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17q11.1
A chromosome band present on 17q
National Institutes of Health
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Related topics
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3 relations
17q
Chromosomes
KSR1 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
ERα-related chromothripsis enhances concordant gene transcription on chromosome 17q11.1-q24.1 in luminal breast cancer
Chun-Lin Lin
,
Xi Tan
,
+13 authors
T. Huang
BMC Medical Genomics
2020
Corpus ID: 255852782
Chromothripsis is an event of genomic instability leading to complex chromosomal alterations in cancer. Frequent long-range…
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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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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
2008
2008
Association study of serotonin transporter gene polymorphisms with obstructive sleep apnea syndrome in Chinese Han population.
W. Yue
,
Hui-guo Liu
,
+5 authors
W. Hao
Sleep
2008
Corpus ID: 7766526
BACKGROUND Since the serotonin (5-HT) is associated with circadian rhythm and breathing regulation, the serotonin transporter (5…
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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 and 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
,
J. Bateman
,
+7 authors
M. Spence
Investigative Ophthalmology and 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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