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1p32.3

A chromosome band present on 1p
National Institutes of Health

Related topics

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4 relations
Chromosome 1 Short ArmChromosomesPCSK9 wt AlleleZFYVE9 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Clinical characteristics and prognostic values of 1p32.3 deletion detected through fluorescence in situ hybridization in patients with newly diagnosed multiple myeloma: a single-center study in China
This study aimed to investigate the prevalence, clinical characteristics, and prognostic impact of 1p32.3 deletion in patients… 
Review
2018
Review
2018
A survey of microRNA single nucleotide polymorphisms identifies novel breast cancer susceptibility loci in a case-control, population-based study of African-American women
MicroRNAs (miRNAs) regulate gene expression and influence cancer. Primary transcripts of miRNAs (pri-miRNAs) are poorly annotated… 
Highly Cited
2009
Highly Cited
2009
Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome.
2009
2009
A new method for measurement of total plasma PCSK 9 : clinical applications
The familial hypercholesterolemia (FH) phenotype is characterized by elevated plasma LDL-cholesterol (LDL-C) levels, xanthomas… 
2007
2007
Detailed assessment of copy number alterations revealing homozygous deletions in 1p and 13q in mantle cell lymphoma.
2007
2007
Genomic alterations in sporadic synchronous primary breast cancer using array and metaphase comparative genomic hybridization.
Synchronous primary breast cancer describes the occurrence of multiple tumors affecting one or both breasts at initial diagnosis… 
2003
2003
Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytoma
objective  Despite the very recent discovery that about 25% of apparently sporadic forms of pheochromocytoma are actually due to… 
2003
2003
Isolation and characterization of a novel human thioredoxin-like gene hTLP19 encoding a secretory protein.
2003
2003
Analysis of 148 kb of Genomic DNA of Tetraodon nigroviridis Covering an Amylase Gene Family*
We have sequenced and analysed a 148 kb genomic region of Tetraodon nigroviridis, a teleost fish with a compact genome. Several… 
1998
1998
Identification and characterization of the gene encoding a second proteolipid subunit of human vacuolar H(+)-ATPase (ATP6F).
The proteolipid domain of vacuolar H(+)-ATPase (V-ATPase) plays a major role in H+ transport in microvesicles and other acidic… 
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