Academic Articles NEW
The following is a chronological list of all of the articles we have been able to find about FOXP1. If you find an article that you think would be useful for us to share here, please contact us.
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[object Object]
2016
The RNA binding protein HuR determines the differential translation of autism-associated FoxP subfamily members in the developing neocortex
T Popovitchenko 1, K Thompson 1, B Viljetic 1, X Jiao 2, D L Kontonyiannis 3, M Kiledjian 2, R P Hart 2, M R Rasin 1
[object Object]
2020
Foxp1 Regulates Neural Stem Cell Self-Renewal and Bias Toward Deep Layer Cortical Fates
Caroline Alayne Pearson 1, Destaye M Moore 1, Haley O Tucker 2, Joseph D Dekker 2, Hui Hu 3, Amaya Miquelajáuregui 4, Bennett G Novitch 5
[object Object]
2019
Differential Song Deficits after Lentivirus-Mediated Knockdown of FoxP1, FoxP2, or FoxP4 in Area X of Juvenile Zebra Finches
Philipp Norton 1, Peggy Barschke 1, Constance Scharff 1, Ezequiel Mendoza 2
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2021
Severe speech impairment is a distinguishing feature of FOXP1-related disorder
Ruth O Braden, David J Amori, Simon E Fisher, Cristina Mei,
Candace T Muers, Heather Mefford, DeepakGill, Siddharth Srivastava,
Lindsay C Swanson, Himanshu Goel, Ingrid E Scheffer, Angela T Morgan
[object Object]
2020
Intrinsically Disordered Regions of the DNA-Binding Domain of Human FoxP1 Facilitate Domain Swapping
ExequielMedina1PabloVillalobos1George L.Hamilton2ElizabethA.Komives3HugoSanabria2César A.Ramírez-Sarmiento45JorgeBabul1
[object Object]
2011
Mild to Moderate Intellectual Disability and Significant Speech and Language Deficits in Patients with FOXP1 Deletions and Mutations
Horn D.
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2012
ASD-relevant Animal Models of the Foxp Family of Transcription Factors
J Michael Bowers 1, Genevieve Konopka 1
[object Object]
2013
Increased gene expression of FOXP1 in patients with autism spectrum disorders
Wei-Hsien Chien 1, Susan Shur-Fen Gau, Chun-Houh Chen, Wen-Che Tsai, Yu-Yu Wu, Po Hsu Chen, Chi-Yung Shang, Chia-Hsiang Chen
[object Object]
2015
Genetic Changes Shaping the Human Brain
lByoung-IlBae1DivyaJayaraman1Christopher A.Walsh1
[object Object]
2017
SUMOylation of FOXP1 regulates transcriptional repression via CtBP1 to drive dendritic morphogenesis
Daniel L Rocca 1, Kevin A Wilkinson 1, Jeremy M Henley
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2017
FOXP1 Promotes Embryonic Neural Stem Cell Differentiation by Repressing Jagged1 Expression
Luca Braccioli 1, Stephin J Vervoort 2, Youri Adolfs 3, Cobi J Heijnen 4, Onur Basak 5, R Jeroen Pasterkamp 3, Cora H Nijboer 6, Paul J Coffer 7
[object Object]
2016
Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder
Elliot Sollis 1, Sarah A Graham 1, Arianna Vino 1, Henning Froehlich 2, Maaike Vreeburg 3, Danai Dimitropoulou 1, Christian Gilissen 4, Rolph Pfundt 4, Gudrun A Rappold 5, Han G Brunner 6, Pelagia Deriziotis 7, Simon E Fisher 8