 102(47):17053-17058.
65. Miller C.T., Mandel K., Wang X. The communicative content of the common marmoset phee call during antiphonal calling. American Journal of Primatology 2010, 72(11):974-980.
66. Miller J.E., Spiteri E., Condro M.C., Dosumu-Johnson R.T., Geschwind D.H., White S.A. Birdsong decreases protein levels of FoxP2, a molecule required for human speech. Journal of Neurophysiology 2008, 100(4):2015-2025.
67. Monaco A.P. Multivariate linkage analysis of specific language impairment (SLI). Annals of Human Genetics 2007, 71(Pt 5):660-673.
68. Newbury D.F., Monaco A.P. Genetic advances in the study of speech and language disorders. Neuron 2010, 68(2):309-320.
69. Newbury D.F., Paracchini S., Scerri T.S., Winchester L., Addis L., Richardson A.J., et al. Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects. Behavior Genetics 2011, 41(1):90-104.
70. Newbury D.F., Winchester L., Addis L., Paracchini S., Buckingham L.L., Clark A., et al. CMIP and ATP2C2 modulate phonological short-term memory in language impairment. American Journal of Human Genetics 2009, 85(2):264-272.
71. Nguyen Ba-Charvet K.T., Brose K., Marillat V., Kidd T., Goodman C.S., Tessier-Lavigne M., et al. Slit2-Mediated chemorepulsion and collapse of developing forebrain axons. Neuron 1999, 22(3):463-473.
72. Okano H., Hikishima K., Iriki A., Sasaki E. The common marmoset as a novel animal model system for biomedical and neuroscience research applications. Seminars in Fetal and Neonatal Medicine 2012, 17(6):336-340.
73. Palumbo O., D'Agruma L., Minenna A.F., Palumbo P., Stallone R., Palladino T., et al. 3p14.1 de novo microdeletion involving the FOXP1 gene in an adult patient with autism, severe speech delay and deficit of motor coordination. Gene 2013, 516(1):107-113.
74. Panaitof S.C., Abrahams B.S., Dong H., Geschwind D.H., White S.A. Language-related Cntnap2 gene is differentially expressed in sexually dimorphic song nuclei essential for vocal learning in songbirds. Journal of Comparative Neurology 2010, 518(11):1995-2018.
75. Paracchini S., Scerri T., Monaco A.P. The genetic lexicon of dyslexia. Annual Review of Genomics and Human Genetics 2007, 8:57-79.
76. Pariani M.J., Spencer A., Graham J.M., Rimoin D.L. A 785kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosis. European Journal of Medical Genetics 2009, 52(2-3):123-127.
77. Paxinos G., Watson C., Petrides M., Rosa M., Tokuno H. The marmoset brain in stereotaxic coordinates 2012, Academic Press.
78. Peter B., Raskind W.H., Matsushita M., Lisowski M., Vu T., Berninger V.W., et al. Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample. Journal of Neurodevelopmental Disorders 2011, 3(1):39-49.
79. Pistorio A.L., Vintch B., Wang X. Acoustic analysis of vocal development in a New World primate, the common marmoset (Callithrix jacchus). Journal of the Acoustical Society of America 2006, 120(3):1655-1670.
80. Poelmans G., Engelen J.J., Van Lent-Albrechts J., Smeets H.J., Schoenmakers E., Franke B., et al. Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 2009, 150B(1):140-147.
81. Poliak S., Salomon D., Elhanany H., Sabanay H., Kiernan B., Pevny L., et al. Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1. Journal of Cell Biology 2003, 162(6):1149-1160.
82. Ramus F., Rosen S., Dakin S.C., Day B.L., Castellote J.M., White S., et al. Theories of developmental dyslexia: Insights from a multiple case study of dyslexic adults. Brain 2003, 126(Pt 4):841-865.
83. Rice M.L., Smith S.D., Gayan J. Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment. Journal of Neurodevelopmental Disorders 2009, 1(4):264-282.
84. Rilling J.K., Glasser M.F., Preuss T.M., Ma X., Zhao T., Hu X., et al. The evolution of the arcuate fasciculus revealed with comparative DTI. Nature Neuroscience 2008, 11(4):426-428.
85. Roberts A.C., Wallis J.D. Inhibitory control and affective processing in the prefrontal cortex: Neuropsychological studies in the common marmoset. Cerebral Cortex 2000, 10(3):252-262.
