202 related articles for article (PubMed ID: 33766516)
1. Novel insights from fetal and placental phenotyping in 3 mouse models of Down syndrome.
Adams AD; Hoffmann V; Koehly L; Guedj F; Bianchi DW
Am J Obstet Gynecol; 2021 Sep; 225(3):296.e1-296.e13. PubMed ID: 33766516
[TBL] [Abstract][Full Text] [Related]
2. Embryonic statistical analyses reveal 2 growth phenotypes in mouse models of Down syndrome.
Adams AD; Lin J; Bianchi DW; Bishop L; Sato T; Baxter LL; Hoffmann V; Koehly L; Guedj F
Am J Obstet Gynecol; 2024 Feb; 230(2):258.e1-258.e11. PubMed ID: 37544351
[TBL] [Abstract][Full Text] [Related]
3. Lifespan analysis of brain development, gene expression and behavioral phenotypes in the Ts1Cje, Ts65Dn and Dp(16)1/Yey mouse models of Down syndrome.
Aziz NM; Guedj F; Pennings JLA; Olmos-Serrano JL; Siegel A; Haydar TF; Bianchi DW
Dis Model Mech; 2018 Jun; 11(6):. PubMed ID: 29716957
[TBL] [Abstract][Full Text] [Related]
4. Visual discrimination and inhibitory control deficits in mouse models of Down syndrome: A pilot study using rodent touchscreen technology.
Siegel AE; Bianchi DW; Guedj F
J Neurosci Res; 2023 Apr; 101(4):492-507. PubMed ID: 36602162
[TBL] [Abstract][Full Text] [Related]
5. The fetal brain transcriptome and neonatal behavioral phenotype in the Ts1Cje mouse model of Down syndrome.
Guedj F; Pennings JL; Ferres MA; Graham LC; Wick HC; Miczek KA; Slonim DK; Bianchi DW
Am J Med Genet A; 2015 Sep; 167A(9):1993-2008. PubMed ID: 25975229
[TBL] [Abstract][Full Text] [Related]
6. Overlapping trisomies for human chromosome 21 orthologs produce similar effects on skull and brain morphology of Dp(16)1Yey and Ts65Dn mice.
Starbuck JM; Dutka T; Ratliff TS; Reeves RH; Richtsmeier JT
Am J Med Genet A; 2014 Aug; 164A(8):1981-1990. PubMed ID: 24788405
[TBL] [Abstract][Full Text] [Related]
7. Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes.
Olson LE; Roper RJ; Baxter LL; Carlson EJ; Epstein CJ; Reeves RH
Dev Dyn; 2004 Jul; 230(3):581-9. PubMed ID: 15188443
[TBL] [Abstract][Full Text] [Related]
8. Perinatal Natural History of the Ts1Cje Mouse Model of Down Syndrome: Growth Restriction, Early Mortality, Heart Defects, and Delayed Development.
Ferrés MA; Bianchi DW; Siegel AE; Bronson RT; Huggins GS; Guedj F
PLoS One; 2016; 11(12):e0168009. PubMed ID: 27930746
[TBL] [Abstract][Full Text] [Related]
9. Skeletal Deficits in Male and Female down Syndrome Model Mice Arise Independent of Normalized Dyrk1a Expression in Osteoblasts.
Thomas JR; Sloan K; Cave K; Wallace JM; Roper RJ
Genes (Basel); 2021 Oct; 12(11):. PubMed ID: 34828335
[TBL] [Abstract][Full Text] [Related]
10. Genetic dissection of region associated with behavioral abnormalities in mouse models for Down syndrome.
Sago H; Carlson EJ; Smith DJ; Rubin EM; Crnic LS; Huang TT; Epstein CJ
Pediatr Res; 2000 Nov; 48(5):606-13. PubMed ID: 11044479
[TBL] [Abstract][Full Text] [Related]
11. Non-trisomic homeobox gene expression during craniofacial development in the Ts65Dn mouse model of Down syndrome.
Billingsley CN; Allen JR; Baumann DD; Deitz SL; Blazek JD; Newbauer A; Darrah A; Long BC; Young B; Clement M; Doerge RW; Roper RJ
Am J Med Genet A; 2013 Aug; 161A(8):1866-74. PubMed ID: 23843306
[TBL] [Abstract][Full Text] [Related]
12. Molecular responses of the Ts65Dn and Ts1Cje mouse models of Down syndrome to MK-801.
Siddiqui A; Lacroix T; Stasko MR; Scott-McKean JJ; Costa AC; Gardiner KJ
Genes Brain Behav; 2008 Oct; 7(7):810-20. PubMed ID: 19125866
[TBL] [Abstract][Full Text] [Related]
13. Perturbation of the immune cells and prenatal neurogenesis by the triplication of the Erg gene in mouse models of Down syndrome.
Ishihara K; Shimizu R; Takata K; Kawashita E; Amano K; Shimohata A; Low D; Nabe T; Sago H; Alexander WS; Ginhoux F; Yamakawa K; Akiba S
Brain Pathol; 2020 Jan; 30(1):75-91. PubMed ID: 31206867
[TBL] [Abstract][Full Text] [Related]
14. Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling Down syndrome.
Duchon A; Raveau M; Chevalier C; Nalesso V; Sharp AJ; Herault Y
Mamm Genome; 2011 Dec; 22(11-12):674-84. PubMed ID: 21953411
[TBL] [Abstract][Full Text] [Related]
15. Synaptic and cognitive abnormalities in mouse models of Down syndrome: exploring genotype-phenotype relationships.
Belichenko PV; Kleschevnikov AM; Salehi A; Epstein CJ; Mobley WC
J Comp Neurol; 2007 Oct; 504(4):329-45. PubMed ID: 17663443
[TBL] [Abstract][Full Text] [Related]
16. The "Down syndrome critical region" is sufficient in the mouse model to confer behavioral, neurophysiological, and synaptic phenotypes characteristic of Down syndrome.
Belichenko NP; Belichenko PV; Kleschevnikov AM; Salehi A; Reeves RH; Mobley WC
J Neurosci; 2009 May; 29(18):5938-48. PubMed ID: 19420260
[TBL] [Abstract][Full Text] [Related]
17. Increased male reproductive success in Ts65Dn "Down syndrome" mice.
Moore CS; Hawkins C; Franca A; Lawler A; Devenney B; Das I; Reeves RH
Mamm Genome; 2010 Dec; 21(11-12):543-9. PubMed ID: 21110029
[TBL] [Abstract][Full Text] [Related]
18. Penetrance of Congenital Heart Disease in a Mouse Model of Down Syndrome Depends on a Trisomic Potentiator of a Disomic Modifier.
Li H; Edie S; Klinedinst D; Jeong JS; Blackshaw S; Maslen CL; Reeves RH
Genetics; 2016 Jun; 203(2):763-70. PubMed ID: 27029737
[TBL] [Abstract][Full Text] [Related]
19. Cardiovascular development and survival during gestation in the Ts65Dn mouse model for Down syndrome.
Lorandeau CG; Hakkinen LA; Moore CS
Anat Rec (Hoboken); 2011 Jan; 294(1):93-101. PubMed ID: 21157920
[TBL] [Abstract][Full Text] [Related]
20. Abnormal mineralization of the Ts65Dn Down syndrome mouse appendicular skeleton begins during embryonic development in a Dyrk1a-independent manner.
Blazek JD; Malik AM; Tischbein M; Arbones ML; Moore CS; Roper RJ
Mech Dev; 2015 May; 136():133-42. PubMed ID: 25556111
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
