234 related articles for article (PubMed ID: 35165191)
1. Mitochondrial dysfunction and oxidative stress contribute to cognitive and motor impairment in FOXP1 syndrome.
Wang J; Fröhlich H; Torres FB; Silva RL; Poschet G; Agarwal A; Rappold GA
Proc Natl Acad Sci U S A; 2022 Feb; 119(8):. PubMed ID: 35165191
[TBL] [Abstract][Full Text] [Related]
2. Disrupted Mitochondrial Network Drives Deficits of Learning and Memory in a Mouse Model of
Wang J; Rappold GA; Fröhlich H
Genes (Basel); 2022 Jan; 13(1):. PubMed ID: 35052467
[TBL] [Abstract][Full Text] [Related]
3.
Meerschaut I; Rochefort D; Revençu N; Pètre J; Corsello C; Rouleau GA; Hamdan FF; Michaud JL; Morton J; Radley J; Ragge N; García-Miñaúr S; Lapunzina P; Bralo MP; Mori MÁ; Moortgat S; Benoit V; Mary S; Bockaert N; Oostra A; Vanakker O; Velinov M; de Ravel TJ; Mekahli D; Sebat J; Vaux KK; DiDonato N; Hanson-Kahn AK; Hudgins L; Dallapiccola B; Novelli A; Tarani L; Andrieux J; Parker MJ; Neas K; Ceulemans B; Schoonjans AS; Prchalova D; Havlovicova M; Hancarova M; Budisteanu M; Dheedene A; Menten B; Dion PA; Lederer D; Callewaert B
J Med Genet; 2017 Sep; 54(9):613-623. PubMed ID: 28735298
[TBL] [Abstract][Full Text] [Related]
4. Prospective investigation of FOXP1 syndrome.
Siper PM; De Rubeis S; Trelles MDP; Durkin A; Di Marino D; Muratet F; Frank Y; Lozano R; Eichler EE; Kelly M; Beighley J; Gerdts J; Wallace AS; Mefford HC; Bernier RA; Kolevzon A; Buxbaum JD
Mol Autism; 2017; 8():57. PubMed ID: 29090079
[TBL] [Abstract][Full Text] [Related]
5. A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment.
Lozano R; Vino A; Lozano C; Fisher SE; Deriziotis P
Eur J Hum Genet; 2015 Dec; 23(12):1702-7. PubMed ID: 25853299
[TBL] [Abstract][Full Text] [Related]
6. Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour.
Bacon C; Schneider M; Le Magueresse C; Froehlich H; Sticht C; Gluch C; Monyer H; Rappold GA
Mol Psychiatry; 2015 May; 20(5):632-9. PubMed ID: 25266127
[TBL] [Abstract][Full Text] [Related]
7. Foxp1 in Forebrain Pyramidal Neurons Controls Gene Expression Required for Spatial Learning and Synaptic Plasticity.
Araujo DJ; Toriumi K; Escamilla CO; Kulkarni A; Anderson AG; Harper M; Usui N; Ellegood J; Lerch JP; Birnbaum SG; Tucker HO; Powell CM; Konopka G
J Neurosci; 2017 Nov; 37(45):10917-10931. PubMed ID: 28978667
[TBL] [Abstract][Full Text] [Related]
8. FoxP1 orchestration of ASD-relevant signaling pathways in the striatum.
Araujo DJ; Anderson AG; Berto S; Runnels W; Harper M; Ammanuel S; Rieger MA; Huang HC; Rajkovich K; Loerwald KW; Dekker JD; Tucker HO; Dougherty JD; Gibson JR; Konopka G
Genes Dev; 2015 Oct; 29(20):2081-96. PubMed ID: 26494785
[TBL] [Abstract][Full Text] [Related]
9. Foxp1 expression is essential for sex-specific murine neonatal ultrasonic vocalization.
Fröhlich H; Rafiullah R; Schmitt N; Abele S; Rappold GA
Hum Mol Genet; 2017 Apr; 26(8):1511-1521. PubMed ID: 28204507
[TBL] [Abstract][Full Text] [Related]
10. Whole genome sequencing identifies a de novo 2.1 Mb balanced paracentric inversion disrupting FOXP1 and leading to severe intellectual disability.