86. Rodenas-Cuadrado P., Ho J., Vernes S.C. Shining a light on CNTNAP2: Complex functions to complex disorders. European Journal of Human Genetics 2014, 22(2):171-178.
87. Rousso D.L., Gaber Z.B., Wellik D., Morrisey E.E., Novitch B.G. Coordinated actions of the forkhead protein Foxp1 and Hox proteins in the columnar organization of spinal motor neurons. Neuron 2008, 59(2):226-240.
88. Sasaki E., Suemizu H., Shimada A., Hanazawa K., Oiwa R., Kamioka M., et al. Generation of transgenic non-human primates with germline transmission. Nature 2009, 459(7246):523-527.
89. Sawamoto K., Hirota Y., Alfaro-Cervello C., Soriano-Navarro M., He X., Hayakawa-Yano Y., et al. Cellular composition and organization of the subventricular zone and rostral migratory stream in the adult and neonatal common marmoset brain. Journal of Comparative Neurology 2011, 519(4):690-713.
90. Schoen J.H. The corticofugal projection on the brain stem and spinal cord in man. Psychiatria, Neurologia, Neurochirurgia 1969, 72(1):121-128.
91. Schulz S.B., Haesler S., Scharff C., Rochefort C. Knockdown of FoxP2 alters spine density in Area X of the zebra finch. Genes, Brain and Behavior 2010, 9(7):732-740.
92. Schumacher J., Anthoni H., Dahdouh F., Konig I.R., Hillmer A.M., Kluck N., et al. Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. American Journal of Human Genetics 2006, 78(1):52-62.
93. Schumacher J., Dahdouh F., Hilmer A.M., Koenig I.R., Anthoni H., Zucchelli M., et al. Independent evidence for the VMP/DCDC2/KAAG1 gene locus on chromosomal region 6p22 as susceptibility factor for dyslexia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 2005, 138B(1). 114-114.
94. Seeger M., Tear G., Ferres-Marco D., Goodman C.S. Mutations affecting growth cone guidance in Drosophila: Genes necessary for guidance toward or away from the midline. Neuron 1993, 10(3):409-426.
95. Shimada H., Okada Y., Ibata K., Ebise H., Ota S., Tomioka I., et al. Efficient derivation of multipotent neural stem/progenitor cells from non-human primate embryonic stem cells. PLoS One 2012, 7(11):e49469.
96. Simoes C.S., Vianney P.V., de Moura M.M., Freire M.A., Mello L.E., Sameshima K., et al. Activation of frontal neocortical areas by vocal production in marmosets. Frontiers in Integrative Neuroscience 2010, 4.
97. Simonyan K., Jurgens U. Cortico-cortical projections of the motorcortical larynx area in the rhesus monkey. Brain Research 2002, 949(1-2):23-31.
98. SLI Consortium (SLIC) A genomewide scan identifies two novel loci involved in specific language impairment. American Journal of Human Genetics 2002, 70(2):384-398.
99. SLI Consortium (SLIC) Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment. American Journal of Human Genetics 2004, 74(6):1225-1238.
100. Sparks D.L. Translation of sensory signals into commands for control of saccadic eye movements: Role of primate superior colliculus. Physiological Reviews 1986, 66(1):118-171.
101. Takahashi K., Liu F.C., Oishi T., Mori T., Higo N., Hayashi M., et al. Expression of FOXP2 in the developing monkey forebrain: Comparison with the expression of the genes FOXP1, PBX3, and MEIS2. Journal of Comparative Neurology 2008, 509(2):180-189.
102. Tatsumoto S., Adati N., Tohtoki Y., Sakaki Y., Boroviak T., Habu S., et al. Development and characterization of cDNA resources for the common marmoset: One of the experimental primate models. DNA Research 2013, 20(3):255-262.
103. Teramitsu I., Kudo L.C., London S.E., Geschwind D.H., White S.A. Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction. Journal of Neuroscience 2004, 24(13):3152-3163.
104. Teramitsu I., Poopatanapong A., Torrisi S., White S.A. Striatal FoxP2 is actively regulated during songbird sensorimotor learning. PLoS One 2010, 5(1):e8548.
105. Teramitsu I., White S.A. FoxP2 regulation during undirected singing in adult songbirds. Journal of Neuroscience 2006, 26(28):7390-7394.
