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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

68 related articles for article (PubMed ID: 25037997)

  • 1. [Clinical phenotype of a patient with FOXP1 deletion].
    Blanco Sánchez T; Duat Rodríguez A; Cantarín Extremera V; Lapunzina P; Palomares Bralo M; Nevado Blanco J
    An Pediatr (Barc); 2015 Apr; 82(4):280-1. PubMed ID: 25037997
    [No Abstract]   [Full Text] [Related]  

  • 2. Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders.
    Sollis E; Deriziotis P; Saitsu H; Miyake N; Matsumoto N; Hoffer MJV; Ruivenkamp CAL; Alders M; Okamoto N; Bijlsma EK; Plomp AS; Fisher SE
    Hum Mutat; 2017 Nov; 38(11):1542-1554. PubMed ID: 28741757
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. FOXP1 Syndrome and Severe Obstructive Sleep Apnea.
    Kritikou I; Afolabi-Brown O
    J Clin Sleep Med; 2018 Aug; 14(8):1432-1434. PubMed ID: 30092897
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. Three Japanese patients with 3p13 microdeletions involving FOXP1.
    Yamamoto-Shimojima K; Okamoto N; Matsumura W; Okazaki T; Yamamoto T
    Brain Dev; 2019 Mar; 41(3):257-262. PubMed ID: 30424912
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia.
    Vernes SC; MacDermot KD; Monaco AP; Fisher SE
    Eur J Hum Genet; 2009 Oct; 17(10):1354-8. PubMed ID: 19352412
    [TBL] [Abstract][Full Text] [Related]  

  • 14. FOXP1 inhibits cell growth and attenuates tumorigenicity of neuroblastoma.
    Ackermann S; Kocak H; Hero B; Ehemann V; Kahlert Y; Oberthuer A; Roels F; Theißen J; Odenthal M; Berthold F; Fischer M
    BMC Cancer; 2014 Nov; 14():840. PubMed ID: 25406647
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Vocal cord immobility as a cause of aphonia in a child with 3p13p12 deletion syndrome encompassing FOXP1 gene.
    Mutlu-Albayrak H; Karaer K
    Int J Pediatr Otorhinolaryngol; 2019 Feb; 117():179-181. PubMed ID: 30579078
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Forkhead box protein P1 expression in mucosa-associated lymphoid tissue lymphomas predicts poor prognosis and transformation to diffuse large B-cell lymphoma.
    Sagaert X; de Paepe P; Libbrecht L; Vanhentenrijk V; Verhoef G; Thomas J; Wlodarska I; De Wolf-Peeters C
    J Clin Oncol; 2006 Jun; 24(16):2490-7. PubMed ID: 16636337
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 6p subtelomere deletion with congenital glaucoma, severe mental retardation, and growth impairment.
    Nakane T; Kousuke N; Sonoko H; Yuko K; Sato H; Kubota T; Sugita K
    Pediatr Int; 2013 Jun; 55(3):376-81. PubMed ID: 23782370
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [FOXP1 in B-lymphoproliferative diseases].
    Mara D
    Lijec Vjesn; 2007 May; 129 Suppl 3():43. PubMed ID: 18959064
    [No Abstract]   [Full Text] [Related]  

  • 19. FOXP1 protein overexpression is associated with inferior outcome in nodal diffuse large B-cell lymphomas with non-germinal centre phenotype, independent of gains and structural aberrations at 3p14.1.
    Hoeller S; Schneider A; Haralambieva E; Dirnhofer S; Tzankov A
    Histopathology; 2010 Jul; 57(1):73-80. PubMed ID: 20579129
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel FOXP1-PDGFRA fusion gene in myeloproliferative neoplasm with eosinophilia.
    Sugimoto Y; Sada A; Shimokariya Y; Monma F; Ohishi K; Masuya M; Nobori T; Matsui T; Katayama N
    Cancer Genet; 2015 Oct; 208(10):508-12. PubMed ID: 26319757
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.