FOXP2 (Dutch Wikipedia)

Analysis of information sources in references of the Wikipedia article "FOXP2" in Dutch language version.

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16nih.gov

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10web.archive.org

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1evolutionpages.com

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1brighthub.com

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1nationalgeographic.com

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1evolutiebiologie.blogspot.com

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1ensembl.org

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1fu-berlin.de

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1biomedcentral.com

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1multilingualarchive.com

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1tamarstelling.nl

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1plosbiology.org

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1els-cdn.com

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1bbc.co.uk

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bbc.co.uk

news.bbc.co.uk

(en) Morgan,James:Neanderthals 'distinct from us'. In: BBC-News; 12 februari 2009. Bezocht 2 april 2012.
Oorspronkelijk citaat: "There is no reason to believe they couldn't speak like us...". Gearchiveerd op 1 november 2022.

biomedcentral.com

(en) Tolosa, Amparo et al.:FOXP2 gene and language impairment inschizophrenia: association and epigenetic studies. In: BMC Medical Genetics 2010, 11(114). Bezocht 1 april 2012

brighthub.com

(en) DulceCorazon: The FOXP2 Gene Mutations’’. In: Bright Hub: The hub for bright minds. 14 juli 2010. Bezocht 30 maart 2012

els-cdn.com

ac.els-cdn.com

(en) Krause,Johannes et al.:Report: The Derived FOXP2 Variant of Modern Humans Was Shared with Neandertals. In: Current Biology 17,6 november 2007; pp. 1908–1912

ensembl.org

(en) Ensembl.org: Ensembl Gene Report for ENSG00000128573

evolutiebiologie.blogspot.com

(nl) Jong de, Gerdien: Echolocatie en geluid: FOXP2. In: Evolutiebiologie: Dit blog gaat over evolutie en evolutiebiologie. Niet over geloof en wetenschap. 20 oktober 2011. Bezocht 30 maart 2012

evolutionpages.com

(en) MacAndrew, Alec: FOXP2 and the Evolution of Language. In: Alec's Evolution Pages: Molecular Biology. Bezocht 30 maart 2012. Gearchiveerd op 8 maart 2023.

fu-berlin.de

bcp.fu-berlin.de

(de) Haesler, S.: Also sprach der Zebrafink.^{[dode link]} In: Gehirn&Geist, 2006;12, pp. 52–57. Bezocht 1 april 2012

multilingualarchive.com

(nl) Multiligual Archive:Erfelijkheid van autisme.^{[dode link]}. Bezocht 3 april 2012

nationalgeographic.com

news.nationalgeographic.com

(en) Tivedi, Bijal P.: Scientists Identify a Language Gene. In: National Geographic Today, 4 oktober 2001. Bezocht 30 maart 2012

nih.gov

ncbi.nlm.nih.gov

(en) Hurst JA et al.: An extended family with a dominantly inherited speech disorder. In: Dev. Med. Child Neurol., vol. 32(4) pp. 352–355. april 1990. Bezocht: 29 maart 2012. Gearchiveerd op 7 januari 2020.
FOXP2 forkhead box P2 (Homo sapiens)’’
(en) MacDermot, K.D.: et al.: Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits. In: Am J Hum Genet, 20005. 74, pp. 1074–1080. PMID 15877281
(en) Fujita E, Tanabe Y, Momoi MY, Momoi T.:Cntnap2 expression in the cerebellum of Foxp2(R552H) mice, with a mutation related to speech-language disorder. In: Neurosci Lett. 11 januari 2012;506(2):pp. 277-280. PMID 22133810
(en) Sanjuán, J et al.: Association between FOXP2 polymorphisms and schizophrenia with auditory hallucinations. In: Psychiatr Genet, 2006, 16. pp. 67–72. PMID 16538183
(en) Shu W. et al.: Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene. In: Proc Natl Acad Sci U S A., 102/2005, pp. 9643–9648. PMID 15983371
(en) Fujita E. et al.: Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells. In: Proc Natl Acad Sci U S A, 105/2008, S. 3117–22. PMID 18287060. Gearchiveerd op 10 juli 2023.
(en) Kumar S., Hedges S. B.: A molecular timescale for vertebrate evolution. In: Nature, 392/1998, pp. 917–20. PMID 9582070
(en) F. C. Chen, F.C. et al.: Genomic divergences between humans and other hominoids and the effective population size of the common ancestor of humans and chimpanzees. In: Am. J.Hum. Genet., 68/2001, pp. 444–456. PMID 11170892
(en) Boughman, J.W. Vocal learning by greater spear-nosed bats. In: Proc Biol Sci, 265/1998, pp. 227–33. PMID 9493408
(en) Moss C.F., Sinha, S.R.: Neurobiology of echolocation in bats. In: Current Opinion in Neurobiology, 13/2003, pp. 751–8. PMID 14662378
(en) G. Li et al.: Accelerated FoxP2 evolution in echolocating bats. In: PLoS ONE, 2/2007, e900. PMID 17878935

