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.
2. FMR1 CGG repeat lengths mediate different regulation of reporter gene expression in comparative transient and locus specific integration assays. Sølvsten C; Nielsen AL Gene; 2011 Oct; 486(1-2):15-22. PubMed ID: 21767618 [TBL] [Abstract][Full Text] [Related]
3. Transcription-associated R-loop formation across the human FMR1 CGG-repeat region. Loomis EW; Sanz LA; Chédin F; Hagerman PJ PLoS Genet; 2014 Apr; 10(4):e1004294. PubMed ID: 24743386 [TBL] [Abstract][Full Text] [Related]
5. Comprehensive analysis of the transcriptional landscape of the human FMR1 gene reveals two new long noncoding RNAs differentially expressed in Fragile X syndrome and Fragile X-associated tremor/ataxia syndrome. Pastori C; Peschansky VJ; Barbouth D; Mehta A; Silva JP; Wahlestedt C Hum Genet; 2014 Jan; 133(1):59-67. PubMed ID: 24005575 [TBL] [Abstract][Full Text] [Related]
6. CGG Repeats in the 5'UTR of FMR1 RNA Regulate Translation of Other RNAs Localized in the Same RNA Granules. Rovozzo R; Korza G; Baker MW; Li M; Bhattacharyya A; Barbarese E; Carson JH PLoS One; 2016; 11(12):e0168204. PubMed ID: 28005950 [TBL] [Abstract][Full Text] [Related]
7. Both cis and trans-acting genetic factors drive somatic instability in female carriers of the FMR1 premutation. Hwang YH; Hayward BE; Zafarullah M; Kumar J; Durbin Johnson B; Holmans P; Usdin K; Tassone F Sci Rep; 2022 Jun; 12(1):10419. PubMed ID: 35729184 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program. Jarmolowicz AI; Baker EK; Bartlett E; Francis D; Ling L; Gamage D; Delatycki MB; Godler DE Am J Med Genet A; 2021 May; 185(5):1498-1503. PubMed ID: 33544979 [TBL] [Abstract][Full Text] [Related]
11. Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles. Nolin SL; Brown WT; Glicksman A; Houck GE; Gargano AD; Sullivan A; Biancalana V; Bröndum-Nielsen K; Hjalgrim H; Holinski-Feder E; Kooy F; Longshore J; Macpherson J; Mandel JL; Matthijs G; Rousseau F; Steinbach P; Väisänen ML; von Koskull H; Sherman SL Am J Hum Genet; 2003 Feb; 72(2):454-64. PubMed ID: 12529854 [TBL] [Abstract][Full Text] [Related]
12. Polymerase chain reaction, nuclease digestion, and mass spectrometry based assay for the trinucleotide repeat status of the fragile X mental retardation 1 gene. Dodds ED; Tassone F; Hagerman PJ; Lebrilla CB Anal Chem; 2009 Jul; 81(13):5533-40. PubMed ID: 19514725 [TBL] [Abstract][Full Text] [Related]
13. Reversion to Normal of Tabolacci E; Pietrobono R; Maneri G; Remondini L; Nobile V; Della Monica M; Pomponi MG; Genuardi M; Neri G; Chiurazzi P Genes (Basel); 2020 Feb; 11(3):. PubMed ID: 32111011 [TBL] [Abstract][Full Text] [Related]
15. Study of telomere length in men who carry a fragile X premutation or full mutation allele. Albizua I; Chopra P; Allen EG; He W; Amin AS; Sherman SL Hum Genet; 2020 Dec; 139(12):1531-1539. PubMed ID: 32533363 [TBL] [Abstract][Full Text] [Related]
16. Differential usage of transcriptional start sites and polyadenylation sites in FMR1 premutation alleles. Tassone F; De Rubeis S; Carosi C; La Fata G; Serpa G; Raske C; Willemsen R; Hagerman PJ; Bagni C Nucleic Acids Res; 2011 Aug; 39(14):6172-85. PubMed ID: 21478165 [TBL] [Abstract][Full Text] [Related]
17. Evaluation of the human fragile X mental retardation 1 polymerase chain reaction reagents to amplify the FMR1 gene: testing in a clinical diagnostic laboratory. Nahhas FA; Monroe TJ; Prior TW; Botma PI; Fang J; Snyder PJ; Talbott SL; Feldman GL Genet Test Mol Biomarkers; 2012 Mar; 16(3):187-92. PubMed ID: 21992462 [TBL] [Abstract][Full Text] [Related]
18. Elevated Fmr1 mRNA levels and reduced protein expression in a mouse model with an unmethylated Fragile X full mutation. Brouwer JR; Mientjes EJ; Bakker CE; Nieuwenhuizen IM; Severijnen LA; Van der Linde HC; Nelson DL; Oostra BA; Willemsen R Exp Cell Res; 2007 Jan; 313(2):244-53. PubMed ID: 17150213 [TBL] [Abstract][Full Text] [Related]
19. Partially methylated alleles, microdeletion, and tissue mosaicism in a fragile X male with tremor and ataxia at 30 years of age: A case report. Hwang YT; Aliaga SM; Arpone M; Francis D; Li X; Chong B; Slater HR; Rogers C; Bretherton L; Hunter M; Heard R; Godler DE Am J Med Genet A; 2016 Dec; 170(12):3327-3332. PubMed ID: 27696642 [TBL] [Abstract][Full Text] [Related]
20. Induction of inclusion formation and disruption of lamin A/C structure by premutation CGG-repeat RNA in human cultured neural cells. Arocena DG; Iwahashi CK; Won N; Beilina A; Ludwig AL; Tassone F; Schwartz PH; Hagerman PJ Hum Mol Genet; 2005 Dec; 14(23):3661-71. PubMed ID: 16239243 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]