Literature library
Case Reports
Topic:
8
2022
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Case report: FOXP1 syndrome caused by a de novo splicing variant (c.1652+5 G>A) of the FOXP1 gene
Min Chen, 1 Yixi Sun, 1 Yeqing Qian, 1 Na Chen, 1 Hongge Li, 1 Liya Wang, 1 and Minyue Dongcorresponding
This paper explores various things
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Developmental biology
Topic:
2
2021
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Autism-linked gene FoxP1 selectively regulates the cultural transmission of learned vocalizations
F Garcia-Oscos 1, T M I Koch 1, H Pancholi 1, M Trusel 1, V Daliparthi 1, M Co 1, S E Park 1, F Ayhan 1, D H Alam 1, J E Holdway 1, G Konopka 1, T F Roberts 2
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Developmental biology
Topic:
12
2020
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Identification of FoxP circuits involved in locomotion and object fixation in Drosophila
Ottavia Palazzo 1, Mathias Rass 1, Björn Brembs 1
This is a paper about neuro development
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Syndrome description
Topic:
9
2021
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Individuals with FOXP1 syndrome present with a complex neurobehavioral profile with high rates of ADHD, anxiety, repetitive behaviors, and sensory symptoms
M. Pilar Trelles, Tess Levy, Bonnie Lerman, Paige Siper, Reymundo Lozano, Danielle Halpern, Hannah Walker, Jessica Zweifach, Yitzchak Frank, Jennifer Foss-Feig, Alexander Kolevzon & Joseph Buxbaum
This study, conducted by the Seaver team, characterized the FOXP1 syndrome
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Syndrome description
Topic:
4
2021
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FOXP1 syndrome: a review of the literature and practice parameters for medical assessment and monitoring
Reymundo Lozano, Catherine Gbekie, Paige M. Siper, Shubhika Srivastava, Jeffrey M. Saland, Swathi Sethuram, Lara Tang, Elodie Drapeau, Yitzchak Frank, Joseph D. Buxbaum & Alexander Kolevzon
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Transcriptional regulation
Topic:
2
2021
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Ensemble Switching of the DNA-Binding Domain of Human FOXP1
Narendar Kolimi, Exequiel Medina, Cesar Ramirez-Sarmiento, Hugo Sanabria, Jorge Babul
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Transcriptional regulation
Topic:
1
2021
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FOXP1 Interacts with MyoD to Repress its Transcription and Myoblast Conversion
Woodring E Wright 1, Chuan Li 2, Chang-Xue Zheng 3, Haley O Tucker 3
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Transcriptional regulation
Topic:
9
2020
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Intrinsically Disordered Regions of the DNA-Binding Domain of Human FoxP1 Facilitate Domain Swapping
ExequielMedina1PabloVillalobos1George L.Hamilton2ElizabethA.Komives3HugoSanabria2César A.Ramírez-Sarmiento45JorgeBabul1
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Z
Topic:
5
2021
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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
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Z
Topic:
4
2021
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A genome-wide association study identifies a gene network associated with paranoid schizophrenia and antipsychotics-induced tardive dyskinesia
Anastasia Levchenko 1, Alexander Kanapin 2, Anastasia Samsonova 2, Olga Yu Fedorenko 3, Elena G Kornetova 4, Timur Nurgaliev 5, Galina E Mazo 6, Arkadiy V Semke 7, Alexander O Kibitov 8, Nikolay A Bokhan 9, Raul R Gainetdinov 10, Svetlana A Ivanova 11
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Z
Topic:
12
2021
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Autism Spectrum Disorder (ASD) and Attention Deficit Hyperactivity Disorder (ADHD) With Language Impairment Accompanied by Developmental Disability Caused by Forkhead Box Protein 1 (FOXP1) Exon Deletion: A Case Report
Shuliweeh Alenezi, Ahmed Alyahya, Hesham Aldhalaan
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Z
Topic:
1
2021
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FOXP1 negatively regulates intrinsic excitability in D2 striatal projection neurons by promoting inwardly rectifying and leak potassium currents
Nitin Khandelwal 1, Sheridan Cavalier 1, Volodymyr Rybalchenko 1, Ashwinikumar Kulkarni 1, Ashley G Anderson 1, Genevieve Konopka 2, Jay R Gibson 3
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Z
Topic:
9
2020
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Peruvian Newborn Male with 3p13 Deletion Syndrome Encompassing the FOXP1 Gene: Review of the Literature
Hugo H. Abarca-Barriga
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Z
Topic:
9
2020
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FOXP transcription factors in vertebrate brain development, function, and disorders
Marissa Co 1, Ashley G Anderson 2, Genevieve Konopka 2
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Z
Topic:
3
2020
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Single-Cell Analysis of Foxp1-Driven Mechanisms Essential for Striatal Development
Ashley G Anderson 1, Ashwinikumar Kulkarni 1, Matthew Harper 1, Genevieve Konopka
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Z
Topic:
2
2020
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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
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Z
Topic:
12
2020
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Coupling of autism genes to tissue-wide expression and dysfunction of synapse, calcium signaling and transcriptional regulation
Jamie Reilly, Louise Gallagher, Geraldine Leader, Sanbing Shen
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Z
Topic:
11
2020
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Dysfunction of the corticostriatal pathway in autism spectrum disorders Wei Li 1, Lucas Pozzo-Miller 1
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Z
Topic:
10
2020
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Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations
Dervla M Connaughton et al.
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Z
Topic:
1
2020
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FOXP transcription factors in vertebrate brain development, function, and disorders
Marissa Co Ashley G. Anderson Genevieve Konopka
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