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12p13

A chromosome band present on 12p
National Institutes of Health

Related topics

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17 relations
AICDA wt AlleleCD27 wt AlleleCHD4 wt AlleleChromosome 12 Short Arm

Papers overview

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Highly Cited
2011
Highly Cited
2011
Genomic 5-hydroxymethylcytosine levels correlate with TET2 mutations and a distinct global gene expression pattern in secondary acute myeloid leukemia
Genomic 5-hydroxymethylcytosine levels correlate with TET2 mutations and a distinct global gene expression pattern in secondary… 
2011
2011
Genetic Variant on Chromosome 12p13 Does Not Show Association to Ischemic Stroke in 3 Swedish Case-Control Studies
Background and Purpose— In a genome-wide association study and subsequent case-control studies, the single-nucleotide… 
Highly Cited
2005
Highly Cited
2005
Multiple Retropseudogenes from Pluripotent Cell-specific Gene Expression Indicates a Potential Signature for Novel Gene Identification*
Oct4, Nanog, and Stella are transcription factors specifically expressed in embryonic stem (ES) cells and germ lineage cells that… 
2001
2001
Chromosomal instability in chromosome band 12p13: multiple breaks leading to complex rearrangements including cytogenetically undetectable sub-clones
During fluorescence in situ hybridization (FISH) analysis of metaphase cells from 70 patients with lymphoid and myeloid… 
1999
1999
Cyclin D2 promoter disrupted by t(12;22)(p13;q11.2) during transformation of chronic lymphocytic leukaemia to non‐Hodgkin's lymphoma
In a unique case of chronic lymphocytic leukaemia (CLL) we performed a longitudinal cytogenetic and molecular genetic study of… 
1995
1995
Genetic susceptibility to lung cancer as determined by lymphocytic chromosome analysis.
Highly Cited
1995
Highly Cited
1995
Mouse lymphotoxin-beta receptor. Molecular genetics, ligand binding, and expression.
Lymphotoxin (LT) -alpha beta heterotrimer is a membrane-anchored ligand expressed by activated T cells which binds specifically… 
Highly Cited
1994
Highly Cited
1994
Fluorescence in situ hybridization mapping of translocations and deletions involving the short arm of human chromosome 12 in malignant hematologic diseases.
Translocations and deletions of the short arm of chromosome 12 [t(12p) and del(12p)] are common recurring abnormalities in a… 
1992
1992
Chromosomal localization of an SH2-containing tyrosine phosphatase (PTPN6).
1989
1989
Members of the human glyceraldehyde-3-phosphate dehydrogenase-related gene family map to dispersed chromosomal locations.
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