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17q11.1
A chromosome band present on 17q
National Institutes of Health
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Related topics
Related topics
3 relations
17q
Chromosomes
KSR1 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Delineation of the frequency and boundary of chromosomal copy number variations in paediatric neuroblastoma
Nicholas Ho
,
Hui Peng
,
+5 authors
Tao Liu
Cell cycle
2018
Corpus ID: 37826709
ABSTRACT Neuroblastoma, the most common solid tumour in early childhood, is characterized by very frequent chromosomal copy…
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Highly Cited
2010
Highly Cited
2010
Integration of DNA Copy Number Alterations and Prognostic Gene Expression Signatures in Breast Cancer Patients
H. Horlings
,
Carmen Lai
,
+9 authors
M. J. van de Vijver
Clinical Cancer Research
2010
Corpus ID: 17762158
Purpose: Several prognostic gene expression profiles have been identified in breast cancer. In spite of this progress in…
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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…
Chih-ping Chen
,
Chyi-chyang Lin
,
+8 authors
Wayseen Wang
Taiwanese journal of obstetrics & gynecology
2010
Corpus ID: 206115710
Highly Cited
2009
Highly Cited
2009
Imaging genetics.
K. Muñoz
,
L. Hyde
,
A. Hariri
Journal of the American Academy of Child and…
2009
Corpus ID: 205551922
As research in developmental and clinical sciences has progressed in the last decades, there have been many important…
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2006
2006
Increased WSB1 copy number correlates with its over‐expression which associates with increased survival in neuroblastoma
Qingrong Chen
,
S. Bilke
,
+5 authors
J. Khan
Genes, chromosomes & cancer
2006
Corpus ID: 3099056
Gain of chromosome 17 is the most prevalent genetic abnormality identified in neuroblastoma (NB) and distal 17q gain has…
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Highly Cited
2003
Highly Cited
2003
A deletion mutation in the βA1/A3 crystallin gene (CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese family
Yanhua Qi
,
H. Jia
,
+8 authors
Y. Li
Human Genetics
2003
Corpus ID: 38106334
Congenital cataracts are an important cause of blindness worldwide. In a family of Chinese descent, a dominant congenital nuclear…
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Highly Cited
2000
Highly Cited
2000
A new betaA1-crystallin splice junction mutation in autosomal dominant cataract.
J. Bateman
,
D. Geyer
,
+6 authors
M. Spence
Investigative ophthalmology & visual science
2000
Corpus ID: 20762429
PURPOSE To map the locus for autosomal dominant cataracts (ADCs) in a Brazilian family using candidate gene linkage analyses…
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Highly Cited
1998
Highly Cited
1998
Serotonin Transporter Gene and Risk for Bipolar Affective Disorder: An Association Study in a Spanish Population
B. Gutiérrez
,
M. Arranz
,
+5 authors
L. Fañanás
Biological Psychiatry
1998
Corpus ID: 6452207
1997
1997
Genomic structure and genetic mapping of the human neutral cysteine protease bleomycin hydrolase.
S. E. Montoya
,
R. Ferrell
,
J. Lazo
Cancer research
1997
Corpus ID: 14064883
Bleomycin hydrolase (BH) is the only known eukaryotic enzyme that inactivates the widely used antineoplastic agent bleomycin (BLM…
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Highly Cited
1993
Highly Cited
1993
Antidepressant- and cocaine-sensitive human serotonin transporter: molecular cloning, expression, and chromosomal localization.
S. Ramamoorthy
,
A. Bauman
,
+5 authors
R. Blakely
Proceedings of the National Academy of Sciences…
1993
Corpus ID: 8313261
A Na(+)- and Cl(-)-coupled serotonin (5-hydroxytryptamine, 5HT) transporter is expressed on human neuronal, platelet, placental…
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