233 related articles for article (PubMed ID: 27245352)
1. Epigenetic dysregulation in the developing Down syndrome cortex.
El Hajj N; Dittrich M; Böck J; Kraus TF; Nanda I; Müller T; Seidmann L; Tralau T; Galetzka D; Schneider E; Haaf T
Epigenetics; 2016 Aug; 11(8):563-78. PubMed ID: 27245352
[TBL] [Abstract][Full Text] [Related]
2. Global hypermethylation in fetal cortex of Down syndrome due to DNMT3L overexpression.
Lu J; Mccarter M; Lian G; Esposito G; Capoccia E; Delli-Bovi LC; Hecht J; Sheen V
Hum Mol Genet; 2016 May; 25(9):1714-27. PubMed ID: 26911678
[TBL] [Abstract][Full Text] [Related]
3. Stable DNMT3L overexpression in SH-SY5Y neurons recreates a facet of the genome-wide Down syndrome DNA methylation signature.
Laufer BI; Gomez JA; Jianu JM; LaSalle JM
Epigenetics Chromatin; 2021 Mar; 14(1):13. PubMed ID: 33750431
[TBL] [Abstract][Full Text] [Related]
4. Whole genome bisulfite sequencing of Down syndrome brain reveals regional DNA hypermethylation and novel disorder insights.
Laufer BI; Hwang H; Vogel Ciernia A; Mordaunt CE; LaSalle JM
Epigenetics; 2019 Jul; 14(7):672-684. PubMed ID: 31010359
[TBL] [Abstract][Full Text] [Related]
5. Engineering DYRK1A overdosage yields Down syndrome-characteristic cortical splicing aberrations.
Toiber D; Azkona G; Ben-Ari S; Torán N; Soreq H; Dierssen M
Neurobiol Dis; 2010 Oct; 40(1):348-59. PubMed ID: 20600907
[TBL] [Abstract][Full Text] [Related]
6. Low-pass whole genome bisulfite sequencing of neonatal dried blood spots identifies a role for RUNX1 in Down syndrome DNA methylation profiles.
Laufer BI; Hwang H; Jianu JM; Mordaunt CE; Korf IF; Hertz-Picciotto I; LaSalle JM
Hum Mol Genet; 2021 Jan; 29(21):3465-3476. PubMed ID: 33001180
[TBL] [Abstract][Full Text] [Related]
7. Epigenome-wide base-resolution profiling of DNA methylation in chorionic villi of fetuses with Down syndrome by methyl-capture sequencing.
Lim JH; Kang YJ; Lee BY; Han YJ; Chung JH; Kim MY; Kim MH; Kim JW; Cho YH; Ryu HM
Clin Epigenetics; 2019 Dec; 11(1):180. PubMed ID: 31801612
[TBL] [Abstract][Full Text] [Related]
8. DYRK1A interacts with the REST/NRSF-SWI/SNF chromatin remodelling complex to deregulate gene clusters involved in the neuronal phenotypic traits of Down syndrome.
Lepagnol-Bestel AM; Zvara A; Maussion G; Quignon F; Ngimbous B; Ramoz N; Imbeaud S; Loe-Mie Y; Benihoud K; Agier N; Salin PA; Cardona A; Khung-Savatovsky S; Kallunki P; Delabar JM; Puskas LG; Delacroix H; Aggerbeck L; Delezoide AL; Delattre O; Gorwood P; Moalic JM; Simonneau M
Hum Mol Genet; 2009 Apr; 18(8):1405-14. PubMed ID: 19218269
[TBL] [Abstract][Full Text] [Related]
9. CpG sites with continuously increasing or decreasing methylation from early to late human fetal brain development.
Schneider E; Dittrich M; Böck J; Nanda I; Müller T; Seidmann L; Tralau T; Galetzka D; El Hajj N; Haaf T
Gene; 2016 Oct; 592(1):110-118. PubMed ID: 27468947
[TBL] [Abstract][Full Text] [Related]
10. Frequent long-range epigenetic silencing of protocadherin gene clusters on chromosome 5q31 in Wilms' tumor.
Dallosso AR; Hancock AL; Szemes M; Moorwood K; Chilukamarri L; Tsai HH; Sarkar A; Barasch J; Vuononvirta R; Jones C; Pritchard-Jones K; Royer-Pokora B; Lee SB; Owen C; Malik S; Feng Y; Frank M; Ward A; Brown KW; Malik K
PLoS Genet; 2009 Nov; 5(11):e1000745. PubMed ID: 19956686
[TBL] [Abstract][Full Text] [Related]
11. Meta-Analysis of DNA Methylation Datasets Shows Aberrant DNA Methylation of Thyroid Development or Function Genes in Down Syndrome.
