399 related articles for article (PubMed ID: 21044947)
1. Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissues.
López Castel A; Nakamori M; Tomé S; Chitayat D; Gourdon G; Thornton CA; Pearson CE
Hum Mol Genet; 2011 Jan; 20(1):1-15. PubMed ID: 21044947
[TBL] [Abstract][Full Text] [Related]
2. Myotonic dystrophy type 1 (DM1) clinical subtypes and CTCF site methylation status flanking the CTG expansion are mutant allele length-dependent.
Morales F; Corrales E; Zhang B; Vásquez M; Santamaría-Ulloa C; Quesada H; Sirito M; Estecio MR; Monckton DG; Krahe R
Hum Mol Genet; 2021 Dec; 31(2):262-274. PubMed ID: 34432028
[TBL] [Abstract][Full Text] [Related]
3. Methylation of the CpG sites in the myotonic dystrophy locus does not correlate with CTG expansion size or with the congenital form of the disease.
Spits C; Seneca S; Hilven P; Liebaers I; Sermon K
J Med Genet; 2010 Oct; 47(10):700-3. PubMed ID: 20644219
[TBL] [Abstract][Full Text] [Related]
4. CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy.
Barbé L; Lanni S; López-Castel A; Franck S; Spits C; Keymolen K; Seneca S; Tomé S; Miron I; Letourneau J; Liang M; Choufani S; Weksberg R; Wilson MD; Sedlacek Z; Gagnon C; Musova Z; Chitayat D; Shannon P; Mathieu J; Sermon K; Pearson CE
Am J Hum Genet; 2017 Mar; 100(3):488-505. PubMed ID: 28257691
[TBL] [Abstract][Full Text] [Related]
5.
Visconti VV; Macrì E; D'Apice MR; Centofanti F; Massa R; Novelli G; Botta A
Int J Mol Sci; 2023 Jun; 24(12):. PubMed ID: 37373276
[TBL] [Abstract][Full Text] [Related]
6. Tissue- and age-specific DNA replication patterns at the CTG/CAG-expanded human myotonic dystrophy type 1 locus.
Cleary JD; Tomé S; López Castel A; Panigrahi GB; Foiry L; Hagerman KA; Sroka H; Chitayat D; Gourdon G; Pearson CE
Nat Struct Mol Biol; 2010 Sep; 17(9):1079-87. PubMed ID: 20711191
[TBL] [Abstract][Full Text] [Related]
7. Stable Longitudinal Methylation Levels at the CpG Sites Flanking the CTG Repeat of
Hildonen M; Knak KL; Dunø M; Vissing J; Tümer Z
Genes (Basel); 2020 Aug; 11(8):. PubMed ID: 32823742
[TBL] [Abstract][Full Text] [Related]
8. Replacement of the myotonic dystrophy type 1 CTG repeat with 'non-CTG repeat' insertions in specific tissues.
Axford MM; López-Castel A; Nakamori M; Thornton CA; Pearson CE
J Med Genet; 2011 Jul; 48(7):438-43. PubMed ID: 21622935
[TBL] [Abstract][Full Text] [Related]
9. DM1 CTG expansions affect insulin receptor isoforms expression in various tissues of transgenic mice.
Guiraud-Dogan C; Huguet A; Gomes-Pereira M; Brisson E; Bassez G; Junien C; Gourdon G
Biochim Biophys Acta; 2007 Dec; 1772(11-12):1183-91. PubMed ID: 17950578
[TBL] [Abstract][Full Text] [Related]
10. MSH2 knock-down shows CTG repeat stability and concomitant upstream demethylation at the DMPK locus in myotonic dystrophy type 1 human embryonic stem cells.
Franck S; Barbé L; Ardui S; De Vlaeminck Y; Allemeersch J; Dziedzicka D; Spits C; Vanroye F; Hilven P; Duqué G; Vermeesch JR; Gheldof A; Sermon K
Hum Mol Genet; 2021 Jan; 29(21):3566-3577. PubMed ID: 33242073
[TBL] [Abstract][Full Text] [Related]
11. Molecular, physiological, and motor performance defects in DMSXL mice carrying >1,000 CTG repeats from the human DM1 locus.
