2p11

A chromosome band present on 2p
National Institutes of Health

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3 relations
Chromosome 2 Short ArmChromosomesFABP1 wt Allele

Papers overview

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Highly Cited
2005
Highly Cited
2005
Genome-wide array-based CGH for mantle cell lymphoma: identification of homozygous deletions of the proapoptotic gene BIM
Mantle cell lymphoma (MCL) is characterized by 11q13 chromosomal translocation and CCND1 overexpression, but additional genomic… Expand
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2005
2005
Punctuated duplication seeding events during the evolution of human chromosome 2p11.
Primate genomic sequence comparisons are becoming increasingly useful for elucidating the evolutionary history and organization… Expand
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Highly Cited
2004
Highly Cited
2004
Comprehensive whole genome array CGH profiling of mantle cell lymphoma model genomes.
Mantle cell lymphoma (MCL) is an aggressive non-Hodgkin's lymphoma with median patient survival times of approximately 3 years… Expand
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2004
2004
Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene
Developmental dyslexia, or reading disability, is a multigenic complex disease for which at least five loci, i.e. DYX1–3 and DYX5… Expand
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Highly Cited
2003
Highly Cited
2003
A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32.
Developmental dyslexia is a distinct learning disability with unexpected difficulty in learning to read despite adequate… Expand
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2002
2002
Interphase FISH assays for the detection of translocations with breakpoints in immunoglobulin light chain loci.
Many B-cell malignancies bear chromosomal translocations juxtaposing immunoglobulin (IG) genes with oncogenes, resulting in… Expand
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Highly Cited
2000
Highly Cited
2000
The mosaic structure of human pericentromeric DNA: a strategy for characterizing complex regions of the human genome.
The pericentromeric regions of human chromosomes pose particular problems for both mapping and sequencing. These difficulties are… Expand
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Highly Cited
1998
Highly Cited
1998
Frequent dysregulation of the c-maf proto-oncogene at 16q23 by translocation to an Ig locus in multiple myeloma.
Dysregulation of oncogenes by translocation to an IgH (14q32) or IgL (kappa, 2p11 or lambda, 22q11) locus is a frequent event in… Expand
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Review
1998
Review
1998
Masquerading repeats: paralogous pitfalls of the human genome.
In its most simple terms, the human genome consists of two distinct fractions of DNA: repetitive and unique sequence… Expand
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Highly Cited
1984
Highly Cited
1984
Chromosome study of Ewing's sarcoma (ES) cell lines. Consistency of a reciprocal translocation t(11;22)(q24;q12).
A detailed banded chromosome analysis was performed in five established Ewing's sarcoma (ES) cell lines originating from four… Expand
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