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 *

166 related articles for article (PubMed ID: 19712568)

  • 61. AMH in women with diminished ovarian reserve: potential differences by FMR1 CGG repeat level.
    Pastore LM; McMurry TL; Williams CD; Baker VL; Young SL
    J Assist Reprod Genet; 2014 Oct; 31(10):1295-301. PubMed ID: 24938362
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Variable expression of the Fragile X Mental Retardation 1 (FMR1) gene in patients with premature ovarian failure syndrome is not dependent on number of (CGG)n triplets in exon 1.
    Schuettler J; Peng Z; Zimmer J; Sinn P; von Hagens C; Strowitzki T; Vogt PH
    Hum Reprod; 2011 May; 26(5):1241-51. PubMed ID: 21335413
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Molecular screening of intellectually disabled patients and those with premature ovarian failure for CGG repeat expansion at FMR1 locus: Implication of combined triplet repeat primed polymerase chain reaction and methylation-specific polymerase chain reaction analysis.
    Muthuswamy S; Dean DD; Agarwal S
    Neurol India; 2016; 64(6):1175-1179. PubMed ID: 27841182
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Distribution of the FMR1 gene in females by race/ethnicity: women with diminished ovarian reserve versus women with normal fertility (SWAN study).
    Pastore LM; Young SL; Manichaikul A; Baker VL; Wang XQ; Finkelstein JS
    Fertil Steril; 2017 Jan; 107(1):205-211.e1. PubMed ID: 27816231
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Evidence of an age-related correlation of ovarian reserve and FMR1 repeat number among women with "normal" CGG repeat status.
    Gustin SL; Ding VY; Desai M; Leader B; Baker VL
    J Assist Reprod Genet; 2015 Nov; 32(11):1669-76. PubMed ID: 26409477
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Population-based estimates of the prevalence of FMR1 expansion mutations in women with early menopause and primary ovarian insufficiency.
    Murray A; Schoemaker MJ; Bennett CE; Ennis S; Macpherson JN; Jones M; Morris DH; Orr N; Ashworth A; Jacobs PA; Swerdlow AJ
    Genet Med; 2014 Jan; 16(1):19-24. PubMed ID: 23703681
    [TBL] [Abstract][Full Text] [Related]  

  • 67. The significance of the number of CGG repeats and autoantibodies in premature ovarian failure.
    Fiçicioglu C; Yildirim G; Attar R; Kumbak B; Yesildaglar N
    Reprod Biomed Online; 2010 Jun; 20(6):776-82. PubMed ID: 20362512
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Genetic analysis of FMR1 repeat expansion in essential tremor.
    Clark LN; Ye X; Liu X; Louis ED
    Neurosci Lett; 2015 Apr; 593():114-7. PubMed ID: 25796179
    [TBL] [Abstract][Full Text] [Related]  

  • 69. 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]  

  • 70. Distribution of CGG/GCC repeats at the FMR1 and FMR2 genes in an Indian population with mental retardation of unknown etiology.
    Katikala L; Guruju MR; Madireddi S; Vallamkonda O; Vallamkonda N; Persha A; Spurgeon AM
    Genet Test Mol Biomarkers; 2011 Apr; 15(4):281-4. PubMed ID: 21254876
    [TBL] [Abstract][Full Text] [Related]  

  • 71. 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]  

  • 72. [Chromatin changes caused by CGG repeat expansion in fmr1 gene].
    Yudkin DV; Lemskaya NA; Grischenko IV; Dolskiy AA
    Mol Biol (Mosk); 2015; 49(2):205-11. PubMed ID: 26065250
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Refining the risk for fragile X-associated primary ovarian insufficiency (FXPOI) by FMR1 CGG repeat size.
    Allen EG; Charen K; Hipp HS; Shubeck L; Amin A; He W; Nolin SL; Glicksman A; Tortora N; McKinnon B; Shelly KE; Sherman SL
    Genet Med; 2021 Sep; 23(9):1648-1655. PubMed ID: 33927378
    [TBL] [Abstract][Full Text] [Related]  

  • 74. A study of the distributional characteristics of FMR1 transcript levels in 238 individuals.
    Allen EG; He W; Yadav-Shah M; Sherman SL
    Hum Genet; 2004 Apr; 114(5):439-47. PubMed ID: 14758538
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Expansion mutation frequency and CGG/GCC repeat polymorphism in FMR1 and FMR2 genes in an Indian population.
    Sharma D; Gupta M; Thelma BK
    Genet Epidemiol; 2001 Jan; 20(1):129-144. PubMed ID: 11119302
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Granulosa cell and oocyte mitochondrial abnormalities in a mouse model of fragile X primary ovarian insufficiency.
    Conca Dioguardi C; Uslu B; Haynes M; Kurus M; Gul M; Miao DQ; De Santis L; Ferrari M; Bellone S; Santin A; Giulivi C; Hoffman G; Usdin K; Johnson J
    Mol Hum Reprod; 2016 Jun; 22(6):384-96. PubMed ID: 26965313
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Is Low FMR1 CGG Repeat Length in Males Correlated with Family History of BRCA-Associated Cancers? An Exploratory Analysis of Medical Records.
    Adamsheck HC; Petty EM; Hong J; Baker MW; Brilliant MH; Mailick MR
    J Genet Couns; 2017 Dec; 26(6):1401-1410. PubMed ID: 28667565
    [TBL] [Abstract][Full Text] [Related]  

  • 78. 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]  

  • 79. 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]  

  • 80. Trisomic pregnancy and intermediate CGG repeat length at the FMR1 locus.
    Kline J; Kinney A; Brown S; Levin B; Oppenheimer K; Warburton D
    Hum Reprod; 2012 Jul; 27(7):2224-32. PubMed ID: 22493044
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.