306 related articles for article (PubMed ID: 34828275)
1. Beyond Trinucleotide Repeat Expansion in Fragile X Syndrome: Rare Coding and Noncoding Variants in
Tekendo-Ngongang C; Grochowsky A; Solomon BD; Yano ST
Genes (Basel); 2021 Oct; 12(11):. PubMed ID: 34828275
[No Abstract] [Full Text] [Related]
2. Spontaneous rescue of a FMR1 repeat expansion and review of deletions in the FMR1 non-coding region.
Erbs E; Fenger-Grøn J; Jacobsen CM; Lildballe DL; Rasmussen M
Eur J Med Genet; 2021 Aug; 64(8):104244. PubMed ID: 34022415
[TBL] [Abstract][Full Text] [Related]
3. CGG-repeat dynamics and
Zhou Y; Kumari D; Sciascia N; Usdin K
Mol Autism; 2016; 7():42. PubMed ID: 27713816
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Epigenetic characterization of the FMR1 gene and aberrant neurodevelopment in human induced pluripotent stem cell models of fragile X syndrome.
Sheridan SD; Theriault KM; Reis SA; Zhou F; Madison JM; Daheron L; Loring JF; Haggarty SJ
PLoS One; 2011; 6(10):e26203. PubMed ID: 22022567
[TBL] [Abstract][Full Text] [Related]
6. Two novel intragenic variants in the FMR1 gene in patients with suspect clinical diagnosis of Fragile X syndrome and no CGG repeat expansion.
Carroll R; Shaw M; Arvio M; Gardner A; Kumar R; Hodgson B; Heron S; McKenzie F; Järvelä I; Gecz J
Eur J Med Genet; 2020 Oct; 63(10):104010. PubMed ID: 32688058
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. Fragile X syndrome: the FMR1 CGG repeat distribution among world populations.
Peprah E
Ann Hum Genet; 2012 Mar; 76(2):178-91. PubMed ID: 22188182
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Maternal FMR1 premutation allele expansion and contraction in fraternal twins.
Alfaro MP; Cohen M; Vnencak-Jones CL
Am J Med Genet A; 2013 Oct; 161A(10):2620-5. PubMed ID: 23949867
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Transcript levels of the intermediate size or grey zone fragile X mental retardation 1 alleles are raised, and correlate with the number of CGG repeats.
Loesch DZ; Bui QM; Huggins RM; Mitchell RJ; Hagerman RJ; Tassone F
J Med Genet; 2007 Mar; 44(3):200-4. PubMed ID: 16905681
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Association between IQ and FMR1 protein (FMRP) across the spectrum of CGG repeat expansions.
Kim K; Hessl D; Randol JL; Espinal GM; Schneider A; Protic D; Aydin EY; Hagerman RJ; Hagerman PJ
PLoS One; 2019; 14(12):e0226811. PubMed ID: 31891607
[TBL] [Abstract][Full Text] [Related]
19. [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]
20. Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients.
Grasso M; Faravelli F; Lo Nigro C; Chiurazzi P; Sperandeo MP; Argusti A; Pomponi MG; Lecora M; Sebastio GF; Perroni L; Andria G; Neri G; Bricarelli FD
Am J Med Genet; 1999 Jul; 85(3):311-6. PubMed ID: 10398249
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
