نتایج جستجو برای: foxp2

تعداد نتایج: 433  

2013
Christopher S. Nelson Chris K. Fuller Polly M. Fordyce Alexander L. Greninger Joseph L. DeRisi

The transcription factor forkhead box P2 (FOXP2) is believed to be important in the evolution of human speech. A mutation in its DNA-binding domain causes severe speech impairment. Humans have acquired two coding changes relative to the conserved mammalian sequence. Despite intense interest in FOXP2, it has remained an open question whether the human protein’s DNAbinding specificity and chromat...

Journal: :American journal of human genetics 2013
Qasim Ayub Bryndis Yngvadottir Yuan Chen Yali Xue Min Hu Sonja C Vernes Simon E Fisher Chris Tyler-Smith

Forkhead box P2 (FOXP2) is a highly conserved transcription factor that has been implicated in human speech and language disorders and plays important roles in the plasticity of the developing brain. The pattern of nucleotide polymorphisms in FOXP2 in modern populations suggests that it has been the target of positive (Darwinian) selection during recent human evolution. In our study, we searche...

2012
Simone Kurt Simon E. Fisher Günter Ehret

Heterozygous mutations of the human FOXP2 transcription factor gene cause the best-described examples of monogenic speech and language disorders. Acquisition of proficient spoken language involves auditory-guided vocal learning, a specialized form of sensory-motor association learning. The impact of etiological Foxp2 mutations on learning of auditory-motor associations in mammals has not been d...

2006
Sonja C. Vernes Jérôme Nicod Fanny M. Elahi Julie A. Coventry Niamh Kenny Anne-Marie Coupe Louise E. Bird Kay E. Davies Simon E. Fisher

Mutations in the FOXP2 gene cause a severe communication disorder involving speech deficits (developmental verbal dyspraxia), accompanied by wide-ranging impairments in expressive and receptive language. The protein encoded by FOXP2 belongs to a divergent subgroup of forkhead-box transcription factors, with a distinctive DNA-binding domain and motifs that mediate hetero-and homodimerisation. He...

2007
Stephanie Hunt Bryn Mawr Donna Jo Napoli David Harrison

The gene FOXP2 was discovered to be mutated in members of a family possessing a severe language disorder. Originally some researchers believed that this gene was responsible for grammar and called it the “language gene”. After further study of the family, researchers determined that the gene itself was not generally responsible for grammar but that it may be responsible for the development of s...

Journal: :Cell 2009
Wolfgang Enard Sabine Gehre Kurt Hammerschmidt Sabine M. Hölter Torsten Blass Mehmet Somel Martina K. Brückner Christiane Schreiweis Christine Winter Reinhard Sohr Lore Becker Victor Wiebe Birgit Nickel Thomas Giger Uwe Müller Matthias Groszer Thure Adler Antonio Aguilar Ines Bolle Julia Calzada-Wack Claudia Dalke Nicole Ehrhardt Jack Favor Helmut Fuchs Valérie Gailus-Durner Wolfgang Hans Gabriele Hölzlwimmer Anahita Javaheri Svetoslav Kalaydjiev Magdalena Kallnik Eva Kling Sandra Kunder Ilona Moßbrugger Beatrix Naton Ildikó Racz Birgit Rathkolb Jan Rozman Anja Schrewe Dirk H. Busch Jochen Graw Boris Ivandic Martin Klingenspor Thomas Klopstock Markus Ollert Leticia Quintanilla-Martinez Holger Schulz Eckhard Wolf Wolfgang Wurst Andreas Zimmer Simon E. Fisher Rudolf Morgenstern Thomas Arendt Martin Hrabé de Angelis Julia Fischer Johannes Schwarz Svante Pääbo

It has been proposed that two amino acid substitutions in the transcription factor FOXP2 have been positively selected during human evolution due to effects on aspects of speech and language. Here, we introduce these substitutions into the endogenous Foxp2 gene of mice. Although these mice are generally healthy, they have qualitatively different ultrasonic vocalizations, decreased exploratory b...

2013
Xiaowei Song Yajun Wang Yezhong Tang

As one of the most conserved genes in vertebrates, FoxP2 is widely involved in a number of important physiological and developmental processes. We systematically studied the evolutionary history and functional adaptations of FoxP2 in teleosts. The duplicated FoxP2 genes (FoxP2a and FoxP2b), which were identified in teleosts using synteny and paralogon analysis on genome databases of eight organ...

Journal: :Current opinion in neurobiology 2005
Constance Scharff Sebastian Haesler

FoxP2 mutations in humans are associated with a disorder that affects both the comprehension of language and its production, speech. This discovery provided the first opportunity to analyze the genetics of language with molecular and neurobiological tools. The amino acid sequence and the neural expression pattern of FoxP2 are extremely conserved, from reptile to man. This suggests an important ...

2017
Xian-Lu Song Yao Tang Xiang-Hui Lei Shan-Chao Zhao Zi-Qing Wu

miRNAs play critical role in the development and progression of prostate cancer. Here we studied the role of miR-618 in prostate cancer migration and invasion. miR-618 was downregulated in metastatic androgen-independent prostate cancer (AIPC), patients with low miR-618 had poor outcome. Overexpression of miR-618 inhibited migration and invasion and induced mesenchymal to epithelial transition ...

Journal: :Brain : a journal of neurology 2003
Cecilia S L Lai Dianne Gerrelli Anthony P Monaco Simon E Fisher Andrew J Copp

Disruption of FOXP2, a gene encoding a forkhead-domain transcription factor, causes a severe developmental disorder of verbal communication, involving profound articulation deficits, accompanied by linguistic and grammatical impairments. Investigation of the neural basis of this disorder has been limited previously to neuroimaging of affected children and adults. The discovery of the gene respo...

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