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Forkhead-Box-Protein P2 (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Forkhead-Box-Protein P2" in German language version.

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36nih.gov
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7doi.org
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4web.archive.org
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3zdb-katalog.de
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2mpg.de
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2zeit.de
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1omabrowser.org
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1ensembl.org
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1genetics.org
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1fu-berlin.de
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1abstractsonline.com
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1wissenschaft-online.de
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1geo.de
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1nationalgeographic.com
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abstractsonline.com (Global: low place; German: low place)

doi.org (Global: 2nd place; German: 3rd place)

  • W. Enard u. a.: Molecular evolution of FOXP2, a gene involved in speech and language. In: Nature, 2002, 418, S. 869–872, PMID 12192408, doi:10.1038/nature01025
  • K. D. MacDermot u. a.: Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits. In: American Journal of Human Genetics. Band 76, 2005, S. 1074–1080, doi:10.1086/430841, PMID 15877281.
  • M. Gopnik: Feature-blind grammar and dysphasia. In: Nature. Nr. 344, 1990, S. 715, doi:10.1038/344715a0.
  • A. Wilcke, C. Ligges, J. Burkhardt, M. Alexander, C. Wolf, E. Quente, P. Ahnert, P. Hoffmann, A. Becker, B. Müller-Myhsok, S. Cichon, J. Boltze, H. Kirsten: Imaging genetics of FOXP2 in dyslexia. In: European journal of human genetics: EJHG. Band 20, Nummer 2, Februar 2012, ISSN 1476-5438, S. 224–229, doi:10.1038/ejhg.2011.160. PMID 21897444, PMC 3260915 (freier Volltext).
  • W. Shu, J. Y. Cho u. a.: Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene. In: PNAS. Band 102, Nummer 27, Juli 2005, S. 9643–9648, ISSN 0027-8424. doi:10.1073/pnas.0503739102. PMID 15983371. PMC 1160518 (freier Volltext).
  • E. Fujita, Y. Tanabe u. a.: Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells. In: PNAS. Band 105, Nummer 8, Februar 2008, S. 3117–3122, ISSN 1091-6490. doi:10.1073/pnas.0712298105. PMID 18287060. PMC 2268594 (freier Volltext).
  • J. Krause u. a.: The derived FOXP2 variant of modern humans was shared with Neandertals. In: Current Biology. Band 17, 2007, S. 1908–1912, doi:10.1016/j.cub.2007.10.008, PMID 17949978.

ensembl.org (Global: 1,626th place; German: 4,988th place)

fu-berlin.de (Global: 3,329th place; German: 378th place)

diss.fu-berlin.de

genetics.org (Global: low place; German: low place)

geo.de (Global: low place; German: 1,059th place)

mpg.de (Global: 1,624th place; German: 377th place)

nationalgeographic.com (Global: 344th place; German: 700th place)

news.nationalgeographic.com

nih.gov (Global: 4th place; German: 7th place)

