These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
114 related articles for article (PubMed ID: 27243896)
1. Hematopoietic Stem Cells from Ts65Dn Mice Are Deficient in the Repair of DNA Double-Strand Breaks. Wang Y; Chang J; Shao L; Feng W; Luo Y; Chow M; Du W; Meng A; Zhou D Radiat Res; 2016 Jun; 185(6):630-7. PubMed ID: 27243896 [TBL] [Abstract][Full Text] [Related]
2. Highly penetrant myeloproliferative disease in the Ts65Dn mouse model of Down syndrome. Kirsammer G; Jilani S; Liu H; Davis E; Gurbuxani S; Le Beau MM; Crispino JD Blood; 2008 Jan; 111(2):767-75. PubMed ID: 17901249 [TBL] [Abstract][Full Text] [Related]
3. Defective hematopoietic stem cell and lymphoid progenitor development in the Ts65Dn mouse model of Down syndrome: potential role of oxidative stress. Lorenzo LP; Chen H; Shatynski KE; Clark S; Yuan R; Harrison DE; Yarowsky PJ; Williams MS Antioxid Redox Signal; 2011 Oct; 15(8):2083-94. PubMed ID: 21504363 [TBL] [Abstract][Full Text] [Related]
4. A sensitive and quantitative polymerase chain reaction-based cell free in vitro non-homologous end joining assay for hematopoietic stem cells. Shao L; Feng W; Lee KJ; Chen BP; Zhou D PLoS One; 2012; 7(3):e33499. PubMed ID: 22448248 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
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. Whole-body proton irradiation causes long-term damage to hematopoietic stem cells in mice. Chang J; Feng W; Wang Y; Luo Y; Allen AR; Koturbash I; Turner J; Stewart B; Raber J; Hauer-Jensen M; Zhou D; Shao L Radiat Res; 2015 Feb; 183(2):240-8. PubMed ID: 25635345 [TBL] [Abstract][Full Text] [Related]
9. The pattern of congenital heart defects arising from reduced Tbx5 expression is altered in a Down syndrome mouse model. Polk RC; Gergics P; Steimle JD; Li H; Moskowitz IP; Camper SA; Reeves RH BMC Dev Biol; 2015 Jul; 15():30. PubMed ID: 26208718 [TBL] [Abstract][Full Text] [Related]
10. Perinatal loss of Ts65Dn Down syndrome mice. Roper RJ; St John HK; Philip J; Lawler A; Reeves RH Genetics; 2006 Jan; 172(1):437-43. PubMed ID: 16172497 [TBL] [Abstract][Full Text] [Related]
11. Developmental instability of the cerebellum and its relevance to Down syndrome. Shapiro BL J Neural Transm Suppl; 2001; (61):11-34. PubMed ID: 11771737 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. Hippocampal hypocellularity in the Ts65Dn mouse originates early in development. Lorenzi HA; Reeves RH Brain Res; 2006 Aug; 1104(1):153-9. PubMed ID: 16828061 [TBL] [Abstract][Full Text] [Related]
14. Age-related impairment of olfactory bulb neurogenesis in the Ts65Dn mouse model of Down syndrome. Bianchi P; Bettini S; Guidi S; Ciani E; Trazzi S; Stagni F; Ragazzi E; Franceschini V; Bartesaghi R Exp Neurol; 2014 Jan; 251():1-11. PubMed ID: 24192151 [TBL] [Abstract][Full Text] [Related]
15. Involvement of Potassium and Cation Channels in Hippocampal Abnormalities of Embryonic Ts65Dn and Tc1 Trisomic Mice. Stern S; Segal M; Moses E EBioMedicine; 2015 Sep; 2(9):1048-62. PubMed ID: 26501103 [TBL] [Abstract][Full Text] [Related]
16. Normalization of Dyrk1A expression by AAV2/1-shDyrk1A attenuates hippocampal-dependent defects in the Ts65Dn mouse model of Down syndrome. Altafaj X; Martín ED; Ortiz-Abalia J; Valderrama A; Lao-Peregrín C; Dierssen M; Fillat C Neurobiol Dis; 2013 Apr; 52():117-27. PubMed ID: 23220201 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. MYBL2 Supports DNA Double Strand Break Repair in Hematopoietic Stem Cells. Bayley R; Blakemore D; Cancian L; Dumon S; Volpe G; Ward C; Almaghrabi R; Gujar J; Reeve N; Raghavan M; Higgs MR; Stewart GS; Petermann E; García P Cancer Res; 2018 Oct; 78(20):5767-5779. PubMed ID: 30082276 [TBL] [Abstract][Full Text] [Related]
19. Impaired plasticity at specific subset of striatal synapses in the Ts65Dn mouse model of Down syndrome. Di Filippo M; Tozzi A; Ghiglieri V; Picconi B; Costa C; Cipriani S; Tantucci M; Belcastro V; Calabresi P Biol Psychiatry; 2010 Apr; 67(7):666-71. PubMed ID: 19818432 [TBL] [Abstract][Full Text] [Related]
20. Disruption of bone development and homeostasis by trisomy in Ts65Dn Down syndrome mice. Blazek JD; Gaddy A; Meyer R; Roper RJ; Li J Bone; 2011 Feb; 48(2):275-80. PubMed ID: 20870049 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]