Results 111 to 120 of about 15,547 (147)

CaMKKβ regulates transcription factor Elf2 gene methylation to maintain endothelial junctional barrier integrity. [PDF]

iScience
Wang DM, Yang J, Ansari MO, Arbieva Z, Maienschein-Cline M, Natarajan V, Malik AB, Tiruppathi C.   +7 more
europepmc   +1 more source

Ethanol Alters DNMT1/3a/3b Expression Profile, Promotes Persistent DNA Hypomethylation in Human Brain Endothelial Cells and Impairs Late Cortical Angiogenesis. [PDF]

J Neurochem
Siqueira M, Barros M, Almeida PL, Dos Santos Heringer L, Mendonça HR, Gomes FCA, Stipursky J.   +6 more
europepmc   +1 more source

Immunomodulation of behavior impairment via spleen-specific targeting lipid nanoparticles in a MeCP2 transgenic mouse model. [PDF]

Sci Rep
Zhang S, Li Y, Yang B, Teymur A, Atrooz F, Majd S, Mohan C, Salim S, Wu T.   +8 more
europepmc   +1 more source

M2-exo promote orthodontic bone remodeling via the MeCP2-TCF20-HDAC1 axis. [PDF]

Stem Cell Res Ther
Chen M, Li Y, Yang Z, Chen M, Li J, Bao G, Ma L, Hu J.   +7 more
europepmc   +1 more source

MeCP2 at the crossroads of hypoxia, oxidative stress, and gene regulation in Rett syndrome. [PDF]

Epigenomics
Huang JL, Sharifi O, Yasui DH, LaSalle JM.   +3 more
europepmc   +1 more source

Double Genetic Diagnosis Involving MECP2 and EPHB4 in a Child with Neurodevelopmental Delay and Vascular Anomalies: A Case Report. [PDF]

Mol Syndromol
Sanri A, Mutlu MB.
europepmc   +1 more source

Dysregulated DNA Methylation in <i>Abca4^-/-</i> Retinal Pigment Epithelium: Insights into Early Stage of Stargardt Disease. [PDF]

Int J Mol Sci
Dave A, Tosevska A, Morselli M, Tom E, Pellegrini M, Skowronska-Krawczyk D, Radu RA.   +6 more
europepmc   +1 more source

Optimized clonal isolation and immortalization of Rett syndrome patient fibroblasts for in vitro modeling of MECP2 mutations. [PDF]

Sci Rep
Sarne V, Huber A, Beribisky AV, Hengstschläger M, Laccone F, Steinkellner H.   +5 more
europepmc   +1 more source

miR-199a functions downstream of MeCP2 in neurons of <i>MECP2</i> duplication syndrome models. [PDF]

iScience
Akaba Y, Takahashi S, Adachi S, Nishimura M, Suzuki K, Nakashima H, Nakashima K, Kira R, Chong PF, Sakai Y, Hayashi Y, Kushima I, Mori D, Arioka Y, Okumura H, Nakayama A, Mizuno S, Yamamoto T, Osakada F, Ozaki N, Tsujimura K.   +20 more
europepmc   +1 more source