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    FMR1 fragile X messenger ribonucleoprotein 1 [ Homo sapiens (human) ]

    Gene ID: 2332, updated on 24-Jun-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    [High expression of fragile X mental retardation protein inhibits ferroptosis of colorectal tumor cells by activating the RAS/MAPK signaling pathway].

    [High expression of fragile X mental retardation protein inhibits ferroptosis of colorectal tumor cells by activating the RAS/MAPK signaling pathway].
    Wang N, Shi B, Man X, Wu W, Cao J., Free PMC Article

    06/21/2024
    Conformational and dynamic properties of the KH1 domain of FMRP and its fragile X syndrome linked G266E variant.

    Conformational and dynamic properties of the KH1 domain of FMRP and its fragile X syndrome linked G266E variant.
    Catalano F, Santorelli D, Astegno A, Favretto F, D'Abramo M, Del Giudice A, De Sciscio ML, Troilo F, Giardina G, Di Matteo A, Travaglini-Allocatelli C.

    06/8/2024
    FMR1 Protein Expression Correlates with Intelligence Quotient in Both Peripheral Blood Mononuclear Cells and Fibroblasts from Individuals with an FMR1 Mutation.

    FMR1 Protein Expression Correlates with Intelligence Quotient in Both Peripheral Blood Mononuclear Cells and Fibroblasts from Individuals with an FMR1 Mutation.
    Jiraanont P, Zafarullah M, Sulaiman N, Espinal GM, Randol JL, Durbin-Johnson B, Schneider A, Hagerman RJ, Hagerman PJ, Tassone F.

    05/24/2024
    LLPS of FXR proteins drives replication organelle clustering for beta-coronaviral proliferation.

    LLPS of FXR proteins drives replication organelle clustering for β-coronaviral proliferation.
    Li M, Hou Y, Zhou Y, Yang Z, Zhao H, Jian T, Yu Q, Zeng F, Liu X, Zhang Z, Zhao YG.,

    04/10/2024
    Variation of FMRP Expression in Peripheral Blood Mononuclear Cells from Individuals with Fragile X Syndrome.

    Variation of FMRP Expression in Peripheral Blood Mononuclear Cells from Individuals with Fragile X Syndrome.
    Randol JL, Kim K, Ponzini MD, Tassone F, Falcon AK, Hagerman RJ, Hagerman PJ., Free PMC Article

    04/1/2024
    FMR1 Carriers Report Executive Function Changes Prior to Fragile X-Associated Tremor/Ataxia Syndrome: A Longitudinal Study.

    FMR1 Carriers Report Executive Function Changes Prior to Fragile X-Associated Tremor/Ataxia Syndrome: A Longitudinal Study.
    Hessl D, Mandujano Rojas K, Ferrer E, Espinal G, Famula J, Schneider A, Hagerman R, Tassone F, Rivera SM.

    03/26/2024
    Stratification of the risk of ovarian dysfunction by studying the complexity of intermediate and premutation alleles of the FMR1 gene.

    Stratification of the risk of ovarian dysfunction by studying the complexity of intermediate and premutation alleles of the FMR1 gene.
    Quilichini J, Perol S, Cuisset L, Grotto S, Fouveaut C, Barbot JC, Verebi C, Jordan P, Héron D, Molina-Gomes D, Pipiras E, Grynberg M, Catteau-Jonard S, Touraine P, Christin-Maître S, Plu-Bureau G, El Khattabi L, Bienvenu T.

    03/11/2024
    Complex interplay between FMRP and DHX9 during DNA replication stress.

    Complex interplay between FMRP and DHX9 during DNA replication stress.
    Chakraborty A, Dutta A, Dettori LG, Daoud R, Li J, Gonzalez L, Xue X, Hehnly H, Sung P, Bah A, Feng W., Free PMC Article

    02/12/2024
    Clinical and molecular characteristics of FMR1 microdeletion in patient with fragile X syndrome and review of the literature.

    Clinical and molecular characteristics of FMR1 microdeletion in patient with fragile X syndrome and review of the literature.
    Hnoonual A, Plong-On O, Worachotekamjorn J, Charalsawadi C, Limprasert P.

    01/27/2024
    FMRP Enhances the Translation of 4EBP2 mRNA during Neuronal Differentiation.

    FMRP Enhances the Translation of 4EBP2 mRNA during Neuronal Differentiation.
    Yu J, Woo Y, Kim H, An S, Park SK, Jang SK., Free PMC Article

    11/28/2023
    Transcriptional Dysregulation and Impaired Neuronal Activity in FMR1 Knock-Out and Fragile X Patients' iPSC-Derived Models.

    Transcriptional Dysregulation and Impaired Neuronal Activity in FMR1 Knock-Out and Fragile X Patients' iPSC-Derived Models.
    Maussion G, Rocha C, Abdian N, Yang D, Turk J, Carrillo Valenzuela D, Pimentel L, You Z, Morquette B, Nicouleau M, Deneault E, Higgins S, Chen CX, Reintsch WE, Ho S, Soubannier V, Lépine S, Modrusan Z, Lund J, Stephenson W, Schubert R, Durcan TM., Free PMC Article

    11/3/2023
    Mortality in Women across the FMR1 CGG Repeat Range: The Neuroprotective Effect of Higher Education.

