458 related articles for article (PubMed ID: 31409060)
1. Genetic Landscape of Rett Syndrome Spectrum: Improvements and Challenges.
Vidal S; Xiol C; Pascual-Alonso A; O'Callaghan M; Pineda M; Armstrong J
Int J Mol Sci; 2019 Aug; 20(16):. PubMed ID: 31409060
[TBL] [Abstract][Full Text] [Related]
2. Role of DNA Methyl-CpG-Binding Protein MeCP2 in Rett Syndrome Pathobiology and Mechanism of Disease.
Pejhan S; Rastegar M
Biomolecules; 2021 Jan; 11(1):. PubMed ID: 33429932
[TBL] [Abstract][Full Text] [Related]
3. Rett Syndrome, a Neurodevelopmental Disorder, Whole-Transcriptome, and Mitochondrial Genome Multiomics Analyses Identify Novel Variations and Disease Pathways.
Aldosary M; Al-Bakheet A; Al-Dhalaan H; Almass R; Alsagob M; Al-Younes B; AlQuait L; Mustafa OM; Bulbul M; Rahbeeni Z; Alfadhel M; Chedrawi A; Al-Hassnan Z; AlDosari M; Al-Zaidan H; Al-Muhaizea MA; AlSayed MD; Salih MA; AlShammari M; Faiyaz-Ul-Haque M; Chishti MA; Al-Harazi O; Al-Odaib A; Kaya N; Colak D
OMICS; 2020 Mar; 24(3):160-171. PubMed ID: 32105570
[TBL] [Abstract][Full Text] [Related]
4. Regulation mechanism and research progress of MeCP2 in Rett syndrome.
Yang W; Pan H
Yi Chuan; 2014 Jul; 36(7):625-30. PubMed ID: 25076025
[TBL] [Abstract][Full Text] [Related]
5. MECP2 mutations in Czech patients with Rett syndrome and Rett-like phenotypes: novel mutations, genotype-phenotype correlations and validation of high-resolution melting analysis for mutation scanning.
Zahorakova D; Lelkova P; Gregor V; Magner M; Zeman J; Martasek P
J Hum Genet; 2016 Jul; 61(7):617-25. PubMed ID: 26984561
[TBL] [Abstract][Full Text] [Related]
6. Rett syndrome and the urge of novel approaches to study MeCP2 functions and mechanisms of action.
Bedogni F; Rossi RL; Galli F; Cobolli Gigli C; Gandaglia A; Kilstrup-Nielsen C; Landsberger N
Neurosci Biobehav Rev; 2014 Oct; 46 Pt 2():187-201. PubMed ID: 24594195
[TBL] [Abstract][Full Text] [Related]
7. Exploring the possible link between MeCP2 and oxidative stress in Rett syndrome.
Filosa S; Pecorelli A; D'Esposito M; Valacchi G; Hajek J
Free Radic Biol Med; 2015 Nov; 88(Pt A):81-90. PubMed ID: 25960047
[TBL] [Abstract][Full Text] [Related]
8. MECP2 mutations and clinical correlations in Greek children with Rett syndrome and associated neurodevelopmental disorders.
Psoni S; Sofocleous C; Traeger-Synodinos J; Kitsiou-Tzeli S; Kanavakis E; Fryssira-Kanioura H
Brain Dev; 2012 Jun; 34(6):487-95. PubMed ID: 21982064
[TBL] [Abstract][Full Text] [Related]
9. RettBASE: Rett syndrome database update.
Krishnaraj R; Ho G; Christodoulou J
Hum Mutat; 2017 Aug; 38(8):922-931. PubMed ID: 28544139
[TBL] [Abstract][Full Text] [Related]
10. Rett syndrome and MeCP2.
Liyanage VR; Rastegar M
Neuromolecular Med; 2014 Jun; 16(2):231-64. PubMed ID: 24615633
[TBL] [Abstract][Full Text] [Related]
11. MeCP2 binds to non-CG methylated DNA as neurons mature, influencing transcription and the timing of onset for Rett syndrome.
