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Records 1 - 36 of 36
Publication Link Title
Journal |
Abstract | PubMed |
ABCA12 Is the Major Harlequin Ichthyosis Gene
Thomas AC et al. J Invest Dermatol. 126 (11): 2408-13, 2006
Abstract | PubMed | Amplified, Lost, and Fused Genes in 11q23-25 Amplicon in Acute Myeloid Leukemia, an Array-CGH Study
Tyybakinoja A et al. Genes Chromosomes Cancer. 45 (3): 257-64, 2006
Abstract | PubMed | An oligonucleotide based array-CGH system for detection of genome wide copy number changes including subtelomeric regions for genetic evaluation of mental retardation.
Toruner GA et al. Am J Med Genet A. 143(8): 824-9, 2007
Journal |
Abstract | PubMed |
Array CGH technologies and their applications to cancer genomes
Davies JJ et al. Chromosome Res. 13 (3): 237-48, 2005
Abstract | PubMed | Array comparative genomic hybridization analysis of chromosomal imbalances and their target genes in gastrointestinal stromal tumors.
Assamaki R et al. Genes Chromosomes Cancer. 46(6): 564-76, 2007
Journal |
Abstract | PubMed |
Array comparative genomic hybridization and its applications in cancer
Pinkel D et al. Nat Genet. 37 Suppl: S11-7, 2005
Abstract | PubMed | Both p16(Ink4a) and the p19(Arf)-p53 pathway constrain progression of pancreatic adenocarcinoma in the mouse.
Bardeesy N et al. Proc Natl Acad Sci U S A. 103(15): 5947-52, 2006
Abstract | PubMed | Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
Kallioniemi A et al. Science. 258 (5083): 818-21, 1992
Journal |
Abstract | PubMed |
Comparative genomic hybridization on mouse cDNA microarrays and its application to a murine lymphoma model
Sander S et al. Oncogene. 24 (40): 6101-7, 2005
Journal |
Abstract | PubMed |
Comparative genomic hybridization using oligonucleotide microarrays and total genomic DNA
Barrett MT et al. Proc Natl Acad Sci U S A. 101 (51): 17765-70, 2004
Abstract | PubMed | Cortical dysplasia of the left temporal lobe might explain severe expressive-language delay in patients with duplication of the Williams-Beuren locus.
Torniero C et al. European Journal of Human Genetics. [Epub ahead of print]: 2006
Abstract | PubMed | Deregulated CDC25A expression promotes mammary tumorigenesis with genomic instability.
Ray D et al. Cancer Research. 67(3): 984-91, 2007
Abstract | PubMed | Gene copy number changes in dermatofibrosarcoma protuberans - a fine-resolution study using array comparative genomic hybridization.
Kaur S et al. Cytogenet Genome Res. 115(3-4): 283-8, 2006
Abstract | PubMed | Gene copy number profiling of soft-tissue leiomyosarcomas by array-comparative genomic hybridization.
Larramendy ML et al. Cancer Genet Cytogenet. 169 (2): 94-101, 2006
Journal |
Abstract | PubMed |
Genome-wide analysis of DNA copy-number changes using cDNA microarrays
Pollack JR et al. Nat Genet. 23 (1): 41-6, 1999
Abstract | PubMed | Genome-Wide Oligonucleotide-Based Array Comparative Genome Hybridization Analysis of Non-Isolated Congenital Diaphragmatic Hernia.
Scott DA et al. Hum Mol Genet. 16(4): 424-30, 2007
Journal |
Abstract | PubMed |
Genomic microarrays in the spotlight
Mantripragada KK et al. Trends Genet. 20 (2): 87-94, 2004
Abstract | PubMed | Heterogeneity of mammary lesions represent molecular differences.
Namba R et al. BMC Cancer. 6: 275, 2006
Journal |
Abstract | PubMed |
High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays
Pinkel D et al. Nat Genet. 20 (2): 207-11, 1998
Journal |
Abstract | PubMed |
High resolution genomic analysis of sporadic breast cancer using array-based comparative genomic hybridization
Naylor TL et al. Breast Cancer Res. 7 (6): R1186-98, 2005
Journal |
Abstract | PubMed |
High-resolution analysis of gene copy number alterations in human prostate cancer using CGH on cDNA microarrays: impact of copy number on gene expression
Wolf M et al. Neoplasia. 6 (3): 240-7, 2004
Abstract | PubMed | High-resolution genomic profiles define distinct clinico-pathogenetic subgroups of multiple myeloma patients.
Carrasco DR et al. Cancer Cell. 9(4): 313-25, 2006
Journal |
Abstract | PubMed |
High-resolution genomic profiles of human lung cancer
Tonon G et al. Proc Natl Acad Sci U S A. 102 (27): 9625-30, 2005
Journal |
Abstract | PubMed |
High-resolution global profiling of genomic alterations with long oligonucleotide microarray
Brennan C et al. Cancer Res. 64 (14): 4744-8, 2004
Abstract | PubMed | Identification of disease genes by whole genome CGH arrays
Vissers LE et al. Hum Mol Genet. 14 Spec No. 2: R215-23, 2005
Abstract | PubMed | Marked genomic differences characterize primary and secondary glioblastoma subtypes and identify two distinct molecular and clinical secondary glioblastoma entities.
Maher EA et al. Cancer Research. 66(23): 11502-13, 2006
Journal |
Abstract | PubMed |
Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances
Solinas-Toldo S et al. Genes Chromosomes Cancer. 20 (4): 399-407, 1997
Journal |
Abstract | PubMed |
Microarray-based comparative genomic hybridization and its applications in human genetics
Oostlander AE et al. Clin Genet. 66 (6): 488-95, 2004
Abstract | PubMed | Oligonucleotide array-based comparative genomic hybridization (aCGH) of 90 neuroblastomas reveals aberration patterns closely associated with relapse pattern and outcome.
Spitz R et al. Genes Chromosomes Cancer. 45 (12): 1130-42, 2006
Abstract | PubMed | Oligonucleotide array-CGH reveals cryptic gene copy number alterations in karyotypically normal acute myeloid leukemia.
Tyybakinoja A et al. Leukemia. 21(3): 571-4, 2007
Abstract | PubMed | Periventricular heterotopia in fragile X syndrome.
Moro F et al. Neurology. 67 (4): 713-5, 2006
Abstract | PubMed | Principle and importance of using the array CGH in hematooncology]
Jarosova M et al. Cas Lek Cesk. 145 (1): 9-13, 2006
Abstract | PubMed | Resolving the resolution of array CGH.
Coe BP et al. Genomics. 89(5): 647-53, 2007
Abstract | PubMed | The cryptic chromosomal deletion del(11)(p12p13) as a new activation mechanism of LMO2 in pediatric T-cell acute lymphoblastic leukemia.
Van Vlierberghe P et al. Blood. 108 (10): 3520-9, 2006
Abstract | PubMed | TMPRSS2 Fusions with Oncogenic ETS Factors in Prostate Cancer Involve Unbalanced Genomic Rearrangements and Are Associated with HDAC1 and Epigenetic Reprogramming.
Iljin K et al. Cancer Res. 66 (21): 10242-6, 2006
Abstract | PubMed | Zoom-in CGH arrays for the characterization of variable breakpoint contiguous gene syndromes.
Johnston JJ et al. J Med Genet. [Epub ahead of print]: 2006