BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

292 related articles for article (PubMed ID: 28183735)

  • 1. New insights into the regulatory function of CYFIP1 in the context of WAVE- and FMRP-containing complexes.
    Abekhoukh S; Sahin HB; Grossi M; Zongaro S; Maurin T; Madrigal I; Kazue-Sugioka D; Raas-Rothschild A; Doulazmi M; Carrera P; Stachon A; Scherer S; Drula Do Nascimento MR; Trembleau A; Arroyo I; Szatmari P; Smith IM; Milà M; Smith AC; Giangrande A; Caillé I; Bardoni B
    Dis Model Mech; 2017 Apr; 10(4):463-474. PubMed ID: 28183735
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP.
    Napoli I; Mercaldo V; Boyl PP; Eleuteri B; Zalfa F; De Rubeis S; Di Marino D; Mohr E; Massimi M; Falconi M; Witke W; Costa-Mattioli M; Sonenberg N; Achsel T; Bagni C
    Cell; 2008 Sep; 134(6):1042-54. PubMed ID: 18805096
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Reducing eIF4E-eIF4G interactions restores the balance between protein synthesis and actin dynamics in fragile X syndrome model mice.
    Santini E; Huynh TN; Longo F; Koo SY; Mojica E; D'Andrea L; Bagni C; Klann E
    Sci Signal; 2017 Nov; 10(504):. PubMed ID: 29114037
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P.
    Schenck A; Bardoni B; Moro A; Bagni C; Mandel JL
    Proc Natl Acad Sci U S A; 2001 Jul; 98(15):8844-9. PubMed ID: 11438699
    [TBL] [Abstract][Full Text] [Related]  

  • 5. CYFIP1 coordinates mRNA translation and cytoskeleton remodeling to ensure proper dendritic spine formation.
    De Rubeis S; Pasciuto E; Li KW; Fernández E; Di Marino D; Buzzi A; Ostroff LE; Klann E; Zwartkruis FJ; Komiyama NH; Grant SG; Poujol C; Choquet D; Achsel T; Posthuma D; Smit AB; Bagni C
    Neuron; 2013 Sep; 79(6):1169-82. PubMed ID: 24050404
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Increased CYFIP1 dosage alters cellular and dendritic morphology and dysregulates mTOR.
    Oguro-Ando A; Rosensweig C; Herman E; Nishimura Y; Werling D; Bill BR; Berg JM; Gao F; Coppola G; Abrahams BS; Geschwind DH
    Mol Psychiatry; 2015 Sep; 20(9):1069-78. PubMed ID: 25311365
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fragile X Mental Retardation Protein positively regulates PKA anchor Rugose and PKA activity to control actin assembly in learning/memory circuitry.
    Sears JC; Choi WJ; Broadie K
    Neurobiol Dis; 2019 Jul; 127():53-64. PubMed ID: 30771457
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Neuronal function and dysfunction of CYFIP2: from actin dynamics to early infantile epileptic encephalopathy.
    Zhang Y; Lee Y; Han K
    BMB Rep; 2019 May; 52(5):304-311. PubMed ID: 30982501
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fragile X-like behaviors and abnormal cortical dendritic spines in cytoplasmic FMR1-interacting protein 2-mutant mice.
    Han K; Chen H; Gennarino VA; Richman R; Lu HC; Zoghbi HY
    Hum Mol Genet; 2015 Apr; 24(7):1813-23. PubMed ID: 25432536
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Fragile X mental retardation protein (FMRP) interacting proteins exhibit different expression patterns during development.
    Bonaccorso CM; Spatuzza M; Di Marco B; Gloria A; Barrancotto G; Cupo A; Musumeci SA; D'Antoni S; Bardoni B; Catania MV
    Int J Dev Neurosci; 2015 May; 42():15-23. PubMed ID: 25681562
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cytoplasmic FMR1 interacting protein (CYFIP) family members and their function in neural development and disorders.
    Biembengut ÍV; Silva ILZ; Souza TACB; Shigunov P
    Mol Biol Rep; 2021 Aug; 48(8):6131-6143. PubMed ID: 34327661
    [TBL] [Abstract][Full Text] [Related]  

  • 12. MD and Docking Studies Reveal That the Functional Switch of CYFIP1 is Mediated by a Butterfly-like Motion.
    Di Marino D; Chillemi G; De Rubeis S; Tramontano A; Achsel T; Bagni C
    J Chem Theory Comput; 2015 Jul; 11(7):3401-10. PubMed ID: 26575774
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The fragile X protein controls microtubule-associated protein 1B translation and microtubule stability in brain neuron development.
    Lu R; Wang H; Liang Z; Ku L; O'donnell WT; Li W; Warren ST; Feng Y
    Proc Natl Acad Sci U S A; 2004 Oct; 101(42):15201-6. PubMed ID: 15475576
    [TBL] [Abstract][Full Text] [Related]  

  • 14. CYFIP family proteins between autism and intellectual disability: links with Fragile X syndrome.
    Abekhoukh S; Bardoni B
    Front Cell Neurosci; 2014; 8():81. PubMed ID: 24733999
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Intellectual Disability and Behavioral Deficits Linked to CYFIP1 Missense Variants Disrupting Actin Polymerization.
    Mariano V; Kanellopoulos AK; Ricci C; Di Marino D; Borrie SC; Dupraz S; Bradke F; Achsel T; Legius E; Odent S; Billuart P; Bienvenu T; Bagni C
    Biol Psychiatry; 2024 Jan; 95(2):161-174. PubMed ID: 37704042
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Expression of fragile X mental retardation-1 gene with nuclear export signal mutation changes the expression profiling of mouse cerebella immortal neuronal cell.
    Hu L; Chen Y; Evers S; Shen Y
    Proteomics; 2005 Oct; 5(15):3979-90. PubMed ID: 16130171
    [TBL] [Abstract][Full Text] [Related]  

  • 17.
    Babbs RK; Beierle JA; Ruan QT; Kelliher JC; Chen MM; Feng AX; Kirkpatrick SL; Benitez FA; Rodriguez FA; Pierre JJ; Anandakumar J; Kumar V; Mulligan MK; Bryant CD
    G3 (Bethesda); 2019 Sep; 9(9):3009-3022. PubMed ID: 31324746
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The fragile X mental retardation protein is a molecular adaptor between the neurospecific KIF3C kinesin and dendritic RNA granules.
    Davidovic L; Jaglin XH; Lepagnol-Bestel AM; Tremblay S; Simonneau M; Bardoni B; Khandjian EW
    Hum Mol Genet; 2007 Dec; 16(24):3047-58. PubMed ID: 17881655
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Co-regulation of mRNA translation by TDP-43 and Fragile X Syndrome protein FMRP.
    Majumder P; Chu JF; Chatterjee B; Swamy KB; Shen CJ
    Acta Neuropathol; 2016 Nov; 132(5):721-738. PubMed ID: 27518042
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizures.
    Myrick LK; Deng PY; Hashimoto H; Oh YM; Cho Y; Poidevin MJ; Suhl JA; Visootsak J; Cavalli V; Jin P; Cheng X; Warren ST; Klyachko VA
    Proc Natl Acad Sci U S A; 2015 Jan; 112(4):949-56. PubMed ID: 25561520
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.