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Concise review: new paradigms for Down syndrome research using induced pluripotent stem cells: tackling complex human genetic diseaseSumoylation in Synaptic Function and DysfunctionDown Syndrome Cognitive Phenotypes Modeled in Mice Trisomic for All HSA 21 HomologuesWhat are genes "for" or where are traits "from"? What is the question?A Critical Evaluation of the Down Syndrome Diagnosis for LB1, Type Specimen of Homo floresiensisAneuploidy Causes Non-genetic IndividualityThe use of mouse models to understand and improve cognitive deficits in Down syndrome.Live imaging of neuronal connections by magnetic resonance: Robust transport in the hippocampal-septal memory circuit in a mouse model of Down syndrome.Trisomy for the Down syndrome 'critical region' is necessary but not sufficient for brain phenotypes of trisomic mice.The burden of trisomy 21 disrupts the proteostasis network in Down syndrome.A critical period in cortical interneuron neurogenesis in down syndrome revealed by human neural progenitor cells.A neural crest deficit in Down syndrome mice is associated with deficient mitotic response to Sonic hedgehogAbnormal microRNA expression in Ts65Dn hippocampus and whole blood: contributions to Down syndrome phenotypes.Genome-wide expression analysis in Down syndrome: insight into immunodeficiency.Cardiovascular development and survival during gestation in the Ts65Dn mouse model for Down syndrome.Integrated differential transcriptome maps of Acute Megakaryoblastic Leukemia (AMKL) in children with or without Down Syndrome (DS)Caries in Portuguese children with Down syndromeShotgun metabolomic profiles in maternal urine identify potential mass spectral markers of abnormal fetal biochemistry - dihydrouracil and progesterone in the metabolism of Down syndrome.The Down syndrome critical region regulates retinogeniculate refinementDisruption of neurogenesis and cortical development in transgenic mice misexpressing Olig2, a gene in the Down syndrome critical regionDosage compensation can buffer copy-number variation in wild yeastTrisomy 21 and early brain developmentThe power of comparative and developmental studies for mouse models of Down syndromeGene expression changes in the MAPK pathway in both Fragile X and Down syndrome human neural progenitor cells.Transcriptional consequences of aneuploidy.Reduced salivary flow and colonization by mutans streptococci in children with Down syndromePerturbation of fetal liver hematopoietic stem and progenitor cell development by trisomy 21Down syndrome critical region-1 is a transcriptional target of nuclear factor of activated T cells-c1 within the endocardium during heart development.Small-scale copy number variation and large-scale changes in gene expression.Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs.Haploinsufficiency of DNA Damage Response Genes and their Potential Influence in Human Genomic Disorders.Usp16: key controller of stem cells in Down syndromeThe "Down syndrome critical region" is sufficient in the mouse model to confer behavioral, neurophysiological, and synaptic phenotypes characteristic of Down syndromeAneuploidy: from a physiological mechanism of variance to Down syndrome.Animal models of human genetic diseases: do they need to be faithful to be useful?The identification of protein biomarkers for oxidative stress in Down syndrome.4-Hydroxy-2-nonenal, a reactive product of lipid peroxidation, and neurodegenerative diseases: a toxic combination illuminated by redox proteomics studiesWhole chromosome aneuploidy: big mutations drive adaptation by phenotypic leapThe impact of trisomy 21 on foetal haematopoiesis.Atypical aging in Down syndrome.
P2860
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P2860
description
2006 nî lūn-bûn
@nan
2006 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի մարտին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Understanding the basis for Down syndrome phenotypes.
@ast
Understanding the basis for Down syndrome phenotypes.
@en
type
label
Understanding the basis for Down syndrome phenotypes.
@ast
Understanding the basis for Down syndrome phenotypes.
@en
prefLabel
Understanding the basis for Down syndrome phenotypes.
@ast
Understanding the basis for Down syndrome phenotypes.
@en
P2860
P1433
P1476
Understanding the basis for Down syndrome phenotypes.
@en
P2093
Roger H Reeves
P2860
P356
10.1371/JOURNAL.PGEN.0020050
P577
2006-03-01T00:00:00Z