Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome. - Wikidata - wikimedia - TriplyDB

Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome.

Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome.

http://www.wikidata.org/entity/Q47584862

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Down syndrome: searching for the genetic culprits Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice.Cranial neural crest ablation of Jagged1 recapitulates the craniofacial phenotype of Alagille syndrome patients A Critical Evaluation of the Down Syndrome Diagnosis for LB1, Type Specimen of Homo floresiensis Subtle Morphological Changes in the Mandible of Tabby Mice Revealed by Micro-CT Imaging and Elliptical Fourier Quantification.Trisomy for the Down syndrome 'critical region' is necessary but not sufficient for brain phenotypes of trisomic mice.Understanding the basis for Down syndrome phenotypes.Semi-automatic classification of skeletal morphology in genetically altered mice using flat-panel volume computed tomography Chromosome 21-derived microRNAs provide an etiological basis for aberrant protein expression in human Down syndrome brains.Gene network disruptions and neurogenesis defects in the adult Ts1Cje mouse model of Down syndrome.A neural crest deficit in Down syndrome mice is associated with deficient mitotic response to Sonic hedgehog GABAergic inhibition in visual cortical plasticity The mouse model of Down syndrome Ts65Dn presents visual deficits as assessed by pattern visual evoked potentials Gene expression profiling in a mouse model identifies fetal liver- and placenta-derived potential biomarkers for Down Syndrome screening.An aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypes.Functional transcriptome analysis of the postnatal brain of the Ts1Cje mouse model for Down syndrome reveals global disruption of interferon-related molecular networks Disruption of bone development and homeostasis by trisomy in Ts65Dn Down syndrome mice.Cardiovascular development and survival during gestation in the Ts65Dn mouse model for Down syndrome.Understanding mental retardation in Down's syndrome using trisomy 16 mouse models.A Sonic hedgehog (Shh) response deficit in trisomic cells may be a common denominator for multiple features of Down syndrome Oxidative Stress and Down Syndrome: A Route toward Alzheimer-Like Dementia.Trisomic and allelic differences influence phenotypic variability during development of Down syndrome mice.Comparative genomic sequence analysis of the human chromosome 21 Down syndrome critical region.Down syndrome and genetics - a case of linked histories.The power of comparative and developmental studies for mouse models of Down syndrome Highly penetrant myeloproliferative disease in the Ts65Dn mouse model of Down syndrome Chronic up-regulation of sonic hedgehog has little effect on postnatal craniofacial morphology of euploid and trisomic mice.Quantitative proteomics characterization of a mouse embryonic stem cell model of Down syndrome.Normal protein composition of synapses in Ts65Dn mice: a mouse model of Down syndrome.2001 William Allan Award Address. From Down syndrome to the "human" in "human genetics"A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome Negative feedback Inhibition of NFATc1 by DYRK1A regulates bone homeostasis.Aneuploidy: from a physiological mechanism of variance to Down syndrome.Nurturing brain plasticity: impact of environmental enrichment.Unraveling the complexity of neurodegeneration in brains of subjects with Down syndrome: insights from proteomics.Stem and progenitor cell dysfunction in human trisomies.Abnormal expression of the G-protein-activated inwardly rectifying potassium channel 2 (GIRK2) in hippocampus, frontal cortex, and substantia nigra of Ts65Dn mouse: a model of Down syndrome.Dentofacial and cranial changes in down syndrome.Apoptosis in Down's syndrome: lessons from studies of human and mouse models.The morphology of the mouse masticatory musculature.

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Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome.

http://www.wikidata.org/entity/Q47584862

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name

Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome.

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Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome.

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type

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Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome.

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Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome.

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Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome.

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Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome.

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American Journal of Medical Genetics Part A

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Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome

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Charles J Epstein

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Elaine J Carlson

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Joan T Richtsmeier

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Roger H Reeves

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P2860

The DNA sequence of human chromosome 21

All for one and one for all: condensations and the initiation of skeletal development

Euclidean distance matrix analysis: a coordinate-free approach for comparing biological shapes using landmark data.

A model for development and evolution of complex morphological structures.

Ts1Cje, a partial trisomy 16 mouse model for Down syndrome, exhibits learning and behavioral abnormalities.

A quantitative study of the face in Down's syndrome.

A coordinate-free approach to the analysis of growth patterns: models and theoretical considerations.

Euclidean distance matrix analysis: confidence intervals for form and growth differences.

Genetic dissection of region associated with behavioral abnormalities in mouse models for Down syndrome.

Parallels of craniofacial maldevelopment in Down syndrome and Ts65Dn mice.

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