345 related articles for article (PubMed ID: 24398265)
1. Altered neural activity in the 'when' pathway during temporal processing in fragile X premutation carriers.
Kim SY; Tassone F; Simon TJ; Rivera SM
Behav Brain Res; 2014 Mar; 261():240-8. PubMed ID: 24398265
[TBL] [Abstract][Full Text] [Related]
2. Altered neural activity of magnitude estimation processing in adults with the fragile X premutation.
Kim SY; Hashimoto R; Tassone F; Simon TJ; Rivera SM
J Psychiatr Res; 2013 Dec; 47(12):1909-16. PubMed ID: 24045061
[TBL] [Abstract][Full Text] [Related]
3. An fMRI study of the prefrontal activity during the performance of a working memory task in premutation carriers of the fragile X mental retardation 1 gene with and without fragile X-associated tremor/ataxia syndrome (FXTAS).
Hashimoto R; Backer KC; Tassone F; Hagerman RJ; Rivera SM
J Psychiatr Res; 2011 Jan; 45(1):36-43. PubMed ID: 20537351
[TBL] [Abstract][Full Text] [Related]
4. CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat size.
Ludwig AL; Espinal GM; Pretto DI; Jamal AL; Arque G; Tassone F; Berman RF; Hagerman PJ
Hum Mol Genet; 2014 Jun; 23(12):3228-38. PubMed ID: 24463622
[TBL] [Abstract][Full Text] [Related]
5. Age- and CGG repeat-related slowing of manual movement in fragile X carriers: A prodrome of fragile X-associated tremor ataxia syndrome?
Shickman R; Famula J; Tassone F; Leehey M; Ferrer E; Rivera SM; Hessl D
Mov Disord; 2018 Apr; 33(4):628-636. PubMed ID: 29389022
[TBL] [Abstract][Full Text] [Related]
6. Cerebral protein synthesis in a knockin mouse model of the fragile X premutation.
Qin M; Huang T; Liu Z; Kader M; Burlin T; Xia Z; Zeidler Z; Hukema RK; Smith CB
ASN Neuro; 2014; 6(5):. PubMed ID: 25290064
[TBL] [Abstract][Full Text] [Related]
7. Fragile X-associated tremor/ataxia syndrome: influence of the FMR1 gene on motor fiber tracts in males with normal and premutation alleles.
Wang JY; Hessl D; Schneider A; Tassone F; Hagerman RJ; Rivera SM
JAMA Neurol; 2013 Aug; 70(8):1022-9. PubMed ID: 23753897
[TBL] [Abstract][Full Text] [Related]
8. Unstable mutations in the FMR1 gene and the phenotypes.
Loesch D; Hagerman R
Adv Exp Med Biol; 2012; 769():78-114. PubMed ID: 23560306
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. Immune dysregulation as a cause of autoinflammation in fragile X premutation carriers: link between FMRI CGG repeat number and decreased cytokine responses.
Careaga M; Rose D; Tassone F; Berman RF; Hagerman R; Ashwood P
PLoS One; 2014; 9(4):e94475. PubMed ID: 24718368
[TBL] [Abstract][Full Text] [Related]
11. Age-related functional brain changes in
Brown SSG; Basu S; Whalley HC; Kind PC; Stanfield AC
Neuroimage Clin; 2018; 17():761-767. PubMed ID: 29527483
[TBL] [Abstract][Full Text] [Related]
12. Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation.
Hessl D; Tassone F; Loesch DZ; Berry-Kravis E; Leehey MA; Gane LW; Barbato I; Rice C; Gould E; Hall DA; Grigsby J; Wegelin JA; Harris S; Lewin F; Weinberg D; Hagerman PJ; Hagerman RJ
Am J Med Genet B Neuropsychiatr Genet; 2005 Nov; 139B(1):115-21. PubMed ID: 16184602
[TBL] [Abstract][Full Text] [Related]
13. Spatiotemporal processing deficits in female CGG KI mice modeling the fragile X premutation.
Borthwell RM; Hunsaker MR; Willemsen R; Berman RF
Behav Brain Res; 2012 Jul; 233(1):29-34. PubMed ID: 22561129
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. FMR1 CGG repeat length predicts motor dysfunction in premutation carriers.
Leehey MA; Berry-Kravis E; Goetz CG; Zhang L; Hall DA; Li L; Rice CD; Lara R; Cogswell J; Reynolds A; Gane L; Jacquemont S; Tassone F; Grigsby J; Hagerman RJ; Hagerman PJ
Neurology; 2008 Apr; 70(16 Pt 2):1397-402. PubMed ID: 18057320
[TBL] [Abstract][Full Text] [Related]
16. Expression of the FMR1 gene.
Tassone F; Hagerman PJ
Cytogenet Genome Res; 2003; 100(1-4):124-8. PubMed ID: 14526172
[TBL] [Abstract][Full Text] [Related]
17. The role of AGG interruptions in the transcription of FMR1 premutation alleles.
Yrigollen CM; Tassone F; Durbin-Johnson B; Tassone F
PLoS One; 2011; 6(7):e21728. PubMed ID: 21818263
[TBL] [Abstract][Full Text] [Related]
18. Mosaicism for a full mutation, premutation, and deletion of the CGG repeats results in 22% FMRP and elevated FMR1 mRNA levels in a high-functioning fragile X male.
Han XD; Powell BR; Phalin JL; Chehab FF
Am J Med Genet A; 2006 Jul; 140(13):1463-71. PubMed ID: 16761284
[TBL] [Abstract][Full Text] [Related]
19. Examination of FMR1 transcript and protein levels among 74 premutation carriers.
Peprah E; He W; Allen E; Oliver T; Boyne A; Sherman SL
J Hum Genet; 2010 Jan; 55(1):66-8. PubMed ID: 19927162
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
