189 related articles for article (PubMed ID: 30396881)
1. The G-rich Repeats in
Abu Diab M; Mor-Shaked H; Cohen E; Cohen-Hadad Y; Ram O; Epsztejn-Litman S; Eiges R
Genetics; 2018 Dec; 210(4):1239-1252. PubMed ID: 30396881
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Processing of double-R-loops in (CAG)·(CTG) and C9orf72 (GGGGCC)·(GGCCCC) repeats causes instability.
Reddy K; Schmidt MH; Geist JM; Thakkar NP; Panigrahi GB; Wang YH; Pearson CE
Nucleic Acids Res; 2014; 42(16):10473-87. PubMed ID: 25147206
[TBL] [Abstract][Full Text] [Related]
5. CGG Repeat-Induced FMR1 Silencing Depends on the Expansion Size in Human iPSCs and Neurons Carrying Unmethylated Full Mutations.
Brykczynska U; Pecho-Vrieseling E; Thiemeyer A; Klein J; Fruh I; Doll T; Manneville C; Fuchs S; Iazeolla M; Beibel M; Roma G; Naumann U; Kelley N; Oakeley EJ; Mueller M; Gomez-Mancilla B; Bühler M; Tabolacci E; Chiurazzi P; Neri G; Bouwmeester T; Di Giorgio FP; Fodor BD
Stem Cell Reports; 2016 Dec; 7(6):1059-1071. PubMed ID: 27840045
[TBL] [Abstract][Full Text] [Related]
6. Regional FMRP deficits and large repeat expansions into the full mutation range in a new Fragile X premutation mouse model.
Entezam A; Biacsi R; Orrison B; Saha T; Hoffman GE; Grabczyk E; Nussbaum RL; Usdin K
Gene; 2007 Jun; 395(1-2):125-34. PubMed ID: 17442505
[TBL] [Abstract][Full Text] [Related]
7. C9orf72 Repeat Expansion Frequency among Patients with Huntington Disease Genetic Testing.
Ida CM; Butz ML; Lundquist PA; Dawson DB
Neurodegener Dis; 2018; 18(5-6):239-253. PubMed ID: 30336474
[TBL] [Abstract][Full Text] [Related]
8. Comparative analysis of DNA methylation in transgenic mice with unstable CGG repeats from FMR1 gene.
Alam MP; Datta S; Majumdar S; Mehta AK; Baskaran S; Gulati N; Brahmachari V
Epigenetics; 2010 Apr; 5(3):241-8. PubMed ID: 20364100
[TBL] [Abstract][Full Text] [Related]
9. Fully expanded FMR1 CGG repeats exhibit a length- and differentiation-dependent instability in cell hybrids that is independent of DNA methylation.
Burman RW; Popovich BW; Jacky PB; Turker MS
Hum Mol Genet; 1999 Nov; 8(12):2293-302. PubMed ID: 10545610
[TBL] [Abstract][Full Text] [Related]
10. Quadruplex formation by both G-rich and C-rich DNA strands of the C9orf72 (GGGGCC)8•(GGCCCC)8 repeat: effect of CpG methylation.
Zamiri B; Mirceta M; Bomsztyk K; Macgregor RB; Pearson CE
Nucleic Acids Res; 2015 Nov; 43(20):10055-64. PubMed ID: 26432832
[TBL] [Abstract][Full Text] [Related]
11. The Emerging Role of DNA Damage in the Pathogenesis of the C9orf72 Repeat Expansion in Amyotrophic Lateral Sclerosis.
Konopka A; Atkin JD
Int J Mol Sci; 2018 Oct; 19(10):. PubMed ID: 30322030
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Increase of FMRP expression, raised levels of FMR1 mRNA, and clonal selection in proliferating cells with unmethylated fragile X repeat expansions: a clue to the sex bias in the transmission of full mutations?
Salat U; Bardoni B; Wöhrle D; Steinbach P
J Med Genet; 2000 Nov; 37(11):842-50. PubMed ID: 11073538
[TBL] [Abstract][Full Text] [Related]
14. Contraction of fully expanded FMR1 alleles to the normal range: predisposing haplotype or rare events?
Maia N; Loureiro JR; Oliveira B; Marques I; Santos R; Jorge P; Martins S
J Hum Genet; 2017 Feb; 62(2):269-275. PubMed ID: 27784894
[TBL] [Abstract][Full Text] [Related]
15. A methylation PCR approach for detection of fragile X syndrome.
Panagopoulos I; Lassen C; Kristoffersson U; Aman P
Hum Mutat; 1999; 14(1):71-9. PubMed ID: 10447261
[TBL] [Abstract][Full Text] [Related]
16. Stable DNA methylation boundaries and expanded trinucleotide repeats: role of DNA insertions.
Naumann A; Kraus C; Hoogeveen A; Ramirez CM; Doerfler W
J Mol Biol; 2014 Jul; 426(14):2554-66. PubMed ID: 24816393
[TBL] [Abstract][Full Text] [Related]
17. Reversion of FMR1 Methylation and Silencing by Editing the Triplet Repeats in Fragile X iPSC-Derived Neurons.
Park CY; Halevy T; Lee DR; Sung JJ; Lee JS; Yanuka O; Benvenisty N; Kim DW
Cell Rep; 2015 Oct; 13(2):234-41. PubMed ID: 26440889
[TBL] [Abstract][Full Text] [Related]
18. 1,3-Di(quinolin-2-yl)guanidine binds to GGCCCC hexanucleotide repeat DNA in C9ORF72.
Shibata T; Murakami E; Nakatani K
Bioorg Med Chem Lett; 2018 Aug; 28(14):2364-2368. PubMed ID: 29929880
[TBL] [Abstract][Full Text] [Related]
19. Stress-induced acidification may contribute to formation of unusual structures in C9orf72-repeats.
Zamiri B; Mirceta M; Abu-Ghazalah R; Wold MS; Pearson CE; Macgregor RB
Biochim Biophys Acta Gen Subj; 2018 Jun; 1862(6):1482-1491. PubMed ID: 29550431
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
