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5q32
A chromosome band present on 5q
National Institutes of Health
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Related topics
Related topics
9 relations
CAMK2A wt Allele
CD74 wt Allele
CDX1 wt Allele
CSNK1A1 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2005
2005
Cloning, cellular localization, genomic organization, and tissue-specific expression of the TGFbeta1-inducible SMAP-5 gene.
Katrin Stolle
,
M. Schnoor
,
+5 authors
S. Lorkowski
Gene
2005
Corpus ID: 11275609
2005
2005
Truncation and fusion of HMGA2 in lipomas with rearrangements of 5q32→q33 and 12q14→q15
M. Nilsson
,
F. Mertens
,
M. Höglund
,
N. Mandahl
,
I. Panagopoulos
Cytogenetic and Genome Research
2005
Corpus ID: 24294314
Chromosome segment 12q13→q15 recombines with many different chromosome bands in lipomas and at least ten recurrent translocations…
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Highly Cited
2002
Highly Cited
2002
Narrowing and genomic annotation of the commonly deleted region of the 5q- syndrome.
J. Boultwood
,
C. Fidler
,
+8 authors
J. Wainscoat
Blood
2002
Corpus ID: 11709936
The 5q- syndrome is the most distinct of the myelodysplastic syndromes, and the molecular basis for this disorder remains unknown…
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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…
S. Wiltshire
,
A. Hattersley
,
+23 authors
M. McCarthy
American journal of human genetics
2001
Corpus ID: 13386889
Improved molecular understanding of the pathogenesis of type 2 diabetes is essential if current therapeutic and preventative…
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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.
E. Sprecher
,
S. Chavanas
,
+17 authors
G. Richard
The Journal of investigative dermatology
2001
Corpus ID: 1836968
The Comèl-Netherton syndrome is an autosomal recessive multisystemic disorder characterized by localized or generalized…
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Highly Cited
2000
Highly Cited
2000
Localization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mapping.
S. Chavanas
,
C. Garner
,
+15 authors
A. Hovnanian
American journal of human genetics
2000
Corpus ID: 27850128
Netherton syndrome (NS [MIM 256500]) is a rare and severe autosomal recessive disorder characterized by congenital ichthyosis, a…
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Highly Cited
1998
Highly Cited
1998
Linkage and allelic association of atopy and markers flanking the IL4‐receptor gene
K. Deichmann
,
A. Heinzmann
,
+6 authors
J. Kuehr
Clinical and experimental allergy : journal of…
1998
Corpus ID: 31612545
Atopy, a clinical syndrome characterized by heightened IgE responsiveness, is largely determined by genetic factors. The disease…
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Highly Cited
1997
Highly Cited
1997
Identification and Functional Expression of HAH1, a Novel Human Gene Involved in Copper Homeostasis*
L. Klomp
,
Su-Ju Lin
,
Daniel S.Yuan
,
R. Klausner
,
V. Culotta
,
J. Gitlin
The Journal of Biological Chemistry
1997
Corpus ID: 7033581
To search for a mammalian homologue of ATX1, a human liver cDNA library was screened and a cDNA clone was isolated, which encodes…
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Highly Cited
1990
Highly Cited
1990
Chromosomal organization of adrenergic receptor genes.
T. Yang-Feng
,
F. Y. Xue
,
+5 authors
U. Francke
Proceedings of the National Academy of Sciences…
1990
Corpus ID: 9943719
The adrenergic receptors (ARs) (subtypes alpha 1, alpha 2, beta 1, and beta 2) are a prototypic family of guanine nucleotide…
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Highly Cited
1985
Highly Cited
1985
The human gene encoding GM-CSF is at 5q21-q32, the chromosome region deleted in the 5q- anomaly.
K. Huebner
,
M. Isobe
,
C. Croce
,
D. Golde
,
S. Kaufman
,
J. Gasson
Science
1985
Corpus ID: 22032772
Human granulocyte-macrophage colony-stimulating factor (GM-CSF) is a 22,000-dalton glycoprotein that stimulates the growth of…
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