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5q31-q32
A chromosome band present on 5q
National Institutes of Health
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Related topics
Related topics
4 relations
Chromosomes
ITK wt Allele
PDGFRB wt Allele
chromosome 5q
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2017
Review
2017
Netherton’s syndrome: a case report
H. Nabi
,
Z. Rani
,
A. Shahzad
2017
Corpus ID: 55156984
Netherton’s syndrome is a rare, autosomal recessive disorder of keratinization characterized by trichorrhexis invaginata…
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2016
2016
IL9 Single Nucleotide Polymorphism and Serum Levels of Interleukin 9 in Children with Asthma
Bahrami MahnehSedigheh
,
MovahediMasoud
,
+4 authors
RezaeiNima
2016
Corpus ID: 74508950
Asthma is an inflammatory disease of the lower airway and the most common chronic disease in childhood. Interleukin 9 (IL-9), as…
Expand
Review
2011
Review
2011
CSF1R (colony stimulating factor 1 receptor, formerly McDonough feline sarcoma viral (v-fms) oncogene homolog)
J. Fischer
,
Stefano Rossetti
,
N. Sacchi
2011
Corpus ID: 13866464
Review on CSF1R (colony stimulating factor 1 receptor, formerly McDonough feline sarcoma viral (v-fms) oncogene homolog), with…
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2008
2008
Genetic association between 5′-upstream single-nucleotide polymorphisms of PDGFRB and schizophrenia in a Korean population
Hak‐Jae Kim
,
Min‐ho Kim
,
+9 authors
J. Chung
Schizophrenia Research
2008
Corpus ID: 31120984
Highly Cited
2002
Highly Cited
2002
A polymorphism in the human UGRP1 gene promoter that regulates transcription is associated with an increased risk of asthma.
T. Niimi
,
M. Munakata
,
+4 authors
S. Kimura
American Journal of Human Genetics
2002
Corpus ID: 42363450
Several traits associated with asthma phenotypes, such as high total serum immunoglobulin E and bronchial hyperresponsiveness…
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Review
2002
Review
2002
Novel autosomal dominant mandibulofacial dysostosis with ptosis: clinical description and exclusion of TCOF1
P. Hedera
,
H. Toriello
,
Elizabeth M. Petty
Journal of Medical Genetics
2002
Corpus ID: 43299536
Background: Treacher Collins syndrome (TCS), the most common type of mandibulofacial dysostosis (MFD), is genetically homogeneous…
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2000
2000
Transcription mapping of the 5q- syndrome critical region: cloning of two novel genes and sequencing, expression, and mapping of a further six novel cDNAs.
J. Boultwood
,
C. Fidler
,
+5 authors
J. Wainscoat
Genomics
2000
Corpus ID: 34922705
The 5q- syndrome is a myelodysplastic syndrome with the 5q deletion ¿del(5q) as the sole karyotypic abnormality. We are using the…
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1997
1997
Chromosome localization and structure of the murine cyclin G1 gene promoter sequence.
M. Jensen
,
V. Factor
,
D. Zimonjic
,
M. Miller
,
C. Keck
,
S. Thorgeirsson
Genomics
1997
Corpus ID: 42678979
Cyclins play an essential role in the control of the cell cycle. In this study the murine cyclin G1 gene expression, structure…
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1991
1991
Genetic changes at the beta-2-adrenergic receptor locus on chromosome 5 in human colorectal carcinomas.
R. Gope
,
M. Gope
,
+6 authors
B. Boman
Anticancer Research
1991
Corpus ID: 30262474
Matched normal/tumor DNA pairs from 44 colorectal carcinoma patients were examined for tumor-specific genetic changes using a…
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1989
1989
The glucocorticoid receptor gene is in 5q31-q32 [corrected].
U. Francke
,
B. Foellmer
Genomics
1989
Corpus ID: 34652672
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