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Results 1 to 25 of 43

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Gene amplification in cancerALBERTSON, Donna G.Trends in genetics (Regular ed.). 2006, Vol 22, Num 8, pp 447-455, issn 0168-9525, 9 p.Article

Array comparative genomic hybridization and its applications in cancerPINKEL, Daniel; ALBERTSON, Donna G.Nature genetics. 2005, Vol 37, pp S11-S17, issn 1061-4036, SUPArticle

Genomic microarrays in human genetic disease and cancerALBERTSON, Donna G; PINKEL, Daniel.Human molecular genetics (Print). 2003, Vol 12, pp R145-R152, issn 0964-6906, NS2Article

Profiling breast cancer by array CGHALBERTSON, Donna G.Breast cancer research and treatment. 2003, Vol 78, Num 3, pp 289-298, issn 0167-6806, 10 p.Article

Chromosome aberrations in solid tumorsALBERTSON, Donna G; COLLINS, Colin; MCCORMICK, Frank et al.Nature genetics. 2003, Vol 34, Num 4, pp 369-376, issn 1061-4036, 8 p.Article

Xq chromosome duplication in males : Clinical, cytogenetic and array CGH characterization of a new case and reviewCHENG, Sabrina F; RAUEN, Katherine A; PINKEL, Daniel et al.American journal of medical genetics. 2005, Vol 135A, Num 3, pp 308-313, issn 0148-7299, 6 p.Article

Additional patient with del(12)(q21.2q22): Further evidence for a candidate region for cardio-facio-cutaneous syndrome?RAUEN, Katherine A; ALBERTSON, Donna G; PINKEL, Daniel et al.American journal of medical genetics. 2002, Vol 110, Num 1, pp 51-56, issn 0148-7299Article

ErbB2 activation of ESX gene expressionNEVE, Richard M; YLSTRA, Bauke; CHANG, Chuan-Hsiung et al.Oncogene (Basingstoke). 2002, Vol 21, Num 24, pp 3934-3938, issn 0950-9232Article

FBXW7 and DNA copy number instabilityBYRD, Kristin N; HUEY, Bing; ROYDASGUPTA, Ritu et al.Breast cancer research and treatment. 2008, Vol 109, Num 1, pp 47-54, issn 0167-6806, 8 p.Article

Hidden Markov models approach to the analysis of array CGH dataFRIDLYAND, Jane; SNIJDERS, Antoine M; PINKEL, Dan et al.Journal of multivariate analysis. 2004, Vol 90, Num 1, pp 132-153, issn 0047-259X, 22 p.Article

Shaping of tumor and drug-resistant genomes by instability and selectionSNIJDERS, Antoine M; FRIDLYAND, Jane; MANS, Dorus A et al.Oncogene (Basingstoke). 2003, Vol 22, Num 28, pp 4370-4379, issn 0950-9232, 10 p.Article

Determinants of BRAF mutations in primary melanomasMALDONADO, Janet L; FRIDLYAND, Jane; PATEL, Hetal et al.Journal of the National Cancer Institute. 2003, Vol 95, Num 24, pp 1878-1880, issn 0027-8874, 3 p.Article

Integration of high-resolution array comparative genomic hybridization analysis of chromosome 16q with expression array data refines common regions of loss at 16q23-qter and identifies underlying candidate tumor suppressor genes in prostate cancerWATSON, J. E; DOGGETT, Norman A; KOWBEL, David et al.Oncogene (Basingstoke). 2004, Vol 23, Num 19, pp 3487-3494, issn 0950-9232, 8 p.Article

Whole genome scanning identifies genotypes associated with recurrence and metastasis in prostate tumorsPARIS, Pamela L; ANDAYA, Armann; ALBERTSON, Donna G et al.Human molecular genetics (Print). 2004, Vol 13, Num 13, pp 1303-1313, issn 0964-6906, 11 p.Article

Genome-wide-array-based comparative genomic hybridization reveals genetic homogeneity and frequent copy number increases encompassing CCNE1 in fallopian tube carcinomaSNIJDERS, Antoine M; NOWEE, Marlies E; FRIDLYAND, Jane et al.Oncogene (Basingstoke). 2003, Vol 22, Num 27, pp 4281-4286, issn 0950-9232, 6 p.Article

Ring 21 chromosome and a satellited 1p in the same patient: Novel origin for an ectopic NOREI, Anita; RAUEN, Katherine A; BLACK, Lauri D et al.American journal of medical genetics. 2003, Vol 120A, Num 3, pp 365-369, issn 0148-7299, 5 p.Article

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genomeSHARP, Andrew J; HANSEN, Sierra; FITZPATRICK, Carrie A et al.Nature genetics. 2006, Vol 38, Num 9, pp 1038-1042, issn 1061-4036, 5 p.Article

Interstitial deletion of chromosome 12q : Genotype-phenotype correlation of two patients utilizing array comparative genomic hybridizationKLEIN, Ophir D; COTTER, Philip D; SCHMIDT, Ann M et al.American journal of medical genetics. 2005, Vol 138A, Num 4, pp 349-354, issn 0148-7299, 6 p.Article

Rare amplicons implicate frequent deregulation of cell fate specification pathways in oral squamous cell carcinomaSNIJDERS, Antoine M; SCHMIDT, Brian L; FRIDLYAND, Jane et al.Oncogene (Basingstoke). 2005, Vol 24, Num 26, pp 4232-4242, issn 0950-9232, 11 p.Article

High-resolution analysis of paraffin-embedded and formalin-fixed prostate tumors using comparative genomic hybridization to genomic microarraysPARIS, Pamela L; ALBERTSON, Donna G; PINKEL, Daniel et al.The American journal of pathology. 2003, Vol 162, Num 3, pp 763-770, issn 0002-9440, 8 p.Article

High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGHBRUDER, Carl E. G; HIRVELÄ, Carina; ZUCMAN-ROSSI, Jessica et al.Human molecular genetics (Print). 2001, Vol 10, Num 3, pp 271-282, issn 0964-6906Article

Long-lived Min Mice Develop Advanced Intestinal Cancers through a Genetically Conservative PathwayHALBERG, Richard B; WAGGONER, Jesse; PETRINI, John H. J et al.Cancer research (Chicago, Ill.). 2009, Vol 69, Num 14, pp 5768-5775, issn 0008-5472, 8 p.Article

Deletion of chromosome 11q predicts response to anthracycline-based chemotherapy in early breast cancerCLIMENT, Joan; DIMITROW, Peter; FNDLYAND, Jane et al.Cancer research (Baltimore). 2007, Vol 67, Num 2, pp 818-826, issn 0008-5472, 9 p.Article

Raclb and reactive oxygen species mediate MMP-3- induced EMT and genomic instabilityRADISKY, Derek C; LEVY, Dinah D; WERB, Zena et al.Nature (London). 2005, Vol 436, Num 7047, pp 123-127, issn 0028-0836, 5 p.Article

A tiling resolution DNA microarray with complete coverage of the human genomeISHKANIAN, Adrian S; MALLOFF, Chad A; LING, Victor et al.Nature genetics. 2004, Vol 36, Num 3, pp 299-303, issn 1061-4036, 5 p.Article

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