ncbi.nlm.nih.gov

  • L. Feuk u. a.: Absence of a Paternally Inherited FOXP2 Gene in Developmental Verbal Dyspraxia. In: American Journal of Human Genetics. Band 79, 2006, S. 965–972, PMID 17033973.
  • J. Zhang u. a.: Accelerated Protein Evolution and Origins of Human-Specific Features: FOXP2 as an Example. In: Genetics. Band 162, 2002, S. 1825–1835, PMID 12524352.
  • W. Enard u. a.: Molecular evolution of FOXP2, a gene involved in speech and language. In: Nature, 2002, 418, S. 869–872, PMID 12192408, doi:10.1038/nature01025
  • K. D. MacDermot u. a.: Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits. In: American Journal of Human Genetics. Band 76, 2005, S. 1074–1080, doi:10.1086/430841, PMID 15877281.
  • E. K. O’Brien u. a.: Association of Specific Language Impairment (SLI) to the Region of 7q31. In: Am. J. Hum. Genet., 72/2003, S. 1536–1543, PMID 12721956
  • T. H. Wassink u. a.: Evaluation of FOXP2 as an autism susceptibility gene. In: American Journal of Medical Genetics. Band 114, 2002, S. 566–569, PMID 12116195.
  • J. Sanjuán u. a.: Association between FOXP2 polymorphisms and schizophrenia with auditory hallucinations. In: Psychiatric Genetics. Band 16, 2006, S. 67–72, PMID 16538183.
  • S. E. Fisher u. a.: Localisation of a gene implicated in a severe speech and language disorder. In: Nature Genetics. Band 18, 1998, S. 168–170, PMID 9462748.
  • A. Wilcke, C. Ligges, J. Burkhardt, M. Alexander, C. Wolf, E. Quente, P. Ahnert, P. Hoffmann, A. Becker, B. Müller-Myhsok, S. Cichon, J. Boltze, H. Kirsten: Imaging genetics of FOXP2 in dyslexia. In: European journal of human genetics: EJHG. Band 20, Nummer 2, Februar 2012, ISSN 1476-5438, S. 224–229, doi:10.1038/ejhg.2011.160. PMID 21897444, PMC 3260915 (freier Volltext).
  • K. E. Watkins u. a.: Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia. In: Brain. Band 125, 2002, S. 452–464, PMID 11872604.
  • K. J. Alcock u. a.: Oral dyspraxia in inherited speech and language impairment and acquired dysphasia. In: Brain and language. Band 75, 2000, S. 17–33, PMID 11023636.
  • F. Vargha-Khadem u. a.: Neural basis of an inherited speech and language disorder. In: Proceedings of the National Academy of Sciences of the United States of America. Band 95, 1998, S. 12695–12700, PMID 9770548.
  • E. Belton u. a.: Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia. In: Human Brain Mapping. Band 18, 2003, S. 194–200, PMID 12599277.
  • A. M. Graybiel: Building action repertoires: memory and learning functions of the basal ganglia. In: Current Opinion in Neurobiology. Band 5, 1995, S. 733–741, PMID 8805417.
  • S. Zeesman u. a.: Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2. In: American Journal of Medical Genetics. Band 140, 2006, S. 509–514, PMID 16470794.
  • W. Shu, J. Y. Cho u. a.: Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene. In: PNAS. Band 102, Nummer 27, Juli 2005, S. 9643–9648, ISSN 0027-8424. doi:10.1073/pnas.0503739102. PMID 15983371. PMC 1160518 (freier Volltext).
  • E. Fujita, Y. Tanabe u. a.: Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells. In: PNAS. Band 105, Nummer 8, Februar 2008, S. 3117–3122, ISSN 1091-6490. doi:10.1073/pnas.0712298105. PMID 18287060. PMC 2268594 (freier Volltext).
  • S. Haesler u. a.: FoxP2 expression in avian vocal learners and non-learners. In: Journal of Neuroscience. Band 24, 2004, S. 3164–3175, PMID 15056696.
  • S. A. White u. a.: Singing Mice, Songbirds, and More: Models for FOXP2 Function and Dysfunction in Human Speech and Language. In: The Journal of Neuroscience. Band 26, 2006, S. 10376–10379, PMID 17035521.
  • S. Haesler u. a.: Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X. In: PLOS Biology. Band 5, 2007, e321, PMID 18052609.
  • G. Li u. a.: Accelerated FoxP2 evolution in echolocating bats. In: PLoS ONE. Band 2, 2007, e900, PMID 17878935.
  • D. M. Webb, J. Zhang: FoxP2 in song-learning birds and vocal-learning mammals. In: J Hered., 96/2005, S. 212–216, PMID 15618302
  • C. Scharff, S. Haesler: An evolutionary perspective on FoxP2: strictly for the birds? In: Current Opinion in Neurobiology . Band 15, 2004, S. 694–703, PMID 16266802.
  • I. Teramitsu u. a.: Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction. In: Journal of Neuroscience. Band 24, 2004, S. 3152–3163, PMID 15056695.
  • S. Haesler u. a.: FoxP2 expression in avian vocal learners and non-learners. In: Journal of Neuroscience. Band 24, 2004, S. 3164–3175, PMID 15056696.
  • W. Enard u. a. Molecular evolution of FOXP2, a gene involved in speech and language. In: Nature. Band 418, 2002, S. 869–872, PMID 12192408.
  • G. J. Kops u. a.: Control of cell cycle exit and entry by protein kinase b-regulated forkhead transcription factors. In: Molecular and Cellular Biology. Band 22, 2002, S. 2025–2036, PMID 11884591.
  • A. Brunet u. a. Akt promotes cell survival by phosphorylating and inhibiting a Forkhead transcription factor. In: Cell. Band 96, 1999, S. 857–868, PMID 10102273.
  • J. W. Boughman: Vocal learning by greater spear-nosed bats. In: Proceedings of the Royal Society B: Biological Sciences. Band 265, 1998, S. 227–233, PMID 9493408.
  • G. Jones, R. D. Ransome: Echolocation calls of bats are influenced by maternal effects and change over a lifetime. In: Proceedings of the Royal Society B: Biological Sciences. Band 252, 1993, S. 125–128, PMID 8391702.
  • C. F. Moss, S. R. Sinha: Neurobiology of echolocation in bats. In: Current Opinion in Neurobiology. Band 13, 2003, S. 751–758, PMID 14662378.
  • J. Krause u. a.: The derived FOXP2 variant of modern humans was shared with Neandertals. In: Current Biology. Band 17, 2007, S. 1908–1912, doi:10.1016/j.cub.2007.10.008, PMID 17949978.
  • M. Hofreiter u. a.; Ancient DNA. In: Nature Reviews Genetics. Band 2, 2001, S. 353–359, PMID 11331901
  • S. Pääbo: Human evolution. In: Trends in Cell Biology. Band 9, 1999, M13–16, PMID 10611673.
  • A. Rosas u. a.: Paleobiology and comparative morphology of a late Neandertal sample from El Sidron, Asturias, Spain. In: Proceedings of the National Academy of Sciences USA. Band 103, 2006, S. 19266–71, PMID 17164326.
  • R. E. Green u. a.: Analysis of one million base pairs of Neanderthal DNA. In: Nature, 444/2006, S. 330–336, PMID 17108958

omabrowser.org (Global: low place; German: 8,112th place)

web.archive.org (Global: 1st place; German: 1st place)

wissenschaft-online.de (Global: low place; German: 2,288th place)

zdb-katalog.de (Global: 123rd place; German: 6th place)

zeit.de (Global: 267th place; German: 15th place)