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 Scholar Results 1 - 12 of 12 for MEIS1 and TP53. (0.06 seconds) 

[CITATION] Acute Lymphoblastic Leukemia
MG Alterations
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High-resolution detection and mapping of genomic DNA alterations in neuroblastoma.
YP Mosse, J Greshock, A Margolin, T Naylor, K Cole … - GENES, CHROMOSOMES & CANCER, 2005 - doi.wiley.com
... neuroblastoma-suppressor gene has been unequivocally identified, and inactivation
of tumor-suppressor genes commonly mutated in human cancer (TP53, RB1, CDKN2A ...
Web Search - ncbi.nlm.nih.gov - Get it from MIT Libraries

Analysis of genomic and proteomic data using advanced literature mining - Full text - MIT Libraries
Y Hu, LM Hines, H Weng, D Zuo, M Rivera, A … - J Proteome Res, 2003 - canis.uiuc.edu
... unofficial gene name/symbol false negative P53 instead of TP53 add all gene nicknames ...
PSEN2 S100A6 TNF REM LPL TP53 BDK IL6 KCNN3 PON1 plasminogen ...
Cited by 15 - View as HTML - Web Search - ncbi.nlm.nih.gov - ncbi.nlm.nih.gov

Neuroblastoma tumour genetics: clinical and biological aspects - Full text - MIT Libraries
N Bown - J Clin Pathol, 2001 - jcp.bmjjournals.com
... both MYCN and sequences derived from other sites—for example, MYCN plus MDM2 in
the 12q hsr of the LS cell line, 65 or MYCN plus the MEIS1 homeobox gene from ...
Cited by 25 - Web Search - doccancers.info - doccancers.info - ncbi.nlm.nih.gov - all 6 versions »

Microarrays as Cancer Keys: An Array of Possibilities - Full text - MIT Libraries
S Mohr, GD Leikauf, G Keith, BH Rihn - Journal of Clinical Oncology, 2002 - jco.org
... Wen WH, Bernstein L, Lescallett J, et al: Comparison of TP53 mutations identified
by ... Rozovskaia T, Feinstein E, Mor O, et al: Upregulation of Meis1 and HoxA9 ...
Cited by 30 - Web Search - dx.doi.org - jco.org - ncbi.nlm.nih.gov - all 5 versions »

Transcript map of the 3.7-Mb D19S112-D19S246 candidate tumor suppressor region on the long arm of … - Full text - MIT Libraries
C Hartmann, L Johnk, G Kitange, Y Wu, LK Ashworth, … - Cancer Res, 2002 - cancerres.aacrjournals.org
... suppressor gene, depending on type and location of the mutation (eg, TP53). ...
Interestingly, the highly similar family member Meis1 was isolated as a common site ...
Cited by 10 - Web Search - cancerres.aacrjournals.org - ncbi.nlm.nih.gov - ncbi.nlm.nih.gov

An Efficient and Robust Statistical Modeling Approach to Discover Differentially Expressed Genes … - Full text - MIT Libraries
JG Thomas, JM Olson, SJ Tapscott, LP Zhao - METHODS, 2001 - genome.org
... of clustered breakpoints in 17p11 and is not associated with coding TP53 mutations ...
Frequent co-expression of the HOXA9 and MEIS1 homeobox genes in human myeloid ...
Cited by 86 - Web Search - sullivan.bu.edu - vision.ime.usp.br - xobi.net - all 10 versions »

Bibliography Current World Literature
MR Baer, LA Pixley, LA Ford… - Current Opinion in Oncology, 2002 - co-oncology.com
... R, Blechman J, Nakamura T, Croce CM, et al.: Upregulation of Meis1 and HoxA9 ... Appelbaum
FR, Slovak ML, Willman CL, Radich JP: FLT3, RAS, and TP53 mutations in ...
Web Search - co-rheumatology.com - co-gastroenterology.com - co-endocrinology.com - all 9 versions »

SEROLOGIC ANALYSIS OF OVARIAN TUMOR ANTIGENS REVEALS A BIAS TOWARD ANTIGENS ENCODED ON 17q - Full text - MIT Libraries
N Urban, K O’Briant, BH Nelson - Int. J. Cancer, 2003 - doi.wiley.com
... n 20) H3907 p53 p53 TP53 2 4 0 H3907 Topoisomerase II TOP2A TOP2A 2 1 0 H3907
Putative helicase RUVBL RUVBL WH1P 2 0 0 H3907 Nucleolar ...
Cited by 6 - Web Search - ncbi.nlm.nih.gov

Gene expression profiling and its application in studies of haematological malignancy - Full text - MIT Libraries
M Hubank - British Journal of Haematology, 2004 - blackwell-synergy.com
Full Article. View/Print PDF article (438K). Download to reference manager.
British Journal of Haematology Volume 124 Issue 5 Page ...
Cited by 2 - Web Search - ncbi.nlm.nih.gov - ncbi.nlm.nih.gov

POSTER SESSION I
CD Baldus, SM Tanner, A Ruppert, SP Whitman, G … - springerlink.com
... on the following chromosome arms: 2p (n=2, hMSH2), 5q (n=9, APC), 7q (n=5, D5486,
c-met), 8q (n=8, Eto), 11q (n=6, MLL), 17q (n=6, BRCA1), 17p (n=3, TP53). ...
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[BOOK] Cytogenetic and molecular genetic changes in childhood acute leukaemias
T Niini - 2002 - ethesis.helsinki.fi
Page 1. Department of Medical Genetics Haartman Institute University of Helsinki
Finland Cytogenetic and Molecular Genetic Changes in Childhood Acute Leukaemias ...
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