Molecular evolution of FOXP2, a gene involved in speech and language.

Molecular evolution of FOXP2, a gene involved in speech and language.

Language is a uniquely human trait likely to have been a prerequisite for the development of human culture. The ability to develop articulate speech relies on capabilities, such as fine control of the larynx and mouth, that are absent in chimpanzees and other great apes. FOXP2 is the first gene rele...

Volledige beschrijving

Bibliografische gegevens
Hoofdauteurs:	Enard, W, Przeworski, M, Fisher, S, Lai, C, Wiebe, V, Kitano, T, Monaco, A, Pääbo, S
Formaat:	Journal article
Taal:	English
Gepubliceerd in:	2002

Gelijkaardige items

FOXP2 as a molecular window into speech and language.
door: Fisher, S, et al.
Gepubliceerd in: (2009)

FOXP2 in focus: what can genes tell us about speech and language?
door: Marcus, G, et al.
Gepubliceerd in: (2003)

FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder.
door: Lai, C, et al.
Gepubliceerd in: (2003)

Functional dissection of two amino acid substitutions unique to the human FOXP2 protein
door: Ulrich Bornschein, et al.
Gepubliceerd in: (2023-03-01)

FOXP2 gene and language development: the molecular substrate of the gestural-origin theory of speech?
door: Carmelo Mario Vicario
Gepubliceerd in: (2013-08-01)

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits.
door: MacDermot, K, et al.
Gepubliceerd in: (2005)

Correction: Loss of Olfactory Receptor Genes Coincides with the Acquisition of Full Trichromatic Vision in Primates.
door: Yoav Gilad, et al.
Gepubliceerd in: (2007-06-01)

FOXP2 is not a major susceptibility gene for autism or specific language impairment.
door: Newbury, D, et al.
Gepubliceerd in: (2002)

Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain.
door: Spiteri, E, et al.
Gepubliceerd in: (2007)

Identification of foxp2 truncation as a novel cause of developmental speech disorder.
door: MacDermot, K, et al.
Gepubliceerd in: (2004)

Deciphering the genetic basis of speech and language disorders.
door: Fisher, S, et al.
Gepubliceerd in: (2003)

Singing mice, songbirds, and more: models for FOXP2 function and dysfunction in human speech and language.
door: White, SA, et al.
Gepubliceerd in: (2006)

On genes, speech, and language.
door: Fisher, S
Gepubliceerd in: (2005)

A forkhead-domain gene is mutated in a severe speech and language disorder.
door: Lai, C, et al.
Gepubliceerd in: (2001)

Molecular genetics of speech and language disorders.
door: Newbury, D, et al.
Gepubliceerd in: (2002)

A novel forkhead-domain gene is mutated in a severe speech and language disorder.
door: Fisher, S, et al.
Gepubliceerd in: (2001)

High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders.
door: Vernes, S, et al.
Gepubliceerd in: (2007)

MOLECULAR WINDOWS INTO SPEECH AND LANGUAGE DISORDERS
door: Fisher, S
Gepubliceerd in: (2011)

Molecular windows into speech and language disorders.
door: Fisher, S
Gepubliceerd in: (2007)

Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits.
door: Horn, D, et al.
Gepubliceerd in: (2010)

Humanized Foxp2 accelerates learning by enhancing transitions from declarative to procedural performance
door: Bornschein, U., et al.
Gepubliceerd in: (2015)

Localisation of a gene implicated in a severe speech and language disorder.
door: Fisher, S, et al.
Gepubliceerd in: (1997)

Localisation of a gene implicated in a severe speech and language disorder.
door: Fisher, S, et al.
Gepubliceerd in: (1998)

A Molecular Genetic Perspective on Speech and Language
door: Simon E. Fisher
Gepubliceerd in: (2018-09-01)

Dissection of molecular mechanisms underlying speech and language disorders
door: Fisher, S
Gepubliceerd in: (2005)

Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex.
door: Roll, P, et al.
Gepubliceerd in: (2010)

Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia.
door: Vernes, S, et al.
Gepubliceerd in: (2009)

Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia
door: Vernes, S, et al.
Gepubliceerd in: (2009)

Case Report: Expressive Speech Disorder in a Family as a Hallmark of 7q31 Deletion Involving the FOXP2 Gene
door: Orsolya Nagy, et al.
Gepubliceerd in: (2021-08-01)

A novel transcription factor is mutated in a severe speech and language disorder
door: Lai, C, et al.
Gepubliceerd in: (2001)

Next stop: Language. The ‘FOXP2’ gene’s journey through time
door: Adriana Schatton, et al.
Gepubliceerd in: (2017-06-01)

<it>FOXP2 </it>gene and language impairment in schizophrenia: association and epigenetic studies
door: Moltó María D, et al.
Gepubliceerd in: (2010-07-01)

Analysis of Codon Usage of Speech Gene <i>FoxP2</i> among Animals
door: Tarikul Huda Mazumder, et al.
Gepubliceerd in: (2021-10-01)

Neocerebellar Crus I abnormalities associated with a speech and language disorder due to a mutation in FOXP2
door: Argyropoulos, G, et al.
Gepubliceerd in: (2018)

Talking genes - the molecular basis of language impairment.
door: Newbury, D, et al.
Gepubliceerd in: (2002)

The eloquent ape: genes, brains and the evolution of language.
door: Fisher, S, et al.
Gepubliceerd in: (2006)

Genetic advances in the study of speech and language disorders.
door: Newbury, D, et al.
Gepubliceerd in: (2010)

A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice.
door: Enard, W, et al.
Gepubliceerd in: (2009)

A Foxp2 mutation implicated in human speech deficits alters sequencing of ultrasonic vocalizations in adult male mice
door: Jonathan Chabout, et al.
Gepubliceerd in: (2016-10-01)

The Association Between Genetic Variation in FOXP2 and Sensorimotor Control of Speech Production
door: Siyun Zhang, et al.
Gepubliceerd in: (2018-09-01)