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3. 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]
4. Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects. Ramachandran D; Zeng Z; Locke AE; Mulle JG; Bean LJ; Rosser TC; Dooley KJ; Cua CL; Capone GT; Reeves RH; Maslen CL; Cutler DJ; Feingold E; Sherman SL; Zwick ME G3 (Bethesda); 2015 Jul; 5(10):1961-71. PubMed ID: 26194203 [TBL] [Abstract][Full Text] [Related]
5. Genetic variation in the COL6A1 region is associated with congenital heart defects in trisomy 21 (Down's syndrome). Davies GE; Howard CM; Farrer MJ; Coleman MM; Bennett LB; Cullen LM; Wyse RK; Burn J; Williamson R; Kessling AM Ann Hum Genet; 1995 Jul; 59(3):253-69. PubMed ID: 7486833 [TBL] [Abstract][Full Text] [Related]
6. Influence of allelic differences in Down syndrome. Roper RJ; Hawley L; Goodlett CR Prog Brain Res; 2020; 251():29-54. PubMed ID: 32057311 [TBL] [Abstract][Full Text] [Related]
7. Trisomy 21-associated increases in chromosomal instability are unmasked by comparing isogenic trisomic/disomic leukocytes from people with mosaic Down syndrome. Rafferty K; Archer KJ; Turner K; Brown R; Jackson-Cook C PLoS One; 2021; 16(7):e0254806. PubMed ID: 34283872 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Genetic modifiers predisposing to congenital heart disease in the sensitized Down syndrome population. Li H; Cherry S; Klinedinst D; DeLeon V; Redig J; Reshey B; Chin MT; Sherman SL; Maslen CL; Reeves RH Circ Cardiovasc Genet; 2012 Jun; 5(3):301-8. PubMed ID: 22523272 [TBL] [Abstract][Full Text] [Related]
14. Beta 1 integrin activation mediates adhesive differences between trisomy 21 and non-trisomic fibroblasts on type VI collagen. Jongewaard IN; Lauer RM; Behrendt DA; Patil S; Klewer SE Am J Med Genet; 2002 May; 109(4):298-305. PubMed ID: 11992484 [TBL] [Abstract][Full Text] [Related]
15. Restoration of DSCR1 to disomy in the trisomy 16 mouse model of Down syndrome does not correct cardiac or craniofacial development anomalies. Lange AW; Rothermel BA; Yutzey KE Dev Dyn; 2005 Jul; 233(3):954-63. PubMed ID: 15906378 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. Statistical multilocus methods for disequilibrium analysis in complex traits. Ott J; Hoh J Hum Mutat; 2001 Apr; 17(4):285-8. PubMed ID: 11295826 [TBL] [Abstract][Full Text] [Related]
18. Methods for genetic linkage analysis using trisomies. Feingold E; Lamb NE; Sherman SL Am J Hum Genet; 1995 Feb; 56(2):475-83. PubMed ID: 7847384 [TBL] [Abstract][Full Text] [Related]
19. Linkage disequilibrium mapping for complex disease genes. DeWan A; Klein RJ; Hoh J Methods Mol Biol; 2007; 376():85-107. PubMed ID: 17984540 [TBL] [Abstract][Full Text] [Related]
20. Chronic pro-oxidative state and mitochondrial dysfunctions are more pronounced in fibroblasts from Down syndrome foeti with congenital heart defects. Piccoli C; Izzo A; Scrima R; Bonfiglio F; Manco R; Negri R; Quarato G; Cela O; Ripoli M; Prisco M; Gentile F; Calì G; Pinton P; Conti A; Nitsch L; Capitanio N Hum Mol Genet; 2013 Mar; 22(6):1218-32. PubMed ID: 23257287 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]