106. Thiebaut de Schotten M., Dell'Acqua F., Valabregue R., Catani M. Monkey to human comparative anatomy of the frontal lobe association tracts. Cortex 2012, 48(1):82-96.
107. Tomioka I., Maeda T., Shimada H., Kawai K., Okada Y., Igarashi H., et al. Generating induced pluripotent stem cells from common marmoset (Callithrix jacchus) fetal liver cells using defined factors, including Lin28. Genes to Cells 2010, 15(9):959-969.
108. Usunoff K.G., Schmitt O., Itzev D.E., Rolfs A., Wree A. Efferent connections of the parabigeminal nucleus to the amygdala and the superior colliculus in the rat: A double-labeling fluorescent retrograde tracing study. Brain Research 2007, 1133(1):87-91.
109. Vargha-Khadem F., Gadian D.G., Copp A., Mishkin M. FOXP2 and the neuroanatomy of speech and language. Nature Reviews Neuroscience 2005, 6(2):131-138.
110. Vargha-Khadem F., Watkins K., Alcock K., Fletcher P., Passingham R. Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder. Proceedings of the National Academy of Sciences of the United States of America 1995, 92(3):930-933.
111. Vernes S.C., MacDermot K.D., Monaco A.P., Fisher S.E. Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia. European Journal of Human Genetics 2009, 17(10):1354-1358.
112. Vernes S.C., Newbury D.F., Abrahams B.S., Winchester L., Nicod J., Groszer M., et al. A functional genetic link between distinct developmental language disorders. New England Journal of Medicine 2008, 359(22):2337-2345.
113. Vernes S.C., Spiteri E., Nicod J., Groszer M., Taylor J.M., Davies K.E., et al. High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders. American Journal of Human Genetics 2007, 81(6):1232-1250.
114. Wang X., Merzenich M.M., Beitel R., Schreiner C.E. Representation of a species-specific vocalization in the primary auditory cortex of the common marmoset: Temporal and spectral characteristics. Journal of Neurophysiology 1995, 74(6):2685-2706.
115. Watkins K.E., Dronkers N.F., Vargha-Khadem F. Behavioural analysis of an inherited speech and language disorder: Comparison with acquired aphasia. Brain 2002, 125(Pt 3):452-464.
116. Watkins K.E., Vargha-Khadem F., Ashburner J., Passingham R.E., Connelly A., Friston K.J., et al. MRI analysis of an inherited speech and language disorder: Structural brain abnormalities. Brain 2002, 125(Pt 3):465-478.
117. White S.A., Fisher S.E., Geschwind D.H., Scharff C., Holy T.E. Singing mice, songbirds, and more: Models for FOXP2 function and dysfunction in human speech and language. Journal of Neuroscience 2006, 26(41):10376-10379.
118. Wickelgren B.G. Superior colliculus: Some receptive field properties of bimodally responsive cells. Science 1971, 173(3991):69-72.
119. Wilcke A., Ligges C., Burkhardt J., Alexander M., Wolf C., Quente E., et al. Imaging genetics of FOXP2 in dyslexia. European Journal of Human Genetics 2012, 20(2):224-229.
120. Wright B.A., Lombardino L.J., King W.M., Puranik C.S., Leonard C.M., Merzenich M.M. Deficits in auditory temporal and spectral resolution in language-impaired children. Nature 1997, 387(6629):176-178.
121. Yamazaki Y., Echigo C., Saiki M., Inada M., Watanabe S., Iriki A. Tool-use learning by common marmosets (Callithrix jacchus). Experimental Brain Research 2011, 213(1):63-71.
122. Yamazaki Y., Iriki A., Watanabe S. Modulation of physical understanding by common marmosets (Callithrix jacchus). Animal Cognition 2011, 14(2):175-186.
123. Yamazaki Y., Watanabe S. Marmosets as a next-generation model of comparative cognition. Japanese Psychological Research 2009, 51(3):182-196.
124. Yokoyama C., Yamanaka H., Onoe K., Kawasaki A., Nagata H., Shirakami K., et al. Mapping of serotonin transporters by positron emission tomography with [11C]DASB in conscious common marmosets: Comparison with rhesus monkeys. Synapse 2010, 64(8):594-601.
125. Zweier C., de Jong E.K., Zweier M., Orrico A., Ousager L.B., Collins A.L., et al. CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila. American Journal of Human Genetics 2009, 85(5):655-666.