Reference health
Gene expression variation in Down's syndrome mice allows prioritization of candidate genes
34/34 checkable references clean · checked 2026-07-26
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
4 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.
The 34 checked references that resolve
resolves10.1016/j.pedhc.2006.02.006
Part II: Clinical Practice Guidelines for Adolescents and Young Adults With Down Syndrome: 12 to 21 Years
resolves10.1016/j.pedhc.2005.10.004
Part I: Clinical Practice Guidelines for Children With Down Syndrome From Birth to 12 Years
resolves10.1073/pnas.86.15.5958
Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome.
resolves10.1016/0888-7543(89)90065-7
Molecular genetic approach to the characterization of the “Down syndrome region” of chromosome 21
resolves10.1126/science.1098992
A Chromosome 21 Critical Region Does Not Cause Specific Down Syndrome Phenotypes
resolves10.1016/S0304-3940(98)00641-7
Hippocampal volume and neuronal number in Ts65Dn mice: a murine model of down syndrome
resolves10.1016/S0006-8993(00)01984-3
Synaptic deficit in the temporal cortex of partial trisomy 16 (Ts65Dn) mice
resolves10.1093/hmg/9.2.195
Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouse
resolves10.1073/pnas.181219298
Failed retrograde transport of NGF in a mouse model of Down's syndrome: Reversal of cholinergic neurodegenerative phenotypes following NGF infusion
resolves10.1016/0304-3940(95)12052-6
A behavioral assessment of Ts65Dn mice: a putative Down syndrome model
resolves10.1073/pnas.93.23.13333
Developmental abnormalities and age-related neurodegeneration in a mouse model of Down syndrome
resolves10.1016/S0166-4328(97)00116-2
Impaired spatial working and reference memory in segmental trisomy (Ts65Dn) mice
resolves10.1101/gr.2090904
Gene Expression From the Aneuploid Chromosome in a Trisomy Mouse Model of Down Syndrome
resolves10.1101/gr.1951304
Transcript Level Alterations Reflect Gene Dosage Effects Across Multiple Tissues in a Mouse Model of Down Syndrome
resolves10.1093/hmg/ddi033
The cerebellar transcriptome during postnatal development of the Ts1Cje mouse, a segmental trisomy model for Down syndrome
resolves10.1186/gb-2005-6-13-r107
Primary and secondary transcriptional effects in the developing human Down syndrome brain and heart
resolves10.1038/ng1955
Common genetic variants account for differences in gene expression among ethnic groups
resolves10.1016/S0888-7543(03)00035-1
Global up-regulation of chromosome 21 gene expression in the developing down syndrome brain
resolves10.1093/hmg/ddg217
Global disruption of the cerebellar transcriptome in a Down syndrome mouse model
resolves10.1093/hmg/ddi404
Gene expression variation and expression quantitative trait mapping of human chromosome 21 genes
resolves10.1126/science.1114535
An Aneuploid Mouse Strain Carrying Human Chromosome 21 with Down Syndrome Phenotypes
resolves10.1002/dvdy.20079
Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes
resolves10.1073/pnas.0510750103
Defective cerebellar response to mitogenic Hedgehog signaling in Down's syndrome mice
resolves10.1016/j.neuron.2006.05.022
Increased App Expression in a Mouse Model of Down's Syndrome Disrupts NGF Transport and Causes Cholinergic Neuron Degeneration
resolves10.1016/j.arr.2005.11.001
Alzheimer's disease and endocytic dysfunction: Clues from the Down syndrome-related proteins, DSCR1 and ITSN1
resolves10.1093/nar/gkl136
Analysis of pooled DNA samples on high density arrays without prior knowledge of differential hybridization rates
resolves10.1038/nature04559
Expression profiling in primates reveals a rapid evolution of human transcription factors
resolves10.1186/gb-2002-3-7-research0034
Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes
resolves10.1093/nar/29.23.e117
Statistical evaluation of differential expression on cDNA nylon arrays with replicated experiments
The 4 references without a DOI — listed, not checked
no DOI — not checkedEpstein CJ: Down syndrome (trisomy 21). The Metabolic and Molecular Bases of Inherited Disease. Edited by: Scriver CRE. 1995, New York, NY: McGraw-Hill, 749-794.
no DOI — not checkedDavisson MT, Schmidt C, Akeson EC: Segmental trisomy of murine chromosome 16: a new model system for studying Down syndrome. Prog Clin Biol Res. 1990, 360: 263-280.
no DOI — not checkedLorenzi H, Reeves RH: Hippocampal hypocellularity in the adult Ts65Dn mouse begins early in development. Brain Res.
no DOI — not checkedApplied Biosystems Homepage. [http://www.appliedbiosystems.com]
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