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Results: 1 to 20 of 33

1.

Whole genome SNP arrays as a potential diagnostic tool for the detection of characteristic chromosomal aberrations in renal epithelial tumors.

Monzon FA, Hagenkord JM, Lyons-Weiler MA, Balani JP, Parwani AV, Sciulli CM, Li J, Chandran UR, Bastacky SI, Dhir R.

Mod Pathol. 2008 May;21(5):599-608. doi: 10.1038/modpathol.2008.20. Epub 2008 Feb 8.

PMID:
18246049
[PubMed - indexed for MEDLINE]
Free Article
2.

Clinical genomics of renal epithelial tumors.

Hagenkord JM, Gatalica Z, Jonasch E, Monzon FA.

Cancer Genet. 2011 Jun;204(6):285-97. doi: 10.1016/j.cancergen.2011.06.001. Review.

PMID:
21763625
[PubMed - indexed for MEDLINE]
3.

Single nucleotide polymorphism array analysis of cancer.

Dutt A, Beroukhim R.

Curr Opin Oncol. 2007 Jan;19(1):43-9. Review.

PMID:
17133111
[PubMed - indexed for MEDLINE]
4.

[Genomic classification of renal cell tumors in adults].

Couturier J.

Ann Pathol. 2008 Oct;28(5):402-8. doi: 10.1016/j.annpat.2008.06.032. Epub 2008 Oct 9. Review. French.

PMID:
19068394
[PubMed - indexed for MEDLINE]
5.

High-resolution mapping of copy number aberrations and identification of target genes in hepatocellular carcinoma.

Midorikawa Y, Tang W, Sugiyama Y.

Biosci Trends. 2007 Aug;1(1):26-32. Review.

PMID:
20103863
[PubMed - indexed for MEDLINE]
Free Article
6.

[Genetics of renal tumors].

Oláh E, Jakab Z, Balogh E.

Orv Hetil. 2001 Jul 1;142(26):1367-73. Review. Hungarian.

PMID:
11478032
[PubMed - indexed for MEDLINE]
7.

[Molecular genetics and diagnosis of renal cell tumors].

Kovacs G.

Urologe A. 1999 Sep;38(5):433-41. Review. German.

PMID:
10501701
[PubMed - indexed for MEDLINE]
8.

Progress in concurrent analysis of loss of heterozygosity and comparative genomic hybridization utilizing high density single nucleotide polymorphism arrays.

Zhou X, Rao NP, Cole SW, Mok SC, Chen Z, Wong DT.

Cancer Genet Cytogenet. 2005 May;159(1):53-7. Review.

PMID:
15860358
[PubMed - indexed for MEDLINE]
9.

Array comparative genomic hybridization copy number profiling: a new tool for translational research in solid malignancies.

Costa JL, Meijer G, Ylstra B, Caldas C.

Semin Radiat Oncol. 2008 Apr;18(2):98-104. doi: 10.1016/j.semradonc.2007.10.005. Review.

PMID:
18314064
[PubMed - indexed for MEDLINE]
10.

Application of array-based whole genome scanning technologies as a cytogenetic tool in haematological malignancies.

Maciejewski JP, Tiu RV, O'Keefe C.

Br J Haematol. 2009 Sep;146(5):479-88. doi: 10.1111/j.1365-2141.2009.07757.x. Epub 2009 Jun 26. Review.

PMID:
19563474
[PubMed - indexed for MEDLINE]
11.

Genome-wide SNP analysis in cancer: leukemia shows the way.

Wang Y, Armstrong SA.

Cancer Cell. 2007 Apr;11(4):308-9. Review.

PMID:
17418407
[PubMed - indexed for MEDLINE]
Free Article
12.

Use of single nucleotide polymorphism-based mapping arrays to detect copy number changes and loss of heterozygosity in multiple myeloma.

Walker BA, Morgan GJ.

Clin Lymphoma Myeloma. 2006 Nov;7(3):186-91. Review.

PMID:
17229333
[PubMed - indexed for MEDLINE]
13.

Genomic assessment of pediatric acute leukemia.

Mullighan CG, Flotho C, Downing JR.

Cancer J. 2005 Jul-Aug;11(4):268-82. Review.

PMID:
16197717
[PubMed - indexed for MEDLINE]
14.

Application of oligonucleotides arrays for coincident comparative genomic hybridization, ploidy status and loss of heterozygosity studies in human cancers.

Cowell JK, Lo KC.

Methods Mol Biol. 2009;556:47-65. doi: 10.1007/978-1-60327-192-9_5. Review.

PMID:
19488871
[PubMed - indexed for MEDLINE]
15.

Molecular karyotyping: from microscope to SNP arrays.

Gijsbers AC, Ruivenkamp CA.

Horm Res Paediatr. 2011;76(3):208-13. doi: 10.1159/000330406. Epub 2011 Aug 25. Review.

PMID:
21865676
[PubMed - indexed for MEDLINE]
16.

The evolving concept of renal neoplasia: impact of emerging molecular and electron microscopic studies.

Picken MM.

Ultrastruct Pathol. 2005 May-Aug;29(3-4):277-82. Review.

PMID:
16036881
[PubMed - indexed for MEDLINE]
17.

Identification of structural aberrations in cancer by SNP array analysis.

Heinrichs S, Look AT.

Genome Biol. 2007;8(7):219. Review.

PMID:
17666119
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Clinical utility of single nucleotide polymorphism arrays.

Schwartz S.

Clin Lab Med. 2011 Dec;31(4):581-94, viii. doi: 10.1016/j.cll.2011.09.002. Review.

PMID:
22118738
[PubMed - indexed for MEDLINE]
19.

Use of interphase cytogenetics in demonstrating specific chromosomal aberrations in solid tumors--new insights in the pathogenesis of malignant melanoma and head and neck squamous cell carcinoma.

Poetsch M, Dittberner T, Woenckhaus C, Kleist B.

Histol Histopathol. 2000 Oct;15(4):1225-31. Review.

PMID:
11005247
[PubMed - indexed for MEDLINE]
20.

Whole genome scanning as a cytogenetic tool in hematologic malignancies.

Maciejewski JP, Mufti GJ.

Blood. 2008 Aug 15;112(4):965-74. doi: 10.1182/blood-2008-02-130435. Epub 2008 May 27. Review.

PMID:
18505780
[PubMed - indexed for MEDLINE]
Free PMC Article

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