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5q32

A chromosome band present on 5q
National Institutes of Health

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9 relations
CAMK2A wt AlleleCD74 wt AlleleCDX1 wt AlleleCSNK1A1 wt Allele
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Papers overview

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2005
2005
Cloning, cellular localization, genomic organization, and tissue-specific expression of the TGFbeta1-inducible SMAP-5 gene.
2005
2005
Truncation and fusion of HMGA2 in lipomas with rearrangements of 5q32→q33 and 12q14→q15
Chromosome segment 12q13→q15 recombines with many different chromosome bands in lipomas and at least ten recurrent translocations… 
Highly Cited
2002
Highly Cited
2002
Narrowing and genomic annotation of the commonly deleted region of the 5q- syndrome.
The 5q- syndrome is the most distinct of the myelodysplastic syndromes, and the molecular basis for this disorder remains unknown… 
Highly Cited
2001
Highly Cited
2001
A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility…
Improved molecular understanding of the pathogenesis of type 2 diabetes is essential if current therapeutic and preventative… 
Highly Cited
2001
Highly Cited
2001
The spectrum of pathogenic mutations in SPINK5 in 19 families with Netherton syndrome: implications for mutation detection and first case of prenatal diagnosis.
The Comèl-Netherton syndrome is an autosomal recessive multisystemic disorder characterized by localized or generalized… 
Highly Cited
2000
Highly Cited
2000
Localization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mapping.
Netherton syndrome (NS [MIM 256500]) is a rare and severe autosomal recessive disorder characterized by congenital ichthyosis, a… 
Highly Cited
1998
Highly Cited
1998
Linkage and allelic association of atopy and markers flanking the IL4‐receptor gene
Atopy, a clinical syndrome characterized by heightened IgE responsiveness, is largely determined by genetic factors. The disease… 
Highly Cited
1997
Highly Cited
1997
Identification and Functional Expression of HAH1, a Novel Human Gene Involved in Copper Homeostasis*
To search for a mammalian homologue of ATX1, a human liver cDNA library was screened and a cDNA clone was isolated, which encodes… 
Highly Cited
1990
Highly Cited
1990
Chromosomal organization of adrenergic receptor genes.
The adrenergic receptors (ARs) (subtypes alpha 1, alpha 2, beta 1, and beta 2) are a prototypic family of guanine nucleotide… 
Highly Cited
1985
Highly Cited
1985
The human gene encoding GM-CSF is at 5q21-q32, the chromosome region deleted in the 5q- anomaly.
Human granulocyte-macrophage colony-stimulating factor (GM-CSF) is a 22,000-dalton glycoprotein that stimulates the growth of… 
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