Huguet A; Medja F; Nicole A; Vignaud A; Guiraud-Dogan C; Ferry A; Decostre V; Hogrel JY; Metzger F; Hoeflich A; Baraibar M; Gomes-Pereira M; Puymirat J; Bassez G; Furling D; Munnich A; Gourdon G
PLoS Genet; 2012; 8(11):e1003043. PubMed ID: 23209425
[TBL] [Abstract][Full Text] [Related]
12. CTCF-binding sites flank CTG/CAG repeats and form a methylation-sensitive insulator at the DM1 locus.
Filippova GN; Thienes CP; Penn BH; Cho DH; Hu YJ; Moore JM; Klesert TR; Lobanenkov VV; Tapscott SJ
Nat Genet; 2001 Aug; 28(4):335-43. PubMed ID: 11479593
[TBL] [Abstract][Full Text] [Related]
13. Molecular genetics of congenital myotonic dystrophy.
Lanni S; Pearson CE
Neurobiol Dis; 2019 Dec; 132():104533. PubMed ID: 31326502
[TBL] [Abstract][Full Text] [Related]
14. Length-dependent CTG·CAG triplet-repeat expansion in myotonic dystrophy patient-derived induced pluripotent stem cells.
Du J; Campau E; Soragni E; Jespersen C; Gottesfeld JM
Hum Mol Genet; 2013 Dec; 22(25):5276-87. PubMed ID: 23933738
[TBL] [Abstract][Full Text] [Related]
15. MSH2 ATPase domain mutation affects CTG*CAG repeat instability in transgenic mice.
Tomé S; Holt I; Edelmann W; Morris GE; Munnich A; Pearson CE; Gourdon G
PLoS Genet; 2009 May; 5(5):e1000482. PubMed ID: 19436705
[TBL] [Abstract][Full Text] [Related]
16. 250 CTG repeats in DMPK is a threshold for correlation of expansion size and age at onset of juvenile-adult DM1.
Savić D; Rakocvic-Stojanovic V; Keckarevic D; Culjkovic B; Stojkovic O; Mladenovic J; Todorovic S; Apostolski S; Romac S
Hum Mutat; 2002 Feb; 19(2):131-9. PubMed ID: 11793472
[TBL] [Abstract][Full Text] [Related]
17. Progressive skeletal muscle weakness in transgenic mice expressing CTG expansions is associated with the activation of the ubiquitin-proteasome pathway.
Vignaud A; Ferry A; Huguet A; Baraibar M; Trollet C; Hyzewicz J; Butler-Browne G; Puymirat J; Gourdon G; Furling D
Neuromuscul Disord; 2010 May; 20(5):319-25. PubMed ID: 20346670
[TBL] [Abstract][Full Text] [Related]
18. Molecular, clinical, and muscle studies in myotonic dystrophy type 1 (DM1) associated with novel variant CCG expansions.
Santoro M; Masciullo M; Pietrobono R; Conte G; Modoni A; Bianchi ML; Rizzo V; Pomponi MG; Tasca G; Neri G; Silvestri G
J Neurol; 2013 May; 260(5):1245-57. PubMed ID: 23263591
[TBL] [Abstract][Full Text] [Related]
19. Unusual association of a unique CAG interruption in 5' of DM1 CTG repeats with intergenerational contractions and low somatic mosaicism.
Tomé S; Dandelot E; Dogan C; Bertrand A; Geneviève D; Péréon Y; ; Simon M; Bonnefont JP; Bassez G; Gourdon G
Hum Mutat; 2018 Jul; 39(7):970-982. PubMed ID: 29664219
[TBL] [Abstract][Full Text] [Related]
20. Individual-specific levels of CTG•CAG somatic instability are shared across multiple tissues in myotonic dystrophy type 1.
Morales F; Corrales E; Vásquez M; Zhang B; Fernández H; Alvarado F; Cortés S; Santamaría-Ulloa C; Initiative-Mmdbdi MMDBD; Krahe R; Monckton DG
Hum Mol Genet; 2023 Jan; 32(4):621-631. PubMed ID: 36099027
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
