PRECISION FMR1 METHYLATION ASSAY IN FRAGILE X SYNDROME

被引：0
|
作者：
Erickson, Craig [1 ]
Schmitt, Lauren [1 ]
Pilito, Sebastian [1 ]
Cullion, Kyle [1 ]
Horn, Paul [1 ]
Shanahan, Matilyn [1 ]
Gross, Christina [1 ]
机构：
[1] Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH 45229 USA
来源：
NEUROPSYCHOPHARMACOLOGY | 2024年 / 49卷
关键词：
fragile X syndrome; CpG Methylation; Molecular Genetics;
D O I：
暂无
中图分类号：
Q189 [神经科学];
学科分类号：
071006 ;
摘要：
P459
引用
收藏
页码：325 / 325
页数：1
相关论文
共 50 条
  • [41] The FMR1 Gene and Fragile X-Associated Tremor/Ataxia Syndrome
    Brouwer, J. R.
    Willemsen, R.
    Oostra, B. A.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2009, 150B (06) : 782 - 798
  • [42] Incidence of Fragile X Syndrome by Newborn Screening for Methylated FMR1 DNA
    Coffee, Bradford
    Keith, Krayton
    Albizua, Igor
    Malone, Tamika
    Mowrey, Julie
    Sherman, Stephanie L.
    Warren, Stephen T.
    AMERICAN JOURNAL OF HUMAN GENETICS, 2009, 85 (04) : 503 - 514
  • [43] THE MULTIPLE MOLECULAR FACETS OF FRAGILE X SYNDROME AND FMR1 ASSOCIATED DISORDERS
    Tassone, F. T.
    JOURNAL OF INTELLECTUAL DISABILITY RESEARCH, 2014, 58 (10) : 888 - 888
  • [44] Frontostriatal deficits in fragile X syndrome:: Relation to FMR1 gene expression
    Menon, V
    Leroux, J
    White, CD
    Reiss, AL
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (10) : 3615 - 3620
  • [45] Germinal mosaicism for a deletion of the FMR1 gene leading to fragile X syndrome
    Jiraanont, P.
    Hagerman, R. J.
    Neri, G.
    Zollino, M.
    Murdolo, M.
    Tassone, F.
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2016, 59 (09) : 459 - 462
  • [46] Fragile X syndrome and deletions in FMR1: New case and review of the literature
    Hammond, LS
    Macias, MM
    Tarleton, JC
    Pai, GS
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1997, 72 (04): : 430 - 434
  • [47] Penetrance of FMR1 premutation associated pathologies in fragile X syndrome families
    Laia Rodriguez-Revenga
    Irene Madrigal
    Javier Pagonabarraga
    Mar Xunclà
    Celia Badenas
    Jaime Kulisevsky
    Beatriz Gomez
    Montserrat Milà
    European Journal of Human Genetics, 2009, 17 : 1359 - 1362
  • [48] Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate alleles
    Castellví-Bel, S
    Fernández-Burriel, M
    Rifé, M
    Jiménez, D
    Mallolas, J
    Sánchez, A
    Ramos, F
    Milà, M
    HUMAN GENETICS, 2000, 107 (02) : 195 - 196
  • [49] Pirenperone relieves the symptoms of fragile X syndrome in Fmr1 knockout mice
    Yujeong Kim
    Se Jin Jeon
    Edson Luck Gonzales
    Dongpil Shin
    Chilly Gay Remonde
    TaeJin Ahn
    Chan Young Shin
    Scientific Reports, 12
  • [50] Analysis of FMR 1 methylation in Fragile X syndrome in Iranian population
    Hasanzad, M
    Amini, SH
    Taghizadeh, F
    Teimourian, S
    Karimi-Nejad, R
    Shafeghati, Y
    Karimi-Nejad, M
    Najmabadi, H
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2002, 10 : 229 - 229
12345