Chen L; Chen K; Lavery LA; Baker SA; Shaw CA; Li W; Zoghbi HY
Proc Natl Acad Sci U S A; 2015 Apr; 112(17):5509-14. PubMed ID: 25870282
[TBL] [Abstract][Full Text] [Related]
12. Rett syndrome - biological pathways leading from MECP2 to disorder phenotypes.
Ehrhart F; Coort SL; Cirillo E; Smeets E; Evelo CT; Curfs LM
Orphanet J Rare Dis; 2016 Nov; 11(1):158. PubMed ID: 27884167
[TBL] [Abstract][Full Text] [Related]
13. Technological Improvements in the Genetic Diagnosis of Rett Syndrome Spectrum Disorders.
Xiol C; Heredia M; Pascual-Alonso A; Oyarzabal A; Armstrong J
Int J Mol Sci; 2021 Sep; 22(19):. PubMed ID: 34638716
[TBL] [Abstract][Full Text] [Related]
14. Towards a better diagnosis and treatment of Rett syndrome: a model synaptic disorder.
Banerjee A; Miller MT; Li K; Sur M; Kaufmann WE
Brain; 2019 Feb; 142(2):239-248. PubMed ID: 30649225
[TBL] [Abstract][Full Text] [Related]
15. Rett syndrome: new clinical and molecular insights.
Williamson SL; Christodoulou J
Eur J Hum Genet; 2006 Aug; 14(8):896-903. PubMed ID: 16865103
[TBL] [Abstract][Full Text] [Related]
16. Rett syndrome like phenotypes in the R255X Mecp2 mutant mouse are rescued by MECP2 transgene.
Pitcher MR; Herrera JA; Buffington SA; Kochukov MY; Merritt JK; Fisher AR; Schanen NC; Costa-Mattioli M; Neul JL
Hum Mol Genet; 2015 May; 24(9):2662-72. PubMed ID: 25634563
[TBL] [Abstract][Full Text] [Related]
17. MeCP2 dysfunction in Rett syndrome and related disorders.
Moretti P; Zoghbi HY
Curr Opin Genet Dev; 2006 Jun; 16(3):276-81. PubMed ID: 16647848
[TBL] [Abstract][Full Text] [Related]
18. De novo mutations in SCN1A are associated with classic Rett syndrome: a case report.
Henriksen MW; Ravn K; Paus B; von Tetzchner S; Skjeldal OH
BMC Med Genet; 2018 Oct; 19(1):184. PubMed ID: 30305042
[TBL] [Abstract][Full Text] [Related]
19. A RETT SYNDROME CASE WITH NOVEL NON-IDENTICAL MUTATION IN MECP2 GENE.
Güngör O; Kirik S; Cevizli D; Karaokur F; Ozer L; Uysal S; Dilber C
Genet Couns; 2015; 26(4):387-92. PubMed ID: 26852508
[TBL] [Abstract][Full Text] [Related]
20. Genetic landscape of Rett syndrome-like phenotypes revealed by whole exome sequencing.
Iwama K; Mizuguchi T; Takeshita E; Nakagawa E; Okazaki T; Nomura Y; Iijima Y; Kajiura I; Sugai K; Saito T; Sasaki M; Yuge K; Saikusa T; Okamoto N; Takahashi S; Amamoto M; Tomita I; Kumada S; Anzai Y; Hoshino K; Fattal-Valevski A; Shiroma N; Ohfu M; Moroto M; Tanda K; Nakagawa T; Sakakibara T; Nabatame S; Matsuo M; Yamamoto A; Yukishita S; Inoue K; Waga C; Nakamura Y; Watanabe S; Ohba C; Sengoku T; Fujita A; Mitsuhashi S; Miyatake S; Takata A; Miyake N; Ogata K; Ito S; Saitsu H; Matsuishi T; Goto YI; Matsumoto N
J Med Genet; 2019 Jun; 56(6):396-407. PubMed ID: 30842224
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