pubmedcentral.nih.gov

(en) Shu W. et al.: Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene. In: Proc Natl Acad Sci U S A., 102/2005, pp. 9643–9648. PMID 15983371
(en) F. C. Chen, F.C. et al.: Genomic divergences between humans and other hominoids and the effective population size of the common ancestor of humans and chimpanzees. In: Am. J.Hum. Genet., 68/2001, pp. 444–456. PMID 11170892
(en) Boughman, J.W. Vocal learning by greater spear-nosed bats. In: Proc Biol Sci, 265/1998, pp. 227–33. PMID 9493408
(en) G. Li et al.: Accelerated FoxP2 evolution in echolocating bats. In: PLoS ONE, 2/2007, e900. PMID 17878935

plosbiology.org

(en) Scharrf, Constance et al.: Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X. In: PLoS Biol. 2007; 5, e321

tamarstelling.nl

(nl) Stelling, Tamar: Praten is net tjilpen’’^{[dode link]}. In: Nwtmagazine. Juli/augustus 2010. Bezocht 2 april 2012

web.archive.org

(en) Hurst JA et al.: An extended family with a dominantly inherited speech disorder. In: Dev. Med. Child Neurol., vol. 32(4) pp. 352–355. april 1990. Bezocht: 29 maart 2012. Gearchiveerd op 7 januari 2020.
(en) Itzhaki, Jane: The FOXP2 story: A single family with speech abnormalities may hold one of the keys to the origin of human culture. In: The Human genome, 28 april 2003. Bezocht: 29 maart 2012.
(en) MacAndrew, Alec: FOXP2 and the Evolution of Language. In: Alec's Evolution Pages: Molecular Biology. Bezocht 30 maart 2012. Gearchiveerd op 8 maart 2023.
(en) MacDermot, K.D.: et al.: Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits. In: Am J Hum Genet, 20005. 74, pp. 1074–1080. PMID 15877281
(en) Newbury, D.F., et al.:FOXP2 Is Not a Major Susceptibility Gene for Autism or Specific Language Impairment. In: American Journal of Human Genetics, 70(5); pp. 1318-1327. doi:10.1086/339931
(en) Katsnelson, Alla: Scientists link new deficits to FOXP2 mutations in mice. 22 maart 2012. Bezocht 20 april 2012
(en) Fujita E. et al.: Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells. In: Proc Natl Acad Sci U S A, 105/2008, S. 3117–22. PMID 18287060. Gearchiveerd op 10 juli 2023.
(en) Scharff, Constance; Fisher, Simon E.: FOXP2 as a molecular window into speech and language". In: Trends in Genetics. 25(4), 21 maart 2009. Bezocht 2 april 2012
(en) Anthropology.net (2007):Neandertals have the same mutations in FOXP2, the language gene, as modern humans. Bezocht 2 april 2012
(en) Morgan,James:Neanderthals 'distinct from us'. In: BBC-News; 12 februari 2009. Bezocht 2 april 2012.
Oorspronkelijk citaat: "There is no reason to believe they couldn't speak like us...". Gearchiveerd op 1 november 2022.