Lauffer P; Zwaveling-Soonawala N; Li S; Bacalini MG; Naumova OY; Wiemels J; Boelen A; Henneman P; de Smith AJ; van Trotsenburg ASP
Thyroid; 2023 Jan; 33(1):53-62. PubMed ID: 36326208
[No Abstract] [Full Text] [Related]
12. Comparative genome-wide DNA methylation analysis in myocardial tissue from donors with and without Down syndrome.
Cejas RB; Wang J; Hageman-Blair R; Liu S; Blanco JG
Gene; 2021 Jan; 764():145099. PubMed ID: 32861879
[TBL] [Abstract][Full Text] [Related]
13. Constitutive Dyrk1A is abnormally expressed in Alzheimer disease, Down syndrome, Pick disease, and related transgenic models.
Ferrer I; Barrachina M; Puig B; Martínez de Lagrán M; Martí E; Avila J; Dierssen M
Neurobiol Dis; 2005 Nov; 20(2):392-400. PubMed ID: 16242644
[TBL] [Abstract][Full Text] [Related]
14. Widespread domain-like perturbations of DNA methylation in whole blood of Down syndrome neonates.
Henneman P; Bouman A; Mul A; Knegt L; van der Kevie-Kersemaekers AM; Zwaveling-Soonawala N; Meijers-Heijboer HEJ; van Trotsenburg ASP; Mannens MM
PLoS One; 2018; 13(3):e0194938. PubMed ID: 29601581
[TBL] [Abstract][Full Text] [Related]
15. DYRK1A-mediated Cyclin D1 Degradation in Neural Stem Cells Contributes to the Neurogenic Cortical Defects in Down Syndrome.
Najas S; Arranz J; Lochhead PA; Ashford AL; Oxley D; Delabar JM; Cook SJ; Barallobre MJ; Arbonés ML
EBioMedicine; 2015; 2(2):120-34. PubMed ID: 26137553
[TBL] [Abstract][Full Text] [Related]
16. [Molecular Mechanism Underlying Abnormal Differentiation of Neural Progenitor Cells in the Developing Down Syndrome Brain].
Kurabayashi N; Sanada K
Yakugaku Zasshi; 2017; 137(7):795-800. PubMed ID: 28674289
[TBL] [Abstract][Full Text] [Related]
17. Trisomy-driven overexpression of DYRK1A kinase in the brain of subjects with Down syndrome.
Dowjat WK; Adayev T; Kuchna I; Nowicki K; Palminiello S; Hwang YW; Wegiel J
Neurosci Lett; 2007 Feb; 413(1):77-81. PubMed ID: 17145134
[TBL] [Abstract][Full Text] [Related]
18. Identification of hypo- and hypermethylated genes related to atherosclerosis by a genome-wide analysis of DNA methylation.
Yamada Y; Nishida T; Horibe H; Oguri M; Kato K; Sawabe M
Int J Mol Med; 2014 May; 33(5):1355-63. PubMed ID: 24626634
[TBL] [Abstract][Full Text] [Related]
19. Trans effects of chromosome aneuploidies on DNA methylation patterns in human Down syndrome and mouse models.
Mendioroz M; Do C; Jiang X; Liu C; Darbary HK; Lang CF; Lin J; Thomas A; Abu-Amero S; Stanier P; Temkin A; Yale A; Liu MM; Li Y; Salas M; Kerkel K; Capone G; Silverman W; Yu YE; Moore G; Wegiel J; Tycko B
Genome Biol; 2015 Nov; 16():263. PubMed ID: 26607552
[TBL] [Abstract][Full Text] [Related]
20. DNA methylation changes in Down syndrome derived neural iPSCs uncover co-dysregulation of ZNF and HOX3 families of transcription factors.
Laan L; Klar J; Sobol M; Hoeber J; Shahsavani M; Kele M; Fatima A; Zakaria M; Annerén G; Falk A; Schuster J; Dahl N
Clin Epigenetics; 2020 Jan; 12(1):9. PubMed ID: 31915063
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
