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Copy Number

Title Body Taxonomy Tags Year
Towards a comprehensive structural variation map of an individual human genome

Pang AW, MacDonald JR, Pinto D, Wei J, Rafiq MA, Conrad DF, Park H, Hurles ME, Lee C, Venter JC, Kirkness EF, Levy S, Feuk L, Scherer SW.

Towards a comprehensive structural variation map of an individual human genome.


Genome Biol. 2010;11(5):R52


Copy Number 2010
Lung cancer genomes of smokers and never smokers harbor differential regions of copy number alteration

Thu KL, Chari R, Zhang W, MacAulay C, Gazdar AF, Lam A, Lam WL.
Lung cancer genomes of smokers and never smokers harbor differential regions of copy number alteration
. Cancer Prevention Research. 2010; 3:A15.


Copy Number 2010
Somatic Mutation Profiles of MSI and MSS Colorectal Cancer Identified by Whole Exome Next Generation Sequencing and...

Timmermann B, Kerick M, Roehr C, Fischer A, Isau M, Boerno ST, Wunderlich A, Barmeyer C, Seemann P, Koenig J, Lappe M, Kuss AW, Garshasbi M, Bertram L, Trappe K, Werber M, Herrmann BG, Zatloukal K, Lehrach H, Schweiger MR.

Somatic Mutation Profiles of MSI and MSS Colorectal Cancer Identified by Whole Exome Next Generation Sequencing and Bioinformatics Analysis.


PLoS One. 2010 Dec 22;5(12):e15661


Copy Number 2010
Gene amplification as double minutes or homogeneously staining regions in solid tumors: origin and structure

Storlazzi CT, Lonoce A, Guastadisegni MC, Trombetta D, D'Addabbo P, Daniele G, L'Abbate A, Macchia G, Surace C, Kok K, Ullmann R, Purgato S, Palumbo O, Carella M, Ambros PF, Rocchi M.

Gene amplification as double minutes or homogeneously staining regions in solid tumors: origin and structure.

Genome Res. 2010 Sep;20(9):1198-206


Copy Number 2010
Germline mutations of the CBL gene define a new genetic syndrome with predisposition to juvenile myelomonocytic leukaemia

Pérez B, Mechinaud F, Galambrun C, Ben Romdhane N, Isidor B, Philip N, Derain-Court J, Cassinat B, Lachenaud J, Kaltenbach S, Salmon A, Désirée C, Pereira S, Menot ML, Royer N, Fenneteau O, Baruchel A, Chomienne C, Verloes A, Cavé H.

Germline mutations of the CBL gene define a new genetic syndrome with predisposition to juvenile myelomonocytic leukaemia.

J Med Genet. 2010 Oct;47(10):686-91


Copy Number 2010
Whole-Genome Microarray Detects Deletions and Loss of Heterozygosity of Chromosome 3 Occurring Exclusively in Metastasizing ...

Lake SL, Coupland SE, Taktak AF, Damato BE.

Whole-Genome Microarray Detects Deletions and Loss of Heterozygosity of Chromosome 3 Occurring Exclusively in Metastasizing Uveal Melanoma

Invest Ophthalmol Vis Sci. 2010 Oct;51(10):4884-91


Copy Number 2010
The PAX5 gene is frequently rearranged in BCR-ABL1-positive acute lymphoblastic leukemia but is not associated with outcome...

Iacobucci I, Lonetti A, Paoloni F, Papayannidis C, Ferrari A, Storlazzi CT, Vignetti M, Cilloni D, Messa F, Guadagnuolo V, Paolini S, Elia L, Messina M, Vitale A, Meloni G, Soverini S, Pane F, Baccarani M, Foà R, Martinelli G.

The PAX5 gene is frequently rearranged in BCR-ABL1-positive acute lymphoblastic leukemia but is not associated with outcome. A report on behalf of the GIMEMA Acute Leukemia Working Party

Haematologica. 2010 Oct;95(10):1683-90.


Copy Number 2010
High resolution analysis of follicular lymphoma genomes reveals somatic recurrent sites of copy-neutral loss of heterozygosity..

Cheung, K-J.J., Delaney, A., Ben-Neriah, S., Schein, J., Lee, T., Shah, S.P., Cheung, D., Johnson, N.A., Mungall, A.J., Telenius, A., Lai, B., Boyle, M., Connors, J.M., Gascoyne, R.D., Marra, M.A., & Horsman, D.E. High resolution analysis of follicular lymphoma genomes reveals somatic recurrent sites of copy-neutral loss of heterozygosity and copy number alterations that target single genes. doi:10.1002/gcc.20780.


Copy Number 2010
Deletion of Keap1 in the Lung Attenuates Acute Cigarette Smoke-induced Oxidative Stress and Inflammation

Blake, D.J., Singh, A., Kombairaju, P., Malhotra, D., Mariani, T.J., Tuder, R.M., Gabrielson, E., & Biswal, S. Deletion of Keap1 in the Lung Attenuates Acute Cigarette Smoke-induced Oxidative Stress and Inflammation. Am. J. Respir. Cell Mol. Biol. 2010; 42:524-536. doi:10.1165/rcmb.2009-0054OC.


Copy Number 2010
Human Embryonic Stem Cells as Models for Aneuploid Chromosomal Syndromes

Biancotti, J-C., Narwani, K., Buehler, N., Mandefro, B., Golan-Lev, T., Yanuka, O., Clark, A.T., Hill, D., Benvenisty, N., & Lavon, N. Human Embryonic Stem Cells as Models for Aneuploid Chromosomal Syndromes. Stem Cells, 2010. doi:10.1002/stem.483.


Copy Number 2010

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