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.
92 related articles for article (PubMed ID: 14872338)
1. Detection of DNA copy number abnormality by microarray expression analysis. Zhou X; Cole SW; Hu S; Wong DT Hum Genet; 2004 Apr; 114(5):464-7. PubMed ID: 14872338 [TBL] [Abstract][Full Text] [Related]
2. Dosage-dependent over-expression of genes in the trisomic region of Ts1Cje mouse model for Down syndrome. Amano K; Sago H; Uchikawa C; Suzuki T; Kotliarova SE; Nukina N; Epstein CJ; Yamakawa K Hum Mol Genet; 2004 Jul; 13(13):1333-40. PubMed ID: 15138197 [TBL] [Abstract][Full Text] [Related]
3. Identification of discrete chromosomal deletion by binary recursive partitioning of microarray differential expression data. Zhou X; Cole SW; Rao NP; Cheng Z; Li Y; McBride J; Wong DT J Med Genet; 2005 May; 42(5):416-9. PubMed ID: 15863671 [TBL] [Abstract][Full Text] [Related]
4. Specific transcriptional changes in human fetuses with autosomal trisomies. Altug-Teber O; Bonin M; Walter M; Mau-Holzmann UA; Dufke A; Stappert H; Tekesin I; Heilbronner H; Nieselt K; Riess O Cytogenet Genome Res; 2007; 119(3-4):171-84. PubMed ID: 18253026 [TBL] [Abstract][Full Text] [Related]
5. Engineering of Systematic Elimination of a Targeted Chromosome in Human Cells. Sato H; Kato H; Yamaza H; Masuda K; Nguyen HT; Pham TT; Han X; Hirofuji Y; Nonaka K Biomed Res Int; 2017; 2017():6037159. PubMed ID: 28401157 [TBL] [Abstract][Full Text] [Related]
6. The shaping and functional consequences of the dosage effect landscape in multiple myeloma. Samur MK; Shah PK; Wang X; Minvielle S; Magrangeas F; Avet-Loiseau H; Munshi NC; Li C BMC Genomics; 2013 Oct; 14():672. PubMed ID: 24088394 [TBL] [Abstract][Full Text] [Related]
7. Single cell transcriptome in aneuploidies reveals mechanisms of gene dosage imbalance. Stamoulis G; Garieri M; Makrythanasis P; Letourneau A; Guipponi M; Panousis N; Sloan-Béna F; Falconnet E; Ribaux P; Borel C; Santoni F; Antonarakis SE Nat Commun; 2019 Oct; 10(1):4495. PubMed ID: 31582743 [TBL] [Abstract][Full Text] [Related]
8. High-resolution analysis of DNA copy number alterations and gene expression in renal clear cell carcinoma. Yoshimoto T; Matsuura K; Karnan S; Tagawa H; Nakada C; Tanigawa M; Tsukamoto Y; Uchida T; Kashima K; Akizuki S; Takeuchi I; Sato F; Mimata H; Seto M; Moriyama M J Pathol; 2007 Dec; 213(4):392-401. PubMed ID: 17922474 [TBL] [Abstract][Full Text] [Related]
9. Gene-dosage effects in Down syndrome and trisomic mouse models. Gardiner K Genome Biol; 2004; 5(10):244. PubMed ID: 15461808 [TBL] [Abstract][Full Text] [Related]
10. Candidate glioblastoma development gene identification using concordance between copy number abnormalities and gene expression level changes. Lo KC; Rossi MR; LaDuca J; Hicks DG; Turpaz Y; Hawthorn L; Cowell JK Genes Chromosomes Cancer; 2007 Oct; 46(10):875-94. PubMed ID: 17620294 [TBL] [Abstract][Full Text] [Related]
11. [Detection of mosaic trisomy 9 missed by conventional cytogenetics using SNP-array and fluorescence in situ hybridization]. Luo Y; Chen S; Li H; Pan L; Shen M; Jin F; Xu C Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Aug; 31(4):469-71. PubMed ID: 25119912 [TBL] [Abstract][Full Text] [Related]
12. Partial trisomy 9q syndrome with a de novo tandem duplication of 9q22.2-q31.1. Utine GE; Melotte C; Vermeesch JR; Fryns JP Genet Couns; 2005; 16(4):407-12. PubMed ID: 16440884 [TBL] [Abstract][Full Text] [Related]
13. Transcriptome analysis of genetically matched human induced pluripotent stem cells disomic or trisomic for chromosome 21. Gonzales PK; Roberts CM; Fonte V; Jacobsen C; Stein GH; Link CD PLoS One; 2018; 13(3):e0194581. PubMed ID: 29584757 [TBL] [Abstract][Full Text] [Related]
14. Clonal heterogeneity in childhood myelodysplastic syndromes--challenge for the detection of chromosomal imbalances by array-CGH. Praulich I; Tauscher M; Göhring G; Glaser S; Hofmann W; Feurstein S; Flotho C; Lichter P; Niemeyer CM; Schlegelberger B; Steinemann D Genes Chromosomes Cancer; 2010 Oct; 49(10):885-900. PubMed ID: 20589934 [TBL] [Abstract][Full Text] [Related]
15. Resolution of trisomic mosaicism in prenatal diagnosis: estimated performance of a 50K SNP microarray. Cross J; Peters G; Wu Z; Brohede J; Hannan GN Prenat Diagn; 2007 Dec; 27(13):1197-204. PubMed ID: 17994637 [TBL] [Abstract][Full Text] [Related]
16. Genomic gains and losses influence expression levels of genes located within the affected regions: a study on acute myeloid leukemias with trisomy 8, 11, or 13, monosomy 7, or deletion 5q. Schoch C; Kohlmann A; Dugas M; Kern W; Hiddemann W; Schnittger S; Haferlach T Leukemia; 2005 Jul; 19(7):1224-8. PubMed ID: 15902281 [TBL] [Abstract][Full Text] [Related]
17. Primary and secondary transcriptional effects in the developing human Down syndrome brain and heart. Mao R; Wang X; Spitznagel EL; Frelin LP; Ting JC; Ding H; Kim JW; Ruczinski I; Downey TJ; Pevsner J Genome Biol; 2005; 6(13):R107. PubMed ID: 16420667 [TBL] [Abstract][Full Text] [Related]
18. Giemsa banding patterns of 13/14, 21/21 translocations, Philadelphia chromosome and trisomy 18. Taysi K; Hatiboğlu N; Halicioglu C; Say B Turk J Pediatr; 1972 Oct; 14(4):141-5. PubMed ID: 16295083 [No Abstract] [Full Text] [Related]
19. Broad copy neutral-loss of heterozygosity regions and rare recurring copy number abnormalities in normal karyotype-acute myeloid leukemia genomes. Barresi V; Romano A; Musso N; Capizzi C; Consoli C; Martelli MP; Palumbo G; Di Raimondo F; Condorelli DF Genes Chromosomes Cancer; 2010 Nov; 49(11):1014-23. PubMed ID: 20725993 [TBL] [Abstract][Full Text] [Related]
20. Error-pooling-based statistical methods for identifying novel temporal replication profiles of human chromosomes observed by DNA tiling arrays. Park T; Kim Y; Bekiranov S; Lee JK Nucleic Acids Res; 2007; 35(9):e69. PubMed ID: 17430969 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]