Altered expression of mitochondrial and extracellular matrix genes in the heart of human fetuses with chromosome 21 trisomy
about
Characterization of PTZ-induced seizure susceptibility in a down syndrome mouse model that overexpresses CSTBValidation of microarray data in human lymphoblasts shows a role of the ubiquitin-proteasome system and NF-kB in the pathogenesis of Down syndrome.Integrating gene and protein expression data with genome-scale metabolic networks to infer functional pathwaysChromosome 21-derived microRNAs provide an etiological basis for aberrant protein expression in human Down syndrome brains.Genome-wide association study of maternal and inherited loci for conotruncal heart defects.Neuropathological role of PI3K/Akt/mTOR axis in Down syndrome brain.Brain phenotype of transgenic mice overexpressing cystathionine β-synthase.The App-Runx1 region is critical for birth defects and electrocardiographic dysfunctions observed in a Down syndrome mouse model.Molecular signatures of cardiac defects in Down syndrome lymphoblastoid cell lines suggest altered ciliome and Hedgehog pathways.Genome-wide expression analysis in Down syndrome: insight into immunodeficiency.Potential contribution of SIM2 and ETS2 functional polymorphisms in Down syndrome associated malignancies.Expression signature as a biomarker for prenatal diagnosis of trisomy 21.Analysis of mtDNA, miR-155 and BACH1 expression in hearts from donors with and without Down syndrome.Defective mitochondrial function in vivo in skeletal muscle in adults with Down's syndrome: a 31P-MRS study.Opposite phenotypes of muscle strength and locomotor function in mouse models of partial trisomy and monosomy 21 for the proximal Hspa13-App region.Intracellular oxidant activity, antioxidant enzyme defense system, and cell senescence in fibroblasts with trisomy 21.Oxidative Stress and Down Syndrome: A Route toward Alzheimer-Like Dementia.Large-scale discovery of enhancers from human heart tissue.Dosage compensation can buffer copy-number variation in wild yeastExplore the dynamic alternation of gene PLAC4 mRNA expression levels in maternal plasma in second trimester for nonivasive detection of trisomy 21Trisomy 21 Alters DNA Methylation in Parent-of-Origin-Dependent and -Independent Manners.Screening key genes associated with congenital heart defects in Down syndrome based on differential expression network.Human gene copy number spectra analysis in congenital heart malformationsSystematic Tracking of Disrupted Modules Identifies Altered Pathways Associated with Congenital Heart Defects in Down Syndrome.Perturbation of fetal liver hematopoietic stem and progenitor cell development by trisomy 21Mitochondrial Factors and VACTERL Association-Related Congenital MalformationsDown's syndrome and myocardial reperfusion injury.An integrative computational analysis provides evidence for FBN1-associated network deregulation in trisomy 21An Integrated Human/Murine Transcriptome and Pathway Approach To Identify Prenatal Treatments For Down Syndrome.Trisomy 21 and Down syndrome: a short review.Mitochondrial dysfunction and Down's syndrome: is there a role for coenzyme Q(10) ?Haematopoietic development and leukaemia in Down syndrome.Stem and progenitor cell dysfunction in human trisomies.Down syndrome-A narrative review with a focus on anatomical features.Tail-anchored Protein Insertion in Mammals: FUNCTION AND RECIPROCAL INTERACTIONS OF THE TWO SUBUNITS OF THE TRC40 RECEPTOR.Impairment of F1F0-ATPase, adenine nucleotide translocator and adenylate kinase causes mitochondrial energy deficit in human skin fibroblasts with chromosome 21 trisomy.Spatiotemporal regulation of cAMP signaling controls the human trophoblast fusionDeficit of complex I activity in human skin fibroblasts with chromosome 21 trisomy and overproduction of reactive oxygen species by mitochondria: involvement of the cAMP/PKA signalling pathway.Systematic proteome and proteostasis profiling in human Trisomy 21 fibroblast cells.Overexpression of Chromosome 21 miRNAs May Affect Mitochondrial Function in the Hearts of Down Syndrome Fetuses.
P2860
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P2860
Altered expression of mitochondrial and extracellular matrix genes in the heart of human fetuses with chromosome 21 trisomy
description
2007 nî lūn-bûn
@nan
2007 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Altered expression of mitochon ...... ses with chromosome 21 trisomy
@ast
Altered expression of mitochon ...... ses with chromosome 21 trisomy
@en
Altered expression of mitochon ...... es with chromosome 21 trisomy.
@nl
type
label
Altered expression of mitochon ...... ses with chromosome 21 trisomy
@ast
Altered expression of mitochon ...... ses with chromosome 21 trisomy
@en
Altered expression of mitochon ...... es with chromosome 21 trisomy.
@nl
prefLabel
Altered expression of mitochon ...... ses with chromosome 21 trisomy
@ast
Altered expression of mitochon ...... ses with chromosome 21 trisomy
@en
Altered expression of mitochon ...... es with chromosome 21 trisomy.
@nl
P2093
P2860
P356
P1433
P1476
Altered expression of mitochon ...... ses with chromosome 21 trisomy
@en
P2093
Carlo Olla
Dario Paladini
Floriana Fabbrini
Lucio Nitsch
Maria D'Armiento
Mariastella Zannini
Paola D'Agostino
Rita Genesio
Rosa Negri
P2860
P2888
P356
10.1186/1471-2164-8-268
P407
P577
2007-08-07T00:00:00Z
P5875
P6179
1004241642