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FOXP2 targets show evidence of positive selection in European populations.
Am J Hum Genet. 2013 May 2;92(5):696-706. doi: 10.1016/j.ajhg.2013.03.019. Epub 2013 Apr 18.
2
A study of the role of the FOXP2 and CNTNAP2 genes in persistent developmental stuttering.
Neurobiol Dis. 2014 Sep;69:23-31. doi: 10.1016/j.nbd.2014.04.019. Epub 2014 May 5.
4
A functional genetic link between distinct developmental language disorders.
N Engl J Med. 2008 Nov 27;359(22):2337-45. doi: 10.1056/NEJMoa0802828. Epub 2008 Nov 5.
6
Analysis of two language-related genes in autism: a case-control association study of FOXP2 and CNTNAP2.
Psychiatr Genet. 2013 Apr;23(2):82-5. doi: 10.1097/YPG.0b013e32835d6fc6.
7
Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain.
PLoS Genet. 2011 Jul;7(7):e1002145. doi: 10.1371/journal.pgen.1002145. Epub 2011 Jul 7.
8
Cntnap2 expression in the cerebellum of Foxp2(R552H) mice, with a mutation related to speech-language disorder.
Neurosci Lett. 2012 Jan 11;506(2):277-80. doi: 10.1016/j.neulet.2011.11.022. Epub 2011 Nov 22.
10
CNTNAP2 is a direct FoxP2 target in vitro and in vivo in zebra finches: complex regulation by age and activity.
Genes Brain Behav. 2017 Jul;16(6):635-642. doi: 10.1111/gbb.12390. Epub 2017 Jun 22.

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MUTAGENESISFORGE: A FRAMEWORK FOR MODELING CODON-LEVEL MUTATIONAL BIASES AND CALCULATING dN/dS.
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Genome-wide relaxation of selection and the evolution of the island syndrome in Orkney voles.
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The adaptive evolution of cancer driver genes.
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The role of contactin-associated protein-like 2 in neurodevelopmental disease and human cerebral cortex evolution.
Front Mol Neurosci. 2022 Oct 20;15:1017144. doi: 10.3389/fnmol.2022.1017144. eCollection 2022.
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Discovery of 42 genome-wide significant loci associated with dyslexia.
Nat Genet. 2022 Nov;54(11):1621-1629. doi: 10.1038/s41588-022-01192-y. Epub 2022 Oct 20.
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A Likelihood Approach for Uncovering Selective Sweep Signatures from Haplotype Data.
Mol Biol Evol. 2020 Oct 1;37(10):3023-3046. doi: 10.1093/molbev/msaa115.
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A population-based approach for gene prioritization in understanding complex traits.
Hum Genet. 2020 May;139(5):647-655. doi: 10.1007/s00439-020-02152-4. Epub 2020 Mar 30.
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Identifying and Classifying Shared Selective Sweeps from Multilocus Data.
Genetics. 2020 May;215(1):143-171. doi: 10.1534/genetics.120.303137. Epub 2020 Mar 9.

本文引用的文献

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A recent evolutionary change affects a regulatory element in the human FOXP2 gene.
Mol Biol Evol. 2013 Apr;30(4):844-52. doi: 10.1093/molbev/mss271. Epub 2012 Nov 28.
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Architecture of the human regulatory network derived from ENCODE data.
Nature. 2012 Sep 6;489(7414):91-100. doi: 10.1038/nature11245.
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Exploration of signals of positive selection derived from genotype-based human genome scans using re-sequencing data.
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Changes in the chondrocyte and extracellular matrix proteome during post-natal mouse cartilage development.
Mol Cell Proteomics. 2012 Jan;11(1):M111.014159. doi: 10.1074/mcp.M111.014159. Epub 2011 Oct 11.
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Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain.
PLoS Genet. 2011 Jul;7(7):e1002145. doi: 10.1371/journal.pgen.1002145. Epub 2011 Jul 7.
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Transcriptomic analysis of autistic brain reveals convergent molecular pathology.
Nature. 2011 May 25;474(7351):380-4. doi: 10.1038/nature10110.
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CNTNAP2 variants affect early language development in the general population.
Genes Brain Behav. 2011 Jun;10(4):451-6. doi: 10.1111/j.1601-183X.2011.00684.x. Epub 2011 Mar 1.
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A map of human genome variation from population-scale sequencing.
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A composite of multiple signals distinguishes causal variants in regions of positive selection.
Science. 2010 Feb 12;327(5967):883-6. doi: 10.1126/science.1183863. Epub 2010 Jan 7.

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