237 related articles for article (PubMed ID: 24419320)
1. Chromosome fragility and the abnormal replication of the FMR1 locus in fragile X syndrome.
Yudkin D; Hayward BE; Aladjem MI; Kumari D; Usdin K
Hum Mol Genet; 2014 Jun; 23(11):2940-52. PubMed ID: 24419320
[TBL] [Abstract][Full Text] [Related]
2. The role of DNA damage response pathways in chromosome fragility in Fragile X syndrome.
Kumari D; Somma V; Nakamura AJ; Bonner WM; D'Ambrosio E; Usdin K
Nucleic Acids Res; 2009 Jul; 37(13):4385-92. PubMed ID: 19465392
[TBL] [Abstract][Full Text] [Related]
3. Establishment of FXS-A9 panel with a single human X chromosome from fragile X syndrome-associated individual.
Nakayama Y; Adachi K; Shioda N; Maeta S; Nanba E; Kugoh H
Exp Cell Res; 2021 Jan; 398(2):112419. PubMed ID: 33296661
[TBL] [Abstract][Full Text] [Related]
4. Mapping of an origin of DNA replication in the promoter of fragile X gene FMR1.
Brylawski BP; Chastain PD; Cohen SM; Cordeiro-Stone M; Kaufman DG
Exp Mol Pathol; 2007 Apr; 82(2):190-6. PubMed ID: 17196195
[TBL] [Abstract][Full Text] [Related]
5. Chromosome fragility at FRAXA in human cleavage stage embryos at risk for fragile X syndrome.
Verdyck P; Berckmoes V; De Vos A; Verpoest W; Liebaers I; Bonduelle M; De Rycke M
Am J Med Genet A; 2015 Oct; 167A(10):2306-13. PubMed ID: 25953684
[TBL] [Abstract][Full Text] [Related]
6. [Method for the Molecular Cytogenetic Visualization of Fragile Site FRAXA].
Bobokova TS; Lemskaya NA; Kolesnikova IS; Yudkin DV
Mol Biol (Mosk); 2017; 51(4):704-709. PubMed ID: 28900090
[TBL] [Abstract][Full Text] [Related]
7. Human chromosome fragility.
Lukusa T; Fryns JP
Biochim Biophys Acta; 2008 Jan; 1779(1):3-16. PubMed ID: 18078840
[TBL] [Abstract][Full Text] [Related]
8. Folate deficiency drives mitotic missegregation of the human
Bjerregaard VA; Garribba L; McMurray CT; Hickson ID; Liu Y
Proc Natl Acad Sci U S A; 2018 Dec; 115(51):13003-13008. PubMed ID: 30509972
[TBL] [Abstract][Full Text] [Related]
9. Mechanisms of Genome Instability in the Fragile X-Related Disorders.
Hayward BE; Usdin K
Genes (Basel); 2021 Oct; 12(10):. PubMed ID: 34681027
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Stability of the FMR1 CGG repeat in a Basque sample.
Arrieta I; Gil A; Nuñez T; Telez M; Martinez B; Criado B; Lostao C
Hum Biol; 1999 Feb; 71(1):55-68. PubMed ID: 9972098
[TBL] [Abstract][Full Text] [Related]
12. The DNA replication program is altered at the FMR1 locus in fragile X embryonic stem cells.
Gerhardt J; Tomishima MJ; Zaninovic N; Colak D; Yan Z; Zhan Q; Rosenwaks Z; Jaffrey SR; Schildkraut CL
Mol Cell; 2014 Jan; 53(1):19-31. PubMed ID: 24289922
[TBL] [Abstract][Full Text] [Related]
13. Instability of the FMR2 trinucleotide repeat region associated with expanded FMR1 alleles.
Brown TC; Tarleton JC; Go RC; Longshore JW; Descartes M
Am J Med Genet; 1997 Dec; 73(4):447-55. PubMed ID: 9415473
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. An origin of DNA replication in the promoter region of the human fragile X mental retardation (FMR1) gene.
Gray SJ; Gerhardt J; Doerfler W; Small LE; Fanning E
Mol Cell Biol; 2007 Jan; 27(2):426-37. PubMed ID: 17101793
[TBL] [Abstract][Full Text] [Related]
16. Reactivation of FMR1 by CRISPR/Cas9-Mediated Deletion of the Expanded CGG-Repeat of the Fragile X Chromosome.
Xie N; Gong H; Suhl JA; Chopra P; Wang T; Warren ST
PLoS One; 2016; 11(10):e0165499. PubMed ID: 27768763
[TBL] [Abstract][Full Text] [Related]
17. Distribution of CGG/GCC repeats at the FMR1 and FMR2 genes in an Indian population with mental retardation of unknown etiology.
Katikala L; Guruju MR; Madireddi S; Vallamkonda O; Vallamkonda N; Persha A; Spurgeon AM
Genet Test Mol Biomarkers; 2011 Apr; 15(4):281-4. PubMed ID: 21254876
[TBL] [Abstract][Full Text] [Related]
18. (Dys)function Follows Form: Nucleic Acid Structure, Repeat Expansion, and Disease Pathology in
Zhao X; Usdin K
Int J Mol Sci; 2021 Aug; 22(17):. PubMed ID: 34502075
[TBL] [Abstract][Full Text] [Related]
19. Instability of the CGG repeat at the FRAXA locus and variable phenotypic expression in a large fragile X pedigree.
Pintado E; de Diego Y; Hmadcha A; Carrasco M; Sierra J; Lucas M
J Med Genet; 1995 Nov; 32(11):907-8. PubMed ID: 8592340
[TBL] [Abstract][Full Text] [Related]
20. Human DNA Helicase B as a Candidate for Unwinding Secondary CGG Repeat Structures at the
Guler GD; Rosenwaks Z; Gerhardt J
Front Mol Neurosci; 2018; 11():138. PubMed ID: 29760651
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
