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5q31.1

A chromosome band present on 5q
National Institutes of Health

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12 relations
CSF2 wt AlleleChromosomesGDF9 wt AlleleH2AFY wt Allele

Papers overview

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2013
2013
Integrative analysis of copy number alteration and gene expression profiling in ovarian clear cell adenocarcinoma.
Review
2011
Review
2011
CSF1R (colony stimulating factor 1 receptor, formerly McDonough feline sarcoma viral (v-fms) oncogene homolog)
Review on CSF1R (colony stimulating factor 1 receptor, formerly McDonough feline sarcoma viral (v-fms) oncogene homolog), with… 
Highly Cited
2007
Highly Cited
2007
DNA profiling analysis of 100 consecutive de novo acute myeloid leukemia cases reveals patterns of genomic instability that affect all cytogenetic risk groups
We have carried out a high-resolution whole genome DNA profiling analysis on 100 bone marrow samples from a consecutive series of… 
2007
2007
Association between the 5q31.1 gene neurogenin1 and schizophrenia
Multiple lines of evidence suggest that schizophrenia results from aberrant neurodevelopment. The neurogenin1 gene (neurog1… 
Review
2005
Review
2005
Hematologic and cytogenetic (CTG) response to lenalidomide (CC-5013) in patients with transfusion-dependent (TD) myelodysplastic syndrome (MDS) and chromosome 5q31.1 deletion: Results of the…
5 Background: Interstitial deletion of chromosome 5q31 is the most common CTG abnormality in MDS characterized by TD-anemia and… 
2002
2002
A novel locus for autosomal dominant nonsyndromic hearing loss identified at 5q31.1-32 in a Chinese pedigree
AbstractHearing impairment is an extremely heterogeneous disorder. A total of 35 loci and 17 related genes for autosomal dominant… 
2000
2000
Lack of association between the interferon regulatory factor-1 (IRF1) locus at 5q31.1 and multiple sclerosis in Germany, Northern Italy, Sardinia and Sweden
Interferon regulatory factor-1 (IRF-1) is a transcriptional inducer of the interferon-β (IFN-β) gene and other interferon… 
1998
1998
Duplication of two distinct regions on chromosome 5Q in non‐papillary renal‐cell carcinomas
RFLP studies have indicated a duplication of DNA sequences at the chromosome 5q22 region and showed a breakpoint cluster between… 
1997
1997
Smad5, a tumor suppressor candidate at 5q31.1, is hemizygously lost and not mutated in the retained allele in human leukemia cell line HL60
Deletions of the long arm of chromosome 5 with common overlapping segment 5q31.1 are among the most frequent cytogenetic… 
1997
1997
Allelic loss on chromosomes 3p, 5q and 17p in renal cell carcinomas
Lossof‐heterozygosity (LOH) has been studied on 3p (von Hippel‐Lindau gene locus), 5q and 17p (p53 gene locus) by a polymerase… 
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