These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
233 related articles for article (PubMed ID: 35165191)
41. [Clinical features and genetic analysis of three children with mental retardation, language impairment and autistic features due to de novo variants of FOXP1 gene]. Hua R; Xu X; Wu D; Yang L; Yuan J; Zhu J Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Dec; 38(12):1194-1198. PubMed ID: 34839505 [TBL] [Abstract][Full Text] [Related]
42. Behavioral training rescues motor deficits in Cyfip1 haploinsufficiency mouse model of autism spectrum disorders. Bachmann SO; Sledziowska M; Cross E; Kalbassi S; Waldron S; Chen F; Ranson A; Baudouin SJ Transl Psychiatry; 2019 Jan; 9(1):29. PubMed ID: 30664619 [TBL] [Abstract][Full Text] [Related]
43. Mitochondrial dysfunction as a central actor in intellectual disability-related diseases: an overview of Down syndrome, autism, Fragile X and Rett syndrome. Valenti D; de Bari L; De Filippis B; Henrion-Caude A; Vacca RA Neurosci Biobehav Rev; 2014 Oct; 46 Pt 2():202-17. PubMed ID: 24548784 [TBL] [Abstract][Full Text] [Related]
44. Case Report of Suspected Gonadal Mosaicism in Zsigmond A; Till Á; Bene J; Czakó M; Mikó A; Hadzsiev K Int J Mol Sci; 2024 May; 25(11):. PubMed ID: 38891897 [TBL] [Abstract][Full Text] [Related]
45. FOXP1 regulates the development of excitatory synaptic inputs onto striatal neurons and induces phenotypic reversal with reinstatement. Khandelwal N; Kulkarni A; Ahmed NI; Harper M; Konopka G; Gibson JR Sci Adv; 2024 May; 10(18):eadm7039. PubMed ID: 38701209 [TBL] [Abstract][Full Text] [Related]
46. Severe speech impairment is a distinguishing feature of FOXP1-related disorder. Braden RO; Amor DJ; Fisher SE; Mei C; Myers CT; Mefford H; Gill D; Srivastava S; Swanson LC; Goel H; Scheffer IE; Morgan AT Dev Med Child Neurol; 2021 Dec; 63(12):1417-1426. PubMed ID: 34109629 [TBL] [Abstract][Full Text] [Related]
47. Chiari I malformation, delayed gross motor skills, severe speech delay, and epileptiform discharges in a child with FOXP1 haploinsufficiency. Carr CW; Moreno-De-Luca D; Parker C; Zimmerman HH; Ledbetter N; Martin CL; Dobyns WB; Abdul-Rahman OA Eur J Hum Genet; 2010 Nov; 18(11):1216-20. PubMed ID: 20571508 [TBL] [Abstract][Full Text] [Related]
48. Identification of a de novo FOXP1 mutation and incidental discovery of inherited genetic variants contributing to a case of autism spectrum disorder and epilepsy. Jay K; Mitra A; Harding T; Matthes D; Van Ness B Mol Genet Genomic Med; 2019 Jul; 7(7):e00751. PubMed ID: 31111659 [TBL] [Abstract][Full Text] [Related]
49. Forkhead Box P1 (FOXP1) Transcription Factor Regulates Hepatic Glucose Homeostasis. Zou Y; Gong N; Cui Y; Wang X; Cui A; Chen Q; Jiao T; Dong X; Yang H; Zhang S; Fang F; Chang Y J Biol Chem; 2015 Dec; 290(51):30607-15. PubMed ID: 26504089 [TBL] [Abstract][Full Text] [Related]
50. Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. Horn D; Kapeller J; Rivera-Brugués N; Moog U; Lorenz-Depiereux B; Eck S; Hempel M; Wagenstaller J; Gawthrope A; Monaco AP; Bonin M; Riess O; Wohlleber E; Illig T; Bezzina CR; Franke A; Spranger S; Villavicencio-Lorini P; Seifert W; Rosenfeld J; Klopocki E; Rappold GA; Strom TM Hum Mutat; 2010 Nov; 31(11):E1851-60. PubMed ID: 20848658 [TBL] [Abstract][Full Text] [Related]
51. Genetic abnormalities in FOXP1 are associated with congenital heart defects. Chang SW; Mislankar M; Misra C; Huang N; Dajusta DG; Harrison SM; McBride KL; Baker LA; Garg V Hum Mutat; 2013 Sep; 34(9):1226-30. PubMed ID: 23766104 [TBL] [Abstract][Full Text] [Related]
52. Dexmedetomidine Protects Against Neurological Dysfunction in a Mouse Intracerebral Hemorrhage Model by Inhibiting Mitochondrial Dysfunction-Derived Oxidative Stress. Huang J; Jiang Q J Stroke Cerebrovasc Dis; 2019 May; 28(5):1281-1289. PubMed ID: 30797643 [TBL] [Abstract][Full Text] [Related]
53. Endothelial Foxp1 Suppresses Atherosclerosis via Modulation of Nlrp3 Inflammasome Activation. Zhuang T; Liu J; Chen X; Zhang L; Pi J; Sun H; Li L; Bauer R; Wang H; Yu Z; Zhang Q; Tomlinson B; Chan P; Zheng X; Morrisey E; Liu Z; Reilly M; Zhang Y Circ Res; 2019 Aug; 125(6):590-605. PubMed ID: 31318658 [TBL] [Abstract][Full Text] [Related]
54. Novel FOXP1 pathogenic variants in two Indian subjects with syndromic intellectual disability. Moirangthem A; Phadke SR Am J Med Genet A; 2021 Apr; 185(4):1324-1327. PubMed ID: 33427368 [TBL] [Abstract][Full Text] [Related]
55. Foxp1 regulates cortical radial migration and neuronal morphogenesis in developing cerebral cortex. Li X; Xiao J; Fröhlich H; Tu X; Li L; Xu Y; Cao H; Qu J; Rappold GA; Chen JG PLoS One; 2015; 10(5):e0127671. PubMed ID: 26010426 [TBL] [Abstract][Full Text] [Related]