    Mortality in Women across the FMR1 CGG Repeat Range: The Neuroprotective Effect of Higher Education.
    Hong J, Dembo RS, DaWalt LS, Baker MW, Berry-Kravis E, Mailick MR., Free PMC Article

    09/15/2023
    Increased degradation of FMRP contributes to neuronal hyperexcitability in tuberous sclerosis complex.

    Increased degradation of FMRP contributes to neuronal hyperexcitability in tuberous sclerosis complex.
    Winden KD, Pham TT, Teaney NA, Ruiz J, Chen R, Chen C, Sahin M., Free PMC Article

    09/6/2023
    Large-Scale Whole Genome Sequence Analysis of >22,000 Subjects Provides no Evidence of FMR1 Premutation Allele Involvement in Autism Spectrum Disorder.

    Large-Scale Whole Genome Sequence Analysis of >22,000 Subjects Provides no Evidence of FMR1 Premutation Allele Involvement in Autism Spectrum Disorder.
    Chubick A, Wang E, Au C, Grody WW, Ophoff RA., Free PMC Article

    08/30/2023
    Atypical vocal quality in women with the FMR1 premutation: an indicator of impaired sensorimotor control.

    Atypical vocal quality in women with the FMR1 premutation: an indicator of impaired sensorimotor control.
    Friedman L, Lauber M, Behroozmand R, Fogerty D, Kunecki D, Berry-Kravis E, Klusek J.,

    08/1/2023
    Elevated levels of FMRP-target MAP1B impair human and mouse neuronal development and mouse social behaviors via autophagy pathway.

    Elevated levels of FMRP-target MAP1B impair human and mouse neuronal development and mouse social behaviors via autophagy pathway.
    Guo Y, Shen M, Dong Q, Méndez-Albelo NM, Huang SX, Sirois CL, Le J, Li M, Jarzembowski ED, Schoeller KA, Stockton ME, Horner VL, Sousa AMM, Gao Y, Birth Defects Research Laboratory, Levine JE, Wang D, Chang Q, Zhao X., Free PMC Article

    07/5/2023
    The association between a carrier state of FMR1 premutation and numeric sex chromosome variations.

    The association between a carrier state of FMR1 premutation and numeric sex chromosome variations.
    Malcov M, Blickstein O, Brabbing-Goldstein D, Reches A, Kalma Y, Fouks Y, Azem F, Cohen Y., Free PMC Article

    03/31/2023
    Characterization of Fragile X Mental Retardation Protein expression in human nociceptors and their axonal projections to the spinal dorsal horn.

    Characterization of Fragile X Mental Retardation Protein expression in human nociceptors and their axonal projections to the spinal dorsal horn.
    Mitchell ME, Cook LC, Shiers S, Tavares-Ferreira D, Akopian AN, Dussor G, Price TJ., Free PMC Article

    03/28/2023
    Altered GnRH neuron and ovarian innervation characterize reproductive dysfunction linked to the Fragile X messenger ribonucleoprotein (Fmr1) gene mutation.

    Altered GnRH neuron and ovarian innervation characterize reproductive dysfunction linked to the Fragile X messenger ribonucleoprotein (Fmr1) gene mutation.
    Villa PA, Lainez NM, Jonak CR, Berlin SC, Ethell IM, Coss D., Free PMC Article

    03/15/2023
    Maternal FMR1 alleles expansion in newborns during transmission: a prospective cohort study.

    Maternal FMR1 alleles expansion in newborns during transmission: a prospective cohort study.
    Shahid R, Yasin M, Rehman ZU, Jadoon H, Tahir H, Meraj N, Khan N, Zubair M, Zulfiqar I, Nowshid M, Azeem A, Jabeen M, Hameed A, Saleha S.

    03/14/2023
    Axonal and presynaptic FMRP: Localization, signal, and functional implications.

    Axonal and presynaptic FMRP: Localization, signal, and functional implications.
    Wang X, Sela-Donenfeld D, Wang Y., Free PMC Article

    03/14/2023
    Screening for the FMR1 premutation in Greek patients with late-onset movement disorders.

    Screening for the FMR1 premutation in Greek patients with late-onset movement disorders.
    Kartanou C, Seferiadi M, Pomoni S, Potagas C, Sofocleous C, Traeger-Synodinos J, Stefanis L, Panas M, Koutsis G, Karadima G.

    02/15/2023
    Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome.

    Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome.
    Baker EK, Arpone M, Bui M, Kraan CM, Ling L, Francis D, Hunter MF, Rogers C, Field MJ, Santa María L, Faundes V, Curotto B, Morales P, Trigo C, Salas I, Alliende AM, Amor DJ, Godler DE., Free PMC Article

    02/11/2023
    FMRP, FXR1 protein and Dlg4 mRNA, which are associated with fragile X syndrome, are involved in the ubiquitin-proteasome system.

    FMRP, FXR1 protein and Dlg4 mRNA, which are associated with fragile X syndrome, are involved in the ubiquitin-proteasome system.
    Shimizu H, Hohjoh H., Free PMC Article

    02/10/2023
    Pumping the brakes: A noncanonical RNA-binding domain in FMRP stalls elongating ribosomes.

    Pumping the brakes: A noncanonical RNA-binding domain in FMRP stalls elongating ribosomes.
    Young-Baird SK., Free PMC Article

    02/4/2023
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