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 *

155 related articles for article (PubMed ID: 31512951)

  • 1. Positive Emotional Support in Premutation Carrier Mothers of Adolescents and Adults With Fragile X Syndrome: Gene by Environment Interactions.
    Hartley SL; DaWalt LS; Hong J; Greenberg JS; Mailick MR
    Am J Intellect Dev Disabil; 2019 Sep; 124(5):411-426. PubMed ID: 31512951
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Differential sensitivity to life stress in FMR1 premutation carrier mothers of children with fragile X syndrome.
    Seltzer MM; Barker ET; Greenberg JS; Hong J; Coe C; Almeida D
    Health Psychol; 2012 Sep; 31(5):612-22. PubMed ID: 22149120
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Inhibition deficits are modulated by age and CGG repeat length in carriers of the FMR1 premutation allele who are mothers of children with fragile X syndrome.
    Klusek J; Hong J; Sterling A; Berry-Kravis E; Mailick MR
    Brain Cogn; 2020 Mar; 139():105511. PubMed ID: 31887710
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Unaffected siblings of adolescents and adults with fragile X syndrome: Effects on maternal well-being.
    Usher LV; DaWalt LS; Greenberg JS; Mailick MR
    J Fam Psychol; 2019 Jun; 33(4):487-492. PubMed ID: 30211570
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Stress and genetics influence hair cortisol in FMR1 premutation carrier mothers of children with fragile X syndrome.
    Hong J; Kapoor A; DaWalt LS; Maltman N; Kim B; Berry-Kravis EM; Almeida D; Coe C; Mailick M
    Psychoneuroendocrinology; 2021 Jul; 129():105266. PubMed ID: 34020265
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analysis of FMR1 gene expression in female premutation carriers using robust segmented linear regression models.
    García-Alegría E; Ibáñez B; Mínguez M; Poch M; Valiente A; Sanz-Parra A; Martinez-Bouzas C; Beristain E; Tejada MI
    RNA; 2007 May; 13(5):756-62. PubMed ID: 17449730
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Preliminary evidence of an effect of cerebellar volume on postural sway in FMR1 premutation males.
    Birch RC; Hocking DR; Cornish KM; Menant JC; Georgiou-Karistianis N; Godler DE; Wen W; Hackett A; Rogers C; Trollor JN
    Genes Brain Behav; 2015 Mar; 14(3):251-9. PubMed ID: 25689687
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Detecting AGG Interruptions in Male and Female FMR1 Premutation Carriers by Single-Molecule Sequencing.
    Ardui S; Race V; Zablotskaya A; Hestand MS; Van Esch H; Devriendt K; Matthijs G; Vermeesch JR
    Hum Mutat; 2017 Mar; 38(3):324-331. PubMed ID: 27883256
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Indicators of anxiety and depression in women with the fragile X premutation: assessment of a clinical sample.
    Lachiewicz A; Dawson D; Spiridigliozzi G; Cuccaro M; Lachiewicz M; McConkie-Rosell A
    J Intellect Disabil Res; 2010 Jul; 54(7):597-610. PubMed ID: 20629912
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Does theFMR1 gene affect IVF success?
    Pastore LM; Christianson MS; McGuinness B; Vaught KC; Maher JY; Kearns WG
    Reprod Biomed Online; 2019 Apr; 38(4):560-569. PubMed ID: 30711457
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Health Effects of Sleep Quality in Premutation Carrier Mothers of Individuals With Fragile X Syndrome.
    Dembo RS; Hong J; DaWalt LS; Berry-Kravis EM; Mailick MR
    Am J Intellect Dev Disabil; 2023 May; 128(3):254-268. PubMed ID: 37104861
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Fragile X-associated tremor/ataxia syndrome: intrafamilial variability and the size of the FMR1 premutation CGG repeat.
    Capelli LP; Gonçalves MR; Kok F; Leite CC; Nitrini R; Barbosa ER; Vianna-Morgante AM
    Mov Disord; 2007 Apr; 22(6):866-70. PubMed ID: 17290448
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [FMR1 PREMUTATION CARRIERS - ARE THEY REALLY ASYMPTOMATIC?].
    Elizur S; Berkenstadt M; Ries-Levavi L; Gruber N; Pinhas-Hamiel O; Hassin-Baer S; Raas-Rothschild A; Raanani H; Cukierman-Yaffe T; Orvieto R; Cohen Y; Gabis L
    Harefuah; 2018 Apr; 157(4):241-244. PubMed ID: 29688643
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pragmatic Language Features of Mothers With the FMR1 Premutation Are Associated With the Language Outcomes of Adolescents and Young Adults With Fragile X Syndrome.
    Klusek J; McGrath SE; Abbeduto L; Roberts JE
    J Speech Lang Hear Res; 2016 Feb; 59(1):49-61. PubMed ID: 26895548
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Use of human-derived stem cells to create a novel, in vitro model designed to explore FMR1 CGG repeat instability amongst female premutation carriers.
    Gustin SLF; Wang G; Baker VM; Latham G; Sebastiano V
    J Assist Reprod Genet; 2018 Aug; 35(8):1443-1455. PubMed ID: 29926373
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular predictors of cognitive involvement in female carriers of fragile X syndrome.
    Taylor AK; Safanda JF; Fall MZ; Quince C; Lang KA; Hull CE; Carpenter I; Staley LW; Hagerman RJ
    JAMA; 1994 Feb; 271(7):507-14. PubMed ID: 8301764
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Diminished ovarian reserve is not observed in infertility patients with high normal CGG repeats on the fragile X mental retardation 1 (FMR1) gene.
    Schufreider A; McQueen DB; Lee SM; Allon R; Uhler ML; Davie J; Feinberg EC
    Hum Reprod; 2015 Nov; 30(11):2686-92. PubMed ID: 26345686
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prevalence and instability of fragile X alleles: implications for offering fragile X prenatal diagnosis.
    Cronister A; Teicher J; Rohlfs EM; Donnenfeld A; Hallam S
    Obstet Gynecol; 2008 Mar; 111(3):596-601. PubMed ID: 18310361
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Robust Polymerase Chain Reaction-based Assay for Quantifying Cytosine-guanine-guanine Trinucleotide Repeats in Fragile X Mental Retardation-1 Gene.
    Wang H; Zhu X; Gui B; Cheung WC; Shi M; Yang Z; Kwok KY; Lim R; Pietilä S; Zhu Y; Choy KW
    J Vis Exp; 2019 Sep; (151):. PubMed ID: 31566610
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A genetic study of the FMR1 gene in a Sardinian multiple sclerosis population.
    Lorefice L; Tranquilli S; Fenu G; Murru MR; Frau J; Rolesu M; Coghe GC; Marrosu F; Marrosu MG; Cocco E
    Neurol Sci; 2015 Dec; 36(12):2213-20. PubMed ID: 26194536
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.