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17q11.1

A chromosome band present on 17q
National Institutes of Health

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3 relations
17qChromosomesKSR1 wt Allele

Papers overview

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2018
2018
Delineation of the frequency and boundary of chromosomal copy number variations in paediatric neuroblastoma.
Neuroblastoma, the most common solid tumour in early childhood, is characterized by very frequent chromosomal copy number… Expand
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2010
2010
Integration of DNA Copy Number Alterations and Prognostic Gene Expression Signatures in Breast Cancer Patients
Purpose: Several prognostic gene expression profiles have been identified in breast cancer. In spite of this progress in… Expand
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2010
2010
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving…
OBJECTIVE Prenatal diagnosis of small supernumerary marker chromosomes (sSMC) gives rise to difficulties in genetic counseling… Expand
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2009
2009
Imaging genetics.
As research in developmental and clinical sciences has progressed in the last decades, there have been many important… Expand
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2006
2006
Increased WSB1 copy number correlates with its over-expression which associates with increased survival in neuroblastoma.
Gain of chromosome 17 is the most prevalent genetic abnormality identified in neuroblastoma (NB) and distal 17q gain has… Expand
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2003
2003
A deletion mutation in the βA1/A3 crystallin gene (CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese family
Congenital cataracts are an important cause of blindness worldwide. In a family of Chinese descent, a dominant congenital nuclear… Expand
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Highly Cited
2000
Highly Cited
2000
A new betaA1-crystallin splice junction mutation in autosomal dominant cataract.
PURPOSE To map the locus for autosomal dominant cataracts (ADCs) in a Brazilian family using candidate gene linkage analyses… Expand
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1998
1998
Serotonin Transporter Gene and Risk for Bipolar Affective Disorder: An Association Study in a Spanish Population
BACKGROUND The serotonin transporter (5-HTT) is an important candidate gene for the genetic transmission of manic depressive… Expand
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1997
1997
Genomic structure and genetic mapping of the human neutral cysteine protease bleomycin hydrolase.
Bleomycin hydrolase (BH) is the only known eukaryotic enzyme that inactivates the widely used antineoplastic agent bleomycin (BLM… Expand
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Highly Cited
1993
Highly Cited
1993
Antidepressant- and cocaine-sensitive human serotonin transporter: molecular cloning, expression, and chromosomal localization.
A Na(+)- and Cl(-)-coupled serotonin (5-hydroxytryptamine, 5HT) transporter is expressed on human neuronal, platelet, placental… Expand
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