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1p31

A chromosome band present on 1p
National Institutes of Health

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9 relations
Chromosome 1 Short ArmChromosomesDIRAS3 wt AlleleDNAJB4 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
The nuclear factor I/A (NFIA) gene is associated with the asthma plus rhinitis phenotype.
Review
2011
Review
2011
Molecular characterization of an interstitial deletion of 1p31.3 in a patient with obesity and psychiatric illness and a review of the literature
We report on the clinical and array‐based characterization of an interstitial 1p31.3 deletion in a 15‐year‐old male patient with… 
Review
2002
Review
2002
Cytogenetic Analysis in Mantle Cell Lymphoma: A Review of 214 Cases
Cytogenetic (CG) analysis was performed in 78 consecutive cases of mantle cell lymphoma (MCL) at the British Columbia Cancer… 
2000
2000
Molecular and cytogenetic analysis of glioblastoma multiforme.
Highly Cited
2000
Highly Cited
2000
ARHI is the center of allelic deletion on chromosome 1p31 in ovarian and breast cancers
In our previous work, we had characterized ARHI as an imprinted putative tumor‐suppressor gene in ovarian and breast cancers… 
2000
2000
Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31.
BACKGROUND Recently a locus for antenatal Bartter syndrome associated with sensorineural deafness was mapped to human chromosome… 
1999
1999
TTC4, a novel human gene containing the tetratricopeptide repeat and mapping to the region of chromosome 1p31 that is frequently deleted in sporadic breast cancer.
The 1p31 region shows loss of heterozygosity in up to 50% of human breast cancers, indicating the presence of a tumor suppressor… 
1990
1990
The locus for the medium-chain acyl-CoA dehydrogenase gene on chromosome 1 is highly polymorphic.
1987
1987
Ribonucleotide reductase M2 subunit sequences mapped to four different chromosomal sites in humans and mice: functional locus identified by its amplification in hydroxyurea-resistant cell lines.
1984
1984
Constitutive fragile sites 1p31, 3p14, 6q26, and 16q23 and their use as controls for false-negative results with the fragile(X).
Fragile(X) estimations in fragile(X)-mental retardation hemizygotes or heterozygotes can become falsely negative in stored blood… 
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