Vuillaume ML; Cogné B; Jeanne M; Boland A; Ung DC; Quinquis D; Besnard T; Deleuze JF; Redon R; Bézieau S; Laumonnier F; Toutain A
Clin Chim Acta; 2018 Oct; 485():218-223. PubMed ID: 29969624
[TBL] [Abstract][Full Text] [Related]
11. Gastrointestinal dysfunction in autism displayed by altered motility and achalasia in
Fröhlich H; Kollmeyer ML; Linz VC; Stuhlinger M; Groneberg D; Reigl A; Zizer E; Friebe A; Niesler B; Rappold G
Proc Natl Acad Sci U S A; 2019 Oct; 116(44):22237-22245. PubMed ID: 31611379
[TBL] [Abstract][Full Text] [Related]
12. Characterization of a recurrent missense mutation in the forkhead DNA-binding domain of FOXP1.
Johnson TB; Mechels K; Anderson RH; Cain JT; Sturdevant DA; Braddock S; Pinz H; Wilson MA; Landsverk M; Roux KJ; Weimer JM
Sci Rep; 2018 Nov; 8(1):16161. PubMed ID: 30385778
[TBL] [Abstract][Full Text] [Related]
13. FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?
Myers A; du Souich C; Yang CL; Borovik L; Mwenifumbo J; Rupps R; Study C; Lehman A; Boerkoel CF
Am J Med Genet A; 2017 Dec; 173(12):3172-3181. PubMed ID: 28884888
[TBL] [Abstract][Full Text] [Related]
14. FOXP1 mutations cause intellectual disability and a recognizable phenotype.
Le Fevre AK; Taylor S; Malek NH; Horn D; Carr CW; Abdul-Rahman OA; O'Donnell S; Burgess T; Shaw M; Gecz J; Bain N; Fagan K; Hunter MF
Am J Med Genet A; 2013 Dec; 161A(12):3166-75. PubMed ID: 24214399
[TBL] [Abstract][Full Text] [Related]
15. An Autism-Related, Nonsense Foxp1 Mutant Induces Autophagy and Delays Radial Migration of the Cortical Neurons.
Li X; Han X; Tu X; Zhu D; Feng Y; Jiang T; Yang Y; Qu J; Chen JG
Cereb Cortex; 2019 Jul; 29(7):3193-3208. PubMed ID: 30124790
[TBL] [Abstract][Full Text] [Related]
16. Identification of a Novel
Benvenuto M; Palumbo P; Di Muro E; Perrotta CS; Mazza T; Mandarà GML; Palumbo O; Carella M
Genes (Basel); 2023 Oct; 14(10):. PubMed ID: 37895307
[TBL] [Abstract][Full Text] [Related]
17. De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment.
Hamdan FF; Daoud H; Rochefort D; Piton A; Gauthier J; Langlois M; Foomani G; Dobrzeniecka S; Krebs MO; Joober R; Lafrenière RG; Lacaille JC; Mottron L; Drapeau P; Beauchamp MH; Phillips MS; Fombonne E; Rouleau GA; Michaud JL
Am J Hum Genet; 2010 Nov; 87(5):671-8. PubMed ID: 20950788
[TBL] [Abstract][Full Text] [Related]
18. 3p14.1 de novo microdeletion involving the FOXP1 gene in an adult patient with autism, severe speech delay and deficit of motor coordination.
Palumbo O; D'Agruma L; Minenna AF; Palumbo P; Stallone R; Palladino T; Zelante L; Carella M
Gene; 2013 Mar; 516(1):107-13. PubMed ID: 23287644
[TBL] [Abstract][Full Text] [Related]
19. Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder.
Sollis E; Graham SA; Vino A; Froehlich H; Vreeburg M; Dimitropoulou D; Gilissen C; Pfundt R; Rappold GA; Brunner HG; Deriziotis P; Fisher SE
Hum Mol Genet; 2016 Feb; 25(3):546-57. PubMed ID: 26647308
[TBL] [Abstract][Full Text] [Related]
20. FOXP1 syndrome: a review of the literature and practice parameters for medical assessment and monitoring.
Lozano R; Gbekie C; Siper PM; Srivastava S; Saland JM; Sethuram S; Tang L; Drapeau E; Frank Y; Buxbaum JD; Kolevzon A
J Neurodev Disord; 2021 Apr; 13(1):18. PubMed ID: 33892622
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]