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9q34.11
Part of the chromosome bands present on the long (q) arm of chromosome 9.
National Institutes of Health
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Related topics
Related topics
5 relations
Chromosomes
PTGES2 wt Allele
SH2D3C wt Allele
SLC27A4 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Multidisciplinary analysis of pediatric T-ALL: 9q34 gene fusions.
P. Papenhausen
,
C. Kelly
,
Zhenxi Zhang
,
J. Tepperberg
,
R. Burnside
,
S. Schwartz
Cancer Genetics
2019
Corpus ID: 73460218
Review
2019
Review
2019
A Rare Case of Acute Myeloid Leukemia With SET-NUP214 Fusion and Massive Hyperdiploidy
In-Hwa Jeong
,
Gyu-Dae An
,
+5 authors
Jin-Yeong Han
Annals of Laboratory Medicine
2019
Corpus ID: 73501565
Dear Editor, The SET-NUP214 fusion gene has been observed most commonly in T-cell ALL (T-ALL) patients, with a frequency of about…
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2014
2014
Genome-Wide Linkage Scan Identifies Two Novel Genetic Loci for Coronary Artery Disease: In GeneQuest Families
Hanxiang Gao
,
Lin Li
,
+9 authors
Q. Wang
PLoS ONE
2014
Corpus ID: 16574948
Coronary artery disease (CAD) is the leading cause of death worldwide. Recent genome-wide association studies (GWAS) identified…
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2014
2014
[A microdeletion of chromosome 9q34.11 may cause suspected cerebral palsy].
Haibo Li
,
Ying Chen
,
+4 authors
Hong Li
Zhonghua yi xue yi chuan xue za zhi = Zhonghua…
2014
Corpus ID: 23770185
OBJECTIVE To identify the genetic cause for a child with mental retardation and dyskinesia. METHODS After the routine genetic…
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2013
2013
Neonatal suppression-burst without epileptic seizures: expanding the electroclinical phenotype of STXBP1-related, early-onset encephalopathy
M. Mastrangelo
,
A. Peron
,
+6 authors
O. Zuffardi
Epileptic disorders
2013
Corpus ID: 28501402
Early-onset epileptic encephalopathies (EOEEs) are characterised by epileptic seizures beginning in the first months of life…
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2012
2012
Monosomy 9pter and trisomy 9q34.11qter in two sisters due to a maternal pericentric inversion.
Farmaditya E. P. Mundhofir
,
D. Smeets
,
+6 authors
B. V. van Bon
Gene
2012
Corpus ID: 23503091
2012
2012
[Hereditary dystonia -- phenotype of DYT1].
F. Yokochi
Rinshō shinkeigaku Clinical neurology
2012
Corpus ID: 2741801
Dystonia is characterized by muscle contractions leading to abnormal postures with involuntary twisting and repetitive movements…
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2006
2006
Overexpression of the novel human gene, nuclear apoptosis-inducing factor 1, induces apoptosis.
Bingfeng Lv
,
T. Shi
,
+5 authors
Ya-xin Lou
International Journal of Biochemistry and Cell…
2006
Corpus ID: 23897799
2005
2005
The locus for ichthyosis prematurity syndrome (IPS) is restricted to 231 kb on chromosome 9q34.11
M. Larsson
,
J. Klar
,
T. Gedde-dahl
,
M. Pigg
,
A. Vahlquist
,
N. Dahl
2005
Corpus ID: 82170382
Positional cloning is a method to identify genes from their position in the genome without prior knowledge about function. We…
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2002
2002
Question 5 Given a fragment of mRNA sequence, how would one find where that piece of DNA mapped in the human genome? Once its position has been determined, how would one find alternatively spliced…
Nature Genetics
2002
Corpus ID: 264676276
For the purpose of this example, the fragment of mRNA of interest is contained within GenBank accession number BG